Usages in wwPDB of concept: c_0741
nUsages: 402; SSE string: EEHEE
4gsw:A     (MET4) to    (GLU55)  CRYSTAL STRUCTURE OF UBIQUITIN FROM ENTAMOEBA HISTOLYTICA TO 2.15 ANGSTROM  |   UBIQUITIN, UBIQUITIN-LIKE MODIFIER, UBIQUITIN FOLD, POST- TRANSLATIONAL MODIFICATION, EHUBC5, EHUBA1, UBIQUITINATION, ISOPEPTIDE BOND, PROTEIN BINDING 
3e7s:B   (TYR250) to   (VAL303)  STRUCTURE OF BOVINE ENOS OXYGENASE DOMAIN WITH INHIBITOR AR- C95791  |   NITRIC OXIDE SYNTHASE, NOS, HEME, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE CALMODULIN-BINDING, FAD, FMN, IRON, METAL- BINDING, NADP, OXIDOREDUCTASE, POLYMORPHISM, ZINC 
3eah:A   (TYR217) to   (LEU270)  STRUCTURE OF INHIBITED HUMAN ENOS OXYGENASE DOMAIN  |   NITRIC OXIDE SYNTHASE, NOS, HEME, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE CALMODULIN-BINDING, FAD, FMN, IRON, METAL- BINDING, NADP, OXIDOREDUCTASE, POLYMORPHISM, ZINC 
3eah:B   (TYR217) to   (LEU270)  STRUCTURE OF INHIBITED HUMAN ENOS OXYGENASE DOMAIN  |   NITRIC OXIDE SYNTHASE, NOS, HEME, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE CALMODULIN-BINDING, FAD, FMN, IRON, METAL- BINDING, NADP, OXIDOREDUCTASE, POLYMORPHISM, ZINC 
2al6:A    (ARG35) to    (LEU98)  FERM DOMAIN OF FOCAL ADHESION KINASE  |   FOCAL ADHESION KINASE FERM DOMAIN AUTOPHOSPHORYLATION SITE SRC SH3 BINDING SITE, TRANSFERASE 
2al6:B    (MET33) to    (LEU98)  FERM DOMAIN OF FOCAL ADHESION KINASE  |   FOCAL ADHESION KINASE FERM DOMAIN AUTOPHOSPHORYLATION SITE SRC SH3 BINDING SITE, TRANSFERASE 
3rnb:C     (ALA2) to    (PHE83)  STRUCTURE OF THE TOLUENE/O-XYLENE MONOOXYGENASE HYDROXYLASE T201S/F176W DOUBLE MUTANT  |   TOLUENE, HYDROXYLASE, FOUR-HELIX BUNDLE, DIIRON, OXYGEN PATHWAY, OXIDOREDUCTASE 
3rqo:A   (TYR253) to   (VAL306)  STRUCTURE OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((1S,2R/1R,2S)-2-(3-CLOROPHENYL) CYCLOPROPYLAMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2- AMINE  |   OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX 
3rqp:A   (TYR253) to   (VAL306)  STRUCTURE OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-{[(3R,4R)-4-(2-{[(2R/2S)-1-(3-FLUOROPHENYL)PROPAN-2- YL]AMINO}ETHOXY)PYRROLIDIN-3-YL]METHYL}-4-METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX 
4wjs:A    (GLY35) to    (GLN98)  CRYSTAL STRUCTURE OF RSA4 FROM CHAETOMIUM THERMOPHILUM  |   RIBOSOME ASSEMBLY, RIBOSOME BIOGENESIS, BIOSYNTHETIC PROTEIN 
2awt:A    (ASN15) to    (GLU69)  SOLUTION STRUCTURE OF HUMAN SMALL UBIQUITIN-LIKE MODIFIER PROTEIN ISOFORM 2 (SUMO-2)  |   UBIQUITIN FOLD, HALF-OPEN BARREL, TWO HELICES, PROTEIN TRANSPORT 
3egw:A   (MET338) to   (ALA385)  THE CRYSTAL STRUCTURE OF THE NARGHI MUTANT NARH - C16A  |   OXIDOREDUCTASE, NITRATE REDUCTION, ELECTRON TRANSFER, MEMBRANE PROTEIN, 4FE-4S, CELL MEMBRANE, ELECTRON TRANSPORT, IRON, IRON-SULFUR, MEMBRANE, METAL-BINDING, MOLYBDENUM, NITRATE ASSIMILATION, TRANSPORT, 3FE-4S, CELL INNER MEMBRANE, FORMYLATION, HEME, TRANSMEMBRANE 
3ehv:A     (MET1) to    (ASP52)  X-RAY STRUCTURE OF HUMAN UBIQUITIN ZN(II) ADDUCT  |   HUMAN UBIQUITIN, ADDUCT, LIGASE 
1nos:A   (ALA262) to   (GLU314)  MURINE INDUCIBLE NITRIC OXIDE SYNTHASE OXYGENASE DOMAIN (DELTA 114), IMIDAZOLE COMPLEX  |   NITRIC OXIDE, L-ARGININE MONOOXYGENASE, HEME, IMIDAZOLE, NOS, NO, OXIDOREDUCTASE 
4wph:A   (ASP684) to   (ILE746)  CRYSTAL STRUCTURE OF USP7 UBIQUITIN-LIKE DOMAINS IN COMPACT CONFORMATION  |   DEUBIQUITINATING (DUB) ENZYME, UBIQUITIN-LIKE (UBL) DOMAINS, ICP0 BINDING SITE, HAUSP, HYDROLASE 
4wph:B   (ASP684) to   (ILE746)  CRYSTAL STRUCTURE OF USP7 UBIQUITIN-LIKE DOMAINS IN COMPACT CONFORMATION  |   DEUBIQUITINATING (DUB) ENZYME, UBIQUITIN-LIKE (UBL) DOMAINS, ICP0 BINDING SITE, HAUSP, HYDROLASE 
2b3a:A    (ASP11) to    (GLU75)  SOLUTION STRUCTURE OF THE RAS-BINDING DOMAIN OF THE RAL GUANOSINE DISSOCIATION STIMULATOR  |   RAS BINDING DOMAIN, UBIQUITIN FOLD, SIGNAL TRANSDUCTION, NMR, AUTOMATICALLY SOLVED, AUREMOL, SIGNALING PROTEIN 
1nse:B   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE  |   NITRIC OXIDE SYNTHASE, ARGININE, HEME PROTEIN, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE 
2bps:A     (SER1) to    (SER60)  UBIQUITIN-LIKE PROTEIN YUKD OF BACILLUS SUBTILIS  |   YUKD, UBIQUITIN-LIKE PROTEIN, UBIQUITIN 
2bps:B     (SER1) to    (SER60)  UBIQUITIN-LIKE PROTEIN YUKD OF BACILLUS SUBTILIS  |   YUKD, UBIQUITIN-LIKE PROTEIN, UBIQUITIN 
2bqq:A    (ALA52) to   (SER129)  X-RAY STRUCTURE OF THE N-TERMINAL DOMAIN OF HUMAN DOUBLECORTIN  |   DCX DOMAIN, UBIQUITIN-LIKE FOLD, MICROTUBULE ASSOCIATED, SIGNALING PROTEIN, TRANSFERASE 
3sdl:C    (LEU82) to   (ASP133)  CRYSTAL STRUCTURE OF HUMAN ISG15 IN COMPLEX WITH NS1 N-TERMINAL REGION FROM INFLUENZA B VIRUS, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET IDS HX6481, HR2873, AND OR2  |   STRUCTURAL GENOMICS, PSI-BIOLOGY, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, PROTEIN COMPLEX, VIRAL PROTEIN/ANTIVIRAL PROTEIN, VIRAL PROTEIN-ANTIVIRAL PROTEIN COMPLEX 
2bye:A    (HIS10) to    (GLY81)  NMR SOLUTION STRUCTURE OF PHOSPHOLIPASE C EPSILON RA 1 DOMAIN  |   PHOSPHOLIPASE C EPSILON, RAS ASSOCIATION DOMAIN, UBIQUITIN SUPERFOLD, LIPASE 
2pph:A     (SER2) to    (LEU53)  SOLUTION STRUCTURE OF HUMAN MEKK3 PB1 DOMAIN  |   KINASE SIGNALING DOMAIN, TRANSFERASE 
4i6p:B     (PHE1) to    (ASP62)  CRYSTAL STRUCTURE OF PAR3-NTD DOMAIN  |   PB1 LIKE MOTIF, DUF3534, CELL POLARITY PROTEIN, SIGNALING PROTEIN 
2c60:A    (ASP44) to    (LEU93)  CRYSTAL STRUCTURE OF HUMAN MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 3 ISOFORM 2 PHOX DOMAIN AT 1.25 A RESOLUTION  |   MAP3K3, MAP/ERK KINASE KINASE 3, MAPKKK3, MEKK3, SERINE THREONINE PHOSPHORYLATION, ATP-BINDING, KINASE, MAGNESIUM, METAL-BINDING, NUCLEOTIDE-BINDING, PHOSPHORYLATION, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE 
2c7h:A     (SER5) to    (ASP64)  SOLUTION NMR STRUCTURE OF THE DWNN DOMAIN FROM HUMAN RBBP6  |   RBBP6, P53-ASSOCIATED, MRNA PROCESSING, SPLICING-ASSOCIATED, OESOPHAGEAL CANCER, UBIQUITIN-LIKE PROTEIN 
3sua:D  (GLU1745) to  (ASP1819)  CRYSTAL STRUCTURE OF THE INTRACELLULAR DOMAIN OF PLEXIN-B1 IN COMPLEX WITH RAC1  |   AXON GUIDANCE, SIGNAL TRANSDUCTION, APOPTOSIS-SIGNALING PROTEIN COMPLEX 
3sua:E  (GLU1745) to  (ASP1819)  CRYSTAL STRUCTURE OF THE INTRACELLULAR DOMAIN OF PLEXIN-B1 IN COMPLEX WITH RAC1  |   AXON GUIDANCE, SIGNAL TRANSDUCTION, APOPTOSIS-SIGNALING PROTEIN COMPLEX 
3sua:F  (GLU1745) to  (ASP1819)  CRYSTAL STRUCTURE OF THE INTRACELLULAR DOMAIN OF PLEXIN-B1 IN COMPLEX WITH RAC1  |   AXON GUIDANCE, SIGNAL TRANSDUCTION, APOPTOSIS-SIGNALING PROTEIN COMPLEX 
1d0c:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 3- BROMO-7-NITROINDAZOLE (H4B FREE)  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1d0o:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 3- BROMO-7-NITROINDAZOLE (H4B PRESENT)  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1d0o:B   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 3- BROMO-7-NITROINDAZOLE (H4B PRESENT)  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1d1v:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH S- ETHYL-N-PHENYL-ISOTHIOUREA (H4B BOUND)  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1d1w:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 2- AMINOTHIAZOLINE (H4B BOUND)  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1d1x:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 1, 4-PBITU (H4B BOUND)  |   AHPHA-BETA FOLD, OXIDOREDUCTASE 
4xol:B     (MET1) to    (ASP52)  OBSERVING THE OVERALL ROCKING MOTION OF A PROTEIN IN A CRYSTAL - CUBIC UBIQUITIN CRYSTALS.  |   SIGNALING PROTEIN 
4xok:A     (MET1) to    (ASP52)  OBSERVING THE OVERALL ROCKING MOTION OF A PROTEIN IN A CRYSTAL.  |   UBIQUITIN, ZINC, SIGNALING PROTEIN 
4xok:B     (MET1) to    (ASP52)  OBSERVING THE OVERALL ROCKING MOTION OF A PROTEIN IN A CRYSTAL.  |   UBIQUITIN, ZINC, SIGNALING PROTEIN 
1p6n:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NOS HEME DOMAIN WITH L-N(OMEGA)-NITROARGININE-(4R)- AMINO-L-PROLINE AMIDE BOUND  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME 
1p6n:B   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NOS HEME DOMAIN WITH L-N(OMEGA)-NITROARGININE-(4R)- AMINO-L-PROLINE AMIDE BOUND  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME 
2chx:A   (ILE220) to   (VAL282)  A PHARMACOLOGICAL MAP OF THE PI3-K FAMILY DEFINES A ROLE FOR P110ALPHA IN SIGNALING: THE STRUCTURE OF COMPLEX OF PHOSPHOINOSITIDE 3-KINASE GAMMA WITH INHIBITOR PIK-90  |   PHOSPHOINOSITIDE, KINASE, LIPID, INHIBITOR, 3-KINASE, SIGNALING, QUINAZOLINONE, TRANSFERASE 
2chz:A   (PHE221) to   (VAL282)  A PHARMACOLOGICAL MAP OF THE PI3-K FAMILY DEFINES A ROLE FOR P110ALPHA IN SIGNALING: THE STRUCTURE OF COMPLEX OF PHOSPHOINOSITIDE 3-KINASE GAMMA WITH INHIBITOR PIK-93  |   PHOSPHOINOSITIDE, KINASE, LIPID, INHIBITOR, 3-KINASE, SIGNALING, PHENYLTHIAZOLE, QUINAZOLINONE, TRANSFERASE 
2cjn:A     (LYS4) to    (ASP58)  STRUCTURE OF FERREDOXIN, NMR, MINIMIZED AVERAGE STRUCTURE  |   FERREDOXIN, ELECTRON TRANSPORT, IRON-SULFUR PROTEIN 
2cjo:A     (ALA1) to    (ASP58)  STRUCTURE OF FERREDOXIN, NMR, 10 STRUCTURES  |   FERREDOXIN, ELECTRON TRANSPORT, IRON-SULFUR PROTEIN 
4imx:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 3,5-BIS(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL) BENZONITRILE  |   OXIDOREDUCTASE NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4imx:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 3,5-BIS(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL) BENZONITRILE  |   OXIDOREDUCTASE NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
2cs4:A     (SER6) to    (HIS59)  SOLUTION STRUCTURE OF N-TERMINAL DOMAIN OF CHROMOSOME 12 OPEN READING FRAME 2  |   GTP BINDING, UBIQUITIN FOLD, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, SIGNALING PROTEIN 
1dm6:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N- (4-CHLOROPHENYL)-N'-HYDROXYGUANIDINE (H4B FREE)  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1dmi:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6S-H4B  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1dmj:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 5, 6-CYCLIC-TETRAHYDROPTERIDINE  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1dmj:B   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 5, 6-CYCLIC-TETRAHYDROPTERIDINE  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1dmk:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 4- AMINO-6-PHENYL-TETRAHYDROPTERIDINE  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
2cu1:A     (SER6) to    (THR59)  SOLUTION STRUCTURE OF THE PB1 DOMAIN OF HUMAN PROTEIN KINASE MEKK2B  |   PB1 DOMAIN, MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 2, MAPK/ERK KINASE KINASE 2, MEK KINASE 2, MEKK 2, SIGNALING PROTEIN, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSFERASE 
3t8m:A   (ASN218) to   (VAL282)  RATIONAL DESIGN OF PI3K-ALPHA INHIBITORS THAT EXHIBIT SELECTIVITY OVER THE PI3K-BETA ISOFORM  |   KINASE P110, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2r2o:A  (ARG1747) to  (ILE1816)  CRYSTAL STRUCTURE OF THE EFFECTOR DOMAIN OF HUMAN PLEXIN B1  |   PLEXIN, EFFECTOR DOMAIN, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, GLYCOPROTEIN, MEMBRANE, PHOSPHORYLATION, RECEPTOR, SECRETED, TRANSMEMBRANE, SIGNALING PROTEIN 
2r2o:B  (ARG1747) to  (ASP1819)  CRYSTAL STRUCTURE OF THE EFFECTOR DOMAIN OF HUMAN PLEXIN B1  |   PLEXIN, EFFECTOR DOMAIN, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, GLYCOPROTEIN, MEMBRANE, PHOSPHORYLATION, RECEPTOR, SECRETED, TRANSMEMBRANE, SIGNALING PROTEIN 
3gs2:C   (GLU225) to   (ASP306)  RING1B C-TERMINAL DOMAIN/CBX7 CBOX COMPLEX  |   RING1B, CBOX, CBX7, POLYCOMB, E3-LIGASE, CHROMOSOMAL PROTEIN, TRANSCRIPTION REGULATION, CHROMATIN REGULATOR, TRANSCRIPTION REPRESSOR, LIGASE, METAL-BINDING, NUCLEUS, PHOSPHOPROTEIN, REPRESSOR, TRANSCRIPTION, UBL CONJUGATION PATHWAY, ZINC-FINGER 
1q0w:B     (MET1) to    (ASP52)  SOLUTION STRUCTURE OF VPS27 AMINO-TERMINAL UIM-UBIQUITIN COMPLEX  |   PROTEIN-PROTEIN COMPLEX, TRANSPORT PROTEIN 
4j6i:A   (ASN218) to   (VAL282)  DISCOVERY OF THIAZOLOBENZOXEPIN PI3-KINASE INHIBITORS THAT SPARE THE PI3-KINASE BETA ISOFORM  |   BETA-SPARING, SBDD, CATALYTIC SUBUNIT GAMMA, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1q16:A   (MET338) to   (ALA385)  CRYSTAL STRUCTURE OF NITRATE REDUCTASE A, NARGHI, FROM ESCHERICHIA COLI  |   MEMBRANE PROTEIN, ELECTRON-TRANSFER, OXIDOREDUCTASE 
1e7u:A   (ASN218) to   (VAL282)  STRUCTURE DETERMINANTS OF PHOSPHOINOSITIDE 3-KINASE INHIBITION BY WORTMANNIN, LY294002, QUERCETIN, MYRICETIN AND STAUROSPORINE  |   PHOSPHOINOSITIDE 3-KINASE GAMMA, SECONDARY MESSENGER GENERATION, PI3K, PI 3K, WORTMANNIN 
1e8w:A   (ASN218) to   (VAL282)  STRUCTURE DETERMINANTS OF PHOSPHOINOSITIDE 3-KINASE INHIBITION BY WORTMANNIN, LY294002, QUERCETIN, MYRICETIN AND STAUROSPORINE  |   PHOSPHOINOSITIDE 3-KINASE GAMMA, SECONDARY MESSENGER GENERATION, PI3K, PI 3K, QUERCETIN 
1q5w:B   (MET101) to   (ASP152)  UBIQUITIN RECOGNITION BY NPL4 ZINC-FINGERS  |   UBIQUITIN, PROTEIN-PROTEIN COMPLEX, ZINC-FINGER, RUBREDOXIN KNUCKLE, NZF DOMAIN, PROTEIN BINDING 
1ed6:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH L- NIO (H4B FREE)  |   NITRIC OXIDE SYNTHASE, HEME PROTEIN, ALPHA-BETA FOLD, OXIDOREDUCTASE 
2dx5:B     (MET1) to    (ASP52)  THE COMPLEX STRUCTURE BETWEEN THE MOUSE EAP45-GLUE DOMAIN AND UBIQUITIN  |   UBIQUITIN, PROTEIN-PROTEIN COMPLEX, PROTEIN TRANSPORT/SIGNALING PROTEIN COMPLEX 
2rex:C  (ARG1747) to  (ASP1819)  CRYSTAL STRUCTURE OF THE EFFECTOR DOMAIN OF PLXNB1 BOUND WITH RND1 GTPASE  |   COMPLEX, STRUCTURAL GENOMICS CONSORTIUM, SGC, GTPASE, GNP, PLEXIN, EFFECTOR DOMAIN, GLYCOPROTEIN, MEMBRANE, PHOSPHORYLATION, RECEPTOR, SECRETED, TRANSMEMBRANE, CYTOSKELETON, GTP-BINDING, LIPOPROTEIN, METHYLATION, NUCLEOTIDE-BINDING, PRENYLATION, SIGNALING PROTEIN- LIPOPROTEIN COMPLEX 
4jps:A   (GLY188) to   (LEU262)  CO-CRYSTAL STRUCTURES OF THE LIPID KINASE PI3K ALPHA WITH PAN AND ISOFORM SELECTIVE INHIBITORS  |   CLASS I PHOSPHATIDYLINOSITOL 3-KINASES, P85 ALPHA, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4jsk:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(PENTANE-1,5-DIYL)BIS(4-METHYLPYRIDIN-2-AMINE)  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4jsl:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(HEPTANE-1,7-DIYL)BIS(4-METHYLPYRIDIN-2-AMINE)  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4jsl:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(HEPTANE-1,7-DIYL)BIS(4-METHYLPYRIDIN-2-AMINE)  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4jsm:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((5-(((3-FLUOROPHENETHYL)AMINO)METHYL)PYRIDIN-3-YL) OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4jsm:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((5-(((3-FLUOROPHENETHYL)AMINO)METHYL)PYRIDIN-3-YL) OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
3h8h:A   (SER224) to   (ASN306)  STRUCTURE OF THE C-TERMINAL DOMAIN OF HUMAN RNF2/RING1B;  |   UBIQUITIN FOLD, LIGASE, RING1B, POLYCOMB, E3-LIGASE, NUCLEAR PROTEIN, CHROMOSOMAL PROTEIN, TRANSCRIPTION REGULATION, METAL-BINDING, PROTO- ONCOGENE, CHROMATIN REGULATOR, UBL CONJUGATION PATHWAY, REPRESSOR, TRANSCRIPTION, TRANSCRIPTION REGULATION COMPLEX, NUCLEUS, PHOSPHOPROTEIN, ZINC-FINGER, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC 
3u8z:A    (LYS20) to    (LEU75)  HUMAN MERLIN FERM DOMAIN  |   NEUROFIBROMATOSIS, TUMOR SUPPRESSOR, SIGNALING PROTEIN 
3u8z:B    (LYS20) to    (LEU75)  HUMAN MERLIN FERM DOMAIN  |   NEUROFIBROMATOSIS, TUMOR SUPPRESSOR, SIGNALING PROTEIN 
3u8z:D    (LYS20) to    (LEU75)  HUMAN MERLIN FERM DOMAIN  |   NEUROFIBROMATOSIS, TUMOR SUPPRESSOR, SIGNALING PROTEIN 
1r4n:I   (MET101) to   (ASP152)  APPBP1-UBA3-NEDD8, AN E1-UBIQUITIN-LIKE PROTEIN COMPLEX WITH ATP  |   CELL CYCLE 
1r4n:J   (MET101) to   (ASP152)  APPBP1-UBA3-NEDD8, AN E1-UBIQUITIN-LIKE PROTEIN COMPLEX WITH ATP  |   CELL CYCLE 
1r4n:K   (MET101) to   (ASP152)  APPBP1-UBA3-NEDD8, AN E1-UBIQUITIN-LIKE PROTEIN COMPLEX WITH ATP  |   CELL CYCLE 
1r4n:L   (MET101) to   (ASP152)  APPBP1-UBA3-NEDD8, AN E1-UBIQUITIN-LIKE PROTEIN COMPLEX WITH ATP  |   CELL CYCLE 
4yoc:C   (LEU563) to   (PRO635)  CRYSTAL STRUCTURE OF HUMAN DNMT1 AND USP7/HAUSP COMPLEX  |   DNA METHYLATION, DEUBIQUITINATION, DNA METHYLTRANSFERASE, MODIFICATION, TRANSFERASE-HYDROLASE COMPLEX 
4yoc:C   (ASP684) to   (ILE746)  CRYSTAL STRUCTURE OF HUMAN DNMT1 AND USP7/HAUSP COMPLEX  |   DNA METHYLATION, DEUBIQUITINATION, DNA METHYLTRANSFERASE, MODIFICATION, TRANSFERASE-HYDROLASE COMPLEX 
4yoc:C   (CYS896) to   (GLU955)  CRYSTAL STRUCTURE OF HUMAN DNMT1 AND USP7/HAUSP COMPLEX  |   DNA METHYLATION, DEUBIQUITINATION, DNA METHYLTRANSFERASE, MODIFICATION, TRANSFERASE-HYDROLASE COMPLEX 
2v4l:A   (ASN218) to   (VAL282)  COMPLEX OF HUMAN PHOSPHOINOSITIDE 3-KINASE CATALYTIC SUBUNIT GAMMA (P110 GAMMA) WITH PIK-284  |   TRANSFERASE, LIPID KINASE, PHOSPHOINOSITIDE, PYRAZOLOPYRIMIDINE, S1, KINASE, PIK-284, 3-KINASE, INHIBITOR, SIGNALING 
4k5h:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-1,2-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)- PROPAN-3-AMINE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4k5h:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-1,2-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)- PROPAN-3-AMINE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4k5i:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (R)-1,2-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)- PROPAN-3-AMINE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4k5j:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-1,3-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)- BUTAN-4-AMINE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4k5j:B   (ALA254) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-1,3-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)- BUTAN-4-AMINE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4k5k:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH ((2S, 3S)-1,3-BIS((6-(2,5-DIMETHYL-1H-PYRROL-1-YL)-4- METHYLPYRIDIN-2-YL)METHOXY)-2-AMINOBUTANE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4k5k:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH ((2S, 3S)-1,3-BIS((6-(2,5-DIMETHYL-1H-PYRROL-1-YL)-4- METHYLPYRIDIN-2-YL)METHOXY)-2-AMINOBUTANE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
1foj:B   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 7- NITROINDAZOLE-2-CARBOXAMIDINE (H4B PRESENT)  |   ALPHA-BETA FOLD, NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE 
3hm6:X  (ARG1747) to  (ASP1819)  CRYSTAL STRUCTURE OF THE CYTOPLASMIC DOMAIN OF HUMAN PLEXIN B1  |   STRUCTURAL GENOMICS CONSORTIUM, SGC, MEMBRANE, TRANSMEMBRANE, RECEPTOR, CELL MEMBRANE, GLYCOPROTEIN, PHOSPHOPROTEIN, SECRETED, SIGNALING PROTEIN 
4k7s:C     (ILE3) to    (ASP52)  CRYSTAL STRUCTURE OF ZN2-HUB (HUMAN UBIQUITIN) ADDUCT FROM A SOLUTION 35 MM ZINC ACETATE/1.3 MM HUB  |   LIGASE, ZN ADDUCT 
4k7w:C     (ILE3) to    (ASP52)  CRYSTAL STRUCTURE OF ZN3-HUB(HUMAN UBIQUITIN) ADDUCT FROM A SOLUTION 100 MM ZINC ACETATE/1.3 MM HUB  |   LIGASE, ZN ADDUCT 
4k81:A   (LYS106) to   (THR163)  CRYSTAL STRUCTURE OF THE GRB14 RA AND PH DOMAINS IN COMPLEX WITH GTP- LOADED H-RAS  |   ADAPTOR PROTEIN, SIGNALING PROTEIN 
4k81:C   (LYS106) to   (THR163)  CRYSTAL STRUCTURE OF THE GRB14 RA AND PH DOMAINS IN COMPLEX WITH GTP- LOADED H-RAS  |   ADAPTOR PROTEIN, SIGNALING PROTEIN 
4k81:E   (LYS106) to   (THR163)  CRYSTAL STRUCTURE OF THE GRB14 RA AND PH DOMAINS IN COMPLEX WITH GTP- LOADED H-RAS  |   ADAPTOR PROTEIN, SIGNALING PROTEIN 
4k81:G   (LYS106) to   (THR163)  CRYSTAL STRUCTURE OF THE GRB14 RA AND PH DOMAINS IN COMPLEX WITH GTP- LOADED H-RAS  |   ADAPTOR PROTEIN, SIGNALING PROTEIN 
1roe:A     (ALA1) to    (LEU76)  NMR STUDY OF 2FE-2S FERREDOXIN OF SYNECHOCOCCUS ELONGATUS  |   ELECTRON TRANSPORT, IRON-SULFUR 
1fxt:B     (MET1) to    (ASP52)  STRUCTURE OF A CONJUGATING ENZYME-UBIQUITIN THIOLESTER COMPLEX  |   MODEL OF THE INTERACTION BETWEEN YEAST UBC1 AND UBIQUITIN AFTER THE FORMATION OF A COVALENT THIOLESTER, LIGASE 
4kcp:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHEIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(4-(2-((3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL)AMINO) ETHYL)PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4kcs:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(3-((ETHYL(3-FLUOROPHENETHYL)AMINO)METHYL)PHENYL) THIOPHENE-2-CARBOXIMIDAMIDE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4kcs:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(3-((ETHYL(3-FLUOROPHENETHYL)AMINO)METHYL)PHENYL) THIOPHENE-2-CARBOXIMIDAMIDE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
1rs8:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NOS HEME DOMAIN WITH D-LYSINE-D-NITROARGININE AMIDE BOUND  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME 
4z96:A   (HIS683) to   (ILE746)  CRYSTAL STRUCTURE OF DNMT1 IN COMPLEX WITH USP7  |   USP7, DNMT1, HYDROLASE 
4z97:A   (ASP684) to   (ILE746)  CRYSTAL STRUCTURE OF USP7 IN COMPLEX WITH DNMT1(K1115Q)  |   COMPLEX, TRANSFERASE, HYDROLASE 
4z97:A   (CYS896) to   (GLU955)  CRYSTAL STRUCTURE OF USP7 IN COMPLEX WITH DNMT1(K1115Q)  |   COMPLEX, TRANSFERASE, HYDROLASE 
2fuh:B     (MET1) to    (ASP52)  SOLUTION STRUCTURE OF THE UBCH5C/UB NON-COVALENT COMPLEX  |   PROTEIN-PROTEIN COMPLEX UBIQUITIN UBIQUITIN-CONJUGATING ENZYME, LIGASE 
1glo:A    (GLY62) to   (LYS112)  CRYSTAL STRUCTURE OF CYS25SER MUTANT OF HUMAN CATHEPSIN S  |   CATHEPSIN S, PROTEINASE, INHIBITOR, HYDROLASE, THIOL PROTEAS 
2g3q:B     (MET1) to    (ASP52)  SOLUTION STRUCTURE OF EDE1 UBA-UBIQUITIN COMPLEX  |   ENDOCYTOSIS, MONOUBIQUITIN SIGNALING, SOLUTION STRUCTURE, UBA DOMAIN, UBIQUITIN-BINDING MOTIF, ENDOCYTOSIS/SIGNALING PROTEIN COMPLEX 
2g6o:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENOS HEME DOMAIN (BH4-FREE) COMPLEXED WITH CO  |   NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE 
2gbm:A     (MET1) to    (ASP60)  CRYSTAL STRUCTURE OF THE 35-36 8 GLYCINE INSERTION MUTANT OF UBIQUITIN  |   LOOP INSERTION, PROTEIN BINDING 
4l1b:A    (PRO18) to    (PHE83)  CRYSTAL STRUCTURE OF P110ALPHA COMPLEXED WITH NISH2 OF P85ALPHA  |   ATP BINDING, SIGNALING PROTEIN-TRANSFERASE-INHIBITOR COMPLEX 
1t0q:C     (THR3) to    (PHE83)  STRUCTURE OF THE TOLUENE/O-XYLENE MONOOXYGENASE HYDROXYLASE  |   DIIRON, CARBOXYLATE BRIDGE, 4-HELIX BUNDLE, CHANNEL, OXIDOREDUCTASE 
4l23:A    (PRO18) to    (ASP84)  CRYSTAL STRUCTURE OF P110ALPHA COMPLEXED WITH NISH2 OF P85ALPHA AND PI-103  |   ATP BINDING, PI-103, SIGNALING PROTEIN-TRANSFERASE-INHIBITOR COMPLEX 
4l2y:A    (PRO18) to    (PHE83)  CRYSTAL STRUCTURE OF P110ALPHA COMPLEXED WITH NISH2 OF P85ALPHA AND COMPOUND 9D  |   ATP BINDING, SIGNALING PROTEIN-TRANSFERASE-INHIBITOR COMPLEX 
3ibe:A   (ILE220) to   (VAL282)  CRYSTAL STRUCTURE OF A PYRAZOLOPYRIMIDINE INHIBITOR BOUND TO PI3 KINASE GAMMA  |   PI3KINASE INHIBITOR, ATP-BINDING, KINASE, NUCLEOTIDE- BINDING, TRANSFERASE 
1h4r:A    (LYS20) to    (LEU75)  CRYSTAL STRUCTURE OF THE FERM DOMAIN OF MERLIN, THE NEUROFIBROMATOSIS 2 TUMOR SUPPRESSOR PROTEIN.  |   FERM, NEUROFIBROMATOSIS, NF2, STRUCTURAL PROTEIN, CYTOSKELETON, ANTI-ONCOGENE 
4zop:A   (GLY188) to   (LEU262)  CO-CRYSTAL STRUCTURE OF LIPID KINASE PI3K ALPHA WITH A SELECTIVE PHOSPHATIDYLINOSITOL-3 KINASE ALPHA INHIBITOR  |   LIPID KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
1t94:B   (ARG454) to   (ILE513)  CRYSTAL STRUCTURE OF THE CATALYTIC CORE OF HUMAN DNA POLYMERASE KAPPA  |   REPLICATION; DNA REPAIR; Y-FAMILY DNA POLYMERASE; TRANSLESION DNA SYNTHESIS; LESION BYPASS 
4zri:B    (VAL24) to    (LEU75)  CRYSTAL STRUCTURE OF MERLIN-FERM AND LATS2  |   MERLIN, FERM, LATS2 
4zrj:A    (VAL24) to    (LEU75)  STRUCTURE OF MERLIN-FERM AND CTD  |   MERLIN, FERM, CTD, SIGNALING PROTEIN 
4zrk:B    (PHE22) to    (LEU75)  MERLIN-FERM AND LATS1 COMPLEX  |   MERLIN, FERM, LATS1, SIGNALING PROTEIN-TRANSFERASE COMPLEX 
4zrk:C    (VAL24) to    (LEU75)  MERLIN-FERM AND LATS1 COMPLEX  |   MERLIN, FERM, LATS1, SIGNALING PROTEIN-TRANSFERASE COMPLEX 
3in5:A   (ARG454) to   (SER514)  STRUCTURE OF HUMAN DNA POLYMERASE KAPPA INSERTING DATP OPPOSITE AN 8-OXOG DNA LESION  |   ALTERNATIVE SPLICING, DNA DAMAGE, DNA REPAIR, DNA REPLICATION, DNA SYNTHESIS, DNA-BINDING, DNA-DIRECTED DNA POLYMERASE, MAGNESIUM, METAL-BINDING, MUTATOR PROTEIN, NUCLEOTIDYLTRANSFERASE, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SCHIFF BASE, TRANSFERASE, ZINC, ZINC-FINGER, TRANSFERASE/DNA COMPLEX 
3in5:B   (ARG454) to   (SER514)  STRUCTURE OF HUMAN DNA POLYMERASE KAPPA INSERTING DATP OPPOSITE AN 8-OXOG DNA LESION  |   ALTERNATIVE SPLICING, DNA DAMAGE, DNA REPAIR, DNA REPLICATION, DNA SYNTHESIS, DNA-BINDING, DNA-DIRECTED DNA POLYMERASE, MAGNESIUM, METAL-BINDING, MUTATOR PROTEIN, NUCLEOTIDYLTRANSFERASE, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, SCHIFF BASE, TRANSFERASE, ZINC, ZINC-FINGER, TRANSFERASE/DNA COMPLEX 
1he8:A   (ASN218) to   (VAL282)  RAS G12V - PI 3-KINASE GAMMA COMPLEX  |   KINASE/HYDROLASE, COMPLEX (PHOSPHOINOSITIDE KINASE/RAS), PHOSPHOINOSITIDE 3-KINASE GAMMA - H-RAS G12V COMPLEX, PHOSPHATIDYLINOSITOL 3-KINASE, PI3K, PI 3-K, PI 3-KINASE, SECOND MESSENGER GENERATION, RAS EFFECTOR, H-RAS G12V, ONCOGENE PROTEIN, GMPPNP, GTP, RAS-BINDING DOMAIN, HEAT DOMAIN 
2w7o:A   (ARG454) to   (ASN518)  STRUCTURE AND ACTIVITY OF BYPASS SYNTHESIS BY HUMAN DNA POLYMERASE KAPPA OPPOSITE THE 7,8-DIHYDRO-8- OXODEOXYGUANOSINE ADDUCT  |   8-OXO-2P-DEOXY-GUANOSINE-5P-MONOPHOSPHATE, TRANSLESION DNA POLYMERASE, HUMAN DNA POLYMERASE KAPPA, DGTP, DNA REPAIR, DNA DAMAGE, DNA-BINDING PROTEIN 
2w7o:B   (ARG454) to   (SER514)  STRUCTURE AND ACTIVITY OF BYPASS SYNTHESIS BY HUMAN DNA POLYMERASE KAPPA OPPOSITE THE 7,8-DIHYDRO-8- OXODEOXYGUANOSINE ADDUCT  |   8-OXO-2P-DEOXY-GUANOSINE-5P-MONOPHOSPHATE, TRANSLESION DNA POLYMERASE, HUMAN DNA POLYMERASE KAPPA, DGTP, DNA REPAIR, DNA DAMAGE, DNA-BINDING PROTEIN 
3ivf:A     (VAL2) to    (ALA64)  CRYSTAL STRUCTURE OF THE TALIN HEAD FERM DOMAIN  |   FERM DOMAIN, CELL MEMBRANE, CELL PROJECTION, CYTOSKELETON, MEMBRANE, PHOSPHOPROTEIN, CELL ADHESION, STRUCTURAL PROTEIN 
1i35:A     (LEU3) to    (THR54)  SOLUTION STRUCTURE OF THE RAS-BINDING DOMAIN OF THE PROTEIN KINASE BYR2 FROM SCHIZOSACCHAROMYCES POMBE  |   UBIQUITIN SUPERFOLD, TRANSFERASE 
4luw:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((((3R,5S)-5-(((6-AMINO-4-METHYLPYRIDIN-2-YL)METHOXY) METHYL)PYRROLIDIN-3-YL)OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
2hx2:A   (TYR253) to   (VAL306)  BOVINE ENOS HEME DOMAIN COMPLEXED WITH (4S)-N-{4-AMINO-5-[(2- AMINOETHYL)-HYDROXYAMINO]-PENTYL}-N'-NITROGUANIDINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, OXIDOREDUCTASE 
1i83:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1,N14-BIS((S-METHYL)ISOTHIOUREIDO)TETRADECANE (H4B FREE)  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1i83:B   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1,N14-BIS((S-METHYL)ISOTHIOUREIDO)TETRADECANE (H4B FREE)  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1uf0:A    (LYS12) to    (SER73)  SOLUTION STRUCTURE OF THE N-TERMINAL DCX DOMAIN OF HUMAN DOUBLECORTIN-LIKE KINASE  |   STRUCTURAL GENOMICS, UBIQUITIN-LIKE FOLD, MICROTUBULE- BINDING, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSFERASE 
1uh6:A    (ILE29) to    (ASP80)  SOLUTION STRUCTURE OF THE MURINE UBIQUITIN-LIKE 5 PROTEIN FROM RIKEN CDNA 0610031K06  |   BETA-GRASP FOLD, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION 
2wxf:A   (ARG188) to   (TYR251)  THE CRYSTAL STRUCTURE OF THE MURINE CLASS IA PI 3-KINASE P110DELTA IN COMPLEX WITH PIK-39.  |   TRANSFERASE, PHOSPHOPROTEIN, ISOFORM-SPECIFIC INHIBITORS, CANCER 
2wxi:A   (ARG188) to   (TYR251)  THE CRYSTAL STRUCTURE OF THE MURINE CLASS IA PI 3-KINASE P110DELTA IN COMPLEX WITH SW30.  |   TRANSFERASE, PHOSPHOPROTEIN, ISOFORM-SPECIFIC INHIBITORS, CANCER 
2wxl:A   (ARG188) to   (TYR251)  THE CRYSTAL STRUCTURE OF THE MURINE CLASS IA PI 3-KINASE P110DELTA IN COMPLEX WITH ZSTK474.  |   TRANSFERASE, PHOSPHOPROTEIN, ISOFORM-SPECIFIC INHIBITORS, CANCER 
3wa0:C    (VAL24) to    (LEU75)  CRYSTAL STRUCTURE OF MERLIN COMPLEXED WITH DCAF1/VPRBP  |   MERLIN FERM DOMAIN, CELL ADHESION 
3wa0:F    (VAL24) to    (LEU75)  CRYSTAL STRUCTURE OF MERLIN COMPLEXED WITH DCAF1/VPRBP  |   MERLIN FERM DOMAIN, CELL ADHESION 
1isn:A    (PHE22) to    (MET77)  CRYSTAL STRUCTURE OF MERLIN FERM DOMAIN  |   FERM DOMAIN, CELL ADHESION 
5adk:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH  7-((3-(DIMETHYLAMINO)METHYL) PHENOXY)METHYL)QUINOLIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
5adl:B   (ALA254) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH  7-((3-(METHYLAMINO)METHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
5adn:B   (ALA254) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(((3-((DIMETHYLAMINO)METHYL) PHENYL)AMINO)METHYL)QUINOLIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
5ae9:A   (ASN187) to   (TYR251)  CRYSTAL STRUCTURE OF MOUSE PI3 KINASE DELTA IN COMPLEX WITH GSK2292767  |   TRANSFERASE 
4mgk:E   (ASP650) to   (LYS706)  SELECTIVE ACTIVATION OF EPAC1 AND EPAC2  |   GUANINE NUCLEOTIDE EXCHANGE FACTOR, NUCLEOTIDE BINDING, SIGNALING PROTEIN-GTP-BINDING PROTEIN COMPLEX 
4mgz:E   (ASP650) to   (LYS706)  SELECTIVE ACTIVATION OF EPAC1 AND EPAC2  |   GUANINE NUCLEOTIDE EXCHANGE FACTOR, NUCLEOTIDE BINDING, SIGNALING PROTEIN-GTP-BINDING PROTEIN COMPLEX 
4mm3:A     (MET1) to    (GLY53)  CRYSTAL STRUCTURE OF SARS-COV PAPAIN-LIKE PROTEASE PLPRO IN COMPLEX WITH UBIQUITIN ALDEHYDE  |   NSP3 PAPAIN-LIKE PROTEASE DOMAIN, SIGNALING PROTEIN-HYDROLASE COMPLEX 
2j0j:A    (ARG35) to    (HIS99)  CRYSTAL STRUCTURE OF A FRAGMENT OF FOCAL ADHESION KINASE CONTAINING THE FERM AND KINASE DOMAINS.  |   CELL MIGRATION, FERM, TRANSFERASE, INTEGRIN SIGNALING 
2j0k:A    (ARG35) to    (HIS99)  CRYSTAL STRUCTURE OF A FRAGMENT OF FOCAL ADHESION KINASE CONTAINING THE FERM AND KINASE DOMAINS.  |   CELL MIGRATION, TRANSFERASE, INTEGRIN SIGNALING 
2j0k:B    (ARG35) to    (LEU98)  CRYSTAL STRUCTURE OF A FRAGMENT OF FOCAL ADHESION KINASE CONTAINING THE FERM AND KINASE DOMAINS.  |   CELL MIGRATION, TRANSFERASE, INTEGRIN SIGNALING 
2j0m:A    (ARG35) to    (LEU98)  CRYSTAL STRUCTURE A TWO-CHAIN COMPLEX BETWEEN THE FERM AND KINASE DOMAINS OF FOCAL ADHESION KINASE.  |   FOCAL ADHESION, CELL MIGRATION, PHOSPHORYLATION, FERM, KINASE, TRANSFERASE, ATP-BINDING, INTEGRIN SIGNALING, NUCLEOTIDE-BINDING, TYROSINE-PROTEIN KINASE 
4mzo:B   (GLY185) to   (SER234)  MOUSE CATHEPSIN S WITH COVALENT LIGAND (3S,4S)-N-[(2E)-2-IMINOETHYL]- 4-(MORPHOLIN-4-YLCARBONYL)-1-(PHENYLSULFONYL)PYRROLIDINE-3- CARBOXAMIDE  |   HYDROLASE, CYSTEINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4mzo:H   (GLY185) to   (SER234)  MOUSE CATHEPSIN S WITH COVALENT LIGAND (3S,4S)-N-[(2E)-2-IMINOETHYL]- 4-(MORPHOLIN-4-YLCARBONYL)-1-(PHENYLSULFONYL)PYRROLIDINE-3- CARBOXAMIDE  |   HYDROLASE, CYSTEINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3zdt:B    (ARG35) to    (LEU98)  CRYSTAL STRUCTURE OF BASIC PATCH MUTANT FAK FERM DOMAIN FAK31-405 K216A, K218A, R221A, K222A  |   TRANSFERASE, CELL ADHESION 
5b83:A   (MET153) to   (ASP204)  CRYSTAL STRUCTURE OF OPTINEURIN UBAN IN COMPLEX WITH LINEAR UBIQUITIN  |   UBIQUITIN, COILED-COIL, CELLULAR, SIGNALING, NFKB PATHWAY, SIGNALING PROTEIN 
2jrh:A     (SER2) to    (LEU52)  SOLUTION STURCTURE OF HUMAN MEKK3 PB1 DOMAIN CIS ISOMER  |   KINASE SIGNALING DOMAIN, TRANSFERASE 
2jt4:B     (MET1) to    (ASP52)  SOLUTION STRUCTURE OF THE SLA1 SH3-3-UBIQUITIN COMPLEX  |   ENDOCYTOSIS, MONOUBIQUITIN SIGNALING, UBIQUITIN-BINDING MOTIF, SH3, UBIQUITIN, ACTIN-BINDING, CYTOPLASM, CYTOSKELETON, PHOSPHORYLATION, SH3 DOMAIN, DNA DAMAGE, DNA REPAIR, NUCLEUS, UBL CONJUGATION, SIGNALING PROTEIN 
1wgr:A     (PRO9) to    (GLU67)  SOLUTION STRUCTURE OF THE RA DOMAIN OF HUMAN GRB7 PROTEIN  |   RA DOMAIN, GRB7, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, PROTEIN BINDING 
1wgy:A     (GLY7) to    (GLN65)  RA DOMAIN OF GUANINE NUCLEOTIDE EXCHANGE FACTOR FOR RAP1  |   UBIQUITIN FOLD, RA, GUANINE NUCLEOTIDE EXCHANGE, RAP1, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, SIGNALING PROTEIN 
1wi0:A    (LEU17) to    (SER74)  SOLUTION STRUCTURE OF THE PB1 DOMAIN OF MOUSE MITOGEN ACTIVATED PROTEIN KINASE KINASE 5 (MAP2K5)  |   PB1 DOMAIN, PROTEIN-PROTEIN INTERACTION SITE, CYTOPLASMIC SIGNALLING, STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSFERASE 
2kdb:A     (THR3) to    (ASP57)  SOLUTION STRUCTURE OF HUMAN UBIQUITIN-LIKE DOMAIN OF HERPUD2_9_85, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM (NESG) TARGET HT53A  |   UBL DOMAIN, MEMBRANE, TRANSMEMBRANE, UNFOLDED PROTEIN RESPONSE, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, ONTARIO CENTRE FOR STRUCTURAL PROTEOMICS, OCSP, UNKNOWN FUNCTION, PROTEIN BINDING, SGC 
2kfk:B   (SER104) to   (GLY161)  SOLUTION STRUCTURE OF BEM1P PB1 DOMAIN COMPLEXED WITH CDC24P PB1 DOMAIN  |   PB1, BUDDING, YEAST, PHOX, SIGNALING PROTEIN 
2y3a:A    (GLY22) to    (GLU87)  CRYSTAL STRUCTURE OF P110BETA IN COMPLEX WITH ICSH2 OF P85BETA AND THE DRUG GDC-0941  |   TRANSFERASE, PHOSPHOINOSITIDE 3-KINASE, RTK 
2kk8:A    (HIS10) to    (ARG62)  NMR SOLUTION STRUCTURE OF A PUTATIVE UNCHARACTERIZED PROTEIN OBTAINED FROM ARABIDOPSIS THALIANA: NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET AR3449A  |   SOLUTION NMR, ARABIDOPSIS THALIANA, AR3449A, UNCHARACTERIZED PUTATIVE PROTEIN, NESG, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, UNKNOWN FUNCTION 
2kma:A     (VAL2) to    (ALA64)  NMR STRUCTURE OF THE F0F1 DOUBLE DOMAIN (RESIDUES 1-202) OF THE TALIN FERM DOMAIN  |   TALIN, FERM, F0, N-TERMINAL, F1, ADHESION, CYTOPLASM, CYTOSKELETON, MEMBRANE, STRUCTURAL PROTEIN 
2kma:A    (PRO87) to   (HIS176)  NMR STRUCTURE OF THE F0F1 DOUBLE DOMAIN (RESIDUES 1-202) OF THE TALIN FERM DOMAIN  |   TALIN, FERM, F0, N-TERMINAL, F1, ADHESION, CYTOPLASM, CYTOSKELETON, MEMBRANE, STRUCTURAL PROTEIN 
2kn5:A     (MET1) to    (ASP52)  A CORRESPONDENCE BETWEEN SOLUTION-STATE DYNAMICS OF AN INDIVIDUAL PROTEIN AND THE SEQUENCE AND CONFORMATIONAL DIVERSITY OF ITS FAMILY  |   BACKRUB, RESIDUAL DIPOLAR COUPLING, BACKBONE FLEXIBILITY, PROTEIN DYNAMICS, CYTOPLASM, ISOPEPTIDE BOND, NUCLEUS, PHOSPHOPROTEIN, UBL CONJUGATION, GENE REGULATION 
2knb:A     (MET1) to    (ASN52)  SOLUTION NMR STRUCTURE OF THE PARKIN UBL DOMAIN IN COMPLEX WITH THE ENDOPHILIN-A1 SH3 DOMAIN  |   UBL, SH3, PARKIN, ENDOPHILIN, CELL JUNCTION, CELL MEMBRANE, CELL PROJECTION, ENDOPLASMIC RETICULUM, LIGASE, MEMBRANE, METAL-BINDING, NUCLEUS, POSTSYNAPTIC CELL MEMBRANE, S-NITROSYLATION, SYNAPSE, UBL CONJUGATION PATHWAY, ZINC-FINGER, ENDOCYTOSIS, LIPID-BINDING, PHOSPHOPROTEIN, SH3 DOMAIN, PROTEIN BINDING 
2ktf:A     (MET1) to    (ASP52)  SOLUTION NMR STRUCTURE OF HUMAN POLYMERASE IOTA UBM2 IN COMPLEX WITH UBIQUITIN  |   TRANSLESION SYNTHESIS DNA POLYMERASE, Y-FAMILY DNA POLYMERASE, UBIQUITIN BINDING MOTIF, UBIQUITIN, ISOPEPTIDE BOND, NUCLEUS, PHOSPHOPROTEIN, PROTEIN BINDING 
2l76:A   (LEU267) to   (PRO315)  SOLUTION NMR STRUCTURE OF HUMAN NFATC2IP UBIQUITIN-LIKE DOMAIN, NFATC2IP_244_338, NESG TARGET HT65A/OCSP TARGET HS00387_244_338/SGC- TORONTO  |   UBIQUITIN-LIKE DOMAIN, STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, ONTARIO CENTRE FOR STRUCTURAL PROTEOMICS, OCSP, TRANSCRIPTION 
4nnj:B     (MET1) to    (ASP52)  CRYSTAL STRUCTURE OF UBA1 IN COMPLEX WITH UBIQUITIN-AMP AND THIOESTERIFIED UBIQUITIN  |   UBIQUITIN ACTIVATING ENZYME (E1), UBA1, UBIQUITIN, ACYLADENYLATE, UBIQUITIN THIOESTER, UBIQUITIN ACTIVATION, AMP, THIOESTERIFIED UB, PROTEIN BINDING 
4nnj:D     (MET1) to    (ASP52)  CRYSTAL STRUCTURE OF UBA1 IN COMPLEX WITH UBIQUITIN-AMP AND THIOESTERIFIED UBIQUITIN  |   UBIQUITIN ACTIVATING ENZYME (E1), UBA1, UBIQUITIN, ACYLADENYLATE, UBIQUITIN THIOESTER, UBIQUITIN ACTIVATION, AMP, THIOESTERIFIED UB, PROTEIN BINDING 
1wxa:A    (GLY10) to    (ILE80)  SOLUTION STRUCTURE OF RAS-BINDING DOMAIN IN MOUSE AF-6 PROTEIN  |   RAS-BINDING DOMAIN, UBIQUITIN-LIKE FOLD, AF-6 PROTEIN, STRUCTURAL GENOMICS, AFADIN, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, CELL ADHESION 
3zqj:D   (SER176) to   (GLU253)  MYCOBACTERIUM TUBERCULOSIS UVRA  |   DNA BINDING PROTEIN, NUCLEOTIDE EXCISION REPAIR, 
2lvp:B     (MET1) to    (ASP52)  GP78CUE DOMAIN BOUND TO THE DISTAL UBIQUITIN OF K48-LINKED DIUBIQUITIN  |   CUE DOMAIN, SIGNALING PROTEIN-LIGASE COMPLEX 
2lxa:A    (VAL74) to   (ASP128)  SOLUTION STRUCTURE OF THE GET5 UBIQUITIN-LIKE DOMAIN  |   UBIQUITIN-LIKE DOMAIN, PROTEIN-PROTEIN INTERACTION, SGT2 BINDING DOMAIN, GET PATHWAY, PROTEIN BINDING 
4nse:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE, H4B-FREE, L-ARG COMPLEX  |   NITRIC OXIDE SYNTHASE, HEME PROTEIN, TETRAHYDROBIOPTERIN, COMPLEX (OXIDOREDUCTASE-PEPTIDE), COMPLEX (OXIDOREDUCTASE-PEPTIDE) COMPLEX 
2mh7:A     (VAL3) to    (ASP55)  SOLUTION STRUCTURE OF OXIDIZED [2FE-2S] FERREDOXIN PETF FROM CHLAMYDOMONAS REINHARDTII  |   OXIDOREDUCTASE 
2mlb:A     (ILE4) to    (PRO53)  NMR SOLUTION STRUCTURE OF A COMPUTATIONAL DESIGNED PROTEIN BASED ON TEMPLATE OF HUMAN ERYTHROCYTIC UBIQUITIN  |   PROTEIN DESIGN, STATISTICAL ENERGY FUNCTION, UBIQUITIN, DE NOVO PROTEIN 
3zvv:A   (ASN218) to   (VAL282)  FRAGMENT BOUND TO PI3KINASE GAMMA  |   TRANSFERASE, PI3 KINASE GAMMA 
5c56:A   (ASP684) to   (ILE746)  CRYSTAL STRUCTURE OF USP7/HAUSP IN COMPLEX WITH ICP0  |   VIRUS PROTEIN ICP0, USP7, DEUBIQUITINATION, HYDROLASE 
5c56:A   (ARG891) to   (GLU955)  CRYSTAL STRUCTURE OF USP7/HAUSP IN COMPLEX WITH ICP0  |   VIRUS PROTEIN ICP0, USP7, DEUBIQUITINATION, HYDROLASE 
2mre:A     (ILE3) to    (ASP52)  NMR STRUCTURE OF THE RAD18-UBZ/UBIQUITIN COMPLEX  |   PROTEIN COMPLEX, LIGASE-TRANSLATION COMPLEX, REPLICATION-SIGNALING PROTEIN COMPLEX 
2mur:B   (ILE103) to   (ASP152)  SOLUTION STRUCTURE OF THE HUMAN FAAP20 UBZ-UBIQUITIN COMPLEX  |   UBZ, FAAP20, ZINC-FINGER, FANCONI ANEMIA, PROTEIN BINDING 
2mw5:A    (GLY22) to    (ASP76)  BACKBONE FOLD OF HUMAN SMALL UBIQUITIN LIKE MODIFIER PROTEIN-1 (SUMO- 1) BASED ON PROT3D-NMR APPROACH.  |   HUMAN SUMO, SMALL UBIQUITIN LIKE MODIFIER, SUMO-1, PROTEIN BINDING 
2n13:B   (ILE103) to   (ASP152)  COMPLEX STRUCTURE OF MYUB (1080-1122) OF HUMAN MYOSIN VI WITH K63-DIUB  |   MOTOR PROTEIN-PROTEIN BINDING COMPLEX 
2n13:C   (MET201) to   (ASP252)  COMPLEX STRUCTURE OF MYUB (1080-1122) OF HUMAN MYOSIN VI WITH K63-DIUB  |   MOTOR PROTEIN-PROTEIN BINDING COMPLEX 
4ny0:A    (ARG35) to    (HIS99)  CRYSTAL STRUCTURE OF FERM DOMAIN OF HUMAN FOCAL ADHESION KINASE  |   FERM DOMAIN, FOCAL ADHESION KINASE, FOCAL TARGETING DOMAIN, INTEGRIN SIGNALING, TRANSFERASE 
4ny0:B    (ARG35) to    (LEU98)  CRYSTAL STRUCTURE OF FERM DOMAIN OF HUMAN FOCAL ADHESION KINASE  |   FERM DOMAIN, FOCAL ADHESION KINASE, FOCAL TARGETING DOMAIN, INTEGRIN SIGNALING, TRANSFERASE 
4ny0:C    (ARG35) to    (LEU98)  CRYSTAL STRUCTURE OF FERM DOMAIN OF HUMAN FOCAL ADHESION KINASE  |   FERM DOMAIN, FOCAL ADHESION KINASE, FOCAL TARGETING DOMAIN, INTEGRIN SIGNALING, TRANSFERASE 
2n3u:C     (MET1) to    (ASP52)  SOLUTION STRUCTURE OF THE RPN1 T1 SITE ENGAGING TWO MONOUBIQUITIN MOLECULES  |   PROTEIN BINDING 
2n7k:A     (ILE3) to    (ASP52)  UNVEILING THE STRUCTURAL DETERMINANTS OF KIAA0323 BINDING PREFERENCE FOR NEDD8  |   SIGNALING PROTEIN 
2n9p:C    (VAL19) to    (ASP68)  SOLUTION STRUCTURE OF RNF126 N-TERMINAL ZINC FINGER DOMAIN IN COMPLEX WITH BAG6 UBIQUITIN-LIKE DOMAIN  |   E3 LIGASE, ZINC FINGER, LIGASE 
2nbv:B    (LYS31) to    (ASP83)  SOLUTION STRUCTURE OF THE RPN13 PRU DOMAIN ENGAGING THE HPLIC2 UBL DOMAIN  |   PROTEIN BINDING 
2ns5:A    (GLU17) to    (LEU78)  THE CONSERVED N-TERMINAL DOMAIN OF PAR-3 ADOPTS A NOVEL PB1- LIKE STRUCTURE REQUIRED FOR PAR-3 OLIGOMERIZATION AND APICAL MEMBRANE LOCALIZATION  |   CELL POLARITY, PAR-3, N-TERMINAL DOMAIN, PB1 DOMAIN, ASYMMETRIC MEMBRANE LOCALIZATION, SIGNALING PROTEIN 
2nse:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE SUBSTRATE COMPLEX  |   NITRIC OXIDE SYNTHASE, ARGININE, HEME PROTEIN, TETRAHYDROBIOPTERIN, COMPLEX (OXIDOREDUCTASE-PEPTIDE), COMPLEX (OXIDOREDUCTASE-PEPTIDE) COMPLEX 
2nse:B   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE SUBSTRATE COMPLEX  |   NITRIC OXIDE SYNTHASE, ARGININE, HEME PROTEIN, TETRAHYDROBIOPTERIN, COMPLEX (OXIDOREDUCTASE-PEPTIDE), COMPLEX (OXIDOREDUCTASE-PEPTIDE) COMPLEX 
2ylm:A   (ASP684) to   (ILE746)  MECHANISM OF USP7 (HAUSP) ACTIVATION BY ITS C-TERMINAL UBIQUITIN-LIKE DOMAIN (HUBL) AND ALLOSTERIC REGULATION BY GMP-SYNTHETASE.  |   HYDROLASE, UBL 
2ylm:A   (ARG891) to   (GLU955)  MECHANISM OF USP7 (HAUSP) ACTIVATION BY ITS C-TERMINAL UBIQUITIN-LIKE DOMAIN (HUBL) AND ALLOSTERIC REGULATION BY GMP-SYNTHETASE.  |   HYDROLASE, UBL 
1l7y:A    (THR15) to    (PRO69)  SOLUTION NMR STRUCTURE OF C. ELEGANS PROTEIN ZK652.3. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET WR41.  |   C.ELEGANS, UNKNOWN FUNCTION, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, ZK652.3, UBIQUITIN FOLD, BETA-GRASP FOLD, UFM1, UBIQUITIN-FOLD MODIFIER 1, NESG, STRUCTURAL GENOMICS, STRUCTURAL PROTEOMICS, HYPOTHETICAL, PSI, PROTEIN STRUCTURE INITIATIVE 
3jwx:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1-[(3'R,4'R)-4'-((6"-AMINO-4"-METHYLPYRIDIN-2"-YL)METHYL) PYRROLIDIN-3'-YL]-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE  |   HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3jwx:B   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1-[(3'R,4'R)-4'-((6"-AMINO-4"-METHYLPYRIDIN-2"-YL)METHYL) PYRROLIDIN-3'-YL]-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE  |   HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3jwy:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1-{(3'R,4'S)-4'-[(6"-AMINO-4"-METHYLPYRIDIN-2"-YL) METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE  |   HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3jwz:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1-[(3' S,4' R)-4'-((6"-AMINO-4"-METHYLPYRIDIN-2"-YL)METHYL) PYRROLIDIN-3'-YL]-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE  |   HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
5chw:H    (GLU78) to   (ASP131)  STRUCTURE OF ISG15 IN SPACE GROUP P212121  |   UBIQUITIN-LIKE PROTEIN, INTERFERON INDUCED, SIGNALING PROTEIN 
1m9k:A   (TYR251) to   (LEU304)  HUMAN ENDOTHELIAL NITRIC OXIDE SYNTHASE WITH 7- NITROINDAZOLE BOUND  |   OXIDOREDUCTASE 
1m9r:B   (TYR251) to   (LEU304)  HUMAN ENDOTHELIAL NITRIC OXIDE SYNTHASE WITH 3-BROMO-7- NITROINDAZOLE BOUND  |   OXIDOREDUCTASE 
1xzq:B     (THR3) to    (GLU52)  STRUCTURE OF THE GTP-BINDING PROTEIN TRME FROM THERMOTOGA MARITIMA COMPLEXED WITH 5-FORMYL-THF  |   GTP-BINDING, THF-BINDING, TRNA-MODIFICATION, HYDROLASE 
5d68:B   (LYS417) to   (GLN473)  CRYSTAL STRUCTURE OF KRIT1 ARD-FERM  |   ANKYRIN REPEAT DOMAIN, FERM DOMAIN, CEREBRAL CAVERNOUS MALFORMATIONS, SIGNALING PROTEIN 
1yiw:B     (LEU1) to    (ASP52)  X-RAY CRYSTAL STRUCTURE OF A CHEMICALLY SYNTHESIZED UBIQUITIN  |   UBIQUITIN, STRUCTURAL PROTEIN 
3kuz:A  (GLY1197) to  (ASP1271)  CRYSTAL STRUCTURE OF THE UBIQUITIN LIKE DOMAIN OF PLXNC1  |   PLEXIN, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC 
1yj1:A     (ILE3) to    (ASP52)  X-RAY CRYSTAL STRUCTURE OF A CHEMICALLY SYNTHESIZED [D-GLN35]UBIQUITIN  |   UBIQUITIN, STRUCTURAL PROTEIN 
1yj1:B     (LEU1) to    (ASP52)  X-RAY CRYSTAL STRUCTURE OF A CHEMICALLY SYNTHESIZED [D-GLN35]UBIQUITIN  |   UBIQUITIN, STRUCTURAL PROTEIN 
3l08:A   (ASN218) to   (LEU281)  STRUCTURE OF PI3K GAMMA WITH A POTENT INHIBITOR: GSK2126458  |   PI3K GAMMA, LIPID KINASE, PHOSPHOINOSITIDE, INHIBITOR, GSK2126458, SIGNALING, KINASE, ATP-BINDING, NUCLEOTIDE-BINDING, TRANSFERASE 
3l0w:B     (ILE3) to    (ASP52)  STRUCTURE OF SPLIT MONOUBIQUITINATED PCNA WITH UBIQUITIN IN POSITION TWO  |   REPLICATION, DNA DAMAGE, DNA REPAIR, DNA REPLICATION, DNA- BINDING, ISOPEPTIDE BOND, NUCLEUS, UBL CONJUGATION 
3l13:A   (ASN218) to   (VAL282)  CRYSTAL STRUCTURES OF PAN-PI3-KINASE AND DUAL PAN-PI3-KINASE/MTOR INHIBITORS  |   KINASE, ATP-BINDING, NUCLEOTIDE-BINDING, TRANSFERASE, PI3K-GAMMA P110 GAMMA 
3l54:A   (ASN218) to   (LEU281)  STRUCTURE OF PI3K GAMMA WITH INHIBITOR  |   PI3K, PI3K GAMMA, PHOSPHATIDYLINOSITOL, PI3, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, TRANSFERASE 
1yx6:B     (ILE3) to    (ASP52)  SOLUTION STRUCTURE OF S5A UIM-2/UBIQUITIN COMPLEX  |   NMR, POLYUBIQUITIN, PROTEASOME, S5A, UIM, HYDROLASE 
4ps7:A   (ASN218) to   (VAL282)  STRUCTURE OF PI3K GAMMA IN COMPLEX WITH N-[6-(PYRIDIN-3-YL)-1,3- BENZOTHIAZOL-2-YL]ACETAMIDE  |   SERINE/THREONINE PROTEIN KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4anv:A   (ASN218) to   (VAL282)  COMPLEXES OF PI3KGAMMA WITH ISOFORM SELECTIVE INHIBITORS.  |   TRANSFERASE 
4anw:A   (ASN218) to   (LEU281)  COMPLEXES OF PI3KGAMMA WITH ISOFORM SELECTIVE INHIBITORS.  |   TRANSFERASE 
4anx:A   (ASN218) to   (VAL282)  COMPLEXES OF PI3KGAMMA WITH ISOFORM SELECTIVE INHIBITORS.  |   TRANSFERASE 
4py5:A    (ALA38) to    (GLU98)  THERMOVIBRIO AMMONIFICANS RNASE H3 IN COMPLEX WITH 19-MER RNA/DNA  |   RNASE H FOLD, RNA/DNA HYBRID, HYDROLASE-DNA-RNA COMPLEX 
4pyu:A     (ILE2) to    (ASP53)  THE CONSERVED UBIQUITIN-LIKE PROTEIN HUB1 PLAYS A CRITICAL ROLE IN SPLICING IN HUMAN CELLS  |   UBIQUITIN-LIKE, PRE-MRNA SPLICING, PROTEIN BINDING-ALLERGEN COMPLEX 
4pyu:B     (ILE2) to    (ASP53)  THE CONSERVED UBIQUITIN-LIKE PROTEIN HUB1 PLAYS A CRITICAL ROLE IN SPLICING IN HUMAN CELLS  |   UBIQUITIN-LIKE, PRE-MRNA SPLICING, PROTEIN BINDING-ALLERGEN COMPLEX 
4pyu:K     (HIS0) to    (ASP53)  THE CONSERVED UBIQUITIN-LIKE PROTEIN HUB1 PLAYS A CRITICAL ROLE IN SPLICING IN HUMAN CELLS  |   UBIQUITIN-LIKE, PRE-MRNA SPLICING, PROTEIN BINDING-ALLERGEN COMPLEX 
4pyz:A   (HIS683) to   (ILE746)  CRYSTAL STRUCTURE OF THE FIRST TWO UBL DOMAINS OF DEUBIQUITYLASE USP7  |   DEUBIQUITYLASE, UBIQUITIN-LIKE DOMAIN, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, HYDROLASE 
4pyz:B   (ASP684) to   (ILE746)  CRYSTAL STRUCTURE OF THE FIRST TWO UBL DOMAINS OF DEUBIQUITYLASE USP7  |   DEUBIQUITYLASE, UBIQUITIN-LIKE DOMAIN, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, HYDROLASE 
5dxh:D    (PRO18) to    (ASP84)  P110ALPHA/P85ALPHA WITH COMPOUND 5  |   LIPID KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5dxu:A   (ARG188) to   (TYR251)  P110DELTA/P85ALPHA WITH GDC-0326  |   LIPID KINASE, INHIBITOR, TRANSFERASE-INHIBITOR COMPLEX 
4q5h:B     (MET1) to    (ASP52)  SHIGELLA EFFECTOR KINASE OSPG BOUND TO AMPPNP AND E2-UB UBCH7-UB CONJUGATE  |   PROTEIN-PROTEIN COMPLEX, STRUCTURAL GENOMICS, MONTREAL-KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, KINASE FOLD, INHIBITION OF NF-KB PATHWAY, UNKNOWN FUNCTION, PROTEIN BINDING 
2a5u:A   (ASN218) to   (VAL282)  CRYSTAL STRUCTURE OF HUMAN PI3KGAMMA COMPLEXED WITH AS605240  |   PROTEIN-INHIBITOR COMPLEX, PI3KG, TRANSFERASE 
2aeh:A    (MET33) to    (LEU98)  FOCAL ADHESION KINASE 1  |   FERM DOMAIN, TRANSFERASE 
3bc3:A    (GLY61) to   (THR110)  EXPLORING INHIBITOR BINDING AT THE S SUBSITES OF CATHEPSIN L  |   CATHEPSIN L INHIBITOR BINDING AT THE S SUBSITES, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN 
4bpv:B   (GLY185) to   (SER234)  MOUSE CATHEPSIN S WITH COVALENT LIGAND  |   HYDROLASE, CYSTEINE PROTEASE, COVALENT LIGAND 
3n11:A   (GLY230) to   (ARG273)  CRYSTAL STRICTURE OF WILD-TYPE CHITINASE FROM BACILLUS CEREUS NCTU2  |   CHITINASE, CHINCTU2, WILD-TYPE, HYDROLASE 
3n12:A   (GLY230) to   (ARG273)  CRYSTAL STRICTURE OF CHITINASE IN COMPLEX WITH ZINC ATOMS FROM BACILLUS CEREUS NCTU2  |   CHITINASE, CHINCTU2, ZINC ATOMS, COMPLEX, HYDROLASE 
3n1a:A   (GLY230) to   (ARG273)  CRYSTAL STRICTURE OF E145G/Y227F CHITINASE IN COMPLEX WITH CYCLO-(L- HIS-L-PRO) FROM BACILLUS CEREUS NCTU2  |   CHITINASE, CHINCTU2, COMPLEX, CYCLO-(L-HIS-L-PRO), MUTATION, HYDROLASE 
3n5q:B   (ALA254) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE)  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
3n5r:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 4-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)PHENETHYL)-6- METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
3n5s:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 4-(2-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-3-YL) ETHYL)-6-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
3n5t:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6,6'-(2,2'-(PYRIDINE-3,5-DIYL)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE)  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
3n6b:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE H373S SINGLE MUTANT HEME DOMAIN COMPLEXED WITH 6,6'-(2,2'-(PYRIDINE-3,5-DIYL)BIS(ETHANE- 2,1-DIYL))BIS(4-METHYLPYRIDIN-2-AMINE)  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
5fj3:B   (ALA254) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((4-CHLORO-3-((METHYLAMINO)METHYL) PHENOXY)METHYL)QUINOLIN-2-AMINE IN THE ABSENCE OF ACETATE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4c3a:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6-AMINO-4- METHYLPYRIDIN-2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL)OXY) METHYL)-4-METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4c3a:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6-AMINO-4- METHYLPYRIDIN-2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL)OXY) METHYL)-4-METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
3cf6:E   (ASP650) to   (LYS706)  STRUCTURE OF EPAC2 IN COMPLEX WITH CYCLIC-AMP AND RAP  |   EPAC, RAPGEF4, RAP, RAP1B, CAMP, SP-CAMPS, GEF, GUNANINE NUCLEOTIDE EXCHANGE FACTOR, G-PROTEIN, GTP-BINDING, NUCLEOTIDE-BINDING, SIGNALING PROTEIN REGULATOR-GTP-BINDING PROTEIN COMPLEX, SIGNALING PROTEIN-GTP-BINDING PROTEIN COMPLEX 
4rf0:B     (MET1) to    (ASP52)  CRYSTAL STRUCTURE OF THE MIDDLE-EAST RESPIRATORY SYNDROME CORONAVIRUS PAPAIN-LIKE PROTEASE IN COMPLEX WITH UBIQUITIN (SPACE GROUP P6522)  |   ZINC RIBBON, DEUBIQUITINASE, PAPAIN-LIKE PROTEASE, PROTEIN BINDING 
3nlg:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6-{{(3'S,4'R)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3nlf:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6-{{(3'R,4'S)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3nlf:B   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6-{{(3'R,4'S)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3nlh:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN N368D MUTANT COMPLEXED WITH 6-{{(3'S,4'S)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3nli:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE N368D MUTANT HEME DOMAIN COMPLEXED WITH 6-{{(3'R,4'R)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3nli:B   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE N368D MUTANT HEME DOMAIN COMPLEXED WITH 6-{{(3'R,4'R)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3cmm:B     (MET1) to    (ASP52)  CRYSTAL STRUCTURE OF THE UBA1-UBIQUITIN COMPLEX  |   UBIQUITIN, E1, UBA1, PROTEIN TURNOVER, LIGASE, CONFORMATIONAL CHANGE, THIOESTER, ADENYLATION, TRANSTHIOESTERIFICATION, ATP-BINDING, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, UBL CONJUGATION PATHWAY, DNA DAMAGE, DNA REPAIR, LIGASE-PROTEIN BINDING COMPLEX 
3nlu:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1-{(3'R,4'R)-4'-[(6"-AMINO-4"-METHYLPYRIDIN-2"-YL) METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3nob:H     (MET1) to    (ASP52)  STRUCTURE OF K11-LINKED DI-UBIQUITIN  |   UBIQUITIN LYSINE-11, PROTEIN BINDING 
4car:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)METHYL) QUINOLIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4car:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)METHYL) QUINOLIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4rm8:B     (VAL7) to    (LEU61)  CRYSTAL STRUCTURE OF HUMAN EZRIN IN SPACE GROUP P21  |   FERM DOMAIN, C-ERMAD DOMAIN, MEMBRANE CYTOSKELETON LINKERS, ACTIN BINDING, PEPTIDE BINDING PROTEIN 
4rm9:A     (VAL7) to    (LEU61)  CRYSTAL STRUCTURE OF HUMAN EZRIN IN SPACE GROUP C2221  |   FERM DOMAIN, C-ERMAD DOMAIN, MEMBRANE CYTOSKELETON LINKERS, ACTIN BINDING, PEPTIDE BINDING PROTEIN 
3nse:A   (TYR253) to   (VAL306)  BOVINE ENOS, H4B-FREE, SEITU COMPLEX  |   NITRIC OXIDE SYNTHASE, HEME PROTEIN, TETRAHYDROBIOPTERIN, COMPLEX (OXIDOREDUCTASE-PEPTIDE), COMPLEX (OXIDOREDUCTASE-PEPTIDE) COMPLEX 
4cft:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)ETHYL) QUINOLIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4cft:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)ETHYL) QUINOLIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
5fvz:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(2-(5-(3-(DIMETHYLAMINO)PROPYL) PYRIDIN-3-YL)ETHYL)-4-METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
5fvz:B   (ALA254) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(2-(5-(3-(DIMETHYLAMINO)PROPYL) PYRIDIN-3-YL)ETHYL)-4-METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
5fvy:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(4-METHYLPIPERAZIN- 1-YL)PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
3nzs:A   (ASN218) to   (VAL282)  STRUCTURE-BASED OPTIMIZATION OF PYRAZOLO -PYRIMIDINE AND -PYRIDINE INHIBITORS OF PI3-KINASE  |   KINASE P110, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
3nzu:A   (ASN218) to   (VAL282)  STRUCTURE-BASED OPTIMIZATION OF PYRAZOLO -PYRIMIDINE AND -PYRIDINE INHIBITORS OF PI3-KINASE  |   KINASE P110, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5g2n:A   (ASN218) to   (VAL282)  X-RAY STRUCTURE OF PI3KINASE GAMMA IN COMPLEX WITH COPANLISIB  |   TRANSFERASE 
5g55:A   (ASN218) to   (VAL282)  3-QUINOLINE CARBOXAMIDES INHIBITORS OF PI3K  |   TRANSFERASE, ATM 
4ctz:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-6-(2-AMINO-2-(3-(2-(4-METHYLPYRIDIN-2-YL) ETHYL)PHENYL)ETHYL)-4-METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4cty:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (R)-6-(2-AMINO-2-(3-(2-(6-AMINO-4-METHYLPYRIDIN- 2-YL)ETHYL)PHENYL)ETHYL)-4-METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4cu0:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (R)-6-(3-AMINO-2-(5-(2-(6-AMINO-4- METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-3-YL)PROPYL)-4- METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4cu1:B   (ALA254) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-[(2S)-3-AMINO-2-{5-[2-(6-AMINO- 4-METHYLPYRIDIN-2-YL)ETHYL]PYRIDIN-3-YL}PROPYL]-4- METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4cul:B   (ALA254) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-ACETYL-2-AMINO-7,7-DIMETHYL-7,8- DIHYDROPTERIDIN-4(3H)-ONE  |   OXIDOREDUCTASE, COFACTOR ANALOG COMPLEX 
4cum:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (9AS)-2-AMINO-9A-METHYL-6,7,8,9,9A, 10-HEXAHYDROBENZO[G]PTERIDIN-4(3H)-ONE  |   OXIDOREDUCTASE, COFACTOR ANALOG COMPLEX 
4cum:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (9AS)-2-AMINO-9A-METHYL-6,7,8,9,9A, 10-HEXAHYDROBENZO[G]PTERIDIN-4(3H)-ONE  |   OXIDOREDUCTASE, COFACTOR ANALOG COMPLEX 
4cun:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (9AS)-2-AMINO-9A-METHYL-8,9,9A,10- TETRAHYDROBENZO[G]PTERIDINE-4,6(3H,7H)-DIONE  |   OXIDOREDUCTASE, COFACTOR ANALOG COMPLEX 
4cvg:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN (H4B-FREE) SUPPLEMENTED WITH 50UM ZN ACETATE AND WITH POOR BINDING OF 6-ACETYL-2-AMINO-7,7-DIMETHYL-7,8-DIHYDROPTERIDIN-4(3H)-ONE.  |   OXIDOREDUCTASE, COFACTOR ANALOG COMPLEX 
3dbs:A   (ASN218) to   (VAL282)  STRUCTURE OF PI3K GAMMA IN COMPLEX WITH GDC0941  |   PI3K GAMMA, INHIBITOR, KINASE, TRANSFERASE 
4cww:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-((5-(4- METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4cwx:A   (TYR253) to   (VAL306)  ALPHA-KETOGLUTARATE-DEPENDENT DIOXYGENASE COMPLEX1  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4cwy:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(5-(((3R,4R)-4-((6-AMINO-4- METHYLPYRIDIN-2-YL)METHYL)PYRROLIDIN-3-YL)OXY)PENTYL)-4- METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4cwy:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(5-(((3R,4R)-4-((6-AMINO-4- METHYLPYRIDIN-2-YL)METHYL)PYRROLIDIN-3-YL)OXY)PENTYL)-4- METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4cx0:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE Y477A MUTANT HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6- AMINO-4-METHYLPYRIDIN-2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL) OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4cx1:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE L111A MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(4-METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4cx2:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(5-(((3R,4R)-4-((6-AMINO-4- METHYLPYRIDIN-2-YL)METHYL)PYRROLIDIN-3-YL)OXY)PENTYL)-4- METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4cx2:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(5-(((3R,4R)-4-((6-AMINO-4- METHYLPYRIDIN-2-YL)METHYL)PYRROLIDIN-3-YL)OXY)PENTYL)-4- METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
3ddc:B   (GLY229) to   (SER331)  CRYSTAL STRUCTURE OF NORE1A IN COMPLEX WITH RAS  |   ONCOGENE, TUMORSUPPRESSOR, UBIQUITIN FOLD, RAS EFFECTOR, RAP1, H-RAS, RASSF1, RASSF5, RAPL, NORE1, GMPPNP, ADAPTOR, APOPTOSIS, MICROTUBULES, HYDROLASE-APOPTOSIS COMPLEX, DISEASE MUTATION, GOLGI APPARATUS, GTP-BINDING, LIPOPROTEIN, MEMBRANE, METHYLATION, NUCLEOTIDE-BINDING, PALMITATE, PRENYLATION, PROTO-ONCOGENE, ANTI- ONCOGENE, CELL CYCLE, METAL-BINDING, MICROTUBULE, PHORBOL-ESTER BINDING, ZINC-FINGER 
4d1p:A   (TYR251) to   (LEU304)  STRUCTURE OF HUMAN ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6-AMINO-4- METHYLPYRIDIN-2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL)OXY) METHYL)-4-METHYLPYRIDIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, 
4d33:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (N1-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN- 4-YL)-N2-(3-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4d34:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4- YL)-N-(3-FLUOROPHENETHYL)ETHAN-1-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4d34:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4- YL)-N-(3-FLUOROPHENETHYL)ETHAN-1-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4d35:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN- 4-YL)ETHYL-3-(3-FLUOROPHENYL)PROPAN-1-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4d35:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN- 4-YL)ETHYL-3-(3-FLUOROPHENYL)PROPAN-1-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4d37:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH  N-{[(1R,2R)-2-(3-FLUOROPHENYL)CYCLOPROPYL] ETHYL}-2-[2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL]ETHANAMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
3dqt:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NOS HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-N1-{TRANS-4'-[(6"-AMINO-4"-METHYLPYRIDIN-2"-YL) METHYL]PYRROLIDIN-3'-YL}-N2-(3'-CHLOROBENZYL)ETHANE-1,2-DIAMINE  |   NITRIC OXIDE SYNTHASE HEME ENZYME INHIBITOR, BLOOD COAGULATION, CALMODULIN-BINDING, CYTOSKELETON, FAD, FMN, GOLGI APPARATUS, HEME, IRON, LIPOPROTEIN, MEMBRANE, METAL-BINDING, MYRISTATE, NADP, OXIDOREDUCTASE, PALMITATE, PHOSPHOPROTEIN 
4u6p:B   (ARG454) to   (SER514)  STRUCTURAL MECHANISM OF ERROR-FREE BYPASS OF MAJOR BENZO[A]PYRENE ADDUCT BY HUMAN POLYMERASE KAPPA  |   BENZO[A]PYRENE-N2-GUANINE, DNA REPLICATION, DNA DAMAGE TOLERANCE, POLYMERASE KAPPA, ENVIRONMENT POLLUTION, TRANSFERASE-DNA COMPLEX 
4dk5:A   (ILE222) to   (VAL282)  CRYSTAL STRUCTURE OF HUMAN PI3K-GAMMA IN COMPLEX WITH A PYRIDYL- TRIAZINE INHIBITOR  |   PHOSPHOTRANSFERASE, CANCER, P85-ALPHA, P85-BETA, RAS, TRANSFERASE- INHIBITOR COMPLEX 
4u7c:A   (ARG454) to   (SER514)  STRUCTURE OF DNA POLYMERASE KAPPA IN COMPLEX WITH BENZOPYRENE ADDUCTED DNA  |   BENZO[A]PYRENE-N2-GUANINE, DNA REPLICATION, DNA DAMAGE TOLERANCE, POLYMERASE KAPPA, ENVIRONMENT POLLUTION, TRANSFERASE-DNA COMPLEX 
4u7c:B   (ARG454) to   (SER514)  STRUCTURE OF DNA POLYMERASE KAPPA IN COMPLEX WITH BENZOPYRENE ADDUCTED DNA  |   BENZO[A]PYRENE-N2-GUANINE, DNA REPLICATION, DNA DAMAGE TOLERANCE, POLYMERASE KAPPA, ENVIRONMENT POLLUTION, TRANSFERASE-DNA COMPLEX 
4uh7:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2- YL)ETHYL)PHENYL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4uh7:B   (LEU250) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2- YL)ETHYL)PHENYL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4uh8:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2- YL)ETHYL)PYRIDIN-3-YL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4uh8:B   (LEU250) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2- YL)ETHYL)PYRIDIN-3-YL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4uh9:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2- YL)ETHYL)-5-FLUOROPHENYL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4uh9:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2- YL)ETHYL)-5-FLUOROPHENYL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4uha:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)-5-(METHYL(2-(METHYLAMINO)ETHYL)AMINO)BENZONITRILE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
3phx:B    (GLU80) to   (ASP133)  OTU DOMAIN OF CRIMEAN CONGO HEMORRHAGIC FEVER VIRUS IN COMPLEX WITH ISG15  |   OTU DOMAIN, DE-UBIQUITINASE, DE-ISGYLASE, HYDROLASE-PROTEIN BINDING COMPLEX 
3pnh:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2-FLUORO-2-(3-FLUOROPHENYL) ETHYL) AMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE  |   HEME ENZYME, INHIBITOR, OXIDOREDUCTASE-INHIBITOR COMPLEX 
3pnh:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2-FLUORO-2-(3-FLUOROPHENYL) ETHYL) AMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE  |   HEME ENZYME, INHIBITOR, OXIDOREDUCTASE-INHIBITOR COMPLEX 
4upq:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N',N'-{[(2R)-3-AMINOPROPANE-1,2-DIYL] BIS(OXYMETHANEDIYLBENZENE-3,1-DIYL)}DITHIOPHENE-2-CARBOXIMIDAMIDE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4upr:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N,N''-{[(2S)-3-AMINOPROPANE-1,2-DIYL] BIS(OXYMETHANEDIYLBENZENE-3,1-DIYL)}DITHIOPHENE-2-CARBOXIMIDAMIDE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4upr:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N,N''-{[(2S)-3-AMINOPROPANE-1,2-DIYL] BIS(OXYMETHANEDIYLBENZENE-3,1-DIYL)}DITHIOPHENE-2-CARBOXIMIDAMIDE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4upt:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N'-[4-[[(2S,4R)-4-[3-[(C-THIOPHEN-2- YLCARBONIMIDOYL)AMINO]PHENOXY]PYRROLIDIN-2- YL]METHOXY]PHENYL]THIOPHENE-2-CARBOXIMIDAMIDE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4upt:B   (ALA254) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N'-[4-[[(2S,4R)-4-[3-[(C-THIOPHEN-2- YLCARBONIMIDOYL)AMINO]PHENOXY]PYRROLIDIN-2- YL]METHOXY]PHENYL]THIOPHENE-2-CARBOXIMIDAMIDE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4ups:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-[3-({[(3S,5S)-5-{[(3-{[(Z)-IMINO (THIOPHEN-2-YL)METHYL]AMINO}BENZYL)OXY]METHYL}PYRROLIDIN-3 -YL]OXY}METHYL)PHENYL]THIOPHENE-2-CARBOXIMIDAMIDE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4ups:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-[3-({[(3S,5S)-5-{[(3-{[(Z)-IMINO (THIOPHEN-2-YL)METHYL]AMINO}BENZYL)OXY]METHYL}PYRROLIDIN-3 -YL]OXY}METHYL)PHENYL]THIOPHENE-2-CARBOXIMIDAMIDE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
3pre:A   (ASN218) to   (LEU281)  QUINAZOLINES WITH INTRA-MOLECULAR HYDROGEN BONDING SCAFFOLD (IMHBS) AS PI3K/MTOR DUAL INHIBITORS.  |   PHOSPHOINOSITIDE KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5io9:A   (MET132) to   (SER210)  X-RAY STRUCURE OF THE N-TERMINAL DOMAIN OF HUMAN DOUBLECORTIN  |   DCX DOMAIN, UBIQUITIN-LIKE FOLD, MICROTUBULE ASSOCIATED, SIGNALING PROTEIN, TRANSFERASE 
3pzd:A  (GLN1698) to  (ALA1754)  STRUCTURE OF THE MYOSIN X MYTH4-FERM/DCC COMPLEX  |   PROTEIN-PROTEIN COMPLEX, MYTH4 DOMAIN, FERM DOMAIN, CARGO BINDING, MOTOR PROTEIN-APOPTOSIS COMPLEX 
3q3j:A  (LYS1498) to  (ASP1567)  CRYSTAL STRUCTURE OF PLEXIN A2 RBD IN COMPLEX WITH RND1  |   RAS-BINDING DOMAIN, PLEXIN, SMALL GTPASE, STRUCTURAL GENOMICS CONSORTIUM, SGC, MEMBRANE PROTEIN-PROTEIN BINDING COMPLEX 
3q7x:A    (GLU11) to    (SER58)  CRYSTAL STRUCTURE OF SYMFOIL-4P/PV1: DE NOVO DESIGNED BETA-TREFOIL ARCHITECTURE WITH SYMMETRIC PRIMARY STRUCTURE, PRIMITIVE VERSION 1  |   BETA-TREFOIL, BETA-TERFOIL, DE NOVO PROTEIN 
4ezj:A   (ASN218) to   (VAL282)  POTENT AND SELECTIVE INHIBITORS OF PI3K-DELTA: OBTAINING ISOFORM SELECTIVITY FROM THE AFFINITY POCKET AND TRYPTOPHAN SHELF  |   KINASE P110, P110-GAMMA, LIPID KINASE, CYTOPLASMIC, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4ezk:A   (ASN218) to   (VAL282)  POTENT AND SELECTIVE INHIBITORS OF PI3K-DELTA: OBTAINING ISOFORM SELECTIVITY FROM THE AFFINITY POCKET AND TRYPTOPHAN SHELF  |   KINASE P110, P110-GAMMA, LIPID KINASE, CYTOPLASMIC, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4f1s:A   (ILE220) to   (VAL282)  CRYSTAL STRUCTURE OF HUMAN PI3K-GAMMA IN COMPLEX WITH A PYRIDYL- TRIAZINE-SULFONAMIDE INHIBITOR  |   PHOSPHOTRANSFERASE, LIPID KINASE, P85, TRANSFERASE-INHIBITOR COMPLEX 
5j18:A   (PRO155) to   (GLY209)  SOLUTION STRUCTURE OF RAS BINDING DOMAIN (RBD) OF B-RAF COMPLEXED WITH RIGOSERTIB (COMPLEX I)  |   MAPK, PI3K, PROTEIN BINDING 
3qij:A   (HIS211) to   (ASP266)  PRIMITIVE-MONOCLINIC CRYSTAL STRUCTURE OF THE FERM DOMAIN OF PROTEIN 4.1R  |   CYTOSKELETON, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, STRUCTURAL PROTEIN 
5j7t:A   (HIS683) to   (ILE746)  MOLECULAR UNDERSTANDING OF USP7 SUBSTRATE RECOGNITION AND C-TERMINAL ACTIVATION  |   USP7, HAUSP, DUB, ACTIVATION, HYDROLASE 
4fa6:A   (ASN218) to   (VAL282)  DESIGN AND SYNTHESIS OF A NOVEL PYRROLIDINYL PYRIDO PYRIMIDINONE DERIVATIVE AS A POTENT INHIBITOR OF PI3KA AND MTOR  |   PHOSPHOINOSITIDE KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4fad:A   (ILE222) to   (VAL282)  DESIGN AND SYNTHESIS OF A NOVEL PYRROLIDINYL PYRIDO PYRIMIDINONE DERIVATIVE AS A POTENT INHIBITOR OF PI3KA AND MTOR  |   PHOSPHOINOSITIDE KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4v0i:A   (ASN187) to   (TYR251)  WATER NETWORK DETERMINES SELECTIVITY FOR A SERIES OF PYRIMIDONE INDOLINE AMIDE PI3KBETA INHIBITORS OVER PI3K-DELTA  |   TRANSFERASE, PI3K, KINASE SELECTIVITY 
4v0i:B   (SER186) to   (TYR251)  WATER NETWORK DETERMINES SELECTIVITY FOR A SERIES OF PYRIMIDONE INDOLINE AMIDE PI3KBETA INHIBITORS OVER PI3K-DELTA  |   TRANSFERASE, PI3K, KINASE SELECTIVITY 
3qx1:A   (GLU571) to   (THR625)  CRYSTAL STRUCTURE OF FAF1 UBX DOMAIN  |   UBX, PROTEIN BINDING, P97 BINDING 
4flh:A   (ILE220) to   (VAL282)  CRYSTAL STRUCTURE OF HUMAN PI3K-GAMMA IN COMPLEX WITH AMG511  |   P110, PHOSPHOTRANSFERASE, CANCER, P85, PHOSPHORYLATION, TRANSFERASE- INHIBITOR COMPLEX 
3r66:D    (GLU80) to   (ASP133)  CRYSTAL STRUCTURE OF HUMAN ISG15 IN COMPLEX WITH NS1 N-TERMINAL REGION FROM INFLUENZA VIRUS B, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET IDS HX6481, HR2873, AND OR2  |   STRUCTURAL GENOMICS, PSI-BIOLOGY, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, INNATE IMMUNITY, ISG15 CONJUGATION, VIRAL PROTEIN- ANTIVIRAL PROTEIN COMPLEX 
4gb9:A   (ASN218) to   (VAL282)  POTENT AND HIGHLY SELECTIVE BENZIMIDAZOLE INHIBITORS OF PI3K-DELTA  |   KINASE P110 GAMMA-ISOFORM, KINASE, LIPID KINASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
5kho:B   (GLY146) to   (VAL228)  RASIP1 RA DOMAIN IN COMPLEX WITH RAP1B  |   RASIP1, RAS-ASSOCIATION DOMAIN, RAP1B, COMPLEX, SIGNALING PROTEIN 
5khq:B   (GLY146) to   (GLY230)  RASIP1 RA DOMAIN  |   RASIP1, RAS-ASSOCIATION DOMAIN, RAP EFFECTOR, SIGNALING PROTEIN 
5kz6:B   (GLY230) to   (ARG273)  1.25 ANGSTROM CRYSTAL STRUCTURE OF CHITINASE FROM BACILLUS ANTHRACIS.  |   CHITINASE, TIM BARREL, HYDROLASE, STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID 
5lrv:B     (MET1) to    (ASP52)  STRUCTURE OF CEZANNE/OTUD7B OTU DOMAIN BOUND TO LYS11-LINKED DIUBIQUITIN  |   HYDROLASE, PROTEASE, DEUBIQUITINASE, OTU DOMAIN 
6nse:B   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE, H4B-FREE, CANAVANINE COMPLEX  |   NITRIC OXIDE SYNTHASE, HEME PROTEIN, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE 
8nse:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE, NNA COMPLEX  |   NITRIC OXIDE SYNTHASE, HEME PROTEIN, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE 
9nse:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE, ETHYL-ISOSELENOUREA COMPLEX  |   NITRIC OXIDE SYNTHASE, HEME PROTEIN, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE 
3ene:A   (ASN218) to   (VAL282)  COMPLEX OF PI3K GAMMA WITH AN INHIBITOR  |   LIPID KINASE, PHOSPHOINOSITIDE, INHIBITOR, 3-KINASE, SIGNALING, PYRAZOLOPYRIMIDINE, PIK-208, S2, KINASE, TRANSFERASE 
2bhj:A   (TYR261) to   (GLU314)  MURINE INO SYNTHASE WITH COUMARIN INHIBITOR  |   INOS, CALMODULIN-BINDING, FAD, FMN, HEME, METAL-BINDING, NADP, OXIDOREDUCTASE, POLYMORPHISM, ZINC 
1d1y:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 1, 3-PBITU (H4B FREE)  |   ALPHA-BETA FOLD, OXIDOREDUCTASE 
1p6l:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NOS HEME DOMAIN WITH L-N(OMEGA)-NITROARGININE-2,4- L-DIAMINOBUTYRIC AMIDE BOUND  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME 
1q1o:A   (GLY760) to   (GLY829)  SOLUTION STRUCTURE OF THE PB1 DOMAIN OF CDC24P (LONG FORM)  |   PB1 DOMAIN, PCCR, PC MOTIF, OPCA MOTIF, YEAST, CELL POLARITY, PROTEIN-PROTEIN INTERACTION, SIGNALING PROTEIN 
1e8z:A   (ASN218) to   (VAL282)  STRUCTURE DETERMINANTS OF PHOSPHOINOSITIDE 3-KINASE INHIBITION BY WORTMANNIN, LY294002, QUERCETIN, MYRICETIN AND STAUROSPORINE  |   TRANSFERASE, PHOSPHOINOSITIDE 3-KINASE GAMMA, SECONDARY MESSENGER GENERATION, PI3K, PI 3K, STAUROSPORINE 
1e90:A   (ASN218) to   (VAL282)  STRUCTURE DETERMINANTS OF PHOSPHOINOSITIDE 3-KINASE INHIBITION BY WORTMANNIN, LY294002, QUERCETIN, MYRICETIN AND STAUROSPORINE  |   PHOSPHOINOSITIDE 3-KINASE GAMMA, SECONDARY MESSENGER GENERATION, PI3K, PI 3K, MYRICETIN 
2dhz:A     (SER6) to    (GLN71)  SOLUTION STRUCTURE OF THE RA DOMAIN IN THE HUMAN LINK GUANINE NUCLEOTIDE EXCHANGE FACTOR II (LINK-GEFII)  |   LINK GUANINE NUCLEOTIDE EXCHANGE FACTOR II, LINK-GEFII, RA DOMAIN, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, SIGNALING PROTEIN 
3tl5:A   (ASN218) to   (VAL282)  DISCOVERY OF GDC-0980: A POTENT, SELECTIVE, AND ORALLY AVAILABLE CLASS I PHOSPHATIDYLINOSITOL 3-KINASE (PI3K)/MAMMALIAN TARGET OF RAPAMYCIN (MTOR) KINASE INHIBITOR FOR THE TREATMENT OF CANCER  |   TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
2uwq:A     (MET2) to    (ASP58)  SOLUTION STRUCTURE OF ASPP2 N-TERMINUS  |   ASPP2, UBIQUITIN-LIKE, SH3-DOMAIN, APOPTOSIS, CELL CYCLE, ANK REPEAT, SH3-BINDING 
4kcq:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(4-(2-(ETHYL(3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL) AMINO)ETHYL)PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4kcq:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(4-(2-(ETHYL(3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL) AMINO)ETHYL)PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
4kcr:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(3-(((3-FLUOROPHENETHYL)AMINO)METHYL)PHENYL)THIOPHENE- 2-CARBOXIMIDAMIDE  |   NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
2wxo:A   (ASN187) to   (TYR251)  THE CRYSTAL STRUCTURE OF THE MURINE CLASS IA PI 3-KINASE P110DELTA IN COMPLEX WITH AS5.  |   TRANSFERASE, PHOSPHOPROTEIN, ISOFORM-SPECIFIC INHIBITORS, CANCER 
2jy6:A     (ILE3) to    (ASP52)  SOLUTION STRUCTURE OF THE COMPLEX OF UBIQUITIN AND UBIQUILIN 1 UBA DOMAIN  |   UBIQUILIN, UBA, UBIQUITIN, COMPLEX, ALTERNATIVE SPLICING, CYTOPLASM, NUCLEUS, PHOSPHOPROTEIN, PROTEASOME, SIGNALING PROTEIN 
2kde:C    (ILE79) to   (ASP128)  NMR STRUCTURE OF MAJOR S5A (196-306):K48 LINKED DIUBIQUITIN SPECIES  |   PROTEIN COMPLEX, UBIQUITIN INTERACTING MOTIFS, CYTOPLASM, NUCLEUS, UBL CONJUGATION, ALTERNATIVE SPLICING, PHOSPHOPROTEIN, PROTEASOME, PROTEIN BINDING 
4nkx:D    (VAL37) to    (HIS78)  HUMAN STEROIDOGENIC CYTOCHROME P450 17A1 MUTANT A105L WITH SUBSTRATE PROGESTERONE  |   HEME PROTEIN, MONOOXYGENASE, STEROID 17ALPHA-HYDROXYLASE, STEROID C17,20 LYASE, NADPH-CYTOCHROME P450 REDUCTASE, CYTOCHROME B5, ENDOPLASMIC RETICULUM MEMBRANE, OXIDOREDUCTASE, LYASE 
2mbh:A     (ILE3) to    (ASP52)  NMR STRUCTURE OF EKLF(22-40)/UBIQUITIN COMPLEX  |   PROTEIN-PROTEIN COMPLEX, EKLF, UBIQUITIN, UIM/MIU, TRANSCRIPTION FACTOR TAD, TRANSCRIPTION 
3zw3:A   (ASN218) to   (VAL282)  FRAGMENT BASED DISCOVERY OF A NOVEL AND SELECTIVE PI3 KINASE INHIBITOR  |   TRANSFERASE 
3jww:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1-[(3'S,4'S)-4'-((6"-AMINO-4"-METHYLPYRIDIN-2"-YL)METHYL) PYRROLIDIN-3'-YL]-N2- (3'-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE  |   HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3jww:B   (ALA254) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1-[(3'S,4'S)-4'-((6"-AMINO-4"-METHYLPYRIDIN-2"-YL)METHYL) PYRROLIDIN-3'-YL]-N2- (3'-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE  |   HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3jx4:B   (TYR482) to   (GLN535)  STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'R,4'S)-4'-[(6"-AMINO-4"- METHYLPYRIDIN-2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL) ETHANE-1,2-DIAMINE  |   HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
2zcb:A     (MET1) to    (ASP52)  CRYSTAL STRUCTURE OF UBIQUITIN P37A/P38A  |   UB-FOLD, CYTOPLASM, NUCLEUS, PHOSPHORYLATION, UBL CONJUGATION, SIGNALING PROTEIN 
2zcb:B     (MET1) to    (ASP52)  CRYSTAL STRUCTURE OF UBIQUITIN P37A/P38A  |   UB-FOLD, CYTOPLASM, NUCLEUS, PHOSPHORYLATION, UBL CONJUGATION, SIGNALING PROTEIN 
4ovv:A    (ILE20) to    (ASP84)  CRYSTAL STRUCTURE OF PI3KALPHA IN COMPLEX WITH DIC4-PIP2  |   P110, P85, PI3KCA, PI3K, PIK3R1, PHOSPHATIDILYNOSITOL 3, 4, 5 TRIPHOSPHATE, PIP2, PHOSPHATIDYLINOSITOL 4, 5 BISPHOSPHATE, LIPID KINASE, PHOSPHOINOSITIDE, 3-KINASE, SIGNALING, PHOSPHATIDYLINOSITOL 3-KINASE, TRANSFERASE-TRANSFERASE REGULATOR COMPLEX 
4aj3:A    (ARG96) to   (GLU154)  3D STRUCTURE OF E. COLI ISOCITRATE DEHYDROGENASE IN COMPLEX WITH ISOCITRATE, CALCIUM(II) AND NADP - THE PSEUDO-MICHAELIS COMPLEX  |   OXIDOREDUCTASE, OXIDATIVE BETA-DECARBOXYLATION 
3l16:A   (ASN218) to   (LEU281)  DISCOVERY OF (THIENOPYRIMIDIN-2-YL)AMINOPYRIMIDINES AS POTENT, SELECTIVE, AND ORALLY AVAILABLE PAN-PI3-KINASE AND DUAL PAN-PI3- KINASE/MTOR INHIBITORS FOR THE TREATMENT OF CANCER  |   KINASE, ATP-BINDING, NUCLEOTIDE-BINDING, TRANSFERASE, PI3K-GAMMA P110 GAMMA 
5e6p:A  (PRO1466) to  (ASP1532)  PLEXINB2 CYTOPLASMIC REGION/PDZ-RHOGEF PDZ DOMAIN COMPLEX  |   PLEXIN, PDZ, PDZ-RHOGEF, COMPLEX, SIGNALING PROTEIN 
3n13:A   (GLY230) to   (ARG273)  CRYSTAL STRICTURE OF D143A CHITINASE IN COMPLEX WITH NAG FROM BACILLUS CEREUS NCTU2  |   CHITINASE, CHINCTU2, COMPLEX, NAG, MUTATION, HYDROLASE 
3n5p:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 4-(2-(6-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-2-YL) ETHYL)-6-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
3n67:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE N368D/V106M DOUBLE MUTANT HEME DOMAIN COMPLEXED WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE) BIS(ETHANE-2,1-DIYL))BIS(4-METHYLPYRIDIN-2-AMINE)  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
3n68:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN N368D/V106M DOUBLE MUTANT COMPLEXED WITH 4-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PHENETHYL)-6-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX 
3nld:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6-{{(3'S,4'S)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3nle:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6-{{(3'R,4'R)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3nle:B   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6-{{(3'R,4'R)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
3nlt:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1-{(3'S,4'S)-4'-[(6"-AMINO-4"-METHYLPYRIDIN-2"-YL) METHYL]PYRROLIDIN-3'-YL}- N2-(3'-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE  |   NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE 
4cwv:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-((5-(PYRIDIN- 2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL)PYRIDIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4cwv:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-((5-(PYRIDIN- 2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL)PYRIDIN-2-AMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4cwz:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE Y477A MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(4-METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4cwz:B   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE Y477A MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(4-METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE  |   OXIDOREDUCTASE, INHIBITOR COMPLEX 
4tv3:A   (GLY188) to   (GLU263)  ISOLATED P110A SUBUNIT OF PI3KA PROVIDES A PLATFORM FOR STRUCTURE- BASED DRUG DESIGN  |   LIPID KINASE ACTIVITY, ATPASE ACTIVITY, SURFACE PLASMON RESONANCE (SPR), ISOTHERMAL TITRATION CALORIMETRY (ITC)., TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4d38:A   (TYR253) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (1R,2R)-2-(3-FLUOROBENZYL)-N-{2-[2- (1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL]ETHYL}CYCLOPROPANAMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
4d38:B   (ALA254) to   (VAL306)  STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (1R,2R)-2-(3-FLUOROBENZYL)-N-{2-[2- (1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL]ETHYL}CYCLOPROPANAMINE  |   OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX 
3dqs:A   (TYR253) to   (VAL306)  STRUCTURE OF ENDOTHELIAL NOS HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-N1-{CIS-4'-[(6"-AMINO-4"-METHYLPYRIDIN-2"-YL)METHYL]PYRROLIDIN- 3'-YL}-N2-(4'-CHLOROBENZYL)ETHANE-1,2-DIAMINE  |   NITRIC OXIDE SYNTHASE HEME ENZYME INHIBITOR, BLOOD COAGULATION, CALMODULIN-BINDING, CYTOSKELETON, FAD, FMN, GOLGI APPARATUS, HEME, IRON, LIPOPROTEIN, MEMBRANE, METAL-BINDING, MYRISTATE, NADP, OXIDOREDUCTASE, PALMITATE, PHOSPHOPROTEIN 
5j17:A   (PRO155) to   (GLY209)  SOLUTION STRUCTURE OF RAS BINDING DOMAIN (RBD) OF B-RAF  |   MAPK, PI3K, PROTEIN BINDING 
4fhj:A   (ASN218) to   (VAL282)  CRYSTAL STRUCTURE OF PI3K-GAMMA IN COMPLEX WITH IMIDAZOPYRIDINE 2  |   INHIBITOR, P110, KINASE, TRANSFERASE, ATP-BINDING, P84, P101, TRANSFERASE-INHIBITOR COMPLEX 
5jtv:E   (ARG892) to   (GLU955)  USP7CD-UBL45 IN COMPLEX WITH UBIQUITIN  |   USP7, HAUSP, C-TERMINAL ACTIVATION, HYDROLASE 
5jtv:G   (ARG892) to   (GLU955)  USP7CD-UBL45 IN COMPLEX WITH UBIQUITIN  |   USP7, HAUSP, C-TERMINAL ACTIVATION, HYDROLASE 
5l72:A   (ARG188) to   (TYR251)  PI3 KINASE DELTA IN COMPLEX WITH N-[6-(5-METHANESULFONAMIDO-6- METHOXYPYRIDIN-3-YL)-1,3-DIHYDRO-2-BENZOFURAN-4-YL]-2-(MORPHOLIN-4- YL)ACETAMIDE  |   PI3 KINASE DELTA, TRANSFERASE 
5nse:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE, H4B-FREE, HYDROXY-ARG COMPLEX  |   NITRIC OXIDE SYNTHASE, HEME PROTEIN, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE 
7nse:A   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE, H4B-FREE, ADMA COMPLEX  |   NITRIC OXIDE SYNTHASE, HEME PROTEIN, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE 
7nse:B   (TYR253) to   (VAL306)  BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE, H4B-FREE, ADMA COMPLEX  |   NITRIC OXIDE SYNTHASE, HEME PROTEIN, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE