Usages in wwPDB of concept: c_0654
nUsages: 740; SSE string: EEEEE
2o8t:A    (PHE30) to    (GLU84)  CRYSTAL STRUCTURE AND BINDING EPITOPES OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR (C122A/N145Q) IN COMPLEX WITH INHIBITORS  |   UROKINASE-TYPE PLASMINOGEN ACTIVATOR, BENZAMIDINE, PHENYLGUANIDINE, CONTACT AREA, HYDROLASE 
1n8s:A   (HIS354) to   (ALA417)  STRUCTURE OF THE PANCREATIC LIPASE-COLIPASE COMPLEX  |   HYDROLASE, PANCREAS, SIGNAL 
1a3b:H    (GLN30) to    (MET84)  COMPLEX OF HUMAN ALPHA-THROMBIN WITH THE BIFUNCTIONAL BORONATE INHIBITOR BOROLOG1  |   COMPLEX (SERINE PROTEASE-INHIBITOR), HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1a3e:H    (GLN30) to    (MET84)  COMPLEX OF HUMAN ALPHA-THROMBIN WITH THE BIFUNCTIONAL BORONATE INHIBITOR BOROLOG2  |   COMPLEX (SERINE PROTEASE-INHIBITOR), HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1a46:H    (GLN30) to    (MET84)  THROMBIN COMPLEXED WITH HIRUGEN AND A BETA-STRAND MIMETIC INHIBITOR  |   COMPLEX (SERINE PROTEASE-INHIBITOR), HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1a5g:H    (GLN30) to    (MET84)  HUMAN THROMBIN COMPLEXED WITH NOVEL SYNTHETIC PEPTIDE MIMETIC INHIBITOR AND HIRUGEN  |   COMPLEX (SERINE PROTEASE-INHIBITOR),HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1a5h:B    (TRP29) to    (GLU84)  CATALYTIC DOMAIN OF HUMAN TWO-CHAIN TISSUE PLASMINOGEN ACTIVATOR COMPLEX OF A BIS-BENZAMIDINE  |   TRYPSIN LIKE SERINE PROTEASE, FIBRINOLYTIC ENZYME, HYDROLASE 
1nc6:A    (GLN30) to    (SER84)  POTENT, SMALL MOLECULE INHIBITORS OF HUMAN MAST CELL TRYPTASE. ANTI-ASTHMATIC ACTION OF A DIPEPTIDE-BASED TRANSITION STATE ANALOGUE CONTAINING BENZOTHIAZOLE KETONE  |   PROTEIN-INHIBITOR COMPLEX, HYDROLASE 
3eaj:A    (VAL18) to    (ILE78)  CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE QUADRUPLE MUTANT STIF/A WITH TWO MOLECULES IN ONE ASYMMETRIC UNIT  |   SARS CORONAVIRUS MAIN PROTEASE MUTANT EXTRA HELICAL DOMAIN, CYTOPLASM, HYDROLASE, MEMBRANE, METAL-BINDING, PROTEASE, RIBOSOMAL FRAMESHIFTING, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC, ZINC-FINGER 
1a7s:A    (LEU15) to    (SER72)  ATOMIC RESOLUTION STRUCTURE OF HBP  |   SERINE PROTEASE HOMOLOG, ENDOTOXIN BINDING, HEPARIN 
1a8i:A   (LEU198) to   (THR240)  SPIROHYDANTOIN INHIBITOR OF GLYCOGEN PHOSPHORYLASE  |   GLYCOGEN PHOSPHORYLASE, GLUCOPYRANOSE SPIROHYDANTOIN, WATER STRUCTURE, INHIBITOR BINDING, ANTI-HYPERGLYCEMIC AGENT 
2ank:H    (GLN30) to    (MET84)  ORALLY ACTIVE THROMBIN INHIBITORS IN COMPLEX WITH THROMBIN AND AN EXOSITE DECAPEPTIDE  |   BLOOD CLOTTING, HYDROLASE, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3rp2:B    (MET30) to    (LYS84)  THE STRUCTURE OF RAT MAST CELL PROTEASE II AT 1.9-ANGSTROMS RESOLUTION  |   SERINE PROTEINASE 
1ab9:B    (GLN30) to    (LYS84)  CRYSTAL STRUCTURE OF BOVINE GAMMA-CHYMOTRYPSIN  |   HYDROLASE, SERINE PROTEASE, DIGESTION, PANCREAS, ZYMOGEN, COMPLEX (SERINE PROTEASE/PEPTIDE) 
2ok5:A   (TRP470) to   (HIS531)  HUMAN COMPLEMENT FACTOR B  |   PRO-ENZYME, SERINE PROTEASE DOMAIN,VON WILLEBRAND FACTOR-A DOMAIN, CCP DOMAIN, HYDROLASE 
1acb:E    (GLN30) to    (LYS84)  CRYSTAL AND MOLECULAR STRUCTURE OF THE BOVINE ALPHA-CHYMOTRYPSIN-EGLIN C COMPLEX AT 2.0 ANGSTROMS RESOLUTION  |   SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2auk:E    (SER18) to    (LYS57)  STRUCTURE OF E. COLI RNA POLYMERASE BETA' G/G' INSERT  |   SANDWICH-BARREL HYBRID MOTIF, TRANSFERASE 
3ee7:A    (CYS14) to    (GLU68)  CRYSTAL STRUCTURE OF SARS-COV NSP9 G104E  |   GXXXG, DIMERIZATION, SARS-COV, HELIX-HELIX, HYDROLASE, MEMBRANE, METAL-BINDING, PROTEASE, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC-FINGER, VIRAL PROTEIN 
3ee7:D    (CYS14) to    (GLU68)  CRYSTAL STRUCTURE OF SARS-COV NSP9 G104E  |   GXXXG, DIMERIZATION, SARS-COV, HELIX-HELIX, HYDROLASE, MEMBRANE, METAL-BINDING, PROTEASE, RNA-BINDING, THIOL PROTEASE, TRANSMEMBRANE, ZINC-FINGER, VIRAL PROTEIN 
1afe:H    (GLN30) to    (MET84)  HUMAN ALPHA-THROMBIN INHIBITION BY CBZ-PRO-AZALYS-ONP  |   COMPLEX (SERINE PROTEASE-INHIBITOR), BLOOD COAGULATION, N- CARBOBENZOXY-PRO-ALFA-AZALYS-P-NITROPHENYLESTER, SERINE PROTEINASE INHIBITION, GLYCOSYLATED PROTEIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1afq:B    (GLN30) to    (LYS84)  CRYSTAL STRUCTURE OF BOVINE GAMMA-CHYMOTRYPSIN COMPLEXED WITH A SYNTHETIC INHIBITOR  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1aht:H    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH HIRUGEN AND P-AMIDINOPHENYLPYRUVATE AT 1.6 ANGSTROMS RESOLUTION  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1nm6:A    (GLN30) to    (MET84)  THROMBIN IN COMPLEX WITH SELECTIVE MACROCYCLIC INHIBITOR AT 1.8A  |   THROMBIN INHIBITOR COMPLEX, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX 
1aks:A    (GLN30) to    (ASN84)  CRYSTAL STRUCTURE OF THE FIRST ACTIVE AUTOLYSATE FORM OF THE PORCINE ALPHA TRYPSIN  |   HYDROLASE, SERINE PROTEASE 
1amh:B    (GLN30) to    (ASN84)  UNCOMPLEXED RAT TRYPSIN MUTANT WITH ASP 189 REPLACED WITH SER (D189S)  |   SERINE PROTEASE, ACTIVATION DOMAIN, SUBSTRATE SPECIFICITY HYDROLASE 
1ao5:A    (GLN30) to    (LYS87)  MOUSE GLANDULAR KALLIKREIN-13 (PRORENIN CONVERTING ENZYME)  |   GLANDULAR KALLIKREIN, SERINE PROTEASE, PROTEIN MATURATION 
1ao5:B    (GLN30) to    (LEU84)  MOUSE GLANDULAR KALLIKREIN-13 (PRORENIN CONVERTING ENZYME)  |   GLANDULAR KALLIKREIN, SERINE PROTEASE, PROTEIN MATURATION 
2oqu:A    (GLN15) to    (GLY73)  HIGH PRESSURE CRYOCOOLING OF CAPILLARY SAMPLE CRYOPROTECTION AND DIFFRACTION PHASING AT LONG WAVELENGTHS  |   HIGH PRESSURE CRYOCOOLING, XENON, SAD PHASING, HYDROLASE 
4h4f:A    (GLN30) to    (VAL85)  CRYSTAL STRUCTURE OF HUMAN CHYMOTRYPSIN C (CTRC) BOUND TO INHIBITOR EGLIN C FROM HIRUDO MEDICINALIS  |   SERINE PROTEASE, PROTEASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1nrn:H    (GLN30) to    (MET84)  CRYSTALLOGRAPHIC STRUCTURES OF THROMBIN COMPLEXED WITH THROMBIN RECEPTOR PEPTIDES: EXISTENCE OF EXPECTED AND NOVEL BINDING MODES  |   SERINE PROTEINASE/RECEPTOR 
1nrq:H    (GLN30) to    (MET84)  CRYSTALLOGRAPHIC STRUCTURES OF THROMBIN COMPLEXED WITH THROMBIN RECEPTOR PEPTIDES: EXISTENCE OF EXPECTED AND NOVEL BINDING MODES  |   SERINE PROTEINASE, RECEPTOR, HYDROLASE/HYDROLASE RECEPTOR COMPLEX 
1nrr:H    (GLN30) to    (MET84)  CRYSTALLOGRAPHIC STRUCTURES OF THROMBIN COMPLEXED WITH THROMBIN RECEPTOR PEPTIDES: EXISTENCE OF EXPECTED AND NOVEL BINDING MODES  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD CLOTTING 
3s0n:A    (TYR14) to    (GLU71)  CRYSTAL STRUCTURE OF HUMAN CHYMASE WITH BENZIMIDAZOLONE INHIBITOR  |   SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1nt1:A    (GLN30) to    (MET84)  THROMBIN IN COMPLEX WITH SELECTIVE MACROCYCLIC INHIBITOR  |   THROMBIN INHIBITOR COMPLEX, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX 
3ela:H   (GLN167) to   (ARG224)  CRYSTAL STRUCTURE OF ACTIVE SITE INHIBITED COAGULATION FACTOR VIIA MUTANT IN COMPLEX WITH SOLUBLE TISSUE FACTOR  |   SERINE PROTEASE, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2b5t:B    (GLN30) to    (MET84)  2.1 ANGSTROM STRUCTURE OF A NONPRODUCTIVE COMPLEX BETWEEN ANTITHROMBIN, SYNTHETIC HEPARIN MIMETIC SR123781 AND TWO S195A THROMBIN MOLECULES  |   BLOOD COAGULATION, BLOOD CLOTTING 
3ens:D    (GLN30) to    (GLU84)  CRYSTAL STRUCTURE OF HUMAN FXA IN COMPLEX WITH METHYL (2Z)-3-[(3- CHLORO-1H-INDOL-7-YL)AMINO]-2-CYANO-3-{[(3S)-2-OXO-1-(2-OXO-2- PYRROLIDIN-1-YLETHYL)AZEPAN-3-YL]AMINO}ACRYLATE  |   SERINE PROTEASE, HYDROLASE, EPIDERMAL GROWTH FACTOR LIKE DOMAIN, BLOOD COAGULATION FACTOR, CLEAVAGE ON PAIR OF BASIC RESIDUES, EGF- LIKE DOMAIN, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROXYLATION, ZYMOGEN, BLOOD CLOTTING 
1awf:H    (GLN30) to    (MET84)  NOVEL COVALENT THROMBIN INHIBITOR FROM PLANT EXTRACT  |   PROTEINASE, BLOOD COAGULATION, TRYPSIN LIKE PROTEINASE, COMPLEX (PROTEASE-INHIBITOR), HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1ay6:H    (GLN30) to    (MET84)  THROMBIN INHIBITOR FROM THEONALLA, CYCLOTHEANAMIDE-BASED MACROCYCLIC TRIPEPTIDE MOTIF  |   COMPLEX OF SERINE PROTEASE-INHIBITOR, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1azz:A    (HIS29) to    (THR86)  FIDDLER CRAB COLLAGENASE COMPLEXED TO ECOTIN  |   COMPLEX (SERINE PROTEASE/INHIBITOR), SERINE PROTEASE, INHIBITOR, COMPLEX, PROTEASE-SUBSTRATE INTERACTIONS, COLLAGEN 
1b0f:A    (MET30) to    (ALA84)  CRYSTAL STRUCTURE OF HUMAN NEUTROPHIL ELASTASE WITH MDL 101, 146  |   SERINE PROTEASE, FLUOROETHYL KETONES, HYDROLASE 
1nzq:H    (GLN30) to    (MET84)  D-PHE-PRO-ARG-TYPE THROMBIN INHIBITOR  |   THROMBIN, THROMBIN INHIBITOR, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2p3f:H    (GLN30) to    (GLU84)  CRYSTAL STRUCTURE OF THE FACTOR XA/NAP5 COMPLEX  |   FACTOR XA, NEMATODE ANTICOAGULANT PROTEIN, HYDROLASE 
4wwy:B    (GLN30) to    (ASN84)  HUMAN CATIONIC TRYPSIN G193R MUTANT IN COMPLEX WITH BOVINE PANCREATIC TRYPSIN INHIBITOR  |   TRYPSIN INHIBITORS, COMPLEX, BPTI, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4wxk:A    (LEU79) to   (GLY125)  CRYSTAL STRUCTURE OF A PEPTIDE DEFORMYLASE FROM HAEMOPHILUS INFLUENZAE  |   PEPTIDE DEFORMYLASE, HYDROLASE 
4wxk:B    (ASN75) to   (ALA123)  CRYSTAL STRUCTURE OF A PEPTIDE DEFORMYLASE FROM HAEMOPHILUS INFLUENZAE  |   PEPTIDE DEFORMYLASE, HYDROLASE 
4wxk:C    (LEU79) to   (GLY125)  CRYSTAL STRUCTURE OF A PEPTIDE DEFORMYLASE FROM HAEMOPHILUS INFLUENZAE  |   PEPTIDE DEFORMYLASE, HYDROLASE 
4wxl:A    (LEU79) to   (GLY125)  CRYSTAL STRUCTURE OF A PEPTIDE DEFORMYLASE FROM HAEMOPHILUS INFLUENZAE COMPLEX WITH ACTINONIN  |   PEPTIDE DEFORMYLASE, HYDROLASE 
4wxl:B    (ASN75) to   (GLY125)  CRYSTAL STRUCTURE OF A PEPTIDE DEFORMYLASE FROM HAEMOPHILUS INFLUENZAE COMPLEX WITH ACTINONIN  |   PEPTIDE DEFORMYLASE, HYDROLASE 
4wxl:D    (LEU79) to   (GLY125)  CRYSTAL STRUCTURE OF A PEPTIDE DEFORMYLASE FROM HAEMOPHILUS INFLUENZAE COMPLEX WITH ACTINONIN  |   PEPTIDE DEFORMYLASE, HYDROLASE 
1b5g:H    (GLN30) to    (MET84)  HUMAN THROMBIN COMPLEXED WITH NOVEL SYNTHETIC PEPTIDE MIMETIC INHIBITOR AND HIRUGEN  |   SERINE PROTEASE-INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2p8o:B    (GLN30) to    (LYS84)  CRYSTAL STRUCTURE OF A BENZOHYDROXAMIC ACID/VANADATE COMPLEX BOUND TO CHYMOTRYPSIN A  |   PROTEIN-INHIBITOR COMPLEX, HYDROLASE 
1ba8:B    (GLN30) to    (MET84)  THROMBIN INHIBITOR WITH A RIGID TRIPEPTIDYL ALDEHYDES  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1bb0:B    (GLN30) to    (MET84)  THROMBIN INHIBITORS WITH RIGID TRIPEPTIDYL ALDEHYDES  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3f1s:B   (GLN151) to   (LYS203)  CRYSTAL STRUCTURE OF PROTEIN Z COMPLEXED WITH PROTEIN Z-DEPENDENT INHIBITOR  |   PZ, ZPI, COMPLEX, SERPIN, PROTEASE INHIBITOR, PROTEASE, GLYCOPROTEIN, SECRETED, SERINE PROTEASE INHIBITOR, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, EGF-LIKE DOMAIN, GAMMA-CARBOXYGLUTAMIC ACID, HYDROXYLATION, SERINE PROTEASE HOMOLOG, HYDROLASE INHIBITOR- HYDROLASE COMPLEX 
1o2g:H    (GLN30) to    (MET84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, BLOOD CLOTTING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD CLOTTING, HYDROLASE-INHIBITOR COMPLEX 
1o2i:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2j:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2k:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2l:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2m:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2n:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2q:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2s:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2u:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2v:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2w:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2y:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o30:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o31:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o33:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o34:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o35:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o37:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3a:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3c:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3d:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3f:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3e:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3g:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3i:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3j:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3k:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3l:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3m:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3n:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o59:A   (GLN275) to   (GLY342)  CRYSTAL STRUCTURE OF ALLANTOICASE (YIR029W) FROM SACCHAROMYCES CEREVISIAE AT 2.40 A RESOLUTION  |   YIR029W, ALLANTOICASE, STRUCTURAL GENOMICS, JCSG, PSI, PROTEIN STRUCTURE INITIATIVE, JOINT CENTER FOR STRUCTURAL GENOMICS, HYDROLASE 
1bma:A    (GLN30) to    (GLY88)  BENZYL METHYL AMINIMIDE INHIBITOR COMPLEXED TO PORCINE PANCREATIC ELASTASE  |   SERINE PROTEASE,METAL-BINDING, PROTEASE, SECRETED, ZYMOGEN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3s69:A    (LEU30) to    (ASN82)  CRYSTAL STRUCTURE OF SAXTHROMBIN  |   BETA-BARREL, SERINE ENZYMES, FIBRINOGEN BINDING, GLYCOSYLATION, HYDROLASE 
4x6n:A    (GLN30) to    (HIS91)  FACTOR XIA IN COMPLEX WITH THE INHIBITOR 1-{(1S)-1-[4-(3-AMINO-1H- INDAZOL-6-YL)-5-CHLORO-1H-IMIDAZOL-2-YL]-2-PHENYLETHYL}-3-[5-CHLORO- 2-(1H-TETRAZOL-1-YL)BENZYL]UREA  |   SERINE PROTEASE, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2brw:A   (SER704) to   (PHE746)  CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE HYALURONATE LYASE FROM 30PERCENT PEGMME.  |   (ALFA5/ALFA5) BARREL, CELL WALL, LYASE, PEPTIDOGLYCAN-ANCHOR 
2brw:B   (SER704) to   (PHE746)  CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE HYALURONATE LYASE FROM 30PERCENT PEGMME.  |   (ALFA5/ALFA5) BARREL, CELL WALL, LYASE, PEPTIDOGLYCAN-ANCHOR 
1bsz:B   (GLU579) to   (GLY624)  PEPTIDE DEFORMYLASE AS FE2+ CONTAINING FORM (NATIVE) IN COMPLEX WITH INHIBITOR POLYETHYLENE GLYCOL  |   COMPLEX(ENZYME-INHIBITOR), HYDROLASE, IRON METALLOPROTEASE, PROTEIN SYNTHESIS 
1bth:H    (GLN30) to    (MET84)  STRUCTURE OF THROMBIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR  |   THROMBIN INHIBITOR, SERINE PROTEINASE KUNITZ-LIKE INHIBITOR, (SERINE PROTEASE/INHIBITOR), COMPLEX (SERINE PROTEASE/INHIBITOR) COMPLEX 
1bth:K    (GLN30) to    (MET84)  STRUCTURE OF THROMBIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR  |   THROMBIN INHIBITOR, SERINE PROTEINASE KUNITZ-LIKE INHIBITOR, (SERINE PROTEASE/INHIBITOR), COMPLEX (SERINE PROTEASE/INHIBITOR) COMPLEX 
1btx:A    (GLN30) to    (SER84)  EPISELECTION: NOVEL KI ~NANOMOLAR INHIBITORS OF SERINE PROTEASES SELECTED BY BINDING OR CHEMISTRY ON AN ENZYME SURFACE  |   TRIPEPTIDEBORONATE ETHYL ESTER INHIBITED, SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1bty:A    (GLN30) to    (SER84)  CRYSTAL STRUCTURE OF BETA-TRYPSIN IN COMPLEX WITH BENZAMIDINE  |   BENZAMIDINE INHIBITED, HYDROLASE (SERINE PROTEINASE), HYDROLASE 
1bu8:A   (TYR354) to   (ALA417)  RAT PANCREATIC LIPASE RELATED PROTEIN 2  |   HYDROLASE, LIPID DEGRADATION, PANCREATIC LIPASE 
1bwu:Q    (GLY52) to   (SER100)  MANNOSE-SPECIFIC AGGLUTININ (LECTIN) FROM GARLIC (ALLIUM SATIVUM) BULBS COMPLEXED WITH ALPHA-D-MANNOSE  |   BULB LECTIN, MANNOSE, PLANT PROTEIN 
1bx3:A   (LEU198) to   (THR240)  EFFECTS OF COMMONLY USED CRYOPROTECTANTS ON GLYCOGEN PHOSPHORYLASE ACTIVITY AND STRUCTURE  |   PHOSPHORYLASE, INHIBITOR, CRYOPROTECTANT, MPD, DMSO, CRYOCRYSTALLOGRAPHY, TRANSFERASE 
4hsi:D   (GLY205) to   (HIS248)  GLYCOPROTEIN B FROM HERPES SIMPLEX VIRUS TYPE 1, A504P/R505G/Q507G/N511G MUTANT, LOW-PH  |   VIRAL FUSION PROTEIN, VIRAL ENVELOPE, VIRAL PROTEIN 
1c1n:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c1o:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c1q:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c1r:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c1s:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c1u:H    (GLN30) to    (MET84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX 
1c1v:H    (GLN30) to    (MET84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c1w:H    (GLN30) to    (MET84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, BLOOD CLOTTING,HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1c2e:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c2f:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c2g:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1c2h:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c2i:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c2j:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c2k:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c2l:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c2m:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4xcr:B    (GLY41) to   (GLN110)  MONOMERIC HUMAN CU,ZN SUPEROXIDE DISMUTASE, LOOPS IV AND VII DELETED, APO FORM, MUTANT I35A  |   OXIDOREDUCTASE 
2pks:B    (GLN51) to   (MET116)  THROMBIN IN COMPLEX WITH INHIBITOR  |   INHIBITOR COMPLEX, THROMBIN INHIBITOR, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2bxu:H    (GLN30) to    (MET84)  DESIGN AND DISCOVERY OF NOVEL, POTENT THROMBIN INHIBITORS WITH A SOLUBILIZING CATIONIC P1-P2-LINKER  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4xde:A   (TYR367) to   (ALA424)  COAGULATION FACTOR XII PROTEASE DOMAIN CRYSTAL STRUCTURE  |   FACTOR XII, CATALYTIC DOMAIN, ZYMOGENS, HYDROLASE, BLOOD CLOTTING 
3se4:A    (SER35) to    (VAL90)  HUMAN IFNW-IFNAR TERNARY COMPLEX  |   TYPE I INTERFERON SIGNALING COMPLEX, EXTRACELLULAR SPACE, IMMUNE SYSTEM RECEPTOR 
4hzh:B   (GLN335) to   (MET400)  STRUCTURE OF RECOMBINANT GLA-DOMAINLESS PROTHROMBIN MUTANT S525A  |   PROTHROMBIN, KRINGLE, SERINE PROTEASE, COAGULATION, HYDROLASE 
1c4v:2    (GLN30) to    (MET84)  SELECTIVE NON ELECTROPHILIC THROMBIN INHIBITORS WITH CYCLOHEXYL MOIETIES.  |   COMPLEX (SERINE PROTEASE-INHIBITOR), HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3sep:C   (LEU651) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (S796A)  |   DYNAMIC LOOP CONFORMATION, SER-796, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN, BETA SUPERSANDWICH, BETA- GALACTOSIDASE, GLYCOSIDASE, HYDROLASE 
1c5l:H    (GLN30) to    (MET84)  STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB- MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR  |   SELECTIVE, S1 SITE INHIBITOR, STRUCTURE-BASED DRUG DESIGN, UROKINASE, TRYPSIN, THROMBIN, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX 
1c5o:H    (GLN30) to    (MET84)  STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB- MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR  |   SELECTIVE, S1 SITE INHIBITOR, STRUCTURE-BASED DRUG DESIGN, UROKINASE, TRYPSIN, THROMBIN, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX 
1c5q:A    (GLN30) to    (SER84)  STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1- BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR  |   SELECTIVE, S1 SITE INHIBITOR, STRUCTURE-BASED DRUG DESIGN, UROKINASE, TRYPSIN, THROMBIN, HYDROLASE 
1c5s:A    (GLN30) to    (SER84)  STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1- BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR  |   SELECTIVE, S1 SITE INHIBITOR, STRUCTURE-BASED DRUG DESIGN, UROKINASE, TRYPSIN, THROMBIN, HYDROLASE 
1c5t:A    (GLN30) to    (SER84)  STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1- BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR  |   SELECTIVE, S1 SITE INHIBITOR, STRUCTURE-BASED DRUG DESIGN, UROKINASE, TRYPSIN, THROMBIN, HYDROLASE 
1c5v:A    (GLN30) to    (SER84)  STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1- BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR  |   SELECTIVE, S1 SITE INHIBITOR, STRUCTURE-BASED DRUG DESIGN, UROKINASE, TRYPSIN, THROMBIN, HYDROLASE 
1c9t:B    (GLN30) to    (ILE83)  COMPLEX OF BDELLASTASIN WITH BOVINE TRYPSIN  |   COMPLEX (HYDROLASE/INHIBITOR), HYDROLASE, INHIBITOR, ANTISTASIN, PLASMIN, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1c9t:C    (GLN30) to    (ILE83)  COMPLEX OF BDELLASTASIN WITH BOVINE TRYPSIN  |   COMPLEX (HYDROLASE/INHIBITOR), HYDROLASE, INHIBITOR, ANTISTASIN, PLASMIN, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1c9t:E    (GLN30) to    (ILE83)  COMPLEX OF BDELLASTASIN WITH BOVINE TRYPSIN  |   COMPLEX (HYDROLASE/INHIBITOR), HYDROLASE, INHIBITOR, ANTISTASIN, PLASMIN, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1ca8:B    (GLN30) to    (MET84)  THROMBIN INHIBITORS WITH RIGID TRIPEPTIDYL ALDEHYDES  |   SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2ppl:A   (GLN372) to   (ALA434)  HUMAN PANCREATIC LIPASE-RELATED PROTEIN 1  |   HYDROLASE, LIPID DEGRADATION, PANCREATIC LIPASE, STRUCTURAL GENOMICS CONSORTIUM, SGC 
2pv9:B    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF MURINE THROMBIN IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF MURINE PAR4  |   SERINE PROTEASE, HYDROLASE 
2pvs:A   (TYR355) to   (ALA417)  STRUCTURE OF HUMAN PANCREATIC LIPASE RELATED PROTEIN 2 MUTANT N336Q  |   LIPASE, GALACTO LIPIDS HYDROLYSIS, HYDROLASE 
1op2:A    (LEU30) to    (ASN84)  CRYSTAL STRUCTURE OF AAV-SP-II, A GLYCOSYLATED SNAKE VENOM SERINE PROTEINASE FROM AGKISTRODON ACUTUS  |   SNAKE VENOM, SERINE PROTEINASE, GLYCOPROTEIN, AGKISTRODON ACUTUS, HYDROLASE 
1cho:F    (GLN30) to    (LYS84)  CRYSTAL AND MOLECULAR STRUCTURES OF THE COMPLEX OF ALPHA- *CHYMOTRYPSIN WITH ITS INHIBITOR TURKEY OVOMUCOID THIRD DOMAIN AT 1.8 ANGSTROMS RESOLUTION  |   COMPLEX(SERINE PROTEINASE-INHIBITOR) 
1op8:B    (TYR29) to    (MET83)  CRYSTAL STRUCTURE OF HUMAN GRANZYME A  |   GRANZYME A, SERINE PROTEINASE, APOPTOSIS, HYDROLASE 
2pyd:A   (LEU198) to   (THR240)  THE CRYSTAL STRUCTURE OF GLYCOGEN PHOSPHORYLASE IN COMPLEX WITH GLUCOSE AT 100 K  |   GLYCOGENOLYSIS, INHIBITION, TYPE 2 DIABETES, TRANSFERASE 
2pyi:A   (LEU198) to   (THR240)  CRYSTAL STRUCTURE OF GLYCOGEN PHOSPHORYLASE IN COMPLEX WITH GLUCOSYL TRIAZOLEACETAMIDE  |   GLYCOGENOLYSIS, INHIBITION, TYPE 2 DIABETES, TRANSFERASE 
3fp9:F    (PRO98) to   (THR154)  CRYSTAL STRUCTURE OF INTERN DOMAIN OF PROTEASOME-ASSOCIATED ATPASE, MYCOBACTERIUM TUBERCULOSIS  |   FIVE STRAND BETA BARREL, HEXAMER, ATP-BINDING, NUCLEOTIDE- BINDING, HYDROLASE, AAA ATPASE, PROTEASOMAL ATPASE 
3fp9:I    (PRO98) to   (THR154)  CRYSTAL STRUCTURE OF INTERN DOMAIN OF PROTEASOME-ASSOCIATED ATPASE, MYCOBACTERIUM TUBERCULOSIS  |   FIVE STRAND BETA BARREL, HEXAMER, ATP-BINDING, NUCLEOTIDE- BINDING, HYDROLASE, AAA ATPASE, PROTEASOMAL ATPASE 
3so3:A    (GLN30) to    (ARG84)  STRUCTURES OF FAB-PROTEASE COMPLEXES REVEAL A HIGHLY SPECIFIC NON- CANONICAL MECHANISM OF INHIBITION.  |   ANTIBODY-PROTEIN, PROTEIN-PROTEIN, PROTEASE INHIBITOR, DISEASE MUTATION, GLYCOPROTEIN, HYDROLASE, MEMBRANE, SERINE PROTEASE, SIGNAL-ANCHOR, TRANSMEMBRANE 
1oss:A    (PHE29) to    (ARG84)  T190P STREPTOMYCES GRISEUS TRYPSIN IN COMPLEX WITH BENZAMIDINE  |   TRYPSIN, SERINE PROTEASE, MUTANT, HYDROLASE 
4ic5:C   (VAL103) to   (VAL181)  CRYSTAL STRUCTURE OF DEG5  |   BETS-BARREL, ENDOPEPTIDASE, CALCIUM BINDING, CHLOROPLAST, HYDROLASE 
3sti:B    (VAL27) to   (GLY106)  CRYSTAL STRUCTURE OF THE PROTEASE DOMAIN OF DEGQ FROM ESCHERICHIA COLI  |   SERINE PROTEASE, PDZ DOMAIN, PROTEASE, CHAPERONE, HYDROLASE 
1p2n:C    (GLN30) to    (LYS84)  STRUCTURAL CONSEQUENCES OF ACCOMMODATION OF FOUR NON- COGNATE AMINO-ACID RESIDUES IN THE S1 POCKET OF BOVINE TRYPSIN AND CHYMOTRYPSIN  |   TRYPSIN; CHYMOTRYPSIN; SERINE PROTEINASE; BOVINE PANCREATIC TRYPSIN INHIBITOR; PROTEIN-PROTEIN INTERACTION; NON-COGNATE BINDING; S1 POCKET; PRIMARY SPECIFICITY; CRYSTAL STRUCTURE, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1d4p:B    (GLN51) to   (MET116)  CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH 5- AMIDINOINDOLE-4-BENZYLPIPERIDINE INHIBITOR  |   THROMBIN; NONPEPTIDYL INHIBITOR; STRUCTURE-BASED DRUG DESIGN, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1d6w:A    (GLN30) to    (MET84)  STRUCTURE OF THROMBIN COMPLEXED WITH SELECTIVE NON-ELECTROPHILIC INHIBITORS HAVING CYCLOHEXYL MOIETIES AT P1  |   HYDROLASE, THROMBIN, THROMBIN INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2cga:A    (GLN30) to    (LYS84)  BOVINE CHYMOTRYPSINOGEN A. X-RAY CRYSTAL STRUCTURE ANALYSIS AND REFINEMENT OF A NEW CRYSTAL FORM AT 1.8 ANGSTROMS RESOLUTION  |   HYDROLASE(ZYMOGEN) 
2cha:B    (GLN30) to    (LYS84)  THE STRUCTURE OF CRYSTALLINE ALPHA-CHYMOTRYPSIN, $V.THE ATOMIC STRUCTURE OF TOSYL-ALPHA-CHYMOTRYPSIN AT 2 ANGSTROMS RESOLUTION  |   HYDROLASE (SERINE PROTEINASE) 
2cha:F    (GLN30) to    (LYS84)  THE STRUCTURE OF CRYSTALLINE ALPHA-CHYMOTRYPSIN, $V.THE ATOMIC STRUCTURE OF TOSYL-ALPHA-CHYMOTRYPSIN AT 2 ANGSTROMS RESOLUTION  |   HYDROLASE (SERINE PROTEINASE) 
1d9i:A    (GLN30) to    (MET84)  STRUCTURE OF THROMBIN COMPLEXED WITH SELECTIVE NON-ELECTOPHILIC INHIBITORS HAVING CYCLOHEXYL MOIETIES AT P1  |   GLOBULAR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1p8v:C    (GLN15) to    (MET80)  CRYSTAL STRUCTURE OF THE COMPLEX OF PLATELET RECEPTOR GPIB-ALPHA AND ALPHA-THROMBIN AT 2.6A  |   PLATELET GLYCOPROTEIN RECEPTOR, LEUCINE RICH REPEAT DOMAIN, MEMBRANE PROTEIN-HYDROLASE COMPLEX 
1p9m:A   (GLU133) to   (PHE192)  CRYSTAL STRUCTURE OF THE HEXAMERIC HUMAN IL-6/IL-6 ALPHA RECEPTOR/GP130 COMPLEX  |   IG DOMAIN, FOUR HELIX BUNDLE, CYTOKINE, INTERLEUKIN-6, GP130, SIGNALING PROTEIN-CYTOKINE COMPLEX 
1ddj:A   (GLN576) to   (GLU634)  CRYSTAL STRUCTURE OF HUMAN PLASMINOGEN CATALYTIC DOMAIN  |   PLASMINOGEN, CATALYTIC DOMAIN, BLOOD CLOTTING 
1ddj:B   (GLN576) to   (GLU634)  CRYSTAL STRUCTURE OF HUMAN PLASMINOGEN CATALYTIC DOMAIN  |   PLASMINOGEN, CATALYTIC DOMAIN, BLOOD CLOTTING 
1ddj:C   (GLN576) to   (GLU634)  CRYSTAL STRUCTURE OF HUMAN PLASMINOGEN CATALYTIC DOMAIN  |   PLASMINOGEN, CATALYTIC DOMAIN, BLOOD CLOTTING 
1ddj:D   (GLN576) to   (GLU634)  CRYSTAL STRUCTURE OF HUMAN PLASMINOGEN CATALYTIC DOMAIN  |   PLASMINOGEN, CATALYTIC DOMAIN, BLOOD CLOTTING 
1de7:H    (GLN30) to    (MET84)  INTERACTION OF FACTOR XIII ACTIVATION PEPTIDE WITH ALPHA-THROMBIN: CRYSTAL STRUCTURE OF THE ENZYME-SUBSTRATE COMPLEX  |   ENZYME-SUBSTRATE COMPLEX, ALPHA-THROMBIN, FACTOR XIII ACTIVATION PEPTIDE, HYDROLASE/PEPTIDE, BLOOD CLOTTING, HYDROLASE-HYDROLASE SUBSTRATE COMPLEX 
3t0a:C   (LEU651) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (S796T)  |   DYNAMPIC LOOP CONFORMATION, SER-796, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, BETA SUPERSANDWICH, GLYCOSIDASE, HYDROLASE 
3t0b:B   (LEU651) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (S796T) IPTG COMPLEX  |   DYNAMPIC LOOP CONFORMATION, SER-796, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, BETA SUPERSANDWICH, GLYCOSIDASE, HYDROLASE 
3t0d:B   (LEU651) to   (ALA716)  E.COLI (LACZ) BETA-GALACTOSIDASE (S796T) IN COMPLEX WITH GALACTONOLACTONE  |   DYNAMPIC LOOP CONFORMATION, SER-796, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, BETA SUPERSANDWICH, GLYCOSIDASE, HYDROLASE 
2qlv:E   (SER175) to   (ARG246)  CRYSTAL STRUCTURE OF THE HETEROTRIMER CORE OF THE S. CEREVISIAE AMPK HOMOLOG SNF1  |   HETEROTRIMER, ATP-BINDING, CARBOHYDRATE METABOLISM, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHORYLATION, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, LIPOPROTEIN, MYRISTATE, CBS DOMAIN, TRANSCRIPTION, TRANSCRIPTION REGULATION, TRANSFERASE/PROTEIN BINDING COMPLEX 
1dlp:A    (THR56) to   (PRO105)  STRUCTURAL CHARACTERIZATION OF THE NATIVE FETUIN-BINDING PROTEIN SCILLA CAMPANULATA AGGLUTININ (SCAFET): A NOVEL TWO-DOMAIN LECTIN  |   TWO-DOMAIN LECTIN, BETA PRISM II FOLD, NATIVE, SUGAR BINDING PROTEIN 
2qn5:T    (GLN33) to    (SER84)  CRYSTAL STRUCTURE AND FUNCTIONAL STUDY OF THE BOWMAN-BIRK INHIBITOR FROM RICE BRAN IN COMPLEX WITH BOVINE TRYPSIN  |   RBTI, BOWMAN-BIRK INHIBITOR, MONOCOTYLEDONOUS PLANT, REACTIVE-SITE LOOP, PROTEASE-INHIBITOR, PLANT-PEST SYSTEMS, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, CALCIUM, DIGESTION, HYDROLASE, METAL-BINDING, SECRETED, ZYMOGEN, HYDROLASE INHIBITOR/HYDROLASE COMPLEX, HETERO-DIMER 
3gch:B    (GLN30) to    (LYS84)  CHEMISTRY OF CAGED ENZYMES. BINDING OF PHOTOREVERSIBLE CINNAMATES TO CHYMOTRYPSIN  |   HYDROLASE (SERINE PROTEINASE) 
3gct:F    (GLN30) to    (LYS84)  STRUCTURE OF GAMMA-*CHYMOTRYPSIN IN THE RANGE $P*H 2.0 TO $P*H 10.5 SUGGESTS THAT GAMMA-CHYMOTRYPSIN IS A COVALENT ACYL-ENZYME ADDUCT AT LOW $P*H  |   HYDROLASE, SERINE PROTEINASE, HYDROLASE-PEPTIDE COMPLEX 
3t3g:A   (LEU198) to   (THR240)  GLYCOGEN PHOSPHORYLASE B IN COMPLEX WITH GLCBRU  |   A+B PROTEIN, TRANSFERASE, MUSCLE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3t3h:A   (LEU198) to   (THR240)  GLYCOGEN PHOSPHORYLASE B IN COMPLEX WITH GLCIU  |   A+B PROTEIN, TRANSFERASE, MUSCLE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3t3i:A   (LEU198) to   (THR240)  GLYCOGEN PHOSPHORYLASE B IN COMPLEX WITH GLCCF3U  |   A+B PROTEIN, TRANSFERASE, MUSCLE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2cv3:A    (GLN30) to    (GLY88)  CRYSTAL STRUCTURE OF PORCINE PANCREATIC ELASTASE COMPLEXED WITH A MACROCLYCLIC PEPTIDE INHIBITOR  |   PROTEIN-INHIBITOR INTERACTION, MACROCYCLIC PEPTIDE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
2qrp:A   (LEU198) to   (THR240)  GLYCOGEN PHOSPHORYLASE B IN COMPLEX WITH (1R)-3'-(2- NAPHTHYL)-SPIRO[1,5-ANHYDRO-D-GLUCITOL-1,5'-ISOXAZOLINE]  |   GLYCOGENOLYSIS, TYPE 2 DIABETES, ACETYLATION, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHORYLATION, PYRIDOXAL PHOSPHATE, TRANSFERASE 
2qrq:A   (LEU198) to   (THR240)  GLYCOGEN PHOSPHORYLASE B IN COMPLEX WITH (1R)-3'-(4- METHYLPHENYL)-SPIRO[1,5-ANHYDRO-D-GLUCITOL-1,5'- ISOXAZOLINE]  |   GLYCOGENOLYSIS, TYPE 2 DIABETES, ACETYLATION, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHORYLATION, PYRIDOXAL PHOSPHATE, TRANSFERASE 
3t62:C    (GLN30) to    (LYS84)  CRYSTAL STRUCTURE OF RECOMBINANT KUNITZ TYPE SERINE PROTEASE INHIBITOR-1 FROM THE CARIBBEAN SEA ANEMONE STICHODACTYLA HELIANTHUS IN COMPLEX WITH BOVINE CHYMOTRYPSIN  |   CHYMOTRYPSIN-INHIBITOR COMPLEX, KUNITZ-TYPE SERINE PROTEASE INHIBITOR, SECRETED, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3gir:A   (ALA304) to   (SER358)  CRYSTAL STRUCTURE OF GLYCINE CLEAVAGE SYSTEM AMINOMETHYLTRANSFERASE T FROM BARTONELLA HENSELAE  |   BARTONELLA HENSELAE, GLYCINE CLEAVAGE SYSTEM, AMINOMETHYLTRANSFERASE, AMINOTRANSFERASE, TRANSFERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID 
3gis:B    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF NA-FREE THROMBIN IN COMPLEX WITH THROMBOMODULIN  |   PROTEIN-PROTEIN COMPLEX, COAGULATION, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, DISULFIDE BOND, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, EGF-LIKE DOMAIN, HYDROXYLATION, MEMBRANE, RECEPTOR, THROMBOPHILIA, TRANSMEMBRANE, BLOOD CLOTTING 
3gis:F    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF NA-FREE THROMBIN IN COMPLEX WITH THROMBOMODULIN  |   PROTEIN-PROTEIN COMPLEX, COAGULATION, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, DISULFIDE BOND, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, EGF-LIKE DOMAIN, HYDROXYLATION, MEMBRANE, RECEPTOR, THROMBOPHILIA, TRANSMEMBRANE, BLOOD CLOTTING 
1ppf:E    (MET30) to    (ALA84)  X-RAY CRYSTAL STRUCTURE OF THE COMPLEX OF HUMAN LEUKOCYTE ELASTASE (PMN ELASTASE) AND THE THIRD DOMAIN OF THE TURKEY OVOMUCOID INHIBITOR  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1ppg:E    (MET30) to    (ALA84)  THE REFINED 2.3 ANGSTROMS CRYSTAL STRUCTURE OF HUMAN LEUKOCYTE ELASTASE IN A COMPLEX WITH A VALINE CHLOROMETHYL KETONE INHIBITOR  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1ppz:A    (ILE30) to    (SER83)  TRYPSIN COMPLEXES AT ATOMIC AND ULTRA-HIGH RESOLUTION  |   TRYPSIN, SERINE PROTEASE, ATOMIC AND ULTRA-HIGH RESOLUTION, COMPLEX, DFP, HYDROLASE 
1dwb:H    (GLN30) to    (MET84)  CRYSTALLOGRAPHIC ANALYSIS AT 3.0-ANGSTROMS RESOLUTION OF THE BINDING TO HUMAN THROMBIN OF FOUR ACTIVE SITE-DIRECTED INHIBITORS  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1dwc:H    (GLN30) to    (MET84)  CRYSTALLOGRAPHIC ANALYSIS AT 3.0-ANGSTROMS RESOLUTION OF THE BINDING TO HUMAN THROMBIN OF FOUR ACTIVE SITE-DIRECTED INHIBITORS  |   SERINE PROTEINASE, HYDROLASE-HYROLASE INHIBITOR COMPLEX 
1dwd:H    (GLN30) to    (MET84)  CRYSTALLOGRAPHIC ANALYSIS AT 3.0-ANGSTROMS RESOLUTION OF THE BINDING TO HUMAN THROMBIN OF FOUR ACTIVE SITE-DIRECTED INHIBITORS  |   SERINE PROTEINASE, HYDROLASE-HYROLASE INHIBITOR COMPLEX 
1pq5:A    (ILE30) to    (SER83)  TRYPSIN AT PH 5, 0.85 A  |   TRYPSIN, ULTRA-HIGH RESOLUTION, SERINE PROTEASE, CATALYSIS, HYDROLASE 
1pq7:A    (ILE30) to    (SER83)  TRYPSIN AT 0.8 A, PH5 / BORAX  |   TRYPSIN, ULTRA-HIGH RESOLUTION, CATALYSIS, HYDROLASE 
1pqa:A    (ILE30) to    (SER83)  TRYPSIN WITH PMSF AT ATOMIC RESOLUTION  |   TRYPSIN, ATOMIC RESOLUTION, PMSF, CATALYSIS, HYDROLASE 
1e0f:E    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THE HUMAN ALPHA-THROMBIN-HAEMADIN COMPLEX: AN EXOSITE II-BINDING INHIBITOR  |   COAGULATION/CRYSTAL STRUCTURE/HEPARIN-B, COAGULATION/CRYSTAL STRUCTURE/HEPARIN-BINDING SITE/ HIRUDIN/THROMBIN INHIBITOR, HYDROLASE 
2qxg:A    (GLN30) to    (SER86)  CRYSTAL STRUCTURE OF HUMAN KALLIKREIN 7 IN COMPLEX WITH ALA- ALA-PHE-CHLOROMETHYLKETONE  |   DIMER, 37 LOOP, ACTIVE SITE INHIBITOR, CHLOROMETHYL KETONE, ALTERNATIVE SPLICING, GLYCOPROTEIN, HYDROLASE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN 
2qxg:B    (GLN30) to    (SER86)  CRYSTAL STRUCTURE OF HUMAN KALLIKREIN 7 IN COMPLEX WITH ALA- ALA-PHE-CHLOROMETHYLKETONE  |   DIMER, 37 LOOP, ACTIVE SITE INHIBITOR, CHLOROMETHYL KETONE, ALTERNATIVE SPLICING, GLYCOPROTEIN, HYDROLASE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN 
2r0k:A    (ALA31) to    (GLY84)  PROTEASE DOMAIN OF HGFA WITH INHIBITOR FAB58  |   SERINE PROTEASE, ANTIBODY, INHIBITOR, EGF-LIKE DOMAIN, GLYCOPROTEIN, HYDROLASE, KRINGLE, SECRETED, ZYMOGEN, IMMUNE SYSTEM 
2r0l:A    (ALA31) to    (GLY84)  SHORT FORM HGFA WITH INHIBITORY FAB75  |   SERINE PROTEASE, ANTIBODY, ALLOSTERIC INHIBITOR, EGF-LIKE DOMAIN, GLYCOPROTEIN, HYDROLASE, KRINGLE, SECRETED, ZYMOGEN, IMMUNE SYSTEM 
1px3:A   (ASN649) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (G794A)  |   LOOP CONFORMATION, HYDROLASE 
1px3:D   (LEU651) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (G794A)  |   LOOP CONFORMATION, HYDROLASE 
2de9:A    (GLN15) to    (GLY73)  CRYSTAL STRUCTURE OF PORCINE PANCREATIC ELASTASE COMPLEXED WITH TRIS AFTER SOAKING A TRIS-FREE SOLUTION  |   SERINE PROTEASE, HYDROLASE 
4y76:A    (GLN30) to    (GLU84)  FACTOR XA COMPLEX WITH GTC000401  |   HYDROLASE, INHIBITOR 
3th2:H    (GLN30) to    (ARG84)  MG2+ IS REQUIRED FOR OPTIMAL FOLDING OF THE GAMMA-CARBOXYGLUTAMIC ACID (GLA) DOMAINS OF VITAMIN K-DEPENDENT CLOTTING FACTORS AT PHYSIOLOGICAL CA2+  |   HYDROLASE, BLOOD CLOTTING, SERINE PROTEASE, BLOOD COAGULATION, SOLUBLE TISSUE FACTOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3th4:H    (GLN30) to    (ARG84)  MG2+ IS REQUIRED FOR OPTIMAL FOLDING OF THE GAMMA-CARBOXYGLUTAMIC ACID (GLA) DOMAINS OF VITAMIN K-DEPENDENT CLOTTING FACTORS AT PHYSIOLOGICAL CA2+  |   HYDROLASE, SERINE PROTEASE, BLOOD CLOTTING, SOLUBLE TISSUE FACTOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4y9w:A     (SER2) to    (LYS49)  ASPARTIC PROTEINASE SAPP2 SECRETED FROM CANDIDA PARAPSILOSIS AT 0.82 A RESOLUTION.  |   CANDIDAPEPSIN, ASPARTIC ACID ENDOPEPTIDASE, HYDROLASE 
4jf7:D   (VAL400) to   (GLY486)  STRUCTURE OF THE PARAINFLUENZA VIRUS 5 (PIV5) HEMAGGLUTININ- NEURAMINIDASE (HN) ECTODOMAIN  |   PARAMYXOVIRUS, PIV5, ATTACHMENT PROTEIN, HN, RECEPTOR BINDING PROTEIN, ECTODOMAIN, VIRAL PROTEIN 
4jf7:A   (SER399) to   (GLY486)  STRUCTURE OF THE PARAINFLUENZA VIRUS 5 (PIV5) HEMAGGLUTININ- NEURAMINIDASE (HN) ECTODOMAIN  |   PARAMYXOVIRUS, PIV5, ATTACHMENT PROTEIN, HN, RECEPTOR BINDING PROTEIN, ECTODOMAIN, VIRAL PROTEIN 
2rab:A   (ALA232) to   (THR266)  STRUCTURE OF GLUTATHIONE AMIDE REDUCTASE FROM CHROMATIUM GRACILE IN COMPLEX WITH NAD  |   GLUTATHIONE, SUBSTRATE ANALOG, NAD, FAD, REDOX, OXIDOREDUCTASE 
1qbv:H    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THROMBIN COMPLEXED WITH AN GUANIDINE-MIMETIC INHIBITOR  |   THROMBIN, INHIBITOR, 3DP, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4jjo:A   (ARG136) to   (PRO182)  CRYSTAL STRUCTURE OF APO-CLAVIBACTER MICHIGANENSIS EXPANSIN  |   CELLULOSE BINDING PROTEIN, CELL WALL LOOSENING, SUGAR BINDING PROTEIN 
3h0c:B   (THR221) to   (PRO290)  CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE IV (CD26) IN COMPLEX WITH A REVERSED AMIDE INHIBITOR  |   COMPLEX (HYDROLASE-INHIBITOR), DPP-IV, DIABETES MELLITUS, DRUG DESIGN, HYDROLASE, SERINE PROTEASE, AMINOPEPTIDASE, GLYCOPROTEIN, PROTEASE, SIGNAL-ANCHOR, TRANSMEMBRANE, CELL MEMBRANE, DISULFIDE BOND, MEMBRANE, SECRETED 
1ela:A    (GLN30) to    (GLY88)  ANALOGOUS INHIBITORS OF ELASTASE DO NOT ALWAYS BIND ANALOGOUSLY  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SERINE PROTEINASE 
1elf:A    (GLN30) to    (GLY88)  NATURE OF THE INACTIVATION OF ELASTASE BY N-PEPTIDYL-O- AROYL HYDROXYLAMINE AS A FUNCTION OF PH  |   COMPLEX (HYDROLASE/INHIBITOR) 
1eoj:A    (GLN30) to    (MET84)  DESIGN OF P1' AND P3' RESIDUES OF TRIVALENT THROMBIN INHIBITORS AND THEIR CRYSTAL STRUCTURES  |   THROMBIN INHIBITORS, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1esa:A    (GLN30) to    (GLY88)  DIRECT STRUCTURE OBSERVATION OF AN ACYL-ENZYME INTERMEDIATE IN THE HYDROLYSIS OF AN ESTER SUBSTRATE BY ELASTASE  |   HYDROLASE(SERINE PROTEINASE) 
1eth:A   (HIS355) to   (GLY415)  TRIACYLGLYCEROL LIPASE/COLIPASE COMPLEX  |   COMPLEX (HYDROLASE-COFACTOR), LIPID DEGRADATION, COMPLEX (HYDROLASE- COFACTOR) COMPLEX 
1eth:C   (HIS355) to   (GLY415)  TRIACYLGLYCEROL LIPASE/COLIPASE COMPLEX  |   COMPLEX (HYDROLASE-COFACTOR), LIPID DEGRADATION, COMPLEX (HYDROLASE- COFACTOR) COMPLEX 
1ets:H    (GLN30) to    (MET84)  REFINED 2.3 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF BOVINE THROMBIN COMPLEXES FORMED WITH THE BENZAMIDINE AND ARGININE-BASED THROMBIN INHIBITORS NAPAP, 4-TAPAP AND MQPA: A STARTING POINT FOR IMPROVING ANTITHROMBOTICS  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1ett:H    (GLN30) to    (MET84)  REFINED 2.3 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF BOVINE THROMBIN COMPLEXES FORMED WITH THE BENZAMIDINE AND ARGININE-BASED THROMBIN INHIBITORS NAPAP, 4-TAPAP AND MQPA: A STARTING POINT FOR IMPROVING ANTITHROMBOTICS  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1ex3:A    (GLN30) to    (LYS84)  CRYSTAL STRUCTURE OF BOVINE CHYMOTRYPSINOGEN A (TETRAGONAL)  |   HYDROLASE 
2snv:A   (GLY187) to   (GLY232)  THE REFINED STRUCTURE OF SINDBIS VIRUS CORE PROTEIN IN COMPARISON WITH OTHER CHYMOTRYPSIN-LIKE SERINE PROTEINASE STRUCTURES  |   VIRAL PROTEIN 
3h43:I    (PRO91) to   (LEU151)  N-TERMINAL DOMAIN OF THE PROTEASOME-ACTIVATING NUCLEOTIDASE OF METHANOCALDOCOCCUS JANNASCHII  |   PROTEASOME, REGULATORY PARTICLE, NUCLEOSIDASE, ATP-BINDING, CYTOPLASM, NUCLEOTIDE-BINDING, HYDROLASE 
1ezu:C   (GLN430) to   (ASN484)  ECOTIN Y69F, D70P BOUND TO D102N TRYPSIN  |   MACROMOLECULAR COMPLEX, PROTEASE INHIBITOR, PROTEIN-PROTEIN INTERACTIONS, HYDROLASE/INHIBITOR COMPLEX 
2e5y:B    (GLU21) to    (ALA62)  EPSILON SUBUNIT AND ATP COMPLEX OF F1F0-ATP SYNTHASE FROM THE THERMOPHILIC BACILLUS PS3  |   ATP SYNTHASE, F1FO ATP SYNTHASE, F1-ATPASE, EPSILON SUBUNIT, ATP, HYDROLASE 
1qrz:A   (GLN576) to   (GLU634)  CATALYTIC DOMAIN OF PLASMINOGEN  |   MICROPLASMINOGEN, SERINE PROTEASE, ZYMOGEN, CHYMOTRYPSIN FAMILY, HYDROLASE 
1qrz:B   (GLN576) to   (GLU634)  CATALYTIC DOMAIN OF PLASMINOGEN  |   MICROPLASMINOGEN, SERINE PROTEASE, ZYMOGEN, CHYMOTRYPSIN FAMILY, HYDROLASE 
1qrz:D   (GLN576) to   (GLU634)  CATALYTIC DOMAIN OF PLASMINOGEN  |   MICROPLASMINOGEN, SERINE PROTEASE, ZYMOGEN, CHYMOTRYPSIN FAMILY, HYDROLASE 
3h7l:A    (THR31) to    (SER86)  CRYSTAL STRUCTURE OF ENDOGLUCANASE-RELATED PROTEIN FROM VIBRIO PARAHAEMOLYTICUS  |   ENDOGLUCANASE, DEHYDROGENASE, PSI-2, NYSGXRC, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, HYDROLASE 
3h7o:A    (VAL16) to    (TYR73)  CRYSTAL STRUCTURE OF SCABIES MITE INACTIVATED PROTEASE PARALOGUE S-I1 (SMIPP-S-I1)  |   HYDROLASE 
3h7t:A    (VAL16) to    (MET68)  CRYSTAL STRUCTURE OF SCABIES MITE INACTIVATED PROTEASE PARALOGUE S-D1 (SMIPP-S-D1)  |   HYDROLASE 
3u34:B    (ARG39) to   (GLY105)  CRYSTAL STRUCTURE OF THE GENERAL STRESS FMN/FAD BINDING PROTEIN FROM THE PHYTOPATHOGEN XANTHOMONAS CITRI  |   XANTHOMONAS CITRI GENERAL STRESS PROTEIN FMN BINDING PROTEIN FAD BINDING PROTEIN, PNP-OXIDASE LIKE FOLD, FMN FAD, PROTEIN BINDING 
3u34:C    (ARG39) to   (GLY105)  CRYSTAL STRUCTURE OF THE GENERAL STRESS FMN/FAD BINDING PROTEIN FROM THE PHYTOPATHOGEN XANTHOMONAS CITRI  |   XANTHOMONAS CITRI GENERAL STRESS PROTEIN FMN BINDING PROTEIN FAD BINDING PROTEIN, PNP-OXIDASE LIKE FOLD, FMN FAD, PROTEIN BINDING 
3u35:A    (ARG39) to   (GLY105)  CRYSTAL STRUCTURE OF THE GENERAL STRESS FMN/FAD BINDING PROTEIN FROM THE PHYTOPATHOGEN XANTHOMONAS CITRI  |   XANTHOMONAS CITRI GENERAL STRESS PROTEIN FMN BINDING PROTEIN FAD BINDING PROTEIN, PNP-OXIDASE LIKE FOLD, FMN/FAD, PROTEIN BINDING 
3hat:H    (GLN30) to    (MET84)  ACTIVE SITE MIMETIC INHIBITION OF THROMBIN  |   COMPLEX (SERINE PROTEASE-INHIBITOR), COMPLEX (SERINE PROTEASE- INHIBITOR) COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1qz8:A    (CYS14) to    (GLU68)  CRYSTAL STRUCTURE OF SARS CORONAVIRUS NSP9  |   SARS, REPLICATION, NSP9, CORONAVIRUS, UNKNOWN FUNCTION 
1qz8:B    (CYS14) to    (GLU68)  CRYSTAL STRUCTURE OF SARS CORONAVIRUS NSP9  |   SARS, REPLICATION, NSP9, CORONAVIRUS, UNKNOWN FUNCTION 
4jz1:A    (GLN30) to    (ARG84)  CRYSTAL STRUCTURE OF MATRIPTASE IN COMPLEX WITH INHIBITOR  |   MATRIPTASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2est:E    (GLN30) to    (GLY84)  CRYSTALLOGRAPHIC STUDY OF THE BINDING OF A TRIFLUOROACETYL DIPEPTIDE ANILIDE INHIBITOR WITH ELASTASE  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SERINE PROTEINASE 
4k3j:A   (MET508) to   (ASN566)  CRYSTAL STRUCTURE OF ONARTUZUMAB FAB IN COMPLEX WITH MET AND HGF-BETA  |   ANTIBODY, GLYCOSYLATION, TRANSFERASE-IMMUNE SYSTEM-GROWTH FACTOR COMPLEX 
1fn8:A    (ILE30) to    (SER84)  FUSARIUM OXYSPORUM TRYPSIN AT ATOMIC RESOLUTION  |   BETA BARREL, HYDROLASE, HYDROLASE-HYDROLASE SUBSTRATE COMPLEX 
3hk6:B    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF MURINE THROMBIN MUTANT W215A/E217A (TWO MOLECULES IN THE ASYMMETRIC UNIT)  |   SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CALCIUM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISULFIDE BOND, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, ZYMOGEN 
3hk6:D    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF MURINE THROMBIN MUTANT W215A/E217A (TWO MOLECULES IN THE ASYMMETRIC UNIT)  |   SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CALCIUM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISULFIDE BOND, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, ZYMOGEN 
3ufi:A    (ASP65) to   (GLY167)  CRYSTAL STRUCTURE OF A PUTATIVE CELL ADHESION PROTEIN (BACOVA_04980) FROM BACTEROIDES OVATUS ATCC 8483 AT 2.18 A RESOLUTION  |   FIMBRIAL PROTEIN, CELL ADHESION, MAJOR FIMBRIAL SUBUNIT PROTEIN (FIMA),, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY 
3hkj:E    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF HUMAN THROMBIN MUTANT W215A/E217A IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF HUMAN PAR1  |   SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, DISULFIDE BOND, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, ZYMOGEN, CELL MEMBRANE, G-PROTEIN COUPLED RECEPTOR, MEMBRANE, PHOSPHOPROTEIN, RECEPTOR, TRANSDUCER, TRANSMEMBRANE 
4yt7:H    (GLN30) to    (ARG84)  FACTOR VIIA IN COMPLEX WITH THE INHIBITOR 2-(2-{(R)-[(4- CARBAMIMIDOYLPHENYL)AMINO][5-ETHOXY-2-FLUORO-3-(PROPAN-2-YLOXY) PHENYL]METHYL}-1H-IMIDAZOL-4-YL)BENZAMIDE  |   GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
4yta:A    (GLN30) to    (SER84)  BOND LENGTH ANALYSIS OF ASP, GLU AND HIS RESIDUES IN TRYPSIN AT 1.2A RESOLUTION  |   SERINE PROTEASE, HYDROLASE 
4k5z:A    (TYR29) to    (GLU84)  CRYSTAL STRUCTURE OF HUMAN CHYMASE IN COMPLEX WITH FRAGMENT INHIBITOR 6-CHLORO-2,3-DIHYDRO-1H-ISOINDOL-1-ONE  |   SERINE PROTEASE, GLYCOSYLATED, MAST CELLS, SECRETED, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
4k60:A    (TYR29) to    (GLU84)  CRYSTAL STRUCTURE OF HUMAN CHYMASE IN COMPLEX WITH FRAGMENT 6-BROMO-1, 3-DIHYDRO-2H-INDOL-2-ONE  |   SERINE PROTEASE, GLYCOSYLATED, MAST CELLS, SECRETED, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1rd3:D    (GLN30) to    (MET84)  2.5A STRUCTURE OF ANTICOAGULANT THROMBIN VARIANT E217K  |   HYDROLASE 
4k69:A    (TYR29) to    (GLU84)  CRYSTAL STRUCTURE OF HUMAN CHYMASE IN COMPLEX WITH FRAGMENT LINKED BENZIMIDAZOLONE INHIBITOR: (3S)-3-{3-[(6-BROMO-2-OXO-2,3-DIHYDRO-1H- INDOL-4-YL)METHYL]-2-OXO-2,3-DIHYDRO-1H-BENZIMIDAZOL-1-YL}HEXANOIC ACID  |   SERINE PROTEASE, GLYCOSYLATED, MAST CELLS, SECRETED, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1fq3:A    (TYR29) to    (PRO84)  CRYSTAL STRUCTURE OF HUMAN GRANZYME B  |   CHYMOTRYPSIN-LIKE SERINE PROTEINASE, HYDROLASE 
1fq3:B    (TYR29) to    (PRO84)  CRYSTAL STRUCTURE OF HUMAN GRANZYME B  |   CHYMOTRYPSIN-LIKE SERINE PROTEINASE, HYDROLASE 
1rfn:A    (GLN30) to    (ASN84)  HUMAN COAGULATION FACTOR IXA IN COMPLEX WITH P-AMINO BENZAMIDINE  |   SERINE PROTEINASE, BLOOD COAGULATION, COAGULATION FACTOR 
1riw:B    (GLN51) to   (MET116)  THROMBIN IN COMPLEX WITH NATURAL PRODUCT INHIBITOR OSCILLARIN  |   PROTEASE, THROMBIN, INHIBITOR COMPLEX, OSCILLARIN, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1fuj:A    (MET30) to    (SER84)  PR3 (MYELOBLASTIN)  |   HYDROLASE, SERINE PROTEASE, GLYCOPROTEIN, ZYMOGEN, HYDROLASE (SERINE PROTEASE) 
1rp1:A   (GLN354) to   (ALA417)  DOG PANCREATIC LIPASE RELATED PROTEIN 1  |   HYDROLASE, LIPID DEGRADATION, PANCREATIC LIPASE 
1fy3:A    (LEU15) to    (SER72)  [G175Q]HBP, A MUTANT OF HUMAN HEPARIN BINDING PROTEIN (CAP37)  |   SERINE PROTEASE HOMOLOG, BPTI BINDING SITE, ANTIMICROBIAL PROTEIN 
1fy4:A    (ILE30) to    (SER84)  FUSARIUM OXYSPORUM TRYPSIN AT ATOMIC RESOLUTION  |   BETA BARREL, HYDROLASE 
1fy5:A    (ILE30) to    (SER84)  FUSARIUM OXYSPORUM TRYPSIN AT ATOMIC RESOLUTION  |   BETA BARREL, HYDROLASE 
1rqc:A   (VAL143) to   (GLY190)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   HYDROLASE 
1rqc:B   (VAL143) to   (GLY190)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   HYDROLASE 
1rqc:C   (VAL143) to   (GLY190)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   HYDROLASE 
1rqc:D   (VAL143) to   (GLY190)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   HYDROLASE 
1rqc:F   (VAL143) to   (GLY190)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   HYDROLASE 
1rqc:H   (VAL143) to   (GLY190)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   HYDROLASE 
1rqc:J   (VAL143) to   (GLY190)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   HYDROLASE 
1rrh:A    (SER57) to   (VAL128)  SOYBEAN LIPOXYGENASE (LOX-3) AT AMBIENT TEMPERATURES AT 2.0 A RESOLUTION  |   OXIDOREDUCTASE, IRON METALLOPROTEIN, LIPOXYGENASE 
2f91:A    (GLN30) to    (THR84)  1.2A RESOLUTION STRUCTURE OF A CRAYFISH TRYPSIN COMPLEXED WITH A PEPTIDE INHIBITOR, SGTI  |   SERINE PROTEASE, TRYPSIN, CANONICAL INHIBITOR, ATOMIC RESOLUTION, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1g27:A    (LEU78) to   (GLY124)  CRYSTAL STRUCTURE OF E.COLI POLYPEPTIDE DEFORMYLASE COMPLEXED WITH THE INHIBITOR BB-3497  |   BB-3497, INHIBITION, POLYPEPTIDE DEFORMYLASE, HYDROLASE 
1g37:A    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH BCH-10556 AND EXOSITE-DIRECTED PEPTIDE  |   PROTEASE, THROMBIN, INHIBITOR, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3unr:A    (GLN30) to    (SER84)  BOND LENGTH ANALYSIS OF ASP, GLU AND HIS RESIDUES IN TRYPSIN AT 1.2A RESOLUTION  |   SERINE PROTEASE, HYDROLASE 
4kga:A    (GLN30) to    (HIS91)  CRYSTAL STRUCTURE OF KALLIKREIN-RELATED PEPTIDASE 4  |   KLK4, KALLIKREIN-4, SERINE PROTEASE, PROTEASE, HYDROLASE 
4kga:B    (GLN30) to    (SER86)  CRYSTAL STRUCTURE OF KALLIKREIN-RELATED PEPTIDASE 4  |   KLK4, KALLIKREIN-4, SERINE PROTEASE, PROTEASE, HYDROLASE 
2fes:H    (GLN30) to    (MET84)  ORALLY ACTIVE THROMBIN INHIBITORS  |   THROMBIN INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2vgc:B    (GLN30) to    (LYS84)  GAMMA-CHYMOTRYPSIN D-PARA-CHLORO-1-ACETAMIDO BORONIC ACID INHIBITOR COMPLEX  |   HYDROLASE, SERINE PROTEASE 
1gct:B    (GLN30) to    (LYS84)  IS GAMMA-CHYMOTRYPSIN A TETRAPEPTIDE ACYL-ENZYME ADDUCT OF GAMMA- CHYMOTRYPSIN?  |   HYDROLASE, SERINE PROTEINASE, HYDROLASE-PEPTIDE COMPLEX 
1gdn:A    (ILE30) to    (SER84)  FUSARIUM OXYSPORUM TRYPSIN AT ATOMIC RESOLUTION  |   BETA BARREL, HYDROLASE, HYDROLASE-HYDROLASE SUBSTRATE COMPLEX 
1gdq:A    (ILE30) to    (SER84)  FUSARIUM OXYSPORUM TRYPSIN AT ATOMIC RESOLUTION  |   BETA-BARREL, HYDROLASE 
1gdu:A    (ILE30) to    (SER84)  FUSARIUM OXYSPORUM TRYPSIN AT ATOMIC RESOLUTION  |   BETA-BARREL, HYDROLASE 
2vkx:C   (LYS534) to   (LYS594)  HUMAN NCAM, FN3 DOMAINS 1 AND 2, M610R MUTANT  |   ADHESION RECEPTOR, CELL ADHESION 
2fmj:A    (PHE29) to    (ARG84)  220-LOOP MUTANT OF STREPTOMYCES GRISEUS TRYPSIN  |   TRYPSIN, SERINE PROTEASE, HYDROLASE 
3uwi:A    (GLN30) to    (SER84)  BOVINE TRYPSIN VARIANT X(TRIPLEGLU217PHE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR  |   TRYPSIN-LIKE SERINE PROTEASE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2fo9:A    (GLN30) to    (GLY88)  STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 95% ACETONE  |   ELASTASE; SOLVENT MAPPING; ORGANIC SOLVENTS; PROTEIN BINDING SITES; MULTIPLE SOLVENT CRYSTAL STRUCTURES, HYDROLASE 
2foa:A    (GLN30) to    (GLY88)  STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 40/50/10 % BENZENE  |   ELASTASE; SOLVENT MAPPING; ORGANIC SOLVENTS; PROTEIN BINDING SITES; MULTIPLE SOLVENT CRYSTAL STRUCTURES, HYDROLASE 
2fob:A    (GLN30) to    (GLY88)  STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 40/50/10 CYCLOHEXANE  |   ELASTASE; SOLVENT MAPPING; ORGANIC SOLVENTS; PROTEIN BINDING SITES; MULTIPLE SOLVENT CRYSTAL STRUCTURES, HYDROLASE 
1ggd:B    (GLN30) to    (LYS84)  CRYSTAL STUCTURE OF GAMMA CHYMOTRYPSIN WITH N-ACETYL-LEUCIL- PHENYLALANINE ALDEHYDE BOUND AT THE ACTIVE SITE  |   CHYMOTRYPSIN, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1gha:F    (GLN30) to    (LYS84)  A SECOND ACTIVE SITE IN CHYMOTRYPSIN? THE X-RAY CRYSTAL STRUCTURE OF N-ACETYL-D-TRYPTOPHAN BOUND TO GAMMA-CHYMOTRYPSIN  |   HYDROLASE, SERINE PROTEINASE 
1ghb:F    (GLN30) to    (LYS84)  A SECOND ACTIVE SITE IN CHYMOTRYPSIN? THE X-RAY CRYSTAL STRUCTURE OF N-ACETYL-D-TRYPTOPHAN BOUND TO GAMMA-CHYMOTRYPSIN  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1ghx:H    (GLN30) to    (MET84)  A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE  |   THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1gi2:A    (GLN30) to    (SER84)  A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI- CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE  |   THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, HYDROLASE 
1gi4:A    (GLN30) to    (SER84)  A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI- CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE  |   THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, HYDROLASE 
1gi5:A    (GLN30) to    (SER84)  A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI- CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE  |   THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, HYDROLASE 
1gi6:A    (GLN30) to    (SER84)  A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI- CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE  |   THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, HYDROLASE 
1gj4:H    (GLN30) to    (MET84)  SELECTIVITY AT S1, H2O DISPLACEMENT, UPA, TPA, SER190/ALA190 PROTEASE, STRUCTURE-BASED DRUG DESIGN  |   THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, BLOOD CLOTTING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1gj5:H    (GLN30) to    (MET84)  SELECTIVITY AT S1, H2O DISPLACEMENT, UPA, TPA, SER190/ALA190 PROTEASE, STRUCTURE-BASED DRUG DESIGN  |   THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, BLOOD CLOTTING, HYDROLASE,HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD CLOTTING,HYDROLASE-INHIBITOR COMPLEX 
1gj6:A    (GLN30) to    (SER84)  ENGINEERING INHIBITORS HIGHLY SELECTIVE FOR THE S1 SITES OF SER190 TRYPSIN-LIKE SERINE PROTEASE DRUG TARGETS  |   SELECTIVITY AT S1, H2O DISPLACEMENT, UPA, TPA, SER190/ALA190 PROTEASE, STRUCTURE-BASED DRUG DESIGN, HYDROLASE 
1gl1:A    (GLN30) to    (LYS84)  STRUCTURE OF THE COMPLEX BETWEEN BOVINE ALPHA-CHYMOTRYPSIN AND PMP-C, AN INHIBITOR FROM THE INSECT LOCUSTA MIGRATORIA  |   HYDROLASE/INHIBITOR, COMPLEX (PROTEASE/INHIBITOR), HYDROLASE, SERINE PROTEASE, SERINE PROTEASE INHIBITOR 
1gl1:B    (GLN30) to    (LYS84)  STRUCTURE OF THE COMPLEX BETWEEN BOVINE ALPHA-CHYMOTRYPSIN AND PMP-C, AN INHIBITOR FROM THE INSECT LOCUSTA MIGRATORIA  |   HYDROLASE/INHIBITOR, COMPLEX (PROTEASE/INHIBITOR), HYDROLASE, SERINE PROTEASE, SERINE PROTEASE INHIBITOR 
1gmd:F    (GLN30) to    (LYS84)  X-RAY CRYSTAL STRUCTURE OF GAMMA-CHYMOTRYPSIN IN HEXANE  |   HYDROLASE, SERINE PROTEASE 
1gmh:F    (GLN30) to    (LYS84)  REFINED CRYSTAL STRUCTURE OF "AGED" AND "NON-AGED" ORGANOPHOSPHORYL CONJUGATES OF GAMMA-CHYMOTRYPSIN  |   HYDROLASE(SERINE PROTEINASE) 
1sgf:A    (TRP29) to    (LEU84)  CRYSTAL STRUCTURE OF 7S NGF: A COMPLEX OF NERVE GROWTH FACTOR WITH FOUR BINDING PROTEINS (SERINE PROTEINASES)  |   GROWTH FACTOR (BETA-NGF), HYDROLASE - SERINE PROTEINASE (GAMMA-NGF), INACTIVE SERINE PROTEINASE (ALPHA-NGF), GROWTH FACTOR 
1sgf:G    (HIS30) to    (PHE84)  CRYSTAL STRUCTURE OF 7S NGF: A COMPLEX OF NERVE GROWTH FACTOR WITH FOUR BINDING PROTEINS (SERINE PROTEINASES)  |   GROWTH FACTOR (BETA-NGF), HYDROLASE - SERINE PROTEINASE (GAMMA-NGF), INACTIVE SERINE PROTEINASE (ALPHA-NGF), GROWTH FACTOR 
1sgf:X    (VAL31) to    (LEU84)  CRYSTAL STRUCTURE OF 7S NGF: A COMPLEX OF NERVE GROWTH FACTOR WITH FOUR BINDING PROTEINS (SERINE PROTEINASES)  |   GROWTH FACTOR (BETA-NGF), HYDROLASE - SERINE PROTEINASE (GAMMA-NGF), INACTIVE SERINE PROTEINASE (ALPHA-NGF), GROWTH FACTOR 
1shh:B    (GLN30) to    (MET84)  SLOW FORM OF THROMBIN BOUND WITH PPACK  |   SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2g00:A    (GLN30) to    (GLU84)  FACTOR XA IN COMPLEX WITH THE INHIBITOR 3-(6-(2'- ((DIMETHYLAMINO)METHYL)-4-BIPHENYLYL)-7-OXO-3- (TRIFLUOROMETHYL)-4,5,6,7-TETRAHYDRO-1H-PYRAZOLO[3,4- C]PYRIDIN-1-YL)BENZAMIDE  |   GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING 
1shy:A   (TRP507) to   (ASN566)  THE CRYSTAL STRUCTURE OF HGF BETA-CHAIN IN COMPLEX WITH THE SEMA DOMAIN OF THE MET RECEPTOR.  |   PROTEASE, SEMA DOMAIN, PSI DOMAIN, RECEPTOR ECTODOMAIN GROWTH FACTOR, GROWTH FACTOR-GROWTH FACTOR RECEPTOR COMPLEX 
1gpl:A   (GLY353) to   (ALA417)  RP2 LIPASE  |   SERINE ESTERASE, HYDROLASE, LIPID DEGRADATION, PANCREAS, GLYCOPROTEIN, CHIMERIC 
2g3x:B    (VAL28) to    (VAL93)  CRYSTAL STRUCTURE OF TRANSTHYRETIN MUTANT I84S AT ACIDIC PH  |   TTR, AMYLOID FIBRILS, POINT MUTATION, TRANSPORT PROTEIN 
3i3b:B   (LEU651) to   (ALA716)  E.COLI (LACZ) BETA-GALACTOSIDASE (M542A) IN COMPLEX WITH D- GALACTOPYRANOSYL-1-ON  |   BETA-GALACTOSIDASE, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN BETA SUPERSANDWHICH, GLYCOSIDASE, HYDROLASE 
1sl3:A    (GLN30) to    (MET84)  CRYSTAL STRUCTUE OF THROMBIN IN COMPLEX WITH A POTENT P1 HETEROCYCLE- ARYL BASED INHIBITOR  |   THROMBIN INHIBITOR COMPLEX, BLOOD CLOTTING, HYDROLASE-INHIBITOR COMPLEX, BLOOD CLOTTING,HYDROLASE-INHIBITOR COMPLEX 
3i3d:B   (LEU651) to   (ARG721)  E. COLI (LACZ) BETA-GALACTOSIDASE (M542A) IN COMPLEX WITH IPTG  |   BETA-GALACTOSIDASE, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN BETA SUPERSANDWHICH, GLYCOSIDASE, HYDROLASE 
3i3d:D   (LEU651) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (M542A) IN COMPLEX WITH IPTG  |   BETA-GALACTOSIDASE, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN BETA SUPERSANDWHICH, GLYCOSIDASE, HYDROLASE 
3i3e:B   (ASN649) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (M542A)  |   BETA-GALACTOSIDASE, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN BETA SUPERSANDWHICH, GLYCOSIDASE, HYDROLASE 
3i3e:C   (ASN649) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (M542A)  |   BETA-GALACTOSIDASE, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN BETA SUPERSANDWHICH, GLYCOSIDASE, HYDROLASE 
2g51:A    (ILE30) to    (SER83)  ANOMALOUS SUBSTRUCTURE OF TRYPSIN (P1)  |   ANOMALOUS SUBSTRUCTURE OF TRYPSIN (P1), HYDROLASE 
2g52:A    (ILE30) to    (SER83)  ANOMALOUS SUBSTRUCTURE OF TRYPSIN (P21)  |   ANOMALOUS SUBSTRUCTURE OF TRYPSIN (P21), HYDROLASE 
1spj:A    (TRP29) to    (VAL83)  STRUCTURE OF MATURE HUMAN TISSUE KALLIKREIN (HUMAN KALLIKREIN 1 OR KLK1) AT 1.70 ANGSTROM RESOLUTION WITH VACANT ACTIVE SITE  |   SERINE PROTEASE, KLK1, HK1, HUMAN KALLIKREIN 1, HUMAN TISSUE KALLIKREIN 1, TISSUE KALLIKREIN, HYDROLASE 
2vu8:E    (VAL31) to    (SER84)  CRYSTAL STRUCTURE OF AN INSECT INHIBITOR WITH A FUNGAL TRYPSIN  |   HYDROLASE/INHIBITOR, CANONICAL INHIBITOR, INHIBITOR, SERINE PROTEASE, SPECIES SELECTIVITY, INSECT, ZYMOGEN, PROTEASE, SECRETED, HYDROLASE 
3vd4:B   (LEU651) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (N460D) IN COMPLEX WITH IPTG  |   TRANSITION STATE STABILIZATION, SUBSTRATE BINDING, 2-STAGE BINDING, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN, BETA SUPERSANDWICH, GLYCOSIDASE, HYDROLASE 
1gvl:A    (GLN30) to    (VAL86)  HUMAN PROKALLIKREIN 6 (HK6)/ PROZYME/ PROPROTEASE M/ PRONEUROSIN  |   HYDROLASE, ZYMOGEN, HUMAN KALLIKREIN 
2gch:F    (GLN30) to    (LYS84)  REFINED CRYSTAL STRUCTURE OF GAMMA-CHYMOTRYPSIN AT 1.9 ANGSTROMS RESOLUTION  |   HYDROLASE (SERINE PROTEINASE) 
2gd4:H    (GLN30) to    (GLU84)  CRYSTAL STRUCTURE OF THE ANTITHROMBIN-S195A FACTOR XA-PENTASACCHARIDE COMPLEX  |   SERPIN, MICHAELIS COMPLEX, HYDROLASE 
2gd4:B    (GLN30) to    (GLU84)  CRYSTAL STRUCTURE OF THE ANTITHROMBIN-S195A FACTOR XA-PENTASACCHARIDE COMPLEX  |   SERPIN, MICHAELIS COMPLEX, HYDROLASE 
3veq:B    (GLN30) to    (SER81)  A BINARY COMPLEX BETWWEN BOVINE PANCREATIC TRYPSIN AND A ENGINEERED MUTANT TRYPSIN INHIBITOR  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3vfe:A    (GLN30) to    (SER84)  VIRTUAL SCREENING AND X-RAY CRYSTALLOGRAPHY FOR HUMAN KALLIKREIN 6 INHIBITORS WITH AN AMIDINOTHIOPHENE P1 GROUP  |   HUMAN KALLIKREIN 6, HK6, SERINE PROTEASE, PROTEIN-LIGAND COMPLEX, AMIDINOTHIOPHENE, HYDROLASE 
3vgc:B    (GLN30) to    (LYS84)  GAMMA-CHYMOTRYPSIN L-NAPHTHYL-1-ACETAMIDO BORONIC ACID ACID INHIBITOR COMPLEX  |   HYDROLASE, SERINE PROTEASE 
4l0z:A   (LEU102) to   (THR161)  CRYSTAL STRUCTURE OF RUNX1 AND ETS1 BOUND TO TCR ALPHA PROMOTER (CRYSTAL FORM 2)  |   RUNT DOMAIN, ETS DOMAIN, TRANSCRIPTION-DNA COMPLEX 
3iaq:B   (LEU651) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (E416V)  |   GLU-416-VAL BETA-GALACTOSIDASE HYDROLASE TIM BARREL(ALPHA/BETA BARREL) JELLY-ROLL BARREL IMMUNOGLOBULIN BETA SUPERSANDWHICH, GLYCOSIDASE, HYDROLASE 
3iaq:C   (ASN649) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (E416V)  |   GLU-416-VAL BETA-GALACTOSIDASE HYDROLASE TIM BARREL(ALPHA/BETA BARREL) JELLY-ROLL BARREL IMMUNOGLOBULIN BETA SUPERSANDWHICH, GLYCOSIDASE, HYDROLASE 
3idb:B   (PHE169) to   (ASN215)  CRYSTAL STRUCTURE OF (108-268)RIIB:C HOLOENZYME OF CAMP- DEPENDENT PROTEIN KINASE  |   PKA, CAMP, SPR, AFFINITY, KINASE, LINKER, CRYSTAL STRUCTURE, RII HOLOENZYME, ALTERNATIVE SPLICING, ATP-BINDING, CYTOPLASM, LIPOPROTEIN, MYRISTATE, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, ACETYLATION, CAMP-BINDING 
2gmt:B    (GLN30) to    (LYS84)  THREE-DIMENSIONAL STRUCTURE OF CHYMOTRYPSIN INACTIVATED WITH (2S) N- ACETYL-L-ALANYL-L-PHENYLALANYL-CHLOROETHYL KETONE: IMPLICATIONS FOR THE MECHANISM OF INACTIVATION OF SERINE PROTEASES BY CHLOROKETONES  |   HYDROLASE(SERINE PROTEINASE) 
2w1u:B   (ASN880) to   (SER945)  A FAMILY 32 CARBOHYDRATE-BINDING MODULE, FROM THE MU TOXIN PRODUCED BY CLOSTRIDIUM PERFRINGENS, IN COMPLEX WITH BETA- D-GLCNAC-BETA(1,3)GALNAC  |   FAMILY 32 CARBOHYDRATE BINDING MODULE, FAMILY 84 GLYCOSIDE HYDROLASE, GLYCOSIDASE, HEXOSAMINIDASE, CLOSTRIDIUM PERFRINGENS, CBM, TOXIN, SECRETED, VIRULENCE, HYDROLASE 
1t7c:C    (GLN30) to    (LYS84)  CRYSTAL STRUCTURE OF THE P1 GLU BPTI MUTANT- BOVINE CHYMOTRYPSIN COMPLEX  |   CHYMOTRYPSIN; SERINE PROTEINASE; BOVINE PANCREATIC TRYPSIN INHIBITOR; BPTI; PROTEIN-PROTEIN INTERACTION; NON-COGNATE BINDING; S1 POCKET; PRIMARY SPECIFICITY; CRYSTAL STRUCTURE, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1h6y:B    (GLN21) to    (GLU81)  THE ROLE OF CONSERVED AMINO ACIDS IN THE CLEFT OF THE C-TERMINAL FAMILY 22 CARBOHYDRATE BINDING MODULE OF CLOSTRIDIUM THERMOCELLUM XYN10B IN LIGAND BINDING  |   XYLAN DEGRADATION, HYDROLASE, GLYCOSIDASE 
1t8o:C    (GLN30) to    (LYS84)  CRYSTAL STRUCTURE OF THE P1 TRP BPTI MUTANT- BOVINE CHYMOTRYPSIN COMPLEX  |   CHYMOTRYPSIN, SERINE PROTEINASE, BOVINE PANCREATIC TRYPSIN INHIBITOR, BPTI, PROTEIN-PROTEIN INTERACTION, NON-COGNATE BINDING, S1 POCKET, PRIMARY SPECIFICITY, CRYSTAL STRUCTURE, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
2w47:A    (ALA66) to   (SER130)  CLOSTRIDIUM THERMOCELLUM CBM35 IN COMPLEX WITH DELTA-4,5- ANHYDROGALACTURONIC ACID  |   HYDROLASE 
1ta2:A    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH COMPOUND 1  |   THROMBIN INHIBITOR COMPLEX, BLOOD CLOTTING, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1ta6:A    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH COMPOUND 14B  |   THROMBIN INHIBITOR COMPLEX, BLOOD CLOTTING, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1h9i:E    (GLN30) to    (ASN84)  COMPLEX OF EETI-II MUTANT WITH PORCINE TRYPSIN  |   HYDROLASE/INHIBITOR, COMPLEX (SERINE PROTEASE/INHIBITOR), TRYPSIN, SQUASH INHIBITOR, CYSTINE KNOT 
1hah:H    (GLN30) to    (MET84)  THE ISOMORPHOUS STRUCTURES OF PRETHROMBIN2, HIRUGEN-AND PPACK- THROMBIN: CHANGES ACCOMPANYING ACTIVATION AND EXOSITE BINDING TO THROMBIN  |   COMPLEX(SERINE PROTEINASE-INHIBITOR), COMPLEX(SERINE PROTEINASE- INHIBITOR) COMPLEX 
2w5e:B   (CYS438) to   (GLU479)  STRUCTURAL AND BIOCHEMICAL ANALYSIS OF HUMAN PATHOGENIC ASTROVIRUS SERINE PROTEASE AT 2.0 ANGSTROM RESOLUTION  |   COILED COIL, TRANSMEMBRANE, THIOL PROTEASE, RNA REPLICATION, RIBOSOMAL FRAMESHIFTING, SERINE PROTEASE, CATALYTIC TRIAD, PROTEASE, MEMBRANE, HYDROLASE, ANTIVIRAL, ASTROVIRUS 
2w5e:C   (CYS438) to   (GLU479)  STRUCTURAL AND BIOCHEMICAL ANALYSIS OF HUMAN PATHOGENIC ASTROVIRUS SERINE PROTEASE AT 2.0 ANGSTROM RESOLUTION  |   COILED COIL, TRANSMEMBRANE, THIOL PROTEASE, RNA REPLICATION, RIBOSOMAL FRAMESHIFTING, SERINE PROTEASE, CATALYTIC TRIAD, PROTEASE, MEMBRANE, HYDROLASE, ANTIVIRAL, ASTROVIRUS 
2w5e:D   (CYS438) to   (GLU479)  STRUCTURAL AND BIOCHEMICAL ANALYSIS OF HUMAN PATHOGENIC ASTROVIRUS SERINE PROTEASE AT 2.0 ANGSTROM RESOLUTION  |   COILED COIL, TRANSMEMBRANE, THIOL PROTEASE, RNA REPLICATION, RIBOSOMAL FRAMESHIFTING, SERINE PROTEASE, CATALYTIC TRIAD, PROTEASE, MEMBRANE, HYDROLASE, ANTIVIRAL, ASTROVIRUS 
2w5e:E   (CYS438) to   (GLU479)  STRUCTURAL AND BIOCHEMICAL ANALYSIS OF HUMAN PATHOGENIC ASTROVIRUS SERINE PROTEASE AT 2.0 ANGSTROM RESOLUTION  |   COILED COIL, TRANSMEMBRANE, THIOL PROTEASE, RNA REPLICATION, RIBOSOMAL FRAMESHIFTING, SERINE PROTEASE, CATALYTIC TRIAD, PROTEASE, MEMBRANE, HYDROLASE, ANTIVIRAL, ASTROVIRUS 
1hb0:B    (GLN30) to    (GLY84)  SNAPSHOTS OF SERINE PROTEASE CATALYSIS: (D) ACYL-ENZYME INTERMEDIATE BETWEEN PORCINE PANCREATIC ELASTASE AND HUMAN BETA-CASOMORPHIN-7 JUMPED TO PH 10 FOR 2 MINUTES  |   HYDROLASE, SERINE PROTEINASE, HYDROLASE (SERINE PROTEINASE) 
1tbr:H    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF INSECT DERIVED DOUBLE DOMAIN KAZAL INHIBITOR RHODNIIN IN COMPLEX WITH THROMBIN  |   COMPLEX (SERINE PROTEASE-INHIBITOR), KAZAL-TYPE INHIBITOR, THROMBIN, COMPLEX (SERINE PROTEASE-INHIBITOR) COMPLEX 
1tfx:B    (GLN30) to    (ASN84)  COMPLEX OF THE SECOND KUNITZ DOMAIN OF TISSUE FACTOR PATHWAY INHIBITOR WITH PORCINE TRYPSIN  |   COMPLEX (SERINE PROTEASE/INHIBITOR), HYDROLASE, INHIBITOR, BLOOD COAGULATION 
1hdt:H    (GLN30) to    (MET84)  STRUCTURE OF A RETRO-BINDING PEPTIDE INHIBITOR COMPLEXED WITH HUMAN ALPHA-THROMBIN  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1tgs:Z    (GLN30) to    (SER84)  THREE-DIMENSIONAL STRUCTURE OF THE COMPLEX BETWEEN PANCREATIC SECRETORY INHIBITOR (KAZAL TYPE) AND TRYPSINOGEN AT 1.8 ANGSTROMS RESOLUTION. STRUCTURE SOLUTION, CRYSTALLOGRAPHIC REFINEMENT AND PRELIMINARY STRUCTURAL INTERPRETATION  |   COMPLEX (PROTEINASE/INHIBITOR) 
1thr:H    (GLN30) to    (MET84)  STRUCTURES OF THROMBIN COMPLEXES WITH A DESIGNED AND A NATURAL EXOSITE INHIBITOR  |   HYDROLASE(SERINE PROTEINASE) 
1ths:H    (GLN30) to    (MET84)  STRUCTURES OF THROMBIN COMPLEXES WITH A DESIGNED AND A NATURAL EXOSITE INHIBITOR  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1hgt:H    (GLN30) to    (MET84)  STRUCTURE OF THE HIRUGEN AND HIRULOG 1 COMPLEXES OF ALPHA- THROMBIN  |   HYDROLASE(SERINE PROTEASE) 
1hlt:H    (GLN30) to    (MET84)  THE STRUCTURE OF A NONADECAPEPTIDE OF THE FIFTH EGF DOMAIN OF THROMBOMODULIN COMPLEXED WITH THROMBIN  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1ton:A    (GLN30) to    (LEU84)  RAT SUBMAXILLARY GLAND SERINE PROTEASE, TONIN. STRUCTURE SOLUTION AND REFINEMENT AT 1.8 ANGSTROMS RESOLUTION  |   HYDROLASE(SERINE PROTEINASE) 
1tq0:B    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THE POTENT ANTICOAGULANT THROMBIN MUTANT W215A/E217A IN FREE FORM  |   THROMBIN, ANTICOAGULANT, BLOOD CLOTTING 
1hne:E    (MET30) to    (ALA84)  STRUCTURE OF HUMAN NEUTROPHIL ELASTASE IN COMPLEX WITH A PEPTIDE CHLOROMETHYL KETONE INHIBITOR AT 1.84-ANGSTROMS RESOLUTION  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4zxx:H    (GLN30) to    (ARG84)  FACTOR VIIA IN COMPLEX WITH THE INHIBITOR N-{3-[(2R)-1-{(2R)-2-[(1- AMINOISOQUINOLIN-6-YL)AMINO]-2-PHENYLACETYL}PYRROLIDIN-2-YL]-4- (PROPAN-2-YLSULFONYL)PHENYL}ACETAMIDE  |   GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
4zxy:H    (GLN30) to    (ARG84)  FACTOR VIIA IN COMPLEX WITH THE INHIBITOR (2R)-2-[(1-AMINOISOQUINOLIN- 6-YL)AMINO]-4,11-DIAZATRICYCLO[14.2.2.1~6,10~]HENICOSA-1(18),6(21),7, 9,16,19-HEXAENE-3,12-DIONE  |   GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1hpl:B   (HIS354) to   (ALA417)  HORSE PANCREATIC LIPASE. THE CRYSTAL STRUCTURE AT 2.3 ANGSTROMS RESOLUTION  |   HYDROLASE(CARBOXYLIC ESTERASE) 
4lk4:A    (ILE47) to   (ALA107)  STRUCTURE OF VIBRIO CHOLERAE VESB PROTEASE  |   TRYPSIN, PEPTIDASE S1 FAMILY, ENDOPEPTIDASE, DUF3466, SECRETED PROTEIN, EXTRACELLULAR, HYDROLASE 
1trn:B    (GLN30) to    (ASN84)  CRYSTAL STRUCTURE OF HUMAN TRYPSIN 1: UNEXPECTED PHOSPHORYLATION OF TYROSINE 151  |   HUMAN TRYPSIN, DFP INHIBITED, HYDROLASE (SERINE PROTEINASE) 
1try:A    (PHE29) to    (SER84)  STRUCTURE OF INHIBITED TRYPSIN FROM FUSARIUM OXYSPORUM AT 1.55 ANGSTROMS  |   HYDROLASE (SERINE PROTEINASE) 
2wfw:C    (PRO80) to   (THR136)  STRUCTURE AND ACTIVITY OF THE N-TERMINAL SUBSTRATE RECOGNITION DOMAINS IN PROTEASOMAL ATPASES - THE ARC DOMAIN STRUCTURE  |   ATP-BINDING PROTEIN, PROTEASOMAL ATPASES, PAN, ARC, AAA, ATP-BINDING, NUCLEOTIDE-BINDING 
2hlc:A    (TYR29) to    (ASN84)  HL COLLAGENASE STRUCTURE AT 1.7A RESOLUTION  |   SERINE PROTEASE, HYDROLASE, COLLAGEN DEGRADATION 
2hlc:B    (TYR29) to    (ASN84)  HL COLLAGENASE STRUCTURE AT 1.7A RESOLUTION  |   SERINE PROTEASE, HYDROLASE, COLLAGEN DEGRADATION 
2wiq:B   (ASP141) to   (ALA222)  FLUORESCENT PROTEIN KILLERRED IN THE NATIVE STATE  |   FLUORESCENT PROTEIN, CALI, ROS, REACTIVE OXYGEN SPECIES 
1txk:A    (PRO77) to   (LEU152)  CRYSTAL STRUCTURE OF ESCHERICHIA COLI OPGG  |   BETA-SANDWICH, BIOSYNTHETIC PROTEIN 
1hxe:H    (GLN30) to    (MET84)  SERINE PROTEASE  |   SERINE PROTEASE IN BLOOD COAGULATION, HYDROLASE, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASEE-HYDROLASE INHIBITOR COMPLEX 
1hxf:H    (GLN30) to    (MET84)  HUMAN THROMBIN COMPLEX WITH HIRUDIN VARIANT  |   COMPLEX (SERINE PROTEASE INHIBITOR), SULFATATION, MULTIGENE FAMILY, BLOOD COAGULATION, PLASMA, CALCIUM-BINDING, GLYCOPROTEIN, DUPLICATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2hpp:H    (GLN30) to    (MET84)  STRUCTURES OF THE NONCOVALENT COMPLEXES OF HUMAN AND BOVINE PROTHROMBIN FRAGMENT 2 WITH HUMAN PPACK-THROMBIN  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SERINE PROTEINASE 
3vxf:H    (GLN30) to    (MET84)  X/N JOINT REFINEMENT OF HUMAN ALPHA-THROMBIN-BIVALIRUDIN COMPLEX PD5  |   SERINE PROTEASE, HYDROLYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4lxb:H    (GLN30) to    (MET84)  CRYSTAL STRUCTURE ANALYSIS OF THROMBIN IN COMPLEX WITH COMPOUND D58  |   SERINE PROTEASES, ANTITHROMBOTIC AGENTS, DUAL THROMBIN/FACTOR XA INHI, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4lz1:H    (GLN30) to    (MET84)  X-RAY STRUCTURE OF THE COMPLEX BETWEEN HUMAN THROMBIN AND THE TBA DELETION MUTANT LACKING THYMINE 12 NUCLEOBASE  |   PROTEIN-DNA COMPLEX, BLOOD COAGULATION, APTAMER, INHIBITOR-DNA COMPLEX, DNA APTAMER, G-QUADRUPLEX, SERINE PROTEASE, HYDROLASE, ABASIC FURAN, DNA THYMINE NUCLEOBASE DELETION, BLOOD, HYDROLASE-DNA COMPLEX, HYDROLASE-HYDROLASE INHIBITOR-DNA COMPLEX 
1icj:B   (GLU579) to   (GLY624)  PDF PROTEIN IS CRYSTALLIZED AS NI2+ CONTAINING FORM, COCRYSTALLIZED WITH INHIBITOR POLYETHYLENE GLYCOL (PEG)  |   HYDROLASE, IRON METALLOPROTEASE, PROTEIN SYNTHESIS 
1uhb:A    (GLN30) to    (ASN84)  CRYSTAL STRUCTURE OF PORCINE ALPHA TRYPSIN BOUND WITH AUTO CATALYTICALY PRODUCED NATIVE PEPTIDE AT 2.15 A RESOLUTION  |   SERINE PROTEASE, HYDROLASE, PEPTIDE TRYPSIN COMPLEX 
2wvx:A   (THR209) to   (PHE253)  STRUCTURE OF THE FAMILY GH92 INVERTING MANNOSIDASE BT3990 FROM BACTEROIDES THETAIOTAOMICRON VPI-5482  |   GLYCOSIDE HYDROLASE FAMILY 92, GH92, HYDROLASE, BT3990 
2wvx:D   (THR209) to   (PHE253)  STRUCTURE OF THE FAMILY GH92 INVERTING MANNOSIDASE BT3990 FROM BACTEROIDES THETAIOTAOMICRON VPI-5482  |   GLYCOSIDE HYDROLASE FAMILY 92, GH92, HYDROLASE, BT3990 
4m37:A   (ASN258) to   (SER314)  CRYSTAL STRUCTURE OF TRYPANOSOMA BRUCEI PROTEIN ARGININE METHYLTRANSFERASE 7 COMPLEX WITH ADOHCY  |   METHYLTRANSFERASE, TRANSFERASE 
4m38:B   (ASN258) to   (SER314)  CRYSTAL STRUCTURE OF TRYPANOSOMA BRUCEI PROTEIN ARGININE METHYLTRANSFERASE 7 COMPLEX WITH ADOHCY AND HISTONE H4 PEPTIDE  |   METHYLTRANSFERASE, TRANSFERASE-TRANSFERASE SUBSTRATE COMPLEX 
5a8x:A    (MET30) to    (ALA84)  CRYSTAL STRUCTURE OF HUMAN NEUTROPHIL ELASTASE IN COMPLEX WITH A DIHYDROPYRIMIDONE INHIBITOR  |   TRYPSIN FAMILY FOLD, PROTEASE, HYDROLASE, HYDROLASE- INHIBITOR COMPLEX 
1uma:H    (GLN30) to    (MET84)  ALPHA-THROMBIN (HIRUGEN) COMPLEXED WITH NA-(N,N-DIMETHYLCARBAMOYL)- ALPHA-AZALYSINE  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, KRINGLE, ALPHA-THROMBIN- HIRUGEN COMPLEX 
1iqn:A    (GLN30) to    (GLU84)  HUMAN COAGULATION FACTOR XA IN COMPLEX WITH M55192  |   HYDROLASE, SERINE PROTEASE, BLOOD COAGULATION FACTOR, COMPLEX 
4m7g:A    (THR15) to    (ASN73)  STREPTOMYCES ERYTHRAEUS TRYPSIN  |   SERINE PROTEASE, HYDROLASE 
3j26:F   (THR196) to   (GLN266)  THE 3.5 A RESOLUTION STRUCTURE OF THE SPUTNIK VIROPHAGE BY CRYO-EM  |   DOUBLE JELLY-ROLL, SINGLE JELLY-ROLL, VIRUS 
5abe:A   (LEU659) to   (GLU714)  STRUCTURE OF GH84 WITH LIGAND  |   HYDROLASE, TIM-BARREL, INHIBITOR 
5abf:A   (LEU659) to   (GLU714)  STRUCTURE OF GH84 WITH LIGAND  |   HYDROLASE, TIM-BARREL, INHIBITOR 
2wzs:G   (THR209) to   (PHE253)  STRUCTURE OF THE FAMILY GH92 INVERTING MANNOSIDASE BT3990 FROM BACTEROIDES THETAIOTAOMICRON VPI-5482 IN COMPLEX WITH MANNOIMIDAZOLE  |   GLYCOSIDE HYDROLASE FAMILY 92, ALPHA-1\,2 LINKAGE, BT3990, HYDROLASE 
1uto:A    (GLN30) to    (SER84)  TRYPSIN SPECIFICITY AS ELUCIDATED BY LIE CALCULATIONS, X-RAY STRUCTURES AND ASSOCIATION CONSTANT MEASUREMENTS  |   HYDROLASE, TRYPSIN, INHIBITOR SPECIFICITY, ELECTROSTATIC INTERACTIONS, COLD-ADAPTATION, MOLECULAR DYNAMICS, BINDING FREE ENERGY 
1utq:A    (GLN30) to    (SER84)  TRYPSIN SPECIFICITY AS ELUCIDATED BY LIE CALCULATIONS, X-RAY STRUCTURES AND ASSOCIATION CONSTANT MEASUREMENTS  |   HYDROLASE, TRYPSIN, INHIBITOR SPECIFICITY, ELECTROSTATIC INTERACTIONS, COLD-ADAPTATION, MOLECULAR DYNAMICS, BINDING FREE ENERGY HYDROLASE 
1j15:A    (GLN30) to    (ASN84)  BENZAMIDINE IN COMPLEX WITH RAT TRYPSIN MUTANT X99/175/190RT  |   SERINE PROTEASE, HYDROLASE, SERINE PROTEINASE 
4mho:A   (LEU198) to   (THR240)  CRYSTAL STRUCTURE OF GPB IN COMPLEX WITH S3, SUGAR (N-[(BIPHENYL-4- YLOXY)ACETYL]-BETA-D-GLUCOPYRANOSYLAMINE)  |   ALPHA AND BETA PROTEIN, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4mi3:A   (LEU198) to   (THR240)  CRYSTAL STRUCTURE OF GPB IN COMPLEX WITH SUGAR (N-{(2R)-2-METHYL-3-[4- (PROPAN-2-YL)PHENYL]PROPANOYL}-BETA-D-GLUCOPYRANOSYLAMINE) (S21)  |   ALPHA AND BETA PROTEIN, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1v2l:T    (GLN30) to    (SER84)  BENZAMIDINE IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(TRIPLE.GLU)BT.D1  |   SERINE PROTEASE, HYDROLASE, SERINE PROTEINASE 
1v2m:T    (GLN30) to    (SER84)  BENZAMIDINE IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(TRIPLE.GLU)BT.A1  |   SERINE PROTEASE, HYDROLASE, SERINE PROTEINASE 
1vgc:B    (GLN30) to    (LYS84)  GAMMA-CHYMOTRYPSIN L-PARA-CHLORO-1-ACETAMIDO BORONIC ACID INHIBITOR COMPLEX  |   HYDROLASE, SERINE PROTEASE 
1jnq:A    (SER57) to   (VAL128)  LIPOXYGENASE-3 (SOYBEAN) COMPLEX WITH EPIGALLOCATHECHIN (EGC)  |   METALLOPROTEIN, FE(II) COMPLEX, PURPLE LIPOXYGENASE, CATECHIN INHIBITOR, GREEN TEA, OXIDOREDUCTASE 
2j97:A    (THR14) to    (GLU64)  HUMAN CORONAVIRUS 229E NON STRUCTURAL PROTEIN 9 (NSP9)  |   SSB, ZINC, HCOV, MEMBRANE, HELICASE, SARS COV, VIRAL REPLICASE, RNA REPLICATION, ATP-BINDING, NUCLEOTIDE-BINDING, RIBOSOMAL FRAMESHIFT, RNA-BINDING PROTEIN 
1jwt:A    (GLN51) to   (MET116)  CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH A NOVEL BICYCLIC LACTAM INHIBITOR  |   HYDROLASE 
1jym:C   (VAL142) to   (GLY188)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   PDF, MALARIA, PLASMODIUM, DEFORMYLATION, METALLOENZYME, HYDROLASE 
1jym:E   (VAL142) to   (GLY188)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   PDF, MALARIA, PLASMODIUM, DEFORMYLATION, METALLOENZYME, HYDROLASE 
1jym:F   (VAL142) to   (GLY188)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   PDF, MALARIA, PLASMODIUM, DEFORMYLATION, METALLOENZYME, HYDROLASE 
1jym:G   (VAL142) to   (GLY188)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   PDF, MALARIA, PLASMODIUM, DEFORMYLATION, METALLOENZYME, HYDROLASE 
1jym:J   (VAL142) to   (GLY188)  CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN  |   PDF, MALARIA, PLASMODIUM, DEFORMYLATION, METALLOENZYME, HYDROLASE 
4n3l:H    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH A NOVEL GLUCOSE- CONJUGATED POTENT INHIBITOR  |   HYDROLASE(SERINE PROTEASE), COMPLEX THROMBIN-GLUCOSE-CONJUGATED INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3zcq:A   (LEU198) to   (THR240)  RABBIT MUSCLE GLYCOGEN PHOSPHORYLASE B IN COMPLEX WITH N-(4- TRIFLUOROMETHYL-BENZOYL)-N-BETA-D-GLUCOPYRANOSYL UREA DETERMINED AT 2.15 A RESOLUTION  |   TRANSFERASE, INHIBITOR, HYPOGLYCAEMIC AGENTS, STRUCTURE-BASED LIGAND DESIGN 
2jet:B    (GLN30) to    (LYS84)  CRYSTAL STRUCTURE OF A TRYPSIN-LIKE MUTANT (S189D, A226G) CHYMOTRYPSIN.  |   SUBSTRATE SPECIFICITY, ZYMOGEN, PROTEASE, HYDROLASE, DIGESTION, SERINE PROTEASE, PROTEIN ENGINEERING 
2jh5:D    (GLN30) to    (MET84)  HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX  |   GLYCOPROTEIN, SERINE PROTEASE, KRINGLE, ZYMOGEN, THROMBIN, PROTEASE, DISEASE MUTATION, BLOOD COAGULATION, GAMMA-CARBOXYGLUTAMIC ACID, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, ACUTE PHASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2xvg:A   (THR809) to   (ALA850)  CRYSTAL STRUCTURE OF ALPHA-XYLOSIDASE (GH31) FROM CELLVIBRIO JAPONICUS  |   HYDROLASE, GLYCOSYL HYDROLASE FAMILY 31, BETA/ALPHA 8 BARREL 
2xvk:A   (THR809) to   (ALA850)  CRYSTAL STRUCTURE OF ALPHA-XYLOSIDASE (GH31) FROM CELLVIBRIO JAPONICUS IN COMPLEX WITH 5-FLUORO-ALPHA-D-XYLOPYRANOSYL FLUORIDE  |   HYDROLASE, GLYCOSYL HYDROLASE FAMILY 31, (BETA/ALPHA) 8 BARREL 
1w8o:A   (GLU584) to   (ALA639)  CONTRIBUTION OF THE ACTIVE SITE ASPARTIC ACID TO CATALYSIS IN THE BACTERIAL NEURAMINIDASE FROM MICROMONOSPORA VIRIDIFACIENS  |   3D-STRUCTURE, GLYCOSIDASE, HYDROLASE, SIALIDASE, BETA- PROPELLER 
2xwb:F   (ALA472) to   (HIS531)  CRYSTAL STRUCTURE OF COMPLEMENT C3B IN COMPLEX WITH FACTORS B AND D  |   IMMUNE SYSTEM, PRO-CONVERTASE, HYDROLASE, SERINE PROTEASE, CONFORMATIONAL CHANGES, ALTERNATIVE PATHWAY 
2xwb:H   (ALA472) to   (HIS531)  CRYSTAL STRUCTURE OF COMPLEMENT C3B IN COMPLEX WITH FACTORS B AND D  |   IMMUNE SYSTEM, PRO-CONVERTASE, HYDROLASE, SERINE PROTEASE, CONFORMATIONAL CHANGES, ALTERNATIVE PATHWAY 
1w9w:A    (ASP21) to    (ASP70)  STRUCTURE OF A BETA-1,3-GLUCAN BINDING CBM6 FROM BACILLUS HALODURANS IN COMPLEX WITH LAMINARIHEXAOSE  |   CARBOHYDRATE-BINDING MODULE, LECTIN, BETA-GLUCAN, CARBOHYDRATE BINDING, GLYCOSIDE HYDROLASE 
1k2i:1    (GLN30) to    (LYS84)  CRYSTAL STRUCTURE OF GAMMA-CHYMOTRYPSIN IN COMPLEX WITH 7- HYDROXYCOUMARIN  |   ENZYME-INHIBITOR COMPLEX, HYDROLASE 
1k32:B   (ASN145) to   (ARG194)  CRYSTAL STRUCTURE OF THE TRICORN PROTEASE  |   PROTEIN DEGRADATION, SUBSTRATE GATING, SERINE PROTEASE, BETA PROPELLER, PROTEASOME, HYDROLASE 
2k1q:A    (GLN34) to    (GLN73)  NMR STRUCTURE OF HEPATITIS C VIRUS NS3 SERINE PROTEASE COMPLEXED WITH THE NON-COVALENTLY BOUND PHENETHYLAMIDE INHIBITOR  |   SERINE PROTEASE, NS3, HEPATITIS C VIRUS, NON COVALENT INHIBITOR, ENVELOPE PROTEIN, HELICASE, HYDROLASE, NUCLEOTIDE-BINDING, RNA REPLICATION, TRANSMEMBRANE, VIRAL PROTEIN 
4niy:A    (GLN30) to    (SER84)  CRYSTAL STRUCTURE OF TRYPSILIGASE (K60E/N143H/Y151H/D189K TRYPSIN) COMPLEXED TO YRH-ECOTIN (M84Y/M85R/A86H ECOTIN)  |   TRYPSIN INHIBITOR, SERINE PROTEINASE, ENZYME DESIGN, ACTIVATION DOMAIN, PEPTIDE LIGATION, REVERSE PROTEOLYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4niy:D    (GLN30) to    (SER84)  CRYSTAL STRUCTURE OF TRYPSILIGASE (K60E/N143H/Y151H/D189K TRYPSIN) COMPLEXED TO YRH-ECOTIN (M84Y/M85R/A86H ECOTIN)  |   TRYPSIN INHIBITOR, SERINE PROTEINASE, ENZYME DESIGN, ACTIVATION DOMAIN, PEPTIDE LIGATION, REVERSE PROTEOLYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2y4y:C   (GLY106) to   (THR169)  STRUCTURE OF A DOMAIN FROM THE TYPE IV PILUS BIOGENESIS LIPOPROTEIN PILP, FROM PSEUDOMONAS AERUGINOSA  |   BIOSYNTHETIC PROTEIN 
1kf9:F  (GLN1565) to  (PHE1623)  PHAGE DISPLAY DERIVED VARIANT OF HUMAN GROWTH HORMONE COMPLEXED WITH TWO COPIES OF THE EXTRACELLULAR DOMAIN OF ITS RECEPTOR  |   CYTOKINE, HORMONE-RECEPTOR COMPLEX, PHAGE DISPLAY MOLECULAR PLASTICITY, RECEPTOR HOMODIMERIZATION, HUMAN GROWTH HORMONE, HORMONE/GROWTH FACTOR COMPLEX 
1wsr:A   (SER306) to   (LYS363)  CRYSTAL STRUCTURE OF HUMAN T-PROTEIN OF GLYCINE CLEAVAGE SYSTEM  |   GLYCINE-CLEAVAGE SYTEM, AMINOMETHYL TRANSFERASE 
1wsv:B   (SER306) to   (LYS363)  CRYSTAL STRUCTURE OF HUMAN T-PROTEIN OF GLYCINE CLEAVAGE SYSTEM  |   GLYCINE-CLEAVAGE SYTEM, AMINOMETHYL TRANSFERASE 
1kj1:D    (GLY52) to   (SER100)  MANNOSE-SPECIFIC AGGLUTININ (LECTIN) FROM GARLIC (ALLIUM SATIVUM) BULBS COMPLEXED WITH ALPHA-D-MANNOSE  |   BULB LECTIN, MANNOSE, PLANT PROTEIN 
1kj1:Q    (GLY52) to   (SER100)  MANNOSE-SPECIFIC AGGLUTININ (LECTIN) FROM GARLIC (ALLIUM SATIVUM) BULBS COMPLEXED WITH ALPHA-D-MANNOSE  |   BULB LECTIN, MANNOSE, PLANT PROTEIN 
4nu3:B    (ALA47) to    (ASP84)  CRYSTAL STRUCTURE OF MFFIBP, A CAPPING HEAD REGION SWAPPED MUTANT OF ICE-BINDING PROTEIN  |   BETA-HELICAL, ANTIFREEZE ACTIVITY, ICE-CRYSTAL, ANTIFREEZE PROTEIN 
1kts:B    (GLN30) to    (MET84)  THROMBIN INHIBITOR COMPLEX  |   BLOOD COAGULATION, INHIBITION, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4nzl:A    (MET44) to   (ALA100)  EXTRACELLULAR PROTEINS OF STAPHYLOCOCCUS AUREUS INHIBIT THE NEUTROPHIL SERINE PROTEASES  |   PRIMARILY BETA, SERINE PROTEASE, PROTEASE INHIBITOR, INNATE IMMUNITY, AZUROPHILIC GRANULES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1kyn:A    (ALA31) to    (THR84)  CATHEPSIN-G  |   SERINE PROTEASE, HYDROLASE 
4o03:A   (GLN335) to   (MET400)  CRYSTAL STRUCTURE OF CA2+ BOUND PROTHROMBIN DELETION MUTANT RESIDUES 146-167  |   PROTHROMBIN, KRINGLE, SERINE PROTEASE, COAGULATION, HYDROLASE 
1xen:A    (ASN74) to   (GLY124)  HIGH RESOLUTION CRYSTAL STRUCTURE OF ESCHERICHIA COLI IRON- PEPTIDE DEFORMYLASE BOUND TO FORMATE  |   IRON DEFORMYLASE, FORMATE, HYDROLASE 
1xeo:A    (ASN74) to   (GLY124)  HIGH RESOLUTION CRYSTALS STRUCTURE OF COBALT- PEPTIDE DEFORMYLASE BOUND TO FORMATE  |   COBALT DEFORMYLASE, FORMATE, HYDROLASE 
1l1g:A    (GLN15) to    (GLY73)  THE STRUCTURE OF PORCINE PANCREATIC ELASTASE COMPLEXED WITH XENON AND BROMIDE, CRYOPROTECTED WITH GLYCEROL  |   XENON, BROMIDE, PPE, HYDROLASE 
1l2e:A    (GLN30) to    (SER84)  HUMAN KALLIKREIN 6 (HK6) ACTIVE FORM WITH BENZAMIDINE INHIBITOR  |   SERINE PROTEASE, KALLIKREIN, HUMAN KALLIKREIN 6, BENZAMIDINE, PROTEASE, MYELENCEPHALON SPECIFIC PROTEASE, ZYME, PROTEASE M, NEUROSIN, HYDROLASE 
4o3u:A   (MET508) to   (ASN566)  ZYMOGEN HGF-BETA/MET WITH ZYMOGEN ACTIVATOR PEPTIDE ZAP2.3  |   TRYPSIN HOMOLOY, RECEPTOR ACTIVATION, TRANSFERASE-GROWTH FACTOR COMPLEX 
1l4z:A   (GLN576) to   (GLU634)  X-RAY CRYSTAL STRUCTURE OF THE COMPLEX OF MICROPLASMINOGEN WITH ALPHA DOMAIN OF STREPTOKINASE IN THE PRESENCE CADMIUM IONS  |   PLASMINOGEN, STREPTOKINASE, PROTEIN COMPLEX, CRYSTAL STRUCTURE, HYDROLASE/BLOOD CLOTTING COMPLEX 
4o9v:A    (GLN30) to    (ARG84)  CRYSTAL STRUCTURE OF MATRIPTASE IN COMPLEX WITH INHIBITOR  |   MATRIPTASE, TRYPSIN-LIKE SERINE PROTEINASE FOLD, PROTEASE, SMALL MOLECULE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1lhc:H    (GLN30) to    (MET84)  HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BOROARG-OH  |   BLOOD COAGULATION, PLASMA, CALCIUM-BINDING, GLYCOPROTEIN, DUPLICATION, VITAMIN K, ZYMOGEN, GAMMA-CARBOXYGLUTAMIC ACID, ACUTE PHASE, LIVER, HYDROLASE, SERINE PROTEASE, KRINGLE, SIGNAL, DISEASE MUTATION, COMPLEX (SERINE PROTEASE/INHIBITOR) 
1lhf:H    (GLN30) to    (MET84)  HUMAN ALPHA-THROMBIN COMPLEXED WITH AC-(D)PHE-PRO-BORO- HOMOLYS-OH  |   BLOOD COAGULATION, PLASMA, CALCIUM-BINDING, GLYCOPROTEIN, DUPLICATION, VITAMIN K, ZYMOGEN, GAMMA-CARBOXYGLUTAMIC ACID, ACUTE PHASE, LIVER, HYDROLASE, SERINE PROTEASE, KRINGLE, SIGNAL, DISEASE MUTATION, COMPLEX (SERINE PROTEASE/INHIBITOR) 
1lnh:A    (SER57) to   (VAL128)  LIPOXYGENASE-3(SOYBEAN) NON-HEME FE(II) METALLOPROTEIN  |   OXIDOREDUCTASE, METALLOPROTEIN, FE(II) COMPLEX 
1lo6:A    (GLN30) to    (SER84)  HUMAN KALLIKREIN 6 (HK6) ACTIVE FORM WITH BENZAMIDINE INHIBITOR AT 1.56 A RESOLUTION  |   SERINE PROTEASE, KALLIKREIN, HUMAN KALLIKREIN 6, HK6, BENZAMIDINE, PROTEASE, BRAIN SERINE PROTEASE, MYELENCEPHALON SPECIFIC PROTEASE, MSP, ZYME, PROTEASE M, NEUROSIN, HYDROLASE 
1lpa:B   (HIS354) to   (ALA417)  INTERFACIAL ACTIVATION OF THE LIPASE-PROCOLIPASE COMPLEX BY MIXED MICELLES REVEALED BY X-RAY CRYSTALLOGRAPHY  |   HYDROLASE(CARBOXYLIC ESTERASE) 
4a5t:S   (GLN576) to   (GLU634)  STRUCTURAL BASIS FOR THE CONFORMATIONAL MODULATION  |   HYDROLASE, MULTI-DOMAIN CONFORMATIONAL CHANGE 
2zcl:P    (GLN30) to    (GLN84)  CRYSTAL STRUCTURE OF HUMAN PROSTATE SPECIFIC ANTIGEN COMPLEXED WITH AN ACTIVATING ANTIBODY  |   HUMAN PSA, ANTIBODIES, KALLIKREIN RELATED PEPTIDASES, PROSTATE CANCER, GLYCOPROTEIN, HYDROLASE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, IMMUNE SYSTEM 
2o7i:A    (MET37) to    (TYR70)  THE X-RAY CRYSTAL STRUCTURE OF A THERMOPHILIC CELLOBIOSE BINDING PROTEIN BOUND WITH CELLOBIOSE  |   PERIPLASMIC BINDING PROTEIN, CELLULOSE, THERMOPHILIC PROTEINS, CELLOBIOSE BINDING PROTEIN, SUGAR BINDING PROTEIN 
2zf0:H    (GLN30) to    (MET84)  EXPLORING THROMBIN S1 POCKET  |   BLOOD CLOTTING/HYDROLASE INHIBITORS, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX 
2zfp:H    (GLN30) to    (MET84)  THROMBIN INIBITION  |   BLOOD CLOTTING/HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX 
2zfq:H    (GLN30) to    (MET84)  EXPLORING THROMBIN S3 POCKET  |   BLOOD COAGULATION/HYDROLASE INHIBITORS, ACUTE PHASE, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
2zgb:H    (GLN30) to    (MET84)  THROMBIN INHIBITION  |   BLOOD CLOTTING, HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2zhe:H    (GLN30) to    (MET84)  EXPLORING THROMBIN S3 POCKET  |   BLOOD COAGULATION, HYDROLASE INHIBITORS, ACUTE PHASE, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3kcg:H    (VAL31) to    (ASN84)  CRYSTAL STRUCTURE OF THE ANTITHROMBIN-FACTOR IXA- PENTASACCHARIDE COMPLEX  |   MICHAELIS COMPLEX, BLOOD COAGULATION, CALCIUM, DISULFIDE BOND, EGF-LIKE DOMAIN, GLYCOPROTEIN, HEMOPHILIA, HYDROLASE, PHARMACEUTICAL, PROTEASE, SECRETED, SERINE PROTEASE, SULFATION, ZYMOGEN, HEPARIN-BINDING, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, THROMBOPHILIA 
4oqw:H   (LEU138) to   (ARG220)  CRYSTAL STRUCTURE OF MCARDINAL FAR-RED FLUORESCENT PROTEIN  |   FLUORESCENT PROTEIN 
1xug:A    (GLN30) to    (SER84)  TRYPSIN-BABIM-ZN+2, PH 8.2  |   COMPLEX, TRYPSIN-ZN+2-SMALL MOLECULE LIGAND, DESIGNED SMALL MOLECULE LIGAND WITH NANOMOLAR AFFINITY, SERINE PROTEASE 
2znk:H    (GLN30) to    (MET84)  THROMBIN INHIBITION  |   BLOOD CLOTTING, HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SERINE PROTEASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
2zo6:A   (SER141) to   (ALA212)  CRYSTAL STRUCTURE OF KUSABIRA-CYAN (KCY), A CYAN-EMITTING GFP-LIKE PROTEIN  |   GFP-LIKE PROTEIN, LUMINESCENT PROTEIN, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES 
2zo7:A   (SER142) to   (ALA213)  CRYSTAL STRUCTURE OF A KUSABIRA-CYAN MUTANT (KCY-R1), A CYAN/GREEN- EMITTING GFP-LIKE PROTEIN  |   GFP-LIKE PROTEIN, LUMINESCENT PROTEIN, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES 
1xvm:A    (ILE30) to    (SER83)  TRYPSIN FROM FUSARIUM OXYSPORUM- ROOM TEMPERATURE TO ATOMIC RESOLUTION  |   ATOMIC RESOLUTION, MOBILITY, ROOM TEMPERATURE, HYDROLASE 
1xvo:A    (ILE30) to    (SER83)  TRYPSIN FROM FUSARIUM OXYSPORUM AT PH 6  |   TRYPSIN, ATOMIC RESOLUTION, HYDROLASE 
2zp0:H    (GLN30) to    (ARG84)  HUMAN FACTOR VIIA-TISSUE FACTOR COMPLEXED WITH BENZYLSULFONAMIDE-D- ILE-GLN-P-AMINOBENZAMIDINE  |   SERINE PROTEASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, EGF-LIKE DOMAIN, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, HYDROXYLATION, PROTEASE, ZYMOGEN, LIPOPROTEIN, MEMBRANE, PALMITATE, TRANSMEMBRANE, HYDROLASE-BLOOD CLOTTING COMPLEX 
3khv:A    (PHE30) to    (GLU84)  CRYSTAL STRUCTURES OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR IN COMPLEX WITH 4-(AMINOMETHYL) BENZOIC ACID AND 4- (AMINOMETHYL-PHENYL)-METHANOL  |   PROTEIN-LIGAND COMPLEX, DISULFIDE BOND, FIBRINOLYSIS, HYDROLASE, PLASMINOGEN ACTIVATION, SERINE PROTEASE 
4ab8:A    (GLN30) to    (SER84)  FRAGMENTS BOUND TO BOVINE TRYPSIN FOR THE SAMPL CHALLENGE  |   HYDROLASE, FRAGMENT SCREENING, MODELLING 
4abg:A    (GLN30) to    (SER84)  FRAGMENTS BOUND TO BOVINE TRYPSIN FOR THE SAMPL CHALLENGE  |   HYDROLASE, FRAGMENT SCREENING, MODELLING 
1max:A    (GLN30) to    (SER84)  BETA-TRYPSIN PHOSPHONATE INHIBITED  |   HYDROLASE, SERINE PROTEASE, DIGESTION, PANCREAS, ZYMOGEN, HYDROLASE (SERINE PROTEASE) 
1mbm:A    (GLY13) to    (THR57)  NSP4 PROTEINASE FROM EQUINE ARTERITIS VIRUS  |   SERINE PROTEINASE, CHYMOTRYPSIN-LIKE PROTEINASE, COLLAPSED OXYANION HOLE, TRANSFERASE 
1mbm:A    (GLY91) to   (THR139)  NSP4 PROTEINASE FROM EQUINE ARTERITIS VIRUS  |   SERINE PROTEINASE, CHYMOTRYPSIN-LIKE PROTEINASE, COLLAPSED OXYANION HOLE, TRANSFERASE 
1mbm:B    (GLY13) to    (THR57)  NSP4 PROTEINASE FROM EQUINE ARTERITIS VIRUS  |   SERINE PROTEINASE, CHYMOTRYPSIN-LIKE PROTEINASE, COLLAPSED OXYANION HOLE, TRANSFERASE 
1mbm:C    (GLY13) to    (THR57)  NSP4 PROTEINASE FROM EQUINE ARTERITIS VIRUS  |   SERINE PROTEINASE, CHYMOTRYPSIN-LIKE PROTEINASE, COLLAPSED OXYANION HOLE, TRANSFERASE 
1mbm:D    (GLY13) to    (LEU56)  NSP4 PROTEINASE FROM EQUINE ARTERITIS VIRUS  |   SERINE PROTEINASE, CHYMOTRYPSIN-LIKE PROTEINASE, COLLAPSED OXYANION HOLE, TRANSFERASE 
4afq:A    (TYR14) to    (GLU71)  HUMAN CHYMASE - FYNOMER COMPLEX  |   HYDROLASE-DE NOVO PROTEIN COMPLEX, INHIBITOR, SERINE PROTEASE 
4afs:A    (TYR14) to    (GLU71)  HUMAN CHYMASE - FYNOMER COMPLEX  |   HYDROLASE-DE NOVO PROTEIN COMPLEX, INHIBITOR, SERINE PROTEASE 
3kqd:A    (GLN30) to    (GLU84)  FACTOR XA IN COMPLEX WITH THE INHIBITOR 1-(3-(5-OXO-4,5- DIHYDRO-1H-1, 2,4-TRIAZOL-3-YL)PHENYL)-6-(2'-(PYRROLIDIN-1- YLMETHYL)BIPHENYL-4- YL)-3-(TRIFLUOROMETHYL)-5,6-DIHYDRO- 1H-PYRAZOLO[3,4-C]PYRIDIN-7(4H)- ONE  |   GLYCOPROTEIN, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING, BLOOD COAGULATION, CALCIUM, PROTEASE, SECRETED, EGF-LIKE DOMAIN, GAMMA-CARBOXYGLUTAMIC ACID, HYDROLASE 
1yc0:A   (ALA423) to   (GLY478)  SHORT FORM HGFA WITH FIRST KUNITZ DOMAIN FROM HAI-1  |   HYDROLASE/INHIBITOR, HYDROLASE-INHIBITOR COMPLEX 
1mtn:F    (GLN30) to    (LYS84)  BOVINE ALPHA-CHYMOTRYPSIN:BPTI CRYSTALLIZATION  |   COMPLEX, PROTEASE INHIBITOR, TRYPSIN, HYDROLASE, SERINE, COMPLEX (HYDROLASE/INHIBITOR) COMPLEX 
1mu6:B    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH L-378,622  |   HYDROLASE, BLOOD CLOTTING, HYDROLASE-BLOOD CLOTTING COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, BLOOD CLOTTING,HYDROLASE- INHIBITOR COMPLEX 
1mu8:B    (GLN30) to    (MET84)  THROMBIN-HIRUGEN_L-378,650  |   THROMBIN-HIRUGEN, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1mue:B    (GLN30) to    (MET84)  THROMBIN-HIRUGEN-L405,426  |   ALPHA THROMBIN-HIRUGEN, BLOOD CLOTTING COMPLEX,HYDROLASE INHIBITOR COMPLEX, HYDROLASE INHIBITOR 
1ylc:A    (GLN30) to    (ASN84)  TRYPSIN/BPTI COMPLEX MUTANT  |   TRYPSIN II, PANCREATIC TRYPSIN INHIBITOR, BPTI, HYDROLASE/INHIBITOR COMPLEX 
1ynj:D   (MET351) to   (LYS397)  TAQ RNA POLYMERASE-SORANGICIN COMPLEX  |   TRANSFERASE 
1ype:H    (GLN30) to    (MET84)  THROMBIN INHIBITOR COMPLEX  |   THROMBIN, INHIBITOR COMPLEX, BARREL, 6 STRANDED BETA-SHEET, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX 
1yph:C    (GLN30) to    (LYS84)  HIGH RESOLUTION STRUCTURE OF BOVINE ALPHA-CHYMOTRYPSIN  |   SERINE PROTEASE, HYDROLASE 
1yph:D    (GLN30) to    (LYS84)  HIGH RESOLUTION STRUCTURE OF BOVINE ALPHA-CHYMOTRYPSIN  |   SERINE PROTEASE, HYDROLASE 
1ypo:G   (GLY205) to   (GLU254)  HUMAN OXIDIZED LOW DENSITY LIPOPROTEIN RECEPTOR LOX-1 P3 1 21 SPACE GROUP  |   OXIDIZED LOW DENSITY LIPOPROTEIN RECEPTOR, LOX-1,CTLD, C- TYPE LECTIN LIKE DOMAIN, NK CELL RECEPTOR, IMMUNE SYSTEM 
5dgr:A    (HIS30) to    (ALA85)  CRYSTAL STRUCTURE OF GH9 EXO-BETA-D-GLUCOSAMINIDASE PBPRA0520, GLUCOSAMINE COMPLEX  |   GLYCOSIDE HYDROLASE FAMILY 9, ALPHA-ALPHA-6 BARREL, EXO-D-BETA- GLUCOSAMINIDASE, HYDROLASE 
5dgr:B    (HIS30) to    (ALA85)  CRYSTAL STRUCTURE OF GH9 EXO-BETA-D-GLUCOSAMINIDASE PBPRA0520, GLUCOSAMINE COMPLEX  |   GLYCOSIDE HYDROLASE FAMILY 9, ALPHA-ALPHA-6 BARREL, EXO-D-BETA- GLUCOSAMINIDASE, HYDROLASE 
5dgq:B    (HIS30) to    (ALA85)  CRYSTAL STRUCTURE OF GH9 EXO-BETA-D-GLUCOSAMINIDASE PBPRA0520  |   GLYCOSIDE HYDROLASE FAMILY 9, ALPHA-ALPHA-6 BARREL, EXO-D-BETA- GLUCOSAMINIDASE, HYDROLASE 
3l33:D    (GLN30) to    (ASN84)  HUMAN MESOTRYPSIN COMPLEXED WITH AMYLOID PRECURSOR PROTEIN INHIBITOR(APPI)  |   HUMAN MESOTRYPSIN, ALZHEIMER'S AMYLOID PRECURSOR PROTEIN INHIBITOR, APPI, SERINE PROTEASE INHIBITOR, HYDROLASE-CELL ADHESION COMPLEX 
3l5n:A   (VAL365) to   (VAL427)  STAPHYLOCOCCAL COMPLEMENT INHIBITOR (SCIN) IN COMPLEX WITH HUMAN COMPLEMENT COMPONENT C3B  |   COMPLEMENT ALTERNATE PATHWAY, COMPLEMENT PATHWAY, CONVERSTASE, IMMUNE RESPONSE, INFLAMMATORY RESPONSE, INNATE IMMUNITY, SECRETED, VIRULENCE, IMMUNE EVASION, IMMUNE SYSTEM 
1n6e:A   (ASN145) to   (ARG194)  TRICORN PROTEASE IN COMPLEX WITH A TRIDECAPEPTIDE CHLOROMETHYL KETONE DERIVATIVE  |   TRICORN PROTEASE, HYDROLASE, PROPELLER 
1n6e:C   (ASN145) to   (ARG194)  TRICORN PROTEASE IN COMPLEX WITH A TRIDECAPEPTIDE CHLOROMETHYL KETONE DERIVATIVE  |   TRICORN PROTEASE, HYDROLASE, PROPELLER 
1n6e:E   (ASN145) to   (ARG194)  TRICORN PROTEASE IN COMPLEX WITH A TRIDECAPEPTIDE CHLOROMETHYL KETONE DERIVATIVE  |   TRICORN PROTEASE, HYDROLASE, PROPELLER 
1n6e:G   (ASN145) to   (ARG194)  TRICORN PROTEASE IN COMPLEX WITH A TRIDECAPEPTIDE CHLOROMETHYL KETONE DERIVATIVE  |   TRICORN PROTEASE, HYDROLASE, PROPELLER 
1n6e:K   (ASN145) to   (ARG194)  TRICORN PROTEASE IN COMPLEX WITH A TRIDECAPEPTIDE CHLOROMETHYL KETONE DERIVATIVE  |   TRICORN PROTEASE, HYDROLASE, PROPELLER 
3lc3:A    (GLN30) to    (ASN84)  BENZOTHIOPHENE INHIBITORS OF FACTOR IXA  |   PROTEIN-INHIBITOR COMPLEX, PEPTIDASE S1, BLOOD COAGULATION, CALCIUM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, DISULFIDE BOND, EGF-LIKE DOMAIN, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HEMOPHILIA, HYDROLASE, HYDROXYLATION, PHARMACEUTICAL, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, SECRETED, SERINE PROTEASE, SULFATION, ZYMOGEN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3lc3:C    (GLN30) to    (ASN84)  BENZOTHIOPHENE INHIBITORS OF FACTOR IXA  |   PROTEIN-INHIBITOR COMPLEX, PEPTIDASE S1, BLOOD COAGULATION, CALCIUM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, DISULFIDE BOND, EGF-LIKE DOMAIN, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HEMOPHILIA, HYDROLASE, HYDROXYLATION, PHARMACEUTICAL, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, SECRETED, SERINE PROTEASE, SULFATION, ZYMOGEN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1z7k:A    (GLN30) to    (ASN84)  CRYSTAL STRUCTURE OF TRYPSIN- OVOMUCOID TURKEY EGG WHITE INHIBITOR COMPLEX  |   SERINE PROTEASE, HYDROLASE, PROTEASE INHIBITOR, DI-NAG, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1z9s:A   (GLY180) to   (LYS231)  CRYSTAL STRUCTURE OF THE NATIVE CHAPERONE:SUBUNIT:SUBUNIT CAF1M:CAF1:CAF1 COMPLEX  |   DONOR STRAND COMPLEMENTATION, NATIVE MINIMAL FIBER, CHAPERONE-USHER PATHWAY, CHAPERONE/IMMUNE SYSTEM COMPLEX 
1zgi:A    (GLN30) to    (MET84)  THROMBIN IN COMPLEX WITH AN OXAZOLOPYRIDINE INHIBITOR 21  |   THROMBIN, THROMBIN INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1zgv:A    (GLN30) to    (MET84)  THROMBIN IN COMPLEX WITH AN OXAZOLOPYRIDINE INHIBITOR 2  |   THROMBIN, THROMBIN INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4arx:C   (ASN480) to   (VAL536)  LEPIDOPTERA-SPECIFIC TOXIN CRY1AC FROM BACILLUS THURINGIENSIS SSP. KURSTAKI HD-73  |   TOXIN, MEMBRANE PORE-FORMING TOXIN, INSECTICIDAL PROTEIN LEPIDOPTERAN SPECIFICITY, RECEPTOR BINDING SITE 
4q2k:B    (GLN30) to    (LYS84)  BOVINE ALPHA CHYMOTRYPSIN BOUND TO A CYCLIC PEPTIDE INHIBITOR, 5B  |   CHYMOTRYPSIN, PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4q2k:C    (GLN30) to    (LYS84)  BOVINE ALPHA CHYMOTRYPSIN BOUND TO A CYCLIC PEPTIDE INHIBITOR, 5B  |   CHYMOTRYPSIN, PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
5dzx:B    (ARG35) to    (ASN99)  PROTOCADHERIN BETA 6 EXTRACELLULAR CADHERIN DOMAINS 1-4  |   CADHERIN, DIMER, EXTRACELLULAR, CELL ADHESION 
1zrb:A    (GLN30) to    (MET84)  THROMBIN IN COMPLEX WITH AN AZAFLUORENYL INHIBITOR 23B  |   THROMBIN; THROMBIN INHIBITOR COMPLEX, BLOOD CLOTTING, HYDROLASE- INHIBITOR COMPLEX, BLOOD CLOTTING,HYDROLASE-INHIBITOR COMPLEX 
5e2o:A    (GLN30) to    (HIS91)  FACTOR XIA IN COMPLEX WITH THE INHIBITOR 4-[(N-{(2E)-3-[5-CHLORO-2- (1H-TETRAZOL-1-YL)PHENYL]PROP-2-ENOYL}-L-PHENYLALANYL)AMINO]BENZOIC ACID  |   HYDROLASE, SERINE PROTEASE, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3lt3:B   (LYS206) to   (GLU253)  CRYSTAL STRUCTURE OF RV3671C FROM M. TUBERCULOSIS H37RV, SER343ALA MUTANT, INACTIVE FORM  |   SERINE PROTEASE, H37RV, HTRA, HYDROLASE, PROTEASE 
5e55:A   (ILE630) to   (LYS688)  CRYSTAL STRUCTURE OF MOUSE CNTN6 FN1-FN3 DOMAINS  |   NEURAL CELL ADHESION MOLECULE, FIBRONECTIN TYPE III DOMAINS, CELL ADHESION 
3arr:A    (THR77) to   (SER124)  CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH PENTOXIFYLLINE  |   TIM BARREL, INHIBITOR COMPLEX, GLYCOSIDASE, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3arp:A    (THR77) to   (ALA125)  CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH DEQUALINIUM  |   TIM BARREL, INHIBITOR COMPLEX, GLYCOSIDASE, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3ars:A    (THR77) to   (ALA125)  CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - APO STRUCTURE OF MUTANT W275G  |   TIM BARREL, INHIBITOR COMPLEX, GLYCOSIDASE, HYDROLASE 
3arw:A    (THR77) to   (ALA125)  CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH CHELERYTHRINE  |   TIM BARREL, INHIBITOR COMPLEX, GLYCOSIDASE, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1zyo:A   (LEU152) to   (ASP203)  CRYSTAL STRUCTURE OF THE SERINE PROTEASE DOMAIN OF SESBANIA MOSAIC VIRUS POLYPROTEIN  |   VIRAL SERINE PROTEASE OF TRYPSIN FOLD, BETA-BARREL, GLUTAMYL ENDOPEPTIDASE, HYDROLASE 
3ary:A    (THR77) to   (SER124)  CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH 2-(IMIDAZOLIN-2-YL)-5- ISOTHIOCYANATOBENZOFURAN  |   TIM BARREL, INHIBITOR COMPLEX, GLYCOSIDASE, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3arz:A    (THR77) to   (SER124)  CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH 2-(IMIDAZOLIN-2-YL)-5- ISOTHIOCYANATOBENZOFURAN  |   TIM BARREL, INHIBITOR COMPLEX, GLYCOSIDASE, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3lvt:A   (GLU682) to   (GLU730)  THE CRYSTAL STRUCTURE OF A PROTEIN IN THE GLYCOSYL HYDROLASE FAMILY 38 FROM ENTEROCOCCUS FAECALIS TO 2.55A  |   GLYCOSYL, HYDROLASE, PSI, MCSG, STRUCTURAL GENOMICS, MIDWEST CENTER FOR STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE 
4ayy:B    (GLN15) to    (MET80)  HUMAN THROMBIN - INHIBITOR COMPLEX  |   HYDROLASE-INHIBITOR COMPLEX 
2a0q:D    (GLN30) to    (MET84)  STRUCTURE OF THROMBIN IN 400 MM POTASSIUM CHLORIDE  |   SERINE PROTEASE, HYDROLASE 
2a2x:H    (GLN30) to    (MET84)  ORALLY ACTIVE THROMBIN INHIBITORS IN COMPLEX WITH THROMBIN INH12  |   BLOOD CLOTTING, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2a31:A    (GLN30) to    (ASN84)  TRYPSIN IN COMPLEX WITH BORATE  |   HYDROLASE, TRYPSIN 
2a32:A    (GLN30) to    (ASN84)  TRYPSIN IN COMPLEX WITH BENZENE BORONIC ACID  |   HYDROLASE 
5ec5:E    (LYS21) to   (MET130)  CRYSTAL STRUCTURE OF LYSENIN PORE  |   INVERTEBRATE CYTOLYSIN, NONAMER, FUNCTIONAL PORE, NANOPORE, TOXIN 
5ec5:G    (LYS21) to   (MET130)  CRYSTAL STRUCTURE OF LYSENIN PORE  |   INVERTEBRATE CYTOLYSIN, NONAMER, FUNCTIONAL PORE, NANOPORE, TOXIN 
5ec5:R    (LYS21) to   (MET130)  CRYSTAL STRUCTURE OF LYSENIN PORE  |   INVERTEBRATE CYTOLYSIN, NONAMER, FUNCTIONAL PORE, NANOPORE, TOXIN 
3m6o:A    (LYS78) to   (ARG125)  CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA PEPTIDE DEFORMYLASE 1B (ATPDF1B)  |   PEPTIDE DEFORMYLASE, 1B, PDF, N-TERMINAL EXCISION PATHWAY, NME, ARABIDOPSIS THALIANA, INDUCED-FIT, HYDROLASE, METAL-BINDING, MITOCHONDRION, PROTEIN BIOSYNTHESIS, TRANSIT PEPTIDE 
5eg4:A    (GLN30) to    (SER84)  BOVINE TRYPSIN IN COMPLEX WITH CYCLIC INHIBITOR  |   METAL-BINDING, DIGESTION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASE 
3m9d:J    (PRO98) to   (PHE155)  CRYSTAL STRUCTURE OF THE PROKARYOTIC UBIQUINTIN-LIKE PROTEIN PUP COMPLEXED WITH THE HEXAMERIC PROTEASOMAL ATPASE MPA WHICH INCLUDES THE AMINO TERMINAL COILED COIL DOMAIN AND THE INTER DOMAIN  |   ALPHA HELIX COIL COIL, 5 BETA-STRAND BARREL, ATP-BINDING, CHAPERONE, NUCLEOTIDE-BINDING, PROTEASOME, S-NITROSYLATION, VIRULENCE, ISOPEPTIDE BOND, UBL CONJUGATION PATHWAY 
4b9i:A    (GLY60) to   (VAL146)  STRUCTURE OF CSSA SUBUNIT COMPLEMENTED WITH DONOR STRAND FROM CSSB SUBUNIT OF ENTEROTOXIGENIC ESCHERICHIA COLI COLONIZATION FACTOR CS6  |   CELL ADHESION, DIARRHEAL DISEASE, FIMBRIAE, FUSION PROTEIN 
4b9j:A    (GLY60) to   (SER174)  STRUCTURE OF SELF-COMPLEMENTED CSSA SUBUNIT OF ENTEROTOXIGENIC ESCHERICHIA COLI COLONIZATION FACTOR CS6  |   CELL ADHESION, DIARRHEAL DISEASE, FIMBRIAE, FUSION PROTEIN 
5ejb:D   (VAL390) to   (SER428)  CRYSTAL STRUCTURE OF PREFUSION HENDRA VIRUS F PROTEIN  |   PREFUSION FORM, VIRAL GLYCOPROTEIN, ECTODOMAIN, VIRAL PROTEIN 
3b8s:A    (THR77) to   (ALA125)  CRYSTAL STRUCTURE OF WILD-TYPE CHITINASE A FROM VIBRIO HARVEYI  |   TIM-BARREL, GLYCOSIDASE, HYDROLASE 
3b8s:B    (THR77) to   (ALA125)  CRYSTAL STRUCTURE OF WILD-TYPE CHITINASE A FROM VIBRIO HARVEYI  |   TIM-BARREL, GLYCOSIDASE, HYDROLASE 
3b9a:A    (THR77) to   (SER124)  CRYSTAL STRUCTURE OF VIBRIO HARVEYI CHITINASE A COMPLEXED WITH HEXASACCHARIDE  |   TIM-BARREL, HEXASACCHARIDE COMPLEX, GLYCOSIDASE, HYDROLASE 
3bcu:A   (LEU198) to   (THR240)  GLUCOGEN PHOSPHORYLASE COMPLEX WITH THYMIDINE  |   GLYCOGENOLYSIS, TYPE 2 DIABETES, ACETYLATION, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHORYLATION, PYRIDOXAL PHOSPHATE, TRANSFERASE 
5est:E    (GLN30) to    (GLY84)  CRYSTALLOGRAPHIC ANALYSIS OF THE INHIBITION OF PORCINE PANCREATIC ELASTASE BY A PEPTIDYL BORONIC ACID: STRUCTURE OF A REACTION INTERMEDIATE  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4qt8:B   (GLN608) to   (ARG677)  CRYSTAL STRUCTURE OF RON SEMA-PSI-IPT1 EXTRACELLULAR DOMAINS IN COMPLEX WITH MSP BETA-CHAIN  |   GROWTH FACTOR RECEPTOR/GROWTH FACTOR, RECEPTOR-LIGAND COMPLEX, RON RECEPTOR TYROSINE KINASE, MACROPHAGE STIMULATING PROTEIN, HYDROLASE- SIGNALING PROTEIN COMPLEX 
4qt8:C   (THR495) to   (PRO556)  CRYSTAL STRUCTURE OF RON SEMA-PSI-IPT1 EXTRACELLULAR DOMAINS IN COMPLEX WITH MSP BETA-CHAIN  |   GROWTH FACTOR RECEPTOR/GROWTH FACTOR, RECEPTOR-LIGAND COMPLEX, RON RECEPTOR TYROSINE KINASE, MACROPHAGE STIMULATING PROTEIN, HYDROLASE- SIGNALING PROTEIN COMPLEX 
4qt8:D   (THR495) to   (PRO556)  CRYSTAL STRUCTURE OF RON SEMA-PSI-IPT1 EXTRACELLULAR DOMAINS IN COMPLEX WITH MSP BETA-CHAIN  |   GROWTH FACTOR RECEPTOR/GROWTH FACTOR, RECEPTOR-LIGAND COMPLEX, RON RECEPTOR TYROSINE KINASE, MACROPHAGE STIMULATING PROTEIN, HYDROLASE- SIGNALING PROTEIN COMPLEX 
3ms4:A   (LEU198) to   (THR240)  GLYCOGEN PHOSPHORYLASE COMPLEXED WITH 4-TRIFLUOROMETHYLBENZALDEHYDE-4- (BETA-D-GLUCOPYRANOSYL)-THIOSEMICARBAZONE  |   GLYCOGENOLYSIS, TYPE 2 DIABETES, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3mt9:A   (LEU198) to   (THR240)  GLYCOGEN PHOSPHORYLASE COMPLEXED WITH 4-NITROBENZALDEHYDE-4-(BETA-D- GLUCOPYRANOSYL)-THIOSEMICARBAZONE  |   GLYCOGENOLYSIS, TYPE 2 DIABETES, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3muj:A   (LEU283) to   (CYS327)  EARLY B-CELL FACTOR 3 (EBF3) IPT/TIG AND DIMERIZATION HELICES  |   IMMUNOGLOBULIN LIKE FOLD, HELIX-LOOP-HELIX, STRUCTURAL GENOMICS CONSORTIUM, SGC, DNA BINDING PROTEIN 
3bn9:B    (GLN30) to    (ARG84)  CRYSTAL STRUCTURE OF MT-SP1 IN COMPLEX WITH FAB INHIBITOR E2  |   ANTIBODY-PROTEASE COMPLEX, PROTEIN-PROTEIN COMPLEX, ENZYME- INHIBITOR COMPLEX, DISEASE MUTATION, GLYCOPROTEIN, HYDROLASE, MEMBRANE, POLYMORPHISM, SERINE PROTEASE, SIGNAL- ANCHOR, TRANSMEMBRANE 
3bn9:A    (GLN30) to    (ARG84)  CRYSTAL STRUCTURE OF MT-SP1 IN COMPLEX WITH FAB INHIBITOR E2  |   ANTIBODY-PROTEASE COMPLEX, PROTEIN-PROTEIN COMPLEX, ENZYME- INHIBITOR COMPLEX, DISEASE MUTATION, GLYCOPROTEIN, HYDROLASE, MEMBRANE, POLYMORPHISM, SERINE PROTEASE, SIGNAL- ANCHOR, TRANSMEMBRANE 
4boh:H   (GLN335) to   (MET400)  MADANINS (MEROPS I53) ARE CLEAVED BY THROMBIN AND FACTOR XA  |   HYDROLASE-INHIBITOR COMPLEX, COAGULATION INHIBITOR, PROTEASE, MACROMOLECULAR RECOGNITION 
4bom:A   (GLY205) to   (THR249)  STRUCTURE OF HERPESVIRUS FUSION GLYCOPROTEIN B-BILAYER COMPLEX REVEALING THE PROTEIN-MEMBRANE AND LATERAL PROTEIN-PROTEIN INTERACTION  |   VIRAL PROTEIN, MEMBRANE PROXIMAL REGION, PROTEIN COAT, PSEUDO-ATOMIC VIRUS-HOST INTERACTION 
3bsq:A    (GLN30) to    (SER82)  CRYSTAL STRUCTURE OF HUMAN KALLIKREIN 7 PRODUCED AS A SECRETION PROTEIN IN E.COLI  |   SERINE PROTEASES, KALLIKREINS, LD6, X-RAY CRYSTAL STRUCTURE, GLYCOPROTEIN, HYDROLASE, SECRETED, ZYMOGEN 
4btt:B    (GLN30) to    (GLU84)  FACTOR XA IN COMPLEX WITH THE DUAL THROMBIN-FXA INHIBITOR 31.  |   HYDROLASE, SAR107375, FACTOR XA INHIBITOR, THROMBIN INHIBITOR, CHLOROTHIOPHENE P1 FRAGMENT, S3 SUBSITE, MICROSOMES STABILITY, ORAL ANTITHROMBOTIC, DUAL INHIBITOR, IV ANTITHROMBOTIC 
4btu:B    (GLN30) to    (GLU84)  FACTOR XA IN COMPLEX WITH THE DUAL THROMBIN-FXA INHIBITOR 57.  |   HYDROLASE, SAR107375, FACTOR XA INHIBITOR, THROMBIN INHIBITOR, CHLOROTHIOPHENE P1 FRAGMENT, S3 SUBSITE, MICROSOMES STABILITY, ORAL ANTITHROMBOTIC, DUAL INHIBITOR, IV ANTITHROMBOTIC 
4r0i:A    (GLN30) to    (ARG84)  CRYSTAL STRUCTURE OF MATRIPTASE IN COMPLEX WITH INHIBITOR  |   HYDROLASE, MATRIPTASE, COMPLEX STRUCTURE, TRYPSIN-LIKE SERINE PROTEINASE FOLD, PROTEASE, SMALL MOLECULE INHIBITOR 
5fah:A    (GLN30) to    (LYS84)  KALLIKREIN-7 IN COMPLEX WITH COMPOUND1  |   HYDROLASE 
3c1k:A    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH INHIBITOR 15  |   THROMBIN, THROMBIN INHIBITOR COMPLEX, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
5fcr:A    (MET30) to    (ASP84)  MOUSE COMPLEMENT FACTOR D  |   HYDROLASE 
3c2u:B   (MET196) to   (HIS263)  STRUCTURE OF THE TWO SUBSITE D-XYLOSIDASE FROM SELENOMONAS RUMINANTIUM IN COMPLEX WITH 1,3-BIS[TRIS(HYDROXYMETHYL) METHYLAMINO]PROPANE  |   TETRAMER; GLYCOSIDE HYDROLASE; GH43; ALPHA-L- ARABINOFURANOSIDASE 
4r5l:C   (LEU397) to   (ASP460)  CRYSTAL STRUCTURE OF THE DNAK C-TERMINUS (DNAK-SBD-C)  |   HELICAL BUNDLE, BETA SHEETS, CHAPERONE, MEMBRANE 
3c5m:A   (TYR254) to   (ASP303)  CRYSTAL STRUCTURE OF OLIGOGALACTURONATE LYASE (VPA0088) FROM VIBRIO PARAHAEMOLYTICUS. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET VPR199  |   7 BLADE-SHAPED BETA-PROPELLER, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, LYASE 
3nbn:A    (GLN84) to   (LYS145)  CRYSTAL STRUCTURE OF A DIMER OF NOTCH TRANSCRIPTION COMPLEX TRIMERS ON HES1 DNA  |   PROMOTER REGIONS, NOTCH1, CSL, RBPJ, MASTERMIND, TRANSCRIPTION FACTORS, TRANSCRIPTION, TRANSCRIPTIONAL ACTIVATION, TRANSCRIPTION- DNA COMPLEX 
3nbn:D    (GLN84) to   (LYS145)  CRYSTAL STRUCTURE OF A DIMER OF NOTCH TRANSCRIPTION COMPLEX TRIMERS ON HES1 DNA  |   PROMOTER REGIONS, NOTCH1, CSL, RBPJ, MASTERMIND, TRANSCRIPTION FACTORS, TRANSCRIPTION, TRANSCRIPTIONAL ACTIVATION, TRANSCRIPTION- DNA COMPLEX 
4c91:A   (TYR692) to   (VAL748)  EVIDENCE THAT GH115 ALPHA-GLUCURONIDASE ACTIVITY IS DEPENDENT ON CONFORMATIONAL FLEXIBILITY  |   HYDROLASE, XYLOSE, GLUCURONIC ACID 
4c91:B   (TYR692) to   (VAL748)  EVIDENCE THAT GH115 ALPHA-GLUCURONIDASE ACTIVITY IS DEPENDENT ON CONFORMATIONAL FLEXIBILITY  |   HYDROLASE, XYLOSE, GLUCURONIC ACID 
3nps:A    (GLN30) to    (ARG84)  CRYSTAL STRUCTURE OF MEMBRANE-TYPE SERINE PROTEASE 1 (MT-SP1) IN COMPLEX WITH THE FAB INHIBITOR S4  |   HYDROLASE, ANTIBODY-PROTEASE COMPLEX, PROTEIN-PROTEIN COMPLEX, ENZYME-INHIBITOR COMPLEX, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, SERINE PROTEASE, SIGNAL-ANCHOR, TRANSMEMBRANE, HYDROLASE - IMMUNE SYSTEM COMPLEX, HYDROLASE-IMMUNE SYSTEM COMPLEX 
4rn6:A    (GLN30) to    (MET84)  STRUCTURE OF PRETHROMBIN-2 MUTANT S195A BOUND TO THE ACTIVE SITE INHIBITOR ARGATROBAN  |   SERINE PROTEASE, PRETHROMBIN-2, AUTOACTIVATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3cuv:A   (LEU198) to   (THR240)  TRACKING STRUCTURE ACTIVITY RELATIONSHIPS OF GLYCOGEN PHOSPHORYLASE INHIBITORS: SYNTHESIS, KINETIC AND CRYSTALLOGRAPHIC EVALUATION OF ANALOGUES OF N-(-D- GLUCOPYRANOSYL)-N'-OXAMIDES  |   GLYCOGEN PHOSPHORYLASE, STRUCTURE, CATALYTIC SITE, RATIONAL INHIBITOR DESIGN, ACETYLATION, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PYRIDOXAL PHOSPHATE, TRANSFERASE 
3d12:A   (GLN450) to   (GLY523)  CRYSTAL STRUCTURES OF NIPAH VIRUS G ATTACHMENT GLYCOPROTEIN IN COMPLEX WITH ITS RECEPTOR EPHRIN-B3  |   BETA PROPELLER, PROTEIN-RECEPTOR COMPLEX, ENVELOPE PROTEIN, GLYCOPROTEIN, HEMAGGLUTININ, HYDROLASE, MEMBRANE, SIGNAL-ANCHOR, TRANSMEMBRANE, VIRION, DEVELOPMENTAL PROTEIN, DIFFERENTIATION, NEUROGENESIS, HYDROLASE-MEMBRANE PROTEIN COMPLEX 
4ctn:A   (LEU198) to   (THR240)  GLUCOPYRANOSYLIDENE-SPIRO-IMINOTHIAZOLIDINONE, A NEW BICYCLIC RING SYSTEM: SYNTHESIS, DERIVATIZATION, AND EVALUATION AS GLYCOGEN PHOSPHORYLASE INHIBITORS BY ENZYME KINETIC AND CRYSTALLOGRAPHIC METHODS  |   TRANSFERASE, TYPE 2 DIABETES, INHIBITOR, STRUCTURE-BASED DRUG DESIGN 
3da9:B    (GLN51) to   (MET116)  CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH INHIBITOR  |   THROMBIN, INHIBITOR COMPLEX, ACUTE PHASE, BLOOD COAGULATION, CALCIUM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PHARMACEUTICAL, POLYMORPHISM, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN 
5gch:F    (GLN30) to    (LYS84)  CHEMISTRY OF CAGED ENZYMES /II$. PHOTOACTIVATION OF INHIBITED CHYMOTRYPSIN  |   HYDROLASE (SERINE PROTEINASE) 
3ooc:A   (GLN263) to   (PRO328)  CRYSTAL STRUCTURE OF THE MEMBRANE FUSION PROTEIN CUSB FROM ESCHERICHIA COLI  |   THREE-HELIX BUNDLE, BETA BARREL, COPPER TRANSPORT, ION TRANSPORT, TRANSPORT, TRANSPORT PROTEIN, CUSA,CUSC 
5gxp:A    (GLN30) to    (SER84)  CATIONIC TRYPSIN WITH GOL/PGE AS DIMER AT PH 4.6  |   CATIONIC TRYPSIN, GOL, PGE, HYDROLASE 
4d8n:A    (GLN30) to    (SER84)  HUMAN KALLIKREIN 6 INHIBITORS WITH A PARA-AMIDOBENZYLANMINE P1 GROUP CARRY A HIGH BINDING EFFICIENCY  |   HUMAN KALLIKREIN 6, HK6, SERINE PROTEASE, PROTEIN-LIGAND COMPLEX, AMIDINOTHIOPHENE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3dt0:H    (GLN30) to    (MET84)  UNDERSTANDING THROMBIN INHIBITION  |   BLOOD CLOTTING, HYDROLASE INHIBITOR, ACUTE PHASE, BLOOD COAGULATION, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4u30:C    (GLN30) to    (ASN84)  HUMAN MESOTRYPSIN COMPLEXED WITH BIKUNIN KUNITZ DOMAIN 2  |   SERINE PROTEASE, PROTEASE INHIBITOR, PROTEIN-PROTEIN INTERACTION, PROTEIN DEGRADATION, PROTEOLYSIS, SUBSTRATE SPECIFICITY, ENZYME KINETICS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4u32:A    (GLN30) to    (ASN84)  HUMAN MESOTRYPSIN COMPLEXED WITH HAI-2 KUNITZ DOMAIN 1  |   SERINE PROTEASE, PROTEASE INHIBITOR, PROTEIN-PROTEIN INTERACTION, PROTEIN DEGRADATION, PROTEOLYSIS, SUBSTRATE SPECIFICITY, ENZYME KINETICS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3owr:C    (THR40) to   (PRO120)  CRYSTAL STRUCTURE OF A PUTATIVE SECRETED PROTEIN (BF4250) FROM BACTEROIDES FRAGILIS NCTC 9343 AT 1.81 A RESOLUTION  |   CARBOHYDRATE METABOLISM, PUTATIVE GLYCOSIDE HYDROLASE, IG-LIKE, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, UNKNOWN FUNCTION 
4dii:H    (GLN30) to    (MET84)  X-RAY STRUCTURE OF THE COMPLEX BETWEEN HUMAN ALPHA THROMBIN AND THROMBIN BINDING APTAMER IN THE PRESENCE OF POTASSIUM IONS  |   PROTEIN-DNA COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, APTAMER, HYDROLASE-HYDROLASE INHIBITOR-DNA COMPLEX, SERINE PROTEASE FOLD, DNA APTAMER, BLOOD, G-QUADRUPLEX 
4u5z:A   (MET151) to   (VAL249)  TRICHODYSPLASIA SPINULOSA-ASSOCIATED POLYOMAVIRUS (TSPYV) VP1  |   VIRAL COAT PROTEIN, JELLY-ROLL FOLD, GLYCAN BINDING, VIRAL PROTEIN 
4u5z:G   (GLY150) to   (LEU250)  TRICHODYSPLASIA SPINULOSA-ASSOCIATED POLYOMAVIRUS (TSPYV) VP1  |   VIRAL COAT PROTEIN, JELLY-ROLL FOLD, GLYCAN BINDING, VIRAL PROTEIN 
4u61:A   (GLY150) to   (VAL249)  TRICHODYSPLASIA SPINULOSA-ASSOCIATED POLYOMAVIRUS (TSPYV) VP1 IN COMPLEX WITH 6'-SIALYLLACTOSE  |   VIRAL COAT PROTEIN, JELLY-ROLL FOLD, GLYCAN BINDING, VIRAL PROTEIN 
3e0p:B    (GLN30) to    (THR84)  THE X-RAY STRUCTURE OF HUMAN PROSTASIN IN COMPLEX WITH A COVALENT BENZOXAZOLE INHIBITOR  |   PROSTASIN, PROTEASE, BENZOXAZOLE, WARHEAD, CHANNEL, ENAC, CELL MEMBRANE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, SECRETED, SERINE PROTEASE, TRANSMEMBRANE, ZYMOGEN 
3p6z:B   (GLN378) to   (MET443)  STRUCTURAL BASIS OF THROMBIN MEDIATED FACTOR V ACTIVATION: ESSENTIAL ROLE OF THE HIRUDIN-LIKE SEQUENCE GLU666-GLU672 FOR PROCESSING AT THE HEAVY CHAIN-B DOMAIN JUNCTION  |   TRYPSIN-LIKE SERINE PROTEINASE, BLOOD COAGULATION, N-GLYCOSYLATION, BLOOD PLASMA, PPACK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3e1f:3   (LEU651) to   (ARG721)  E.COLI (LACZ) BETA-GALACTOSIDASE (H418E) IN COMPLEX WITH GALACTOSE  |   HIS-418-GLU BETA-GALACTOSIDASE HYDROLASE TIM BARREL (ALPHA/BETA BARREL) JELLY-ROLL BARREL IMMUNOGLOBULIN BETA SUPERSANDWICH, GLYCOSIDASE, HYDROLASE 
3e1f:4   (LEU651) to   (ARG721)  E.COLI (LACZ) BETA-GALACTOSIDASE (H418E) IN COMPLEX WITH GALACTOSE  |   HIS-418-GLU BETA-GALACTOSIDASE HYDROLASE TIM BARREL (ALPHA/BETA BARREL) JELLY-ROLL BARREL IMMUNOGLOBULIN BETA SUPERSANDWICH, GLYCOSIDASE, HYDROLASE 
5hoo:A   (LYS158) to   (LYS209)  CRYSTAL STRUCTURE OF THE MOS1 STRAND TRANSFER COMPLEX  |   PROTEIN-DNA COMPLEX, DNA TRANSPOSASE, RECOMBINASE, INTEGRASE, HELIX- TURN-HELIX, BASE FLIPPING, DNA 
3e3l:C   (LEU198) to   (THR240)  THE R-STATE GLYCOGEN PHOSPHORYLASE  |   GLYCOGENOLYSIS, INHIBITION, TYPE 2 DIABETES, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PYRIDOXAL PHOSPHATE, TRANSFERASE 
3pa1:A   (GLY332) to   (PHE434)  CRYSTAL STRUCTURE OF P DOMAIN FROM NORWALK VIRUS STRAIN VIETNAM 026 IN COMPLEX WITH HBGA TYPE A  |   NOROVIRUS, P-DOMAIN, CAPSID, RECEPTOR, HISTO BLOOD GROUP ANTIGEN (HBGA), VIRAL PROTEIN 
3e3o:C   (LEU198) to   (THR240)  GLYCOGEN PHOSPHORYLASE R STATE-IMP COMPLEX  |   GLYCOGENOLYSIS, INHIBITION, TYPE 2 DIABETES, ALLOSTERIC ENZYME, CARBOHYDRATE METABOLISM, GLYCOGEN METABOLISM, GLYCOSYLTRANSFERASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, PYRIDOXAL PHOSPHATE, TRANSFERASE 
4dt7:D    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THROMBIN BOUND TO THE ACTIVATION DOMAIN QEDQVDPRLIDGKMTRRGDS OF PROTEIN C  |   SERINE PROTEASE, HYDROLASE 
5hza:B   (GLY332) to   (PHE434)  CRYSTAL STRUCTURE OF GII.10 P DOMAIN IN COMPLEX WITH 3-FUCOSYLLACTOSE (3 FL)  |   NOROVIRUS, P DOMAIN, HMO, 3-FUCOSYLLACTOSE, HUMAN MILK, VIRUS, VIRAL PROTEIN 
5hzb:B   (GLY332) to   (PHE434)  CRYSTAL STRUCTURE OF GII.10 P DOMAIN IN COMPLEX WITH 2-FUCOSYLLACTOSE (2'FL)  |   NOROVIRUS CAPSID, P DOMAIN, HMO, HUMAN MILK, 2-FUCOSYLLACTOSE, VIRUS, VIRAL PROTEIN 
4uff:H    (GLN30) to    (MET84)  THROMBIN IN COMPLEX WITH (2R)-2-(BENZYLSULFONYLAMINO)-N-(2-( (4-CARBAMIMIDOYLPHENYL)METHYLAMINO)-2-OXO-ETHYL)-N-METHYL- 3-PHENYL-PROPANAMIDE  |   HYDROLASE, HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, PREORGANIZATION, GLYCOSYLATION, BLOOD 
4ufg:H    (GLN30) to    (MET84)  THROMBIN IN COMPLEX WITH (2R)-2-(BENZYLSULFONYLAMINO)-N-(( 1S)-2-((4-CARBAMIMIDOYLPHENYL)METHYLAMINO)-1-METHYL-2-OXO- ETHYL)-N-METHYL-3-PHENYL-PROPANAMIDE ETHANE  |   HYDROLASE, HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, PREORGANIZATION, GLYCOSYLATION, BLOOD 
4dur:A   (GLN576) to   (GLU634)  THE X-RAY CRYSTAL STRUCTURE OF FULL-LENGTH TYPE II HUMAN PLASMINOGEN  |   SERINE PROTEASE, FIBRINOLYSIS, HYDROLASE 
5i46:H    (GLN30) to    (ARG84)  FACTOR VIIA IN COMPLEX WITH THE INHIBITOR (2R,15R)-2-[(1- AMINOISOQUINOLIN-6-YL)AMINO]-8-FLUORO-7-HYDROXY-4,15,17-TRIMETHYL-13- OXA-4,11-DIAZATRICYCLO[14.2.2.1~6,10~]HENICOSA-1(18),6(21),7,9,16,19- HEXAENE-3,12-DIONE  |   GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3pj5:B   (LEU138) to   (ALA219)  CRYSTAL STRUCTURE OF FAR-RED FLUORESCENT PROTEIN KATUSHKA CRYSTALLIZED AT PH 5.0  |   KATUSHKA, FAR-RED FLUORESCENT PROTEIN, BETA-BARREL, BIOMARKER, MUTANT VARIANT OF EQFP578, MET-TYR-GLY CHROMOPHORE, FLUORESCENT PROTEIN 
3pjb:A   (LEU138) to   (ALA219)  CRYSTAL STRUCTURE OF RED FLUORESCENT PROTEIN EQFP578 CRYSTALLIZED AT PH 4.0  |   EQFP578, RED FLUORESCENT PROTEIN, BETA-BARREL, BIOMARKER, MET-TYR-GLY CHROMOPHORE, FLUORESCENT PROTEIN 
3pjb:B   (LEU138) to   (ALA219)  CRYSTAL STRUCTURE OF RED FLUORESCENT PROTEIN EQFP578 CRYSTALLIZED AT PH 4.0  |   EQFP578, RED FLUORESCENT PROTEIN, BETA-BARREL, BIOMARKER, MET-TYR-GLY CHROMOPHORE, FLUORESCENT PROTEIN 
3pma:B    (GLN30) to    (SER83)  2.2 ANGSTROM CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN BOVINE THROMBIN AND SUCROSE OCTASULFATE  |   PROTEASE, THROMBOSIS, FIBRINOLYSIS, AGONIST, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4e7n:A    (LEU30) to    (VAL84)  CRYSTAL STRUCTURE OF AHV_TL-I, A GLYCOSYLATED SNAKE-VENOM THROMBIN- LIKE ENZYME FROM AGKISTRODON HALYS  |   BETA-BARREL, HYDROLASE, ARGININE ESTERASE, GLYCOSYLATION, EXTRACELLULAR 
4e7r:H    (GLN30) to    (MET84)  THROMBIN IN COMPLEX WITH 3-AMIDINOPHENYLALANINE INHIBITOR  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, KRINGLE, HYDROLASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, GLYCOSYLATION, BLOOD 
4e7r:G  (GLN1030) to  (MET1084)  THROMBIN IN COMPLEX WITH 3-AMIDINOPHENYLALANINE INHIBITOR  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SERINE PROTEASE, KRINGLE, HYDROLASE, BLOOD COAGULATION, BLOOD CLOTTING, CONVERTION OF FIBRINOGEN TO FIBRIN, BLOOD CLOTTING INHIBITOR, THROMBIN INHIBITOR, GLYCOSYLATION, BLOOD 
4edo:A   (LEU138) to   (ALA219)  CRYSTAL STRUCTURE OF FAR-RED FLUORESCENT PROTEIN EQFP650  |   BETA BARREL, FLUORESCENT PROTEIN 
4eds:A   (LEU138) to   (ALA219)  CRYSTAL STRUCTURE OF FAR-RED FLUORESCENT PROTEIN EQFP670  |   BETA BARREL, FLUORESCENT PROTEIN 
4eke:A   (LEU198) to   (THR240)  CRYSTAL STRUCTURE OF GPB IN COMPLEX WITH DK11  |   ALPHA/BETA PROTEIN, TRANSFERASE 
4eky:A   (LEU198) to   (THR240)  CRYSTAL STRUCTURE OF GPB IN COMPLEX WITH DK15  |   ALPHA/BETA PROTEIN, TRANSFERASE 
3q39:A   (GLY332) to   (PHE434)  CRYSTAL STRUCTURE OF P DOMAIN FROM NORWALK VIRUS STRAIN VIETNAM 026 IN COMPLEX WITH HBGA TYPE H2 (DIGLYCAN)  |   NOROVIRUS, P-DOMAIN, CAPSID, RECEPTOR, HISTO BLOOD GROUP ANTIGEN (HBGA), VIRAL PROTEIN 
3q6r:A   (GLY332) to   (PHE434)  CRYSTAL STRUCTURE OF P DOMAIN FROM NORWALK VIRUS STRAIN VIETNAM 026 IN COMPLEX WITH DISORDERED HBGA TYPE LEX  |   NOROVIRUS, P-DOMAIN, CAPSID, RECEPTOR, HISTO BLOOD GROUP ANTIGEN (HBGA), VIRAL PROTEIN 
4est:E    (GLN30) to    (GLY84)  CRYSTAL STRUCTURE OF THE COVALENT COMPLEX FORMED BY A PEPTIDYL ALPHA, ALPHA-DIFLUORO-BETA-KETO AMIDE WITH PORCINE PANCREATIC ELASTASE AT 1.78-ANGSTROMS RESOLUTION  |   SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3qum:P    (GLN30) to    (GLN84)  CRYSTAL STRUCTURE OF HUMAN PROSTATE SPECIFIC ANTIGEN (PSA) IN FAB SANDWICH WITH A HIGH AFFINITY AND A PCA SELECTIVE ANTIBODY  |   KALLIKREIN FOLD, PROSTATE-SPECIFIC ANTIGEN, SERINE PROTEASE, NEGATIVE REGULATION OF ANGIOGENESIS, NATURAL POST-TRANSDUCTIONAL MODIFICATION, N-LINKED AND O-LINKED GLYCOSYLATION, IMMUNE SYSTEM 
3qum:Q    (GLN30) to    (GLN84)  CRYSTAL STRUCTURE OF HUMAN PROSTATE SPECIFIC ANTIGEN (PSA) IN FAB SANDWICH WITH A HIGH AFFINITY AND A PCA SELECTIVE ANTIBODY  |   KALLIKREIN FOLD, PROSTATE-SPECIFIC ANTIGEN, SERINE PROTEASE, NEGATIVE REGULATION OF ANGIOGENESIS, NATURAL POST-TRANSDUCTIONAL MODIFICATION, N-LINKED AND O-LINKED GLYCOSYLATION, IMMUNE SYSTEM 
5jb8:S    (GLN30) to    (ASN84)  CRYSTAL STRUCTURE OF FACTOR IXA VARIANT K98T IN COMPLEX WITH EGR- CHLOROMETHYLKETONE  |   BLOOD CLOTTING, HYDROLASE, GLYCOPROTEIN, HAEMOSTASIS 
5jba:S    (GLN30) to    (ASN84)  CRYSTAL STRUCTURE OF FACTOR IXA VARIANT V16I K98T Y177T I212V IN COMPLEX WITH PPACK  |   BLOOD CLOTTING, HYDROLASE, GLYCOPROTEIN, HAEMOSTASIS 
5jbb:S    (VAL31) to    (ASN84)  CRYSTAL STRUCTURE OF FACTOR IXA VARIANT V16I K98T Y177T I213V IN COMPLEX WITH EGR-CHLOROMETHYLKETONE  |   BLOOD CLOTTING, HYDROLASE, GLYCOPROTEIN, HAEMOSTASIS 
5jbc:S    (GLN30) to    (ASN84)  CRYSTAL STRUCTURE OF FACTOR IXA VARIANT V16I K98T Y177T I213V IN COMPLEX WITH PPACK  |   CRYSTAL STRUCTURE OF FACTOR IXA VARIANT K98T IN COMPLEX WITH EGR- CHLOROMETHYLKETONE, HYDROLASE 
5jbt:A    (GLN30) to    (ASN84)  MESOTRYPSIN IN COMPLEX WITH CLEAVED AMYLOID PRECURSOR LIKE PROTEIN 2 INHIBITOR (APLP2)  |   INHIBITOR PROTEASE SERINE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3rgb:I   (LYS120) to   (ASP179)  CRYSTAL STRUCTURE OF PARTICULATE METHANE MONOOXYGENASE FROM METHYLOCOCCUS CAPSULATUS (BATH)  |   MEMBRANE, OXIDOREDUCTASE 
4fs9:B   (ALA289) to   (ASN337)  COMPLEX STRUCTURE OF A BROAD SPECIFICITY AMINO ACID RACEMASE (BAR) WITHIN THE REACTIVE INTERMEDIATE  |   ISOMERASE, PLP BINDING, RACEMIZATION 
4gaw:H    (MET30) to    (PRO85)  CRYSTAL STRUCTURE OF ACTIVE HUMAN GRANZYME H  |   SERINE PROTEASE, CYTOLYSIS, HYDROLASE, CYTOTOXIC GRANULES 
4gaw:J    (TYR29) to    (PRO85)  CRYSTAL STRUCTURE OF ACTIVE HUMAN GRANZYME H  |   SERINE PROTEASE, CYTOLYSIS, HYDROLASE, CYTOTOXIC GRANULES 
4gch:F    (GLN30) to    (LYS84)  STRUCTURE AND ACTIVITY OF TWO PHOTOREVERSIBLE CINNAMATES BOUND TO CHYMOTRYPSIN  |   HYDROLASE (SERINE PROTEINASE) 
5l56:A  (ASN1185) to  (SER1227)  PLEXIN A1 FULL EXTRACELLULAR REGION, DOMAINS 1 TO 10, TO 4 ANGSTROM  |   RECEPTOR, SIGNALING, AXON GUIDANCE, SIGNALING PROTEIN 
5l59:A  (ASN1185) to  (SER1227)  PLEXIN A1 FULL EXTRACELLULAR REGION, DOMAINS 1 TO 10, TO 6 ANGSTROM, SPACEGROUP P2(1)  |   RECEPTOR, SIGNALING, AXON GUIDANCE, SIGNALING PROTEIN 
5l59:B  (ASN1185) to  (SER1227)  PLEXIN A1 FULL EXTRACELLULAR REGION, DOMAINS 1 TO 10, TO 6 ANGSTROM, SPACEGROUP P2(1)  |   RECEPTOR, SIGNALING, AXON GUIDANCE, SIGNALING PROTEIN 
5l5c:A  (ASN1185) to  (SER1227)  PLEXIN A1 FULL EXTRACELLULAR REGION, DOMAINS 1 TO 10, TO 6 ANGSTROM, SPACEGROUP P4(3)2(1)2  |   RECEPTOR, SIGNALING, AXON GUIDANCE, SIGNALING PROTEIN 
5la2:B   (TYR390) to   (ILE452)  THE MECHANISM BY WHICH ARABINOXYLANASES CAN RECOGNISE HIGHLY DECORATED XYLANS  |   ARABINOXYLANASE, GLYCOSIDE HYDROLASE, CARBOHYDRATE BINDING MODULE, ARABINOSE, CLOSTRIDIUM THERMOCELLUM, CELLULOSOME, HYDROLASE 
5lpe:B    (GLN30) to    (ARG84)  KALLIKREIN-RELATED PEPTIDASE 10 COMPLEX WITH ZN2+  |   SERINE PROTEASE, ZYMOGEN-LIKE ENZYME, ZN2+ INHIBITION, TUMOR SUPPRESSOR, HYDROLASE 
5lpf:A    (GLN30) to    (ARG84)  KALLIKREIN-RELATED PEPTIDASE 10  |   SERINE PROTEASE, ZYMOGEN-LIKE ENZYME, ZN2+ INHIBITION, TUMOR SUPPRESSOR, HYDROLASE 
5lpf:B    (GLN30) to    (ARG84)  KALLIKREIN-RELATED PEPTIDASE 10  |   SERINE PROTEASE, ZYMOGEN-LIKE ENZYME, ZN2+ INHIBITION, TUMOR SUPPRESSOR, HYDROLASE 
6cha:B    (GLN30) to    (LYS84)  STRUCTURE OF A TETRAHEDRAL TRANSITION STATE COMPLEX OF ALPHA-*CHYMOTRYPSIN AT 1.8-*ANGSTROMS RESOLUTION  |   HYDROLASE (SERINE PROTEINASE) 
6cha:F    (GLN30) to    (LYS84)  STRUCTURE OF A TETRAHEDRAL TRANSITION STATE COMPLEX OF ALPHA-*CHYMOTRYPSIN AT 1.8-*ANGSTROMS RESOLUTION  |   HYDROLASE (SERINE PROTEINASE) 
7kme:H    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN INHIBITED WITH SEL2711.  |   SELECTIDE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
8gch:F    (GLN30) to    (LYS84)  GAMMA-CHYMOTRYPSIN IS A COMPLEX OF ALPHA-CHYMOTRYPSIN WITH ITS OWN AUTOLYSIS PRODUCTS  |   HYDROLASE, SERINE PROTEINASE, HYDROLASE-PEPTIDE COMPLEX 
8gpb:A   (LEU198) to   (THR240)  STRUCTURAL MECHANISM FOR GLYCOGEN PHOSPHORYLASE CONTROL BY PHOSPHORYLATION AND AMP  |   GLYCOGEN PHOSPHORYLASE 
8kme:2    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN INHIBITED WITH SEL2770.  |   THROMBIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SELECTIDE 
1a0h:B   (GLN335) to   (MET400)  THE X-RAY CRYSTAL STRUCTURE OF PPACK-MEIZOTHROMBIN DESF1: KRINGLE/THROMBIN AND CARBOHYDRATE/KRINGLE/THROMBIN INTERACTIONS AND LOCATION OF THE LINKER CHAIN  |   SERINE PROTEASE, COAGULATION, THROMBIN, PROTHROMBIN, MEIZOTHROMBIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1a0h:E   (GLN335) to   (MET400)  THE X-RAY CRYSTAL STRUCTURE OF PPACK-MEIZOTHROMBIN DESF1: KRINGLE/THROMBIN AND CARBOHYDRATE/KRINGLE/THROMBIN INTERACTIONS AND LOCATION OF THE LINKER CHAIN  |   SERINE PROTEASE, COAGULATION, THROMBIN, PROTHROMBIN, MEIZOTHROMBIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3edx:B    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THE W215A/E217A MUTANT OF MURINE THROMBIN  |   SERINE PROTEASE, ACUTE PHASE, BLOOD COAGULATION, CLEAVAGE ON PAIR OF BASIC RESIDUES, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HYDROLASE, KRINGLE, PROTEASE, ZYMOGEN 
1ae8:H    (GLN30) to    (MET84)  HUMAN ALPHA-THROMBIN INHIBITION BY EOC-D-PHE-PRO-AZALYS-ONP  |   COMPLEX (SERINE PROTEASE-INHIBITOR), BLOOD COAGULATION, N- ETHOXYCARBONYL-D-PHE-PRO-ALFA-AZALYS-P-NITROPHENYLESTER, SERINE PROTEINASE INHIBITION, GLYCOSYLATED PROTEIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2oua:A    (LEU33) to    (VAL87)  CRYSTAL STRUCTURE OF NOCARDIOPSIS PROTEASE (NAPASE)  |   SERINE PROTEASE; KINETIC STABILITY; ACID STABILITY; ELECTROSTATICS, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1ny2:2    (GLN30) to    (MET84)  HUMAN ALPHA THROMBIN INHIBITED BY RPPGF AND HIRUGEN  |   THROMBOSIS, RETRO BINDING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1bjv:A    (GLN30) to    (SER84)  BETA-TRYPSIN COMPLEXED WITH APPU  |   HYDROLASE, SERINE PROTEASE, DIGESTION, PANCREAS, ZYMOGEN 
1o2o:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2p:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2r:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o2x:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o36:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o38:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3b:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3h:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1o3o:A    (GLN30) to    (SER84)  ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS  |   SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE 
1bs5:B   (GLU579) to   (GLY624)  PEPTIDE DEFORMYLASE AS ZN2+ CONTAINING FORM  |   HYDROLASE, IRON METALLOPROTEASE; PROTEIN SYNTHESIS 
2bvx:H    (GLN30) to    (MET84)  DESIGN AND DISCOVERY OF NOVEL, POTENT THROMBIN INHIBITORS WITH A SOLUBILIZING CATIONIC P1-P2-LINKER  |   SERINE PROTEINASE, COAGULATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c1p:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c1t:A    (GLN30) to    (SER84)  RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES  |   ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS, PH DEPENDENCE, ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN, SERINE PROTEASE/INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1c5p:A    (GLN30) to    (SER84)  STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1- BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR  |   SELECTIVE, S1 SITE INHIBITOR, STRUCTURE-BASED DRUG DESIGN, UROKINASE, TRYPSIN, THROMBIN, HYDROLASE 
1c5r:A    (GLN30) to    (SER84)  STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1- BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR  |   SELECTIVE, S1 SITE INHIBITOR, STRUCTURE-BASED DRUG DESIGN, UROKINASE, TRYPSIN, THROMBIN, HYDROLASE 
1c5u:A    (GLN30) to    (SER84)  STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB- MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR  |   SELECTIVE, S1 SITE INHIBITOR, STRUCTURE-BASED DRUG DESIGN, UROKINASE, TRYPSIN, THROMBIN, HYDROLASE 
2pr3:A    (GLN30) to    (GLU84)  FACTOR XA INHIBITOR  |   FXA COAGULATION FACTOR INHIBITOR, BLOOD CLOTTING 
1cbw:B    (GLN30) to    (LYS84)  BOVINE CHYMOTRYPSIN COMPLEXED TO BPTI  |   SERINE PROTEASE, INHIBITOR, PROTEASE-SUBSTRATE INTERACTIONS, COMPLEX (SERINE PROTEASE/INHIBITOR) 
1os8:A    (PHE29) to    (ARG84)  RECOMBINANT STREPTOMYCES GRISEUS TRYPSIN  |   TRYPSIN, SERINE PROTEASE, HYDROLASE 
1pjp:A    (TYR29) to    (GLU84)  THE 2.2 A CRYSTAL STRUCTURE OF HUMAN CHYMASE IN COMPLEX WITH SUCCINYL- ALA-ALA-PRO-PHE-CHLOROMETHYLKETONE  |   HUMAN CHYMASE, SERINE PROTEINASE, DIPEPTIDYL CARBOXYPEPTIDASE, ANGIOTENSIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4iw4:F   (LEU447) to   (ALA518)  CRYSTAL STRUCTURE OF THE SERINE PROTEASE DOMAIN OF MASP-3 IN COMPLEX WITH ECOTIN  |   TRYPSIN-LIKE FOLD, PROTEASE, INHIBITOR, EXTRACELLULAR, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1pq8:A    (ILE30) to    (SER83)  TRYPSIN AT PH 4 AT ATOMIC RESOLUTION  |   TRYPSIN, ATOMIC RESOLUTION, CATALYSIS, HYDROLASE 
2r9p:A    (GLN30) to    (ASN84)  HUMAN MESOTRYPSIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR(BPTI)  |   HUMAN MESOTRYPSIN, SERINE PROTEASE, BOVINE PANCREATIC TRYPSIN INHIBITOR, BPTI, ALTERNATIVE SPLICING, CALCIUM, DIGESTION, HYDROLASE, METAL-BINDING, SECRETED, SULFATION, ZYMOGEN, PHARMACEUTICAL, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
2r9p:C    (GLN30) to    (ASN84)  HUMAN MESOTRYPSIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR(BPTI)  |   HUMAN MESOTRYPSIN, SERINE PROTEASE, BOVINE PANCREATIC TRYPSIN INHIBITOR, BPTI, ALTERNATIVE SPLICING, CALCIUM, DIGESTION, HYDROLASE, METAL-BINDING, SECRETED, SULFATION, ZYMOGEN, PHARMACEUTICAL, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
2r9p:D    (GLN30) to    (ASN84)  HUMAN MESOTRYPSIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR(BPTI)  |   HUMAN MESOTRYPSIN, SERINE PROTEASE, BOVINE PANCREATIC TRYPSIN INHIBITOR, BPTI, ALTERNATIVE SPLICING, CALCIUM, DIGESTION, HYDROLASE, METAL-BINDING, SECRETED, SULFATION, ZYMOGEN, PHARMACEUTICAL, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
1elb:A    (GLN30) to    (GLY88)  ANALOGOUS INHIBITORS OF ELASTASE DO NOT ALWAYS BIND ANALOGOUSLY  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, SERINE PROTEINASE 
1qj1:B    (GLN30) to    (MET84)  NOVEL COVALENT ACTIVE SITE THROMBIN INHIBITORS  |   BLOOD COAGULATION-INHIBITOR, PROTEINASE, TRYPSIN LIKE PROTEINASE, PROTEASE-INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2snw:B   (PHE188) to   (GLY232)  SINDBIS VIRUS CAPSID PROTEIN, TYPE3 CRYSTAL FORM  |   SINDBIS, VIRUS, PROTEINASE, ALPHAVIRUS, CAPSID, CHYMOTRYPSIN, VIRUS COAT PROTEIN, VIRAL PROTEIN 
4k2y:A    (TYR29) to    (GLU84)  CRYSTAL STRUCTURE OF HUMAN CHYMASE IN COMPLEX WITH FRAGMENT INHIBITOR 6-CHLORO-1,3-DIHYDRO-2H-INDOL-2-ONE  |   SERINE PROTEASE, GLYCOSYLATED, MAST CELLS, SECRETED, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3uir:B   (GLN576) to   (GLU634)  CRYSTAL STRUCTURE OF THE PLASMIN-TEXTILININ-1 COMPLEX  |   SERINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1rjx:B   (GLN576) to   (GLU634)  HUMAN PLASMINOGEN CATALYTIC DOMAIN, K698M MUTANT  |   MICROPLASMINOGEN, PLASMINOGEN ACTIVATION, STREPTOKINASE, HYDROLASE 
1fy8:E    (GLN30) to    (ASN84)  CRYSTAL STRUCTURE OF THE DELTAILE16VAL17 RAT ANIONIC TRYPSINOGEN-BPTI COMPLEX  |   PROTEIN-PROTEIN COMPLEX, PROTEASE-INHIBITOR COMPLEX, BETA BARREL, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
3utu:H    (GLN30) to    (MET84)  HIGH AFFINITY INHIBITOR OF HUMAN THROMBIN  |   SERINE PROTEASE, BLOOD CLOTTING, FIBRINOPEPTIDE A, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3uwa:A    (ASN75) to   (LYS123)  CRYSTAL STRUCTURE OF A PROBABLE PEPTIDE DEFORMYLASE FROM SYNECHOCOCCUS PHAGE S-SSM7  |   SYNECHOCOCCUS PHAGE, PROBABLE PEPTIDE DEFORMYLASE, HYDROLASE 
4zae:A    (TRP29) to    (ASN84)  DEVELOPMENT OF A NOVEL CLASS OF POTENT AND SELECTIVE FIXA INHIBITORS  |   SERINE PROTEINASE, BLOOD COAGULATION, COAGULATION FACTOR, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1ghz:A    (GLN30) to    (SER84)  A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI- CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE  |   THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, HYDROLASE 
1gi0:A    (GLN30) to    (SER84)  A NOVEL SERINE PROTEASE INHIBITION MOTIF INVOLVING A MULTI-CENTERED SHORT HYDROGEN BONDING NETWORK AT THE ACTIVE SITE  |   THREE-CENTERED, VERY SHORT HYDROGEN BOND, OXYANION HOLE WATER, SHIFT OF PKA OF HIS57, STRUCTURE-BASED DRUG DESIGN, SPECIFICITY, UROKINASE, TRYPSIN, THROMBIN, ZN+2-MEDIATED INHIBITION, HYDROLASE 
1gmc:F    (GLN30) to    (LYS84)  THE X-RAY CRYSTAL STRUCTURE OF THE TETRAHEDRAL INTERMEDIATE OF GAMMA- CHYMOTRYPSIN IN HEXANE  |   HYDROLASE, SERINE PROTEASE 
1sg8:E    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THE PROCOAGULANT FAST FORM OF THROMBIN  |   THROMBIN, ALLOSTERY, HYDROLASE 
2vnt:A    (PHE24) to    (GLU86)  UROKINASE-TYPE PLASMINOGEN ACTIVATOR INHIBITOR COMPLEX WITH A 1-(7-SULPHOAMIDOISOQUINOLINYL)GUANIDINE  |   UPA, INHIBITOR COMPLEX, HYDROLASE 
2vnt:F    (PHE24) to    (GLU86)  UROKINASE-TYPE PLASMINOGEN ACTIVATOR INHIBITOR COMPLEX WITH A 1-(7-SULPHOAMIDOISOQUINOLINYL)GUANIDINE  |   UPA, INHIBITOR COMPLEX, HYDROLASE 
3vd5:B   (LEU651) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (N460S)  |   TRANSITION STATE STABILIZATION, SUBSTRATE BINDING, 2-STAGE BINDING, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN, BETA SUPERSANDWICH, GLYCOSIDASE, HYDROLASE 
3vd7:A   (LEU651) to   (ALA716)  E. COLI (LACZ) BETA-GALACTOSIDASE (N460S) IN COMPLEX WITH GALACTOTETRAZOLE  |   TRANSITION STATE STABILIZATION, SUBSTRATE BINDING, 2-STAGE BINDING, TIM BARREL (ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN, BETA SUPERSANDWICH, GLYCOSIDASE, HYDROLASE 
1gvz:A    (GLN30) to    (GLN84)  PROSTATE SPECIFIC ANTIGEN (PSA) FROM STALLION SEMINAL PLASMA  |   ANTIGEN, PROSTATE SPECIFIC ANTIGEN, HYDROLASE 
1h1b:A    (MET30) to    (ALA84)  CRYSTAL STRUCTURE OF HUMAN NEUTROPHIL ELASTASE COMPLEXED WITH AN INHIBITOR (GW475151)  |   HYDROLASE, SERINE PROTEASE, 
1h1b:B    (MET30) to    (ALA84)  CRYSTAL STRUCTURE OF HUMAN NEUTROPHIL ELASTASE COMPLEXED WITH AN INHIBITOR (GW475151)  |   HYDROLASE, SERINE PROTEASE, 
1t31:A    (TYR29) to    (GLU84)  A DUAL INHIBITOR OF THE LEUKOCYTE PROTEASES CATHEPSIN G AND CHYMASE WITH THERAPEUTIC EFFICACY IN ANIMALS MODELS OF INFLAMMATION  |   HUMAN CHYMASE, SERINE PROTEINASE, HYDROLASE 
1tgt:A    (GLN30) to    (SER84)  ON THE DISORDERED ACTIVATION DOMAIN IN TRYPSINOGEN. CHEMICAL LABELLING AND LOW-TEMPERATURE CRYSTALLOGRAPHY  |   HYDROLASE ZYMOGEN (SERINE PROTEINASE) 
1toc:B    (GLN30) to    (MET84)  STRUCTURE OF SERINE PROTEINASE  |   VITAMIN K, ZYMOGEN, GAMMA-CARBOXYGLUTAMIC ACID, ACUTE PHASE, LIVER, HYDROLASE, SERINE PROTEASE KUNITZ-LIKE INHIBITOR, KRINGLE, SIGNAL, COMPLEX (HYDROLASE/INHIBITOR) COMPLEX 
1toc:D    (GLN30) to    (MET84)  STRUCTURE OF SERINE PROTEINASE  |   VITAMIN K, ZYMOGEN, GAMMA-CARBOXYGLUTAMIC ACID, ACUTE PHASE, LIVER, HYDROLASE, SERINE PROTEASE KUNITZ-LIKE INHIBITOR, KRINGLE, SIGNAL, COMPLEX (HYDROLASE/INHIBITOR) COMPLEX 
1toc:F    (GLN30) to    (MET84)  STRUCTURE OF SERINE PROTEINASE  |   VITAMIN K, ZYMOGEN, GAMMA-CARBOXYGLUTAMIC ACID, ACUTE PHASE, LIVER, HYDROLASE, SERINE PROTEASE KUNITZ-LIKE INHIBITOR, KRINGLE, SIGNAL, COMPLEX (HYDROLASE/INHIBITOR) COMPLEX 
1toc:H    (GLN30) to    (MET84)  STRUCTURE OF SERINE PROTEINASE  |   VITAMIN K, ZYMOGEN, GAMMA-CARBOXYGLUTAMIC ACID, ACUTE PHASE, LIVER, HYDROLASE, SERINE PROTEASE KUNITZ-LIKE INHIBITOR, KRINGLE, SIGNAL, COMPLEX (HYDROLASE/INHIBITOR) COMPLEX 
1tx6:B    (GLN30) to    (ASN84)  TRYPSIN:BBI COMPLEX  |   ANTICARCINOGENIC ACTIVITY, DOUBLE-HEADED INHIBITOR, GENE DUPLICATION, MONOCOTYLEDONOUS PLANT, INHIBITORY LOOP, HYDROLASE/PROTEIN BINDING COMPLEX 
1tx6:D    (GLN30) to    (ASN84)  TRYPSIN:BBI COMPLEX  |   ANTICARCINOGENIC ACTIVITY, DOUBLE-HEADED INHIBITOR, GENE DUPLICATION, MONOCOTYLEDONOUS PLANT, INHIBITORY LOOP, HYDROLASE/PROTEIN BINDING COMPLEX 
1hyl:A    (TYR29) to    (ASN84)  THE 1.8 A STRUCTURE OF COLLAGENASE FROM HYPODERMA LINEATUM  |   HYDROLASE (SERINE PROTEASE) 
2hvx:A    (TYR29) to    (GLU84)  DISCOVERY OF POTENT, ORALLY ACTIVE, NONPEPTIDE INHIBITORS OF HUMAN MAST CELL CHYMASE BY USING STRUCTURE-BASED DRUG DESIGN  |   SERINE PROTEASE, HYDROLASE 
1id5:H    (GLN30) to    (SER83)  CRYSTAL STRUCTURE OF BOVINE THROMBIN COMPLEX WITH PROTEASE INHIBITOR ECOTIN  |   THROMBIN, ECOTIN M84R, CONFORMATIONAL CHANGES, HYDROLASE 
1ijq:B   (ALA378) to   (SER423)  CRYSTAL STRUCTURE OF THE LDL RECEPTOR YWTD-EGF DOMAIN PAIR  |   BETA-PROPELLER, LIPID TRANSPORT 
1ik3:A    (SER57) to   (VAL128)  LIPOXYGENASE-3 (SOYBEAN) COMPLEX WITH 13(S)-HYDROPEROXY- 9(Z),11(E)-OCTADECADIENOIC ACID  |   OXIDOREDUCTASE, PURPLE LIPOXYGENASE, FE(III) COMPLEX, INTERM 
5a8z:A    (MET30) to    (ALA84)  CRYSTAL STRUCTURE OF HUMAN NEUTROPHIL ELASTASE IN COMPLEX WITH A DIHYDROPYRIMIDONE INHIBITOR  |   TRYPSIN FAMILY FOLD, PROTEASE, HYDROLASE, HYDROLASE- INHIBITOR COMPLEX 
1iqf:A    (GLN30) to    (GLU84)  HUMAN COAGULATION FACTOR XA IN COMPLEX WITH M55165  |   HYDROLASE, SERINE PROTEASE, BLOOD COAGULATION FACTOR, COMPLEX 
1utp:A    (GLN30) to    (SER84)  TRYPSIN SPECIFICITY AS ELUCIDATED BY LIE CALCULATIONS, X-RAY STRUCTURES AND ASSOCIATION CONSTANT MEASUREMENTS  |   HYDROLASE, TRYPSIN, INHIBITOR SPECIFICITY, ELECTROSTATIC INTERACTIONS, COLD-ADAPTATION, MOLECULAR DYNAMICS, BINDING FREE ENERGY HYDROLASE 
1uw7:A    (CYS14) to    (GLU68)  NSP9 PROTEIN FROM SARS-CORONAVIRUS.  |   VIRUS, VIRAL PROTEIN, REPLICASE PROTEIN, SARS, CORONAVIRUS, RNA-BINDING 
1v2r:T    (GLN30) to    (SER84)  TRYPSIN INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(SSRI)BT.B4  |   SERINE PROTEASE, HYDROLASE, SERINE PROTEINASE 
1w8n:A   (GLU584) to   (ALA639)  CONTRIBUTION OF THE ACTIVE SITE ASPARTIC ACID TO CATALYSIS IN THE BACTERIAL NEURAMINIDASE FROM MICROMONOSPORA VIRIDIFACIENS.  |   GLYCOSIDASE, HYDROLASE, NEURAMINIDASE, BETA- PROPELLER FOLD. 
2mqh:A    (GLU14) to    (ALA78)  SOLUTION STRUCTURE OF THE CHLAMYDOMONAS REINHARDTII NAB1 COLD SHOCK DOMAIN, CSD1  |   PROTEIN, COLD SHOCK DOMAIN, RNA-BINDING, CHLAMYDOMONAS REINHARDTII, ALGAE, DNA BINDING PROTEIN 
5c67:B    (GLN30) to    (ASN84)  HUMAN MESOTRYPSIN IN COMPLEX WITH AMYLOID PRECURSOR PROTEIN INHIBITOR VARIANT APPI-M17G/I18F/F34V  |   APPI, KUNITZ DOMAIN, TRYPSIN, HYRDOLASE-HYDROLASE INHIBITOR COMPLEX 
1xem:A    (ASN74) to   (GLY124)  HIGH RESOLUTION CRYSTAL STRUCTURE OF ESCHERICHIA COLI ZINC- PEPTIDE DEFORMYLASE BOUND TO FORMATE  |   ZINC DEFORMYLASE, FORMATE, HYDROLASE 
5cha:B    (GLN30) to    (LYS84)  THE REFINEMENT AND THE STRUCTURE OF THE DIMER OF ALPHA- *CHYMOTRYPSIN AT 1.67-*ANGSTROMS RESOLUTION  |   HYDROLASE (SERINE PROTEINASE) 
5cha:F    (GLN30) to    (LYS84)  THE REFINEMENT AND THE STRUCTURE OF THE DIMER OF ALPHA- *CHYMOTRYPSIN AT 1.67-*ANGSTROMS RESOLUTION  |   HYDROLASE (SERINE PROTEINASE) 
1lxk:A   (SER704) to   (PHE746)  STREPTOCOCCUS PNEUMONIAE HYALURONATE LYASE IN COMPLEX WITH TETRASACCHARIDE HYALURONAN SUBSTRATE  |   PROTEIN-CARBOHYDRATE COMPLEX, LYASE 
2zhf:H    (GLN30) to    (MET84)  EXPLORING THROMBIN S3 POCKET  |   BLOOD COAGULATION, HYDROLASE INHIBITORS, ACUTE PHASE, CLEAVAGE ON PAIR OF BASIC RESIDUES, GAMMA-CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, KRINGLE, PROTEASE, SECRETED, SERINE PROTEASE, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, SULFATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1mcv:A    (GLN30) to    (GLY84)  CRYSTAL STRUCTURE ANALYSIS OF A HYBRID SQUASH INHIBITOR IN COMPLEX WITH PORCINE PANCREATIC ELASTASE  |   ELASTASE-INHIBITOR COMPLEX, HYBRID SQUASH INHIBITOR, HYDROLASE 
1mh0:B    (GLN30) to    (MET84)  CRYSTAL STRUCTURE OF THE ANTICOAGULANT SLOW FORM OF THROMBIN  |   THROMBIN, ALLOSTERY, SODIUM BINDING, SERINE PROTEASE, BLOOD CLOTTING 
4afz:A    (TYR14) to    (GLU71)  HUMAN CHYMASE - FYNOMER COMPLEX  |   HYDROLASE-DE NOVO PROTEIN COMPLEX, INHIBITOR, SERINE PROTEASE 
3kwf:B    (HIS66) to   (GLU117)  HUMAN DPP-IV WITH CARMEGLIPTIN (S)-1-((2S,3S,11BS)-2-AMINO- 9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1- A]ISOQUINOLIN-3-YL)-4-FLUOROMETHYL-PYRROLIDIN-2-ONE  |   DIABETES TYPE II, AMINOPEPTIDASE, CELL MEMBRANE, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PROTEASE, SECRETED, SERINE PROTEASE, SIGNAL-ANCHOR, TRANSMEMBRANE 
1ypm:H    (GLN30) to    (MET84)  X-RAY CRYSTAL STRUCTURE OF THROMBIN INHIBITED BY SYNTHETIC CYANOPEPTIDE ANALOGUE RA-1014  |   THROMBIN, INHIBITOR COMPLEX, BARREL, 6 STRANDED BETA-SHEET, BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX 
3l3t:D    (GLN30) to    (ASN84)  HUMAN MESOTRYPSIN COMPLEXED WITH AMYLOID PRECURSOR PROTEIN INHIBITOR VARIANT (APPIR15K)  |   HUMAN MESOTRYPSIN, CANONICAL INHIBITOR, ALZHEIMER'S AMYLOID PRECURSOR PROTEIN INHIBITOR,APPI, APPI-R15K, HYDROLASE-CELL ADHESION COMPLEX 
3lc5:A    (VAL31) to    (ASN84)  SELECTIVE BENZOTHIOPHINE INHIBITORS OF FACTOR IXA  |   PROTEIN-INHIBITOR COMPLEX, PEPTIDASE S1, BLOOD COAGULATION, CALCIUM, CLEAVAGE ON PAIR OF BASIC RESIDUES, DISEASE MUTATION, DISULFIDE BOND, EGF-LIKE DOMAIN, GAMMA- CARBOXYGLUTAMIC ACID, GLYCOPROTEIN, HEMOPHILIA, HYDROLASE, HYDROXYLATION, PHARMACEUTICAL, PHOSPHOPROTEIN, POLYMORPHISM, PROTEASE, SECRETED, SERINE PROTEASE, SULFATION, ZYMOGEN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3arq:A    (THR77) to   (ALA125)  CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH IDARUBICIN  |   TIM BARREL, INHIBITOR COMPLEX, GLYCOSIDASE, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3arv:A    (THR77) to   (SER124)  CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH SANGUINARINE  |   TIM BARREL, INHIBITOR COMPLEX, GLYCOSIDASE, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
4b30:A   (VAL140) to   (VAL219)  STRUCTURE OF THE MUTANT V44A OF THE FLUORESCENT PROTEIN KILLERRED  |   FLUORESCENT PROTEIN, PHOTOBLEACHING, PHOTOCONVERSION, ROS 
4b30:B   (ASP141) to   (VAL219)  STRUCTURE OF THE MUTANT V44A OF THE FLUORESCENT PROTEIN KILLERRED  |   FLUORESCENT PROTEIN, PHOTOBLEACHING, PHOTOCONVERSION, ROS 
3m6p:A    (LYS78) to   (ARG125)  CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA PEPTIDE DEFORMYLASE 1B (ATPDF1B) IN COMPLEX WITH ACTINONIN  |   PEPTIDE DEFORMYLASE, 1B, PDF, N-TERMINAL EXCISION PATHWAY, NME, ARABIDOPSIS THALIANA, INDUCED-FIT, HYDROLASE, METAL-BINDING, MITOCHONDRION, PROTEIN BIOSYNTHESIS, TRANSIT PEPTIDE, HYDROLASE- ANTIBIOTIC COMPLEX 
5egm:A    (TRP29) to    (ASN84)  DEVELOPMENT OF A NOVEL TRICYCLIC CLASS OF POTENT AND SELECTIVE FIXA INHIBITORS  |   SERINE PROTEINASE, BLOOD COAGULATION, COAGULATION FACTOR, HYDROLASE-2 HYDROLASE INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
5ek5:A    (PRO43) to   (PRO109)  STRUCTURAL CHARACTERIZATION OF IRMA FROM ESCHERICHIA COLI  |   FIBRONECTIN FOLD, VIRULENCE, SECRETED PROTEIN, UNKNOWN FUNCTION 
3bg4:B    (GLN30) to    (LYS84)  THE CRYSTAL STRUCTURE OF GUAMERIN IN COMPLEX WITH CHYMOTRYPSIN AND THE DEVELOPMENT OF AN ELASTASE-SPECIFIC INHIBITOR  |   GUAMERIN, CHYMOTRYPSIN, ELASTASE, INHIBITOR, DIGESTION, HYDROLASE, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, HYDROLASE/HYDROLASE INHIBITOR COMPLEX 
3muz:3   (LEU651) to   (ALA716)  E.COLI (LACZ) BETA-GALACTOSIDASE (R599A) IN COMPLEX WITH IPTG  |   ARG-599-ALA, BETA-GALACTOSIDASE, HYDROLASE TIM BARREL(ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN BETA SUPERSANDWHICH, GLYCOSIDASE, HYDROLASE 
3mv1:3   (ASN649) to   (ALA716)  E.COLI (LACZ) BETA-GALACTOSIDASE (R599A) IN COMPLEX WITH GUANIDINIUM  |   ARG-599-ALA, BETA-GALACTOSIDASE, HYDROLASE TIM BARREL(ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN BETA SUPERSANDWHICH, GLYCOSIDASE, HYDROLASE 
3mv1:4   (ASN649) to   (ALA716)  E.COLI (LACZ) BETA-GALACTOSIDASE (R599A) IN COMPLEX WITH GUANIDINIUM  |   ARG-599-ALA, BETA-GALACTOSIDASE, HYDROLASE TIM BARREL(ALPHA/BETA BARREL), JELLY-ROLL BARREL, IMMUNOGLOBULIN BETA SUPERSANDWHICH, GLYCOSIDASE, HYDROLASE 
3brf:A   (GLU285) to   (GLN361)  CSL (LAG-1) BOUND TO DNA WITH LIN-12 RAM PEPTIDE, C2221  |   PROTEIN-DNA COMPLEX, SIGNALING, TRANSCRIPTION, NOTCH, DNA- BINDING, ANK REPEAT, DEVELOPMENTAL PROTEIN, DIFFERENTIATION, EGF-LIKE DOMAIN, GLYCOPROTEIN, MEMBRANE, TRANSMEMBRANE, DNA BINDING PROTEIN/DNA COMPLEX 
3n50:A   (LEU283) to   (CYS327)  HUMAN EARLY B-CELL FACTOR 3 (EBF3) IPT/TIG AND HLHLH DOMAINS  |   BETA-BARREL, HELIX-LOOP-HELIX-LOOP-HELIX, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSCRIPTION 
3n50:D   (GLN284) to   (CYS327)  HUMAN EARLY B-CELL FACTOR 3 (EBF3) IPT/TIG AND HLHLH DOMAINS  |   BETA-BARREL, HELIX-LOOP-HELIX-LOOP-HELIX, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSCRIPTION 
3n50:F   (GLY282) to   (CYS327)  HUMAN EARLY B-CELL FACTOR 3 (EBF3) IPT/TIG AND HLHLH DOMAINS  |   BETA-BARREL, HELIX-LOOP-HELIX-LOOP-HELIX, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSCRIPTION 
4r5g:B   (PRO396) to   (ASP460)  CRYSTAL STRUCTURE OF THE DNAK C-TERMINUS WITH THE INHIBITOR PET-16  |   HELICAL BUNDLE, BETA SHEETS, CHAPERONE, HSP70/DNAK INHIBITORS, MEMBRANE, CHAPERONE-CHAPERONE INHIBITOR COMPLEX 
3nwf:B   (GLY205) to   (THR249)  GLYCOPROTEIN B FROM HERPES SIMPLEX VIRUS TYPE 1, LOW-PH  |   COILED-COIL, ENVELOPE GLYCOPROTEIN, MEMBRANE FUSION, VIRAL PROTEIN, GLYCOPROTEIN B, HERPESVIRUS 1, HSV-1, MEMBRANE 
3nwf:C   (GLY205) to   (THR249)  GLYCOPROTEIN B FROM HERPES SIMPLEX VIRUS TYPE 1, LOW-PH  |   COILED-COIL, ENVELOPE GLYCOPROTEIN, MEMBRANE FUSION, VIRAL PROTEIN, GLYCOPROTEIN B, HERPESVIRUS 1, HSV-1, MEMBRANE 
4ci8:B   (VAL247) to   (VAL291)  CRYSTAL STRUCTURE OF THE TANDEM ATYPICAL BETA-PROPELLER DOMAIN OF EML1  |   STRUCTURAL PROTEIN, EML1, EML4-ALK, HSP90 INHIBITORS, TUBULIN-BINDING, BETA PROPELLER 
3dfj:A    (GLN59) to   (THR116)  CRYSTAL STRUCTURE OF HUMAN PROSTASIN  |   PROSTASIN, SERINE PROTEASE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, SECRETED, TRANSMEMBRANE, ZYMOGEN 
3p70:F   (GLN378) to   (MET443)  STRUCTURAL BASIS OF THROMBIN-MEDIATED FACTOR V ACTIVATION: ESSENTIAL ROLE OF THE HIRUDIN-LIKE SEQUENCE GLU666-GLU672 FOR PROCESSING AT THE HEAVY CHAIN-B DOMAIN JUNCTION  |   TRYPSIN-LIKE SERINE PROTEINASE, BLOOD COAGULATION, N-GLYCOSYLATION, BLOOD PLASMA, HYDROLASE 
3p70:H   (GLN378) to   (MET443)  STRUCTURAL BASIS OF THROMBIN-MEDIATED FACTOR V ACTIVATION: ESSENTIAL ROLE OF THE HIRUDIN-LIKE SEQUENCE GLU666-GLU672 FOR PROCESSING AT THE HEAVY CHAIN-B DOMAIN JUNCTION  |   TRYPSIN-LIKE SERINE PROTEINASE, BLOOD COAGULATION, N-GLYCOSYLATION, BLOOD PLASMA, HYDROLASE 
3pa2:B   (GLY332) to   (PHE434)  CRYSTAL STRUCTURE OF P DOMAIN FROM NORWALK VIRUS STRAIN VIETNAM 026 IN COMPLEX WITH HBGA TYPE LEY  |   NOROVIRUS, P-DOMAIN, CAPSID, RECEPTOR, HISTO BLOOD GROUP ANTIGEN (HBGA), VIRAL PROTEIN 
4vgc:B    (GLN30) to    (LYS84)  GAMMA-CHYMOTRYPSIN D-NAPHTHYL-1-ACETAMIDO BORONIC ACID INHIBITOR COMPLEX  |   HYDROLASE, SERINE PROTEASE 
5k0h:A    (GLN30) to    (GLU84)  HUMAN FACTOR XA IN COMPLEX WITH SYNTHETIC INHIBITOR BENZYLSULFONYL- DSER(BENZYL)-GLY-4-AMIDINOBENZYLAMIDE  |   HUMAN FACTOR XA, INHIBITOR COMPLEX, BENZAMIDINE INHIBITOR, HYDROLASE, CLOTTING FACTOR 
5kai:B   (HIS343) to   (ASP413)  NH3-BOUND RT XFEL STRUCTURE OF PHOTOSYSTEM II 500 MS AFTER THE 2ND ILLUMINATION (2F) AT 2.8 A RESOLUTION  |   PHOTOSYSTEMS, TRANSMEMBRANE, ROOM TEMPERATURE, ELECTRON TRANSPORT 
5knd:F    (LEU29) to    (ASP91)  CRYSTAL STRUCTURE OF THE PI-BOUND V1 COMPLEX  |   P-LOOP, HYDROLASE, NA(+)-ATPASE, ATP BINDING