12ca:A (ALA115) to (LEU212) ALTERING THE MOUTH OF A HYDROPHOBIC POCKET. STRUCTURE AND KINETICS OF HUMAN CARBONIC ANHYDRASE II MUTANTS AT RESIDUE VAL-121 | LYASE(OXO-ACID)
3rld:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE Y7I MUTANT OF HUMAN CARBONIC ANHYDRASE II | ZINC METALLOENZYME, HISTIDINE LIGANDS, Y7I MUTATION, LYASE
1a42:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH BRINZOLAMIDE | LYASE, ZINC, INHIBITOR
2aw1:A (ALA115) to (LEU212) CARBONIC ANHYDRASE INHIBITORS: VALDECOXIB BINDS TO A DIFFERENT ACTIVE SITE REGION OF THE HUMAN ISOFORM II AS COMPARED TO THE STRUCTURALLY RELATED CYCLOOXYGENASE II "SELECTIVE" INHIBITOR CELECOXIB | CARBONIC ANHYDRASE, PROTEIN-INHIBITOR COMPLEX, LYASE
3efi:A (ALA115) to (LEU212) CARBONIC ANHYDRASE ACTIVATORS: KINETIC AND X-RAY CRYSTALLOGRAPHIC STUDY FOR THE INTERACTION OF D- AND L- TRYPTOPHAN WITH THE MAMMALIAN ISOFORMS I-XIV | CARBONIC ANHYDRASE, ACTIVATORS, CRYSTAL STRUCTURE, AMINOACIDS, OXO-ACID, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC
2ax2:A (ALA115) to (LEU212) PRODUCTION AND X-RAY CRYSTALLOGRAPHIC ANALYSIS OF FULLY DEUTERATED HUMAN CARBONIC ANHYDRASE II | PERDEURATED HUMAN CARBONIC ANHYDRASE II PROTON TRANSFER, LYASE
4wl4:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE 6-HYDROXY-CHROMENE-2-THIONE INHIBITOR | LYASE
1am6:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II INHIBITOR: ACETOHYDROXAMATE | HYDROLASE, CO2 HYDRATION
3ryj:B (ALA115) to (LEU212) CARBONIC ANHYDRASE COMPLEXED WITH 4-SULFAMOYL-N-(2,2,2- TRIFLUOROETHYL)BENZAMIDE | ALPHA BETA, LYASE
3ryv:B (ALA115) to (LEU212) CARBONIC ANHYDRASE COMPLEXED WITH N-ETHYL-4-SULFAMOYLBENZAMIDE | ALPHA BETA, LYASE
3ryx:B (ALA115) to (LEU212) FLUOROALKYL AND ALKYL CHAINS HAVE SIMILAR HYDROPHOBICITIES IN BINDING TO THE HYDROPHOBIC WALL OF CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3ryz:A (ALA115) to (LEU212) FLUOROALKYL AND ALKYL CHAINS HAVE SIMILAR HYDROPHOBICITIES IN BINDING TO THE HYDROPHOBIC WALL OF CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3rz0:B (ALA115) to (LEU212) FLUOROALKYL AND ALKYL CHAINS HAVE SIMILAR HYDROPHOBICITIES IN BINDING TO THE HYDROPHOBIC WALL OF CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3rz1:B (ALA115) to (LEU212) FLUOROALKYL AND ALKYL CHAINS HAVE SIMILAR HYDROPHOBICITIES IN BINDING TO THE HYDROPHOBIC WALL OF CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3rz5:A (ALA115) to (LEU212) FLUOROALKYL AND ALKYL CHAINS HAVE SIMILAR HYDROPHOBICITIES IN BINDING TO THE HYDROPHOBIC WALL OF CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3rz7:A (ALA115) to (LEU212) FLUOROALKYL AND ALKYL CHAINS HAVE SIMILAR HYDROPHOBICITIES IN BINDING TO THE HYDROPHOBIC WALL OF CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3rz8:A (ALA115) to (LEU212) FLUOROALKYL AND ALKYL CHAINS HAVE SIMILAR HYDROPHOBICITIES IN BINDING TO THE HYDROPHOBIC WALL OF CARBONIC ANHYDRASE | ALPHA BETA, LYASE
2osf:A (ALA115) to (LEU211) INHIBITION OF CARBONIC ANHYDRASE II BY THIOXOLONE: A MECHANISTIC AND STRUCTURAL STUDY | CARBONIC ANHYDRASE II, THIOXOLONE, THERAPEUTIC CA INHIBITORS, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC
2osm:A (ALA115) to (LEU211) INHIBITION OF CARBONIC ANHYDRASE II BY THIOXOLONE: A MECHANISTIC AND STRUCTURAL STUDY | HUMAN CARBONIC ANHYDRASE II, 2-HYDROXYTHIOPHENOL, LYASE
4wr7:A (SER115) to (CYS212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME I WITH 2,3,5,6- TETRAFLUORO-4-(PROPYLTHIO)BENZENESULFONAMIDE. | DRUG DESIGN, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
4wr7:B (SER115) to (CYS212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME I WITH 2,3,5,6- TETRAFLUORO-4-(PROPYLTHIO)BENZENESULFONAMIDE. | DRUG DESIGN, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
4wup:A (SER115) to (CYS212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME I WITH 4-[(2- HYDROXYETHYL)THIO]BENZENESULFONAMIDE | DRUG DESIGN, LYASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4wup:B (SER115) to (CYS212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME I WITH 4-[(2- HYDROXYETHYL)THIO]BENZENESULFONAMIDE | DRUG DESIGN, LYASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4wuq:A (SER115) to (CYS212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME I WITH 2,3,5,6- TETRAFLUORO-4-PIPERIDIN-1-YLBENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
4wuq:B (SER115) to (CYS212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME I WITH 2,3,5,6- TETRAFLUORO-4-PIPERIDIN-1-YLBENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
4hba:A (ALA115) to (LEU212) STRUCTURAL AND CATALYTIC CHARACTERIZATION OF A THERMAL AND ACID STABLE VARIANT OF HUMAN CARBONIC ANHYDRASE II CONTAINING AN ENGINEERED DISULFIDE BOND | HUMAN CARBONIC ANHYDRASE II, THERMAL STABILITY, LYASE
4ww6:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 2,3,5,6- TETRAFLUORO-4-(PROPYLTHIO)BENZENESULFONAMIDE | DRUG DESIGN, LYASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4hew:A (ALA115) to (LEU212) ACTIVITY ENHANCERS OF H64A VARIANT OF HUMAN CARBONIC ANHYDRASE II POSSESS MULTIPLE BINDING SITES WITHIN AND AROUND THE ENZYME STRUCTURE | HYDRATION/DEHYDRATION, HIS64ALA, LYASE
4hey:A (ALA115) to (LEU212) ACTIVITY ENHANCERS OF H64A VARIANT OF HUMAN CARBONIC ANHYDRASE II POSSESS MULTIPLE BINDING SITES WITHIN AND AROUND THE ENZYME STRUCTURE | HYDRATION/DEHYDRATION, HIS64ALA, LYASE
4hez:A (ALA115) to (LEU212) ACTIVITY ENHANCERS OF H64A VARIANT OF HUMAN CARBONIC ANHYDRASE II POSSESS MULTIPLE BINDING SITES WITHIN AND AROUND THE ENZYME STRUCTURE | HYDRATION/DEHYDRATION, HIS64ALA, LYASE
4hf3:A (ALA115) to (LEU212) ACTIVITY ENHANCERS OF H64A VARIANT OF HUMAN CARBONIC ANHYDRASE II POSSESS MULTIPLE BINDING SITES WITHIN AND AROUND THE ENZYME STRUCTURE | HYDRATION/DEHYDRATION, HIS64ALA, LYASE
1bcd:A (ALA115) to (LEU212) X-RAY CRYSTALLOGRAPHIC STRUCTURE OF A COMPLEX BETWEEN HUMAN CARBONIC ANHYDRASE II AND A NEW TOPICAL INHIBITOR, TRIFLUOROMETHANE SULPHONAMIDE | LYASE(OXO-ACID)
1bn1:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II INHIBITOR | CO2 HYDRATION, ZINC ENZYME, LYASE
1bn3:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II INHIBITOR | CO2 HYDRATION, ZINC ENZYME, LYASE
1bn4:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II INHIBITOR | CO2 HYDRATION, ZINC ENZYME, LYASE
1bnm:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II INHIBITOR | CO2 HYDRATION, ZINC ENZYME, LYASE
1bnn:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II INHIBITOR | CO2 HYDRATION, ZINC ENZYME, LYASE
1bnq:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II INHIBITOR | CO2 HYDRATION, ZINC ENZYME, LYASE
1bnt:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II INHIBITOR | CO2 HYDRATION, ZINC ENZYME, LYASE
1bnu:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II INHIBITOR | CO2 HYDRATION, ZINC ENZYME, LYASE
1bnv:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II INHIBITOR | CO2 HYDRATION, ZINC ENZYME, LYASE
1bnw:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II INHIBITOR | CO2 HYDRATION, ZINC ENZYME, LYASE
3s72:B (ALA115) to (LEU212) THE ORIGIN OF THE HYDROPHOBIC EFFECT IN THE MOLECULAR RECOGNITION OF ARYLSULFONAMIDES BY CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3s73:B (ALA115) to (LEU212) THE ORIGIN OF THE HYDROPHOBIC EFFECT IN THE MOLECULAR RECOGNITION OF ARYLSULFONAMIDES BY CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3s74:B (ALA115) to (LEU212) THE ORIGIN OF THE HYDROPHOBIC EFFECT IN THE MOLECULAR RECOGNITION OF ARYLSULFONAMIDES BY CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3s75:B (ALA115) to (LEU212) THE ORIGIN OF THE HYDROPHOBIC EFFECT IN THE MOLECULAR RECOGNITION OF ARYLSULFONAMIDES BY CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3s76:A (ALA115) to (LEU212) THE ORIGIN OF THE HYDROPHOBIC EFFECT IN THE MOLECULAR RECOGNITION OF ARYLSULFONAMIDES BY CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3s78:B (ALA115) to (LEU212) THE ORIGIN OF THE HYDROPHOBIC EFFECT IN THE MOLECULAR RECOGNITION OF ARYLSULFONAMIDES BY CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3s8x:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-{[(4- METHYL-6-OXO-1,6-DIHYDRO-2-PYRIMIDINYL) SULFANYL]ACETYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, SULFONAMIDE, METAL-BINDING, LYASE- LYASE INHIBITOR COMPLEX
3s97:A (PRO150) to (PHE249) PTPRZ CNTN1 COMPLEX | CARBONIC ANHDYRASE LIKE IMMUNOGLOBULIN, CELL ADHESION COMPLEX, CELL ADHESION
3s97:B (PRO150) to (PHE249) PTPRZ CNTN1 COMPLEX | CARBONIC ANHDYRASE LIKE IMMUNOGLOBULIN, CELL ADHESION COMPLEX, CELL ADHESION
1bv3:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH UREA | CARBONATE HYDRO-LYASE
3s9t:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 2- CHLORO-5-{[(4,6-DIMETHYL-2-PYRIMIDINYL) SULFANYL]ACETYL}BENZENESULFONAMIDE | DRUG DESIGN, SULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3sap:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-{[(5- BUTYL-2-PYRIMIDINYL)SULFANYL]ACETYL}BENZENESULFONAMIDE | DRUG DESIGN, SULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4ht0:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH THE INHIBITOR. | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, CARBON-OXYGEN LYASE ACTIVITY
3sbh:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-{[(4, 6-DIMETHYL-2-PYRIMIDINYL)SULFANYL]ACETYL}BENZENESULFONAMIDE | DRUG DESIGN, SULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3sbi:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-[(2- PYRIMIDINYLSULFANYL)ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, SULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4hu1:B (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH THE INHIBITOR. | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, CARBONATE DEHYDRATASE ACTIVITY, CARBON-OXYGEN LYASE ACTIVITY
4hu1:A (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH THE INHIBITOR. | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, CARBONATE DEHYDRATASE ACTIVITY, CARBON-OXYGEN LYASE ACTIVITY
3fe4:A (VAL134) to (LEU233) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE VI | CARBONIC ANHYDRASE, SECRETION, METAL BINDING, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, GLYCOPROTEIN, LYASE, METAL- BINDING, SECRETED
4xe1:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 6-SULFAMOYL-SACCHARIN | CYTOPLASM, LYASE, INHIBITOR
2pou:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 4,5-DICHLORO-BENZENE-1,3-DISULFONAMIDE | CARBONIC ANHYDRASE II, PROTEIN-INHIBITOR COMPLEXES, LYASE
2pov:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 4-AMINO-6-CHLORO-BENZENE-1,3-DISULFONAMIDE | CARBONIC ANHYDRASE II, PROTEIN-INHIBITOR COMPLEXES, LYASE
2pow:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 4-AMINO-6-TRIFLUOROMETHYL-BENZENE-1,3- DISULFONAMIDE | CARBONIC ANHYDRASE II, PROTEIN-INHIBITOR COMPLEXES, LYASE
1cah:A (ALA115) to (LEU212) STRUCTURE OF COBALT CARBONIC ANHYDRASE COMPLEXED WITH BICARBONATE | LYASE(OXO-ACID)
1cai:A (ALA115) to (LEU212) STRUCTURAL ANALYSIS OF THE ZINC HYDROXIDE-THR 199-GLU 106 HYDROGEN BONDING NETWORK IN HUMAN CARBONIC ANHYDRASE II | LYASE(OXO-ACID)
1cak:A (ALA115) to (LEU212) STRUCTURAL ANALYSIS OF THE ZINC HYDROXIDE-THR 199-GLU 106 HYDROGEN BONDING NETWORK IN HUMAN CARBONIC ANHYDRASE II | LYASE(OXO-ACID)
1cam:A (ALA115) to (LEU212) STRUCTURAL ANALYSIS OF THE ZINC HYDROXIDE-THR 199-GLU 106 HYDROGEN BONDING NETWORK IN HUMAN CARBONIC ANHYDRASE II | LYASE(OXO-ACID)
1cao:A (ALA115) to (LEU212) CRYSTALLOGRAPHIC STUDIES OF THE BINDING OF PROTONATED AND UNPROTONATED INHIBITORS TO CARBONIC ANHYDRASE USING HYDROGEN SULPHIDE AND NITRATE ANIONS | LYASE(OXO-ACID)
1cct:A (ALA115) to (LEU212) STRUCTURE-ASSISTED REDESIGN OF A PROTEIN-ZINC BINDING SITE WITH FEMTOMOLAR AFFINITY | LYASE (OXO-ACID)
1okl:A (ALA115) to (LEU211) CARBONIC ANHYDRASE II COMPLEX WITH THE 1OKL INHIBITOR 5- DIMETHYLAMINO-NAPHTHALENE-1-SULFONAMIDE | LYASE (OXO-ACID), INHIBITOR
1okm:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEX WITH THE 1OKM INHIBITOR 4- SULFONAMIDE-[1-(4-AMINOBUTANE)]BENZAMIDE | LYASE (OXO-ACID), INHIBITOR
1cil:A (ALA115) to (LEU212) THE POSITIONS OF HIS-64 AND A BOUND WATER IN HUMAN CARBONIC ANHYDRASE II UPON BINDING THREE STRUCTURALLY RELATED INHIBITORS | LYASE(OXO-ACID)
1cim:A (ALA115) to (LEU212) THE POSITIONS OF HIS-64 AND A BOUND WATER IN HUMAN CARBONIC ANHYDRASE II UPON BINDING THREE STRUCTURALLY RELATED INHIBITORS | LYASE(OXO-ACID)
1cin:A (ALA115) to (LEU212) THE POSITIONS OF HIS-64 AND A BOUND WATER IN HUMAN CARBONIC ANHYDRASE II UPON BINDING THREE STRUCTURALLY RELATED INHIBITORS | LYASE(OXO-ACID)
1oq5:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH NANOMOLAR INHIBITOR | 10-STRANDED, TWISTED BETA-SHEET, METAL BINDING PROTEIN
1cnc:A (ALA115) to (LEU212) COMPENSATORY PLASTIC EFFECTS IN THE REDESIGN OF PROTEIN- ZINC BINDING SITES | LYASE(OXO-ACID)
1cng:A (ALA115) to (LEU212) X-RAY CRYSTALLOGRAPHIC STUDIES OF ENGINEERED HYDROGEN BOND NETWORKS IN A PROTEIN-ZINC BINDING SITE | LYASE (OXO-ACID)
1cnh:A (ALA115) to (LEU212) X-RAY CRYSTALLOGRAPHIC STUDIES OF ENGINEERED HYDROGEN BOND NETWORKS IN A PROTEIN-ZINC BINDING SITE | LYASE (OXO-ACID)
1cni:A (ALA115) to (LEU212) X-RAY CRYSTALLOGRAPHIC STUDIES OF ENGINEERED HYDROGEN BOND NETWORKS IN A PROTEIN-ZINC BINDING SITE | LYASE (OXO-ACID)
1cnj:A (ALA115) to (LEU212) X-RAY CRYSTALLOGRAPHIC STUDIES OF ENGINEERED HYDROGEN BOND NETWORKS IN A PROTEIN-ZINC BINDING SITE | LYASE (OXO-ACID)
1cnk:A (ALA115) to (LEU212) X-RAY CRYSTALLOGRAPHIC STUDIES OF ENGINEERED HYDROGEN BOND NETWORKS IN A PROTEIN-ZINC BINDING SITE | LYASE (OXO-ACID)
1cnw:A (ALA115) to (LEU212) SECONDARY INTERACTIONS SIGNIFICANTLY REMOVED FROM THE SULFONAMIDE BINDING POCKET OF CARBONIC ANHYDRASE II INFLUENCE BINDING CONSTANTS | LYASE (OXO-ACID)
1cny:A (ALA115) to (LEU212) SECONDARY INTERACTIONS SIGNIFICANTLY REMOVED FROM THE SULFONAMIDE BINDING POCKET OF CARBONIC ANHYDRASE II INFLUENCE BINDING CONSTANTS | LYASE (OXO-ACID)
2q1b:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH SACCHARIN | 10-STRANDED, TWISTED BETA-SHEET, LYASE
2q1q:A (ALA115) to (LEU212) CARBONIC ANHYDRASE INHIBITORS. INTERACTION OF THE ANTIEPILEPTIC DRUG SULTHIAME WITH TWELVE MAMMALIAN ISOFORMS: KINETIC AND X-RAY CRYSTALLOGRAPHIC STUDIES | ANTIEPILEPTIC, CARBONIC ANHYDRASE, INHIBITORS, CRYSTAL STRUCTURE, LYASE
1cra:A (ALA115) to (LEU212) THE COMPLEX BETWEEN HUMAN CARBONIC ANHYDRASE II AND THE AROMATIC INHIBITOR 1,2,4-TRIAZOLE | LYASE(OXO-ACID)
1crm:A (SER115) to (CYS212) STRUCTURE AND FUNCTION OF CARBONIC ANHYDRASES | LYASE (OXO-ACID)
4idr:X (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II PROTON TRANSFER DOUBLE MUTANT | GOLOBULAR PROTEIN, LYASE
1cvb:A (ALA115) to (LEU212) STRUCTURAL AND FUNCTIONAL IMPORTANCE OF A CONSERVED HYDROGEN BOND NETWORK IN HUMAN CARBONIC ANHYDRASE II | LYASE(OXO-ACID)
1cvd:A (ALA115) to (LEU212) STRUCTURAL CONSEQUENCES OF REDESIGNING A PROTEIN-ZINC BINDING SITE | LYASE(OXO-ACID)
1cve:A (ALA115) to (LEU212) STRUCTURAL CONSEQUENCES OF REDESIGNING A PROTEIN-ZINC BINDING SITE | LYASE(OXO-ACID)
1cvf:A (ALA115) to (LEU212) STRUCTURAL CONSEQUENCES OF REDESIGNING A PROTEIN-ZINC BINDING SITE | LYASE(OXO-ACID)
1cvh:A (ALA115) to (LEU212) STRUCTURAL CONSEQUENCES OF REDESIGNING A PROTEIN-ZINC BINDING SITE | HYDRO-LYASE
2cbd:A (ALA115) to (LEU212) STRUCTURE OF NATIVE AND APO CARBONIC ANHYDRASE II AND SOME OF ITS ANION-LIGAND COMPLEXES | LYASE(OXO-ACID)
2cba:A (ALA115) to (LEU212) STRUCTURE OF NATIVE AND APO CARBONIC ANHYDRASE II AND SOME OF ITS ANION-LIGAND COMPLEXES | LYASE(OXO-ACID)
2cbb:A (ALA115) to (LEU212) STRUCTURE OF NATIVE AND APO CARBONIC ANHYDRASE II AND SOME OF ITS ANION-LIGAND COMPLEXES | LYASE(OXO-ACID)
2cbc:A (ALA115) to (LEU212) STRUCTURE OF NATIVE AND APO CARBONIC ANHYDRASE II AND SOME OF ITS ANION-LIGAND COMPLEXES | LYASE(OXO-ACID)
2cbe:A (ALA115) to (LEU212) STRUCTURE OF NATIVE AND APO CARBONIC ANHYDRASE II AND SOME OF ITS ANION-LIGAND COMPLEXES | LYASE(OXO-ACID)
1dca:A (ALA115) to (LEU212) STRUCTURE OF AN ENGINEERED METAL BINDING SITE IN HUMAN CARBONIC ANHYDRASE II REVEALS THE ARCHITECTURE OF A REGULATORY CYSTEINE SWITCH | LYASE(OXO-ACID)
1dcb:A (ALA115) to (LEU212) STRUCTURE OF AN ENGINEERED METAL BINDING SITE IN HUMAN CARBONIC ANHYDRASE II REVEALS THE ARCHITECTURE OF A REGULATORY CYSTEINE SWITCH | LYASE(OXO-ACID)
1dmx:A (PRO115) to (GLN212) MURINE MITOCHONDRIAL CARBONIC ANYHDRASE V AT 2.45 ANGSTROMS RESOLUTION | PROTON TRANSFER, LYASE (OXO-ACID)
1dmx:B (PRO115) to (GLN212) MURINE MITOCHONDRIAL CARBONIC ANYHDRASE V AT 2.45 ANGSTROMS RESOLUTION | PROTON TRANSFER, LYASE (OXO-ACID)
1dmy:A (PRO115) to (GLN212) COMPLEX BETWEEN MURINE MITOCHONDRIAL CARBONIC ANYHDRASE V AND THE TRANSITION STATE ANALOGUE ACETAZOLAMIDE | PROTON TRANSFER, LYASE (OXO-ACID)
1dmy:B (PRO115) to (GLN212) COMPLEX BETWEEN MURINE MITOCHONDRIAL CARBONIC ANYHDRASE V AND THE TRANSITION STATE ANALOGUE ACETAZOLAMIDE | PROTON TRANSFER, LYASE (OXO-ACID)
2qo8:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE COMPLEX OF HCAII WITH AN INDANE-SULFONAMIDE INHIBITOR | CARBONIC ANHYDRASE II, LYASE
2qoa:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE COMPLEX OF HCAII WITH AN INDANE-SULFONAMIDE INHIBITOR | CARBONIC ANHYDRASE II, LYASE
2qp6:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE COMPLEX OF HCAII WITH A BIOREDUCTIVE ANTITUMOR DERIVATIVE | CARBONIC ANHYDRASE II, LYASE
4ito:A (ALA115) to (LEU212) HUMAN CA II INHIBITION BY NOVEL SULFONAMIDE | ALPHA BETA FOLD, REVERSIBLE HYDRATION OF CARBON DIOXIDE TO BICARBONATE AND PROTON, LYASE-LYASE INHIBITOR COMPLEX
4itp:A (ALA115) to (LEU212) STRUCTURE OF HUMAN CARBONIC ANHYDRASE II BOUND TO A BENZENE SULFONAMIDE | ALPHA BETA FOLD, REVERSIBLE HYDRATION OF CARBON DIOXIDE TO BICARBONATE AND PROTON, LYASE-LYASE INHIBITOR COMPLEX
3t5u:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH N-HYDROXY BENZENESULFONAMIDE | PROTEIN-INHIBITOR COMPLEX, LYASE-LYASE INHIBITOR COMPLEX
3t5z:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH N-METHOXY-BENZENESULFONAMIDE | PROTEIN-INHIBITOR COMPLEX, LYASE-LYASE INHIBITOR COMPLEX
4iwz:A (ALA115) to (LEU212) STRUCTURE OF HCAII IN COMPLEX WITH AN ACETAZOLAMIDE DERIVATIVE | ALPHA BETA FOLD, REVERSIBLE HYDRATION OF CARBON DI OXIDE TO BICARBONATE AND PROTON, LYASE-LYASE INHIBITOR COMPLEX
3t82:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH ACETYLATED CARBOHYDRATE SULFAMATES | ALPHA CARBONIC ANHYDRASE, LYASE-LYASE INHIBITOR COMPLEX
3t83:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH ACETYLATED CARBOHYDRATE SULFAMATES | ALPHA CARBONIC ANHYDRASE, LYASE-LYASE INHIBITOR COMPLEX
3t85:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH ACETYLATED CARBOHYDRATE SULFAMATES | ALPHA CARBONIC ANHYDRASE, LYASE-LYASE INHIBITOR COMPLEX
4y0j:A (ALA115) to (LEU212) H/D EXCHANGED HUMAN CARBONIC ANHYDRASE II PH 6 ROOM TEMPERATURE NEUTRON CRYSTAL STRUCTURE. | NEUTRON, PROTON TRANSFER, H/D EXCHANGED, LYASE
3tmj:A (ALA115) to (LEU212) JOINT X-RAY/NEUTRON STRUCTURE OF HUMAN CARBONIC ANHYDRASE II AT PH 7.8 | H/D EXCHANGED, JOINT NEUTRON/X-RAY REFINEMENT, LYASE
3gz0:A (ALA115) to (LEU212) APO-HUMAN CARBONIC ANHYDRASE II REVISITED: IMPLICATIONS OF THE LOSS OF A METAL IN PROTEIN STRUCTURE, STABILITY AND SOLVENT NETWORK | APO, CARBONIC ANHYDRASE, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC
1eou:A (ALA115) to (LEU211) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH AN ANTICONVULSANT SUGAR SULFAMATE | HYDROLASE, CO2 HYDRATION, PROTEIN-INHIBITOR COMPLEX, LYASE
3tvn:X (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II PROTON TRANSFER MUTANT | GLOBULAR PROTEIN, LYASE
3tvo:X (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II PROTON TRANSFER DOUBLE MUTANT | GLOBULAR PROTEIN, LYASE
4ygn:A (ALA115) to (LEU212) NAI--INTERACTIONS BETWEEN HOFMEISTER ANIONS AND THE BINDING POCKET OF A PROTEIN | LYASE, HOFMEISTER ANIONS, HCAII
4ygj:A (ALA115) to (LEU212) NABR--INTERACTIONS BETWEEN HOFMEISTER ANIONS AND THE BINDING POCKET OF A PROTEIN | LYASE, HOFMEISTER ANIONS, HCAII
4ygk:A (ALA115) to (LEU212) NASCN--INTERACTIONS BETWEEN HOFMEISTER ANIONS AND THE BINDING POCKET OF A PROTEIN | LYASE, HOFMEISTER ANIONS, HCAII
4ygl:A (ALA115) to (LEU212) NACLO4--INTERACTIONS BETWEEN HOFMEISTER ANIONS AND THE BINDING POCKET OF A PROTEIN | LYASE, HOFMEISTER ANIONS, HCAII
4js6:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF INHIBITOR-FREE HCAII H94D | LYASE
4jsa:A (ALA115) to (LEU212) BENZENESULFONAMIDE COMPLEXED WITH HCAII H94D | LYASE-LYASE INHIBITOR COMPLEX
1f2w:A (ALA115) to (LEU212) THE MECHANISM OF CYANAMIDE HYDRATION CATALYZED BY CARBONIC ANHYDRASE II REVEALED BY CRYOGENIC X-RAY DIFFRACTION | PROTEIN-INHIBITOR COMPLEX, LYASE
4jss:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II H94D BOUND TO A BIDENTATE INHIBITOR | LYASE-LYASE INHIBITOR COMPLEX
4jsw:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II H94C | LYASE-LYASE INHIBITOR COMPLEX
4jsz:A (ALA115) to (LEU212) BENZENESULFONAMIDE BOUND TO HCAII H94C | LYASE-LYASE INHIBITOR COMPLEX
3u3a:X (ALA115) to (LEU212) STRUCTURE OF HUMAN CARBONIC ANHYDRASE II V143I | LYASE, ZINC METALLOENZYME, V143I, ESTERASE, SITE DIRECTED MUTAGENESIS, CO2 BINDING POCKET
3u45:X (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II V143A | LYASE, ZINC METALLOENZYME, V143A, ESTERASE, SITE DIRECTED MUTAGENESIS, HYDROPHOBIC POCKET
3u47:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II V143L | LYASE, ZINC METALLOENZYME, V143L, ESTERASE, SITE DIRECTED MUTAGENESIS
2eu2:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH NOVEL INHIBITORS | CARBONIC ANHYDRASE II PROTON TRANSFER INHIBITOR, LYASE
2eu3:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH NOVEL INHIBITORS | CARBONIC ANHYDRASE II PROTON TRANSFER INHIBITOR, LYASE
3hkn:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH (2,3,4,6-TETRA-O-ACETYL- BETA-D-GALACTOPYRANOSYL) -(1-4)-1,2,3,6-TETRA-O-ACETYL-1-THIO-BETA-D- GLUCOPYRANOSYLSULFONAMIDE | CARBONIC ANHYDRASE DRUG DESIGN, DISEASE MUTATION, LYASE, METAL- BINDING
3hkq:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 1-S-D- GALACTOPYRANOSYLSULFONAMIDE | CARBONIC ANHYDRASE DRUG DESIGN, DISEASE MUTATION, LYASE, METAL- BINDING
3hkt:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH ALPHA-D- GLUCOPYRANOSYL-(1->4)-1-THIO-BETA-D- GLUCOPYRANOSYLSULFONAMIDE | CARBONIC ANHYDRASE DRUG DESIGN, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC
3hku:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH TOPIRAMATE | CARBONIC ANHYDRASE DRUG DESIGN, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC
1ray:A (ALA115) to (LEU212) THE STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH BROMIDE AND AZIDE | LYASE(OXO-ACID)
1raz:A (ALA115) to (LEU212) THE STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH BROMIDE AND AZIDE | LYASE(OXO-ACID)
3hlj:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 3- METHYLTHIOBENZIMIDAZO[1,2-C][1,2,3]THIADIAZOL-7-SULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, SULFONAMIDE, THIADIAZOLE, LYASE, DISEASE MUTATION, METAL-BINDING
2ez7:A (ALA115) to (LEU212) CARBONIC ANHYDRASE ACTIVATORS. ACTIVATION OF ISOZYMES I, II, IV, VA, VII AND XIV WITH L- AND D-HISTIDINE AND CRYSTALLOGRAPHIC ANALYSIS OF THEIR ADDUCTS WITH ISOFORM II: ENGINEERING PROTON TRANSFER PROCESSES WITHIN THE ACTIVE SITE OF AN ENZYME | CARBONIC ANHYDRASE II, ACTIVATORS, LYASE
1fql:A (ALA115) to (LEU212) X-RAY CRYSTAL STRUCTURE OF ZINC-BOUND F95M/W97V CARBONIC ANHYDRASE (CAII) VARIANT | CARBONIC ANHYDRASE, METAL BINDING, METAL SPECIFICITY, LYASE
1fqm:A (ALA115) to (LEU212) X-RAY CRYSTAL STRUCTURE OF ZINC-BOUND F93I/F95M/W97V CARBONIC ANHYDRASE (CAII) VARIANT | CARBONIC ANHYDRASE, METAL BINDING, METAL SPECIFICITY, LYASE
1fqr:A (ALA115) to (LEU212) X-RAY CRYSTAL STRUCTURE OF COBALT-BOUND F93I/F95M/W97V CARBONIC ANHYDRASE (CAII) VARIANT | CARBONIC ANHYDRASE, METAL BINDING, METAL SPECIFICITY, COBALT, LYASE
1fr4:A (ALA115) to (LEU212) X-RAY CRYSTAL STRUCTURE OF COPPER-BOUND F93I/F95M/W97V CARBONIC ANHYDRASE (CAII) VARIANT | CARBONIC ANHYDRASE, METAL BINDING, METAL SPECIFICITY, COPPER, LYASE
2f14:A (ALA115) to (LEU212) TNE CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A FLUORESCENT INHIBITOR | CARBONIC ANHYDRASE II, LYASE
1fsr:A (ALA115) to (LEU212) X-RAY CRYSTAL STRUCTURE OF COPPER-BOUND F93S/F95L/W97M CARBONIC ANHYDRASE (CAII) VARIANT | CARBONIC ANHYDRASE, METAL BINDING, METAL SPECIFICITY, COPPER, LYASE
1fsr:B (ALA115) to (LEU212) X-RAY CRYSTAL STRUCTURE OF COPPER-BOUND F93S/F95L/W97M CARBONIC ANHYDRASE (CAII) VARIANT | CARBONIC ANHYDRASE, METAL BINDING, METAL SPECIFICITY, COPPER, LYASE
4yvy:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH HYDROXYLAMINE-O-SULFONAMIDE, A MOLECULE INCORPORATING TWO ZINC- BINDING GROUPS. | PROTEIN-INHIBITOR COMPLEX, LYASE
4yx4:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH AN INHIBITOR WITH A BENZENESULFONAMIDE GROUP (1). | PROTEIN-LIGAND-COMPLEX, LYASE
4yxo:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH AN INHIBITOR WITH A BENZENESULFONAMIDE GROUP (3). | LYASE
4kap:A (ALA115) to (LEU212) THE BINDING OF BENZOARYLSULFONAMIDE LIGANDS TO HUMAN CARBONIC ANHYDRASE IS INSENSITIVE TO FORMAL FLUORINATION OF THE LIGAND | ALPHA BETA, LYASE
4yxi:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH AN INHIBITOR WITH A BENZENESULFONAMIDE GROUP (2). | PROTEIN-INHIBITOR COMPLEX, LYASE
4yxu:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH AN INHIBITOR WITH A BENZENESULFONAMIDE GROUP (4). | LYASE
4yyt:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH AN INHIBITOR WITH A BENZENESULFONAMIDE GROUP (5). | LYASE
1g0e:A (ALA115) to (LEU212) SITE-SPECIFIC MUTANT (HIS64 REPLACED WITH ALA) OF HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH 4-METHYLIMIDAZOLE | TWISTED BETA SHEET, CHEMICAL RESCUE, 4-METHYLIMIDAZOLE, ZINC METALLOENZYME,PROTEIN LIGAND COMPLEX, LYASE
1g0f:A (ALA115) to (LEU212) SITE-SPECIFIC MUTANT (HIS64 REPLACED WITH ALA) OF HUMAN CARBONIC ANHYDRASE II | TWISTED BETA SHEET, ZINC METALLOENZYME, LYASE
4z1e:A (ALA115) to (LEU211) CARBONIC ANHYDRASE INHIBITORS: DESIGN AND SYNTHESIS OF NEW HETEROARYL- N-CARBONYLBENZENESULFONAMIDES TARGETING DRUGGABLE HUMAN CARBONIC ANHYDRASE ISOFORMS (HCA VII, HCA IX, AND HCA XIV) | LYASE, CARBONATE DEHYDRATASE II, CARBONIC ANHYDRASE C, CARBONIC ANHYDRASE II, CA-II, CARBONATE DEHYDRATASE II- INHIBITOR COMPLEX
4z1k:A (ALA115) to (LEU211) CARBONIC ANHYDRASE INHIBITORS: DESIGN AND SYNTHESIS OF NEW HETEROARYL- N-CARBONYLBENZENESULFONAMIDES TARGETING DRUGGABLE HUMAN CARBONIC ANHYDRASE ISOFORMS (HCA VII, HCA IX, AND HCA XIV) | LYASE, CARBONATE DEHYDRATASE II, CARBONIC ANHYDRASE C, CARBONIC ANHYDRASE II, CA-II, CARBONATE DEHYDRATASE II- INHIBITOR COMPLEX
4z1n:A (ALA115) to (LEU211) CARBONIC ANHYDRASE INHIBITORS: DESIGN AND SYNTHESIS OF NEW HETEROARYL- N-CARBONYLBENZENESULFONAMIDES TARGETING DRUGGABLE HUMAN CARBONIC ANHYDRASE ISOFORMS (HCA VII, HCA IX, AND HCA XIV) | LYASE, CARBONATE DEHYDRATASE II, CARBONIC ANHYDRASE C, CARBONIC ANHYDRASE II, CA-II, CARBONATE DEHYDRATASE II- INHIBITOR COMPLEX
1g3z:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) | CARBONIC ANHYDRASE II, F131V, LYASE
1g45:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) COMPLEXED WITH 4- (AMINOSULFONYL)-N-[(2-FLUOROPHENYL)METHYL]-BENZAMIDE | CARBONIC ANHYDRASE II, F131V, 4-(AMINOSULFONYL)-N-[(2- FLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1g4o:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) COMPLEXED WITH 4- (AMINOSULFONYL)-N-PHENYLMETHYLBENZAMIDE | CARBONIC ANHYDRASE II, F131V, 4-(AMINOSULFONYL)-N- PHENYLMETHYLBENZAMIDE, LYASE
1g52:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH 4-(AMINOSULFONYL)-N- [(2,3-DIFLUOROPHENYL)METHYL]-BENZAMIDE | CARBONIC ANHYDRASE II, 4-(AMINOSULFONYL)-N-[(2,3- DIFLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1g53:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH 4-(AMINOSULFONYL)-N- [(2,6-DIFLUOROPHENYL)METHYL]-BENZAMIDE | CARBONIC ANHYDRASE II, 4-(AMINOSULFONYL)-N-[(2,6- DIFLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1g54:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH 4-(AMINOSULFONYL)-N- [(2,3,4,5,6-PENTAFLUOROPHENYL)METHYL]-BENZAMIDE | CARBONIC ANHYDRASE II, 4-(AMINOSULFONYL)-N-[(2,3,4,5,6- PENTAFLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1g6v:A (ALA115) to (LEU212) COMPLEX OF THE CAMELID HEAVY-CHAIN ANTIBODY FRAGMENT CAB- CA05 WITH BOVINE CARBONIC ANHYDRASE | ANTIBODY, ANTIGEN, COMPLEX, IMMUNOGLOBULIN, LYASE/IMMUNE SYSTEM COMPLEX
1rzb:A (ALA115) to (LEU212) X-RAY ANALYSIS OF METAL SUBSTITUTED HUMAN CARBONIC ANHYDRASE II DERIVATIVES | LYASE(OXO-ACID)
1rzc:A (ALA115) to (LEU212) X-RAY ANALYSIS OF METAL SUBSTITUTED HUMAN CARBONIC ANHYDRASE II DERIVATIVES | LYASE(OXO-ACID)
1rzd:A (ALA115) to (LEU212) X-RAY ANALYSIS OF METAL SUBSTITUTED HUMAN CARBONIC ANHYDRASE II DERIVATIVES | LYASE(OXO-ACID)
1rze:A (ALA115) to (LEU212) X-RAY ANALYSIS OF METAL SUBSTITUTED HUMAN CARBONIC ANHYDRASE II DERIVATIVES | LYASE(OXO-ACID)
2fmg:A (ALA115) to (LEU212) CARBONIC ANHYDRASE ACTIVATORS. ACTIVATION OF ISOFORMS I, II, IV, VA, VII AND XIV WITH L- AND D- PHENYLALANINE AND CRYSTALLOGRAPHIC ANALYSIS OF THEIR ADDUCTS WITH ISOZYME II: STEROSPECIFIC RECOGNITION WITHIN THE ACTIVE SITE OF AN ENZYME AND ITS CONSEQUENCES FOR THE DRUG DESIGN, STRUCTURE WITH L-PHENYLALANINE | CARBONIC ANHYDRASE II, ACTIVATORS, LYASE
2fmz:A (ALA115) to (LEU212) CARBONIC ANHYDRASE ACTIVATORS. ACTIVATION OF ISOFORMS I, II, IV, VA, VII AND XIV WITH L- AND D- PHENYLALANINE, STRUCTURE WITH D-PHENYLALANINE. | CARBONIC ANHYDRASE, ACTIVATORS, CRYSTAL STRUCTURE, LYASE
2fnk:A (ALA115) to (LEU212) ACTIVATION OF HUMAN CARBONIC ANHYDRASE II BY EXOGENOUS PROTON DONORS | CARBONIC ANHYDRASE, PROTON TRANSFER, EXOGENOUS PROTON DONOR, LYASE
2fnm:A (ALA115) to (LEU212) ACTIVATION OF HUMAN CARBONIC ANHDYRASE II BY EXOGENOUS PROTON DONORS | CARBONIC ANHYDRASE, PROTON TRANSFER, EXOGENOUS PROTON DONOR, LYASE
2fnn:A (ALA115) to (LEU212) ACTIVATION OF HUMAN CARBONIC ANHYDRASE II BY EXOGENOUS PROTON DONORS | CARBONIC ANHYDRASE, PROTON TRANSFER, EXOGENOUS PROTON DONOR, LYASE
3hs4:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH ACETAZOLAMIDE | CARBONIC ANHYDRASE 2, CARBONIC ANHYDRASE II, LYASE, CA II, CA 2, ACETAZOLAMIDE, 5-ACETAMIDO-1,3,4-THIADIAZOLE-2-SULFONAMIDE, DISEASE MUTATION, METAL-BINDING
2foq:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH TWO-PRONG INHIBITORS | LYASE, INHIBITOR
2fos:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH TWO-PRONG INHIBITORS | LYASE, ZINC, INHIBITOR, COPPER
2fou:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH TWO-PRONG INHIBITORS | LYASE, INHIBITOR
2fov:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH TWO-PRONG INHIBITORS | LYASE, ZINC, INHIBITOR, COPPER
2foy:A (SER115) to (CYS212) HUMAN CARBONIC ANHYDRASE I COMPLEXED WITH A TWO-PRONG INHIBITOR | LYASE, ZINC, INHIBITOR, COPPER
2foy:B (SER115) to (CYS212) HUMAN CARBONIC ANHYDRASE I COMPLEXED WITH A TWO-PRONG INHIBITOR | LYASE, ZINC, INHIBITOR, COPPER
3v2j:A (ALA115) to (LEU212) EFFECT OF SUCROSE AND GLYCEROL AS CRYOPROTECTANS, ON THE INHIBITION OF HUMAN CARBONIC ANHYDRASE II | GLYCEROL, SUCROSE, CRYOPROTECTANT, ACETAZOLAMIDE, HCA II, LYASE
3v2m:A (ALA115) to (LEU212) EFFECT OF SUCROSE AND GLYCEROL AS CRYOPROTECTANS, ON THE INHIBITION OF HUMAN CARBONIC ANHYDRASE II | GLYCEROL, SUCROSE, CRYOPROTECTANT, ACETAZOLAMIDE, HCA II, LYASE
4knn:B (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH 2- CHLORO-4-[(PYRIMIDIN-2-YLSULFANYL)ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4knn:A (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH 2- CHLORO-4-[(PYRIMIDIN-2-YLSULFANYL)ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4knm:A (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH 2- CHLORO-4-{[(4,6-DIMETHYLPYRIMIDIN-2-YL) SULFANYL]ACETYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4knm:B (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH 2- CHLORO-4-{[(4,6-DIMETHYLPYRIMIDIN-2-YL) SULFANYL]ACETYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3v3g:B (ALA115) to (LEU212) KINETIC AND STRUCTURAL STUDIES OF THERMOSTABILIZED MUTANTS OF HCA II. | THERMOSTABILE, LYASE
3v3h:B (ALA115) to (LEU212) KINETIC AND STRUCTURAL STUDIES OF THERMOSTABILIZED MUTANTS OF HCA II. | THERMOSTABILE, LYASE
3v3i:B (ALA115) to (LEU212) KINETIC AND STRUCTURAL STUDIES OF THERMOSTABILIZED MUTANTS OF HCA II. | THERMOSTABILE, LYASE
3v3j:A (ALA115) to (LEU212) KINETIC AND STRUCTURAL STUDIES OF THERMOSTABILIZED MUTANTS OF HCA II. | THERMOSTABILE, LYASE
2fw4:A (SER115) to (CYS212) CARBONIC ANHYDRASE ACTIVATORS. THE FIRST X-RAY CRYSTALLOGRAPHIC STUDY OF AN ACTIVATOR OF ISOFORM I, STRUCTURE WITH L-HISTIDINE. | CARBONIC ANHYDRASE I, ACTIVATORS, CRYSTAL STRUCTURE, LYASE
2fw4:B (SER115) to (CYS212) CARBONIC ANHYDRASE ACTIVATORS. THE FIRST X-RAY CRYSTALLOGRAPHIC STUDY OF AN ACTIVATOR OF ISOFORM I, STRUCTURE WITH L-HISTIDINE. | CARBONIC ANHYDRASE I, ACTIVATORS, CRYSTAL STRUCTURE, LYASE
3v5g:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE 4-SULFAMIDO-BENZENESULFONAMIDE INHIBITOR | LYASE-LYASE INHIBITOR COMPLEX
3v7x:A (ALA1115) to (LEU1212) COMPLEX OF HUMAN CARBONIC ANHYDRASE II WITH N-[2-(3,4- DIMETHOXYPHENYL)ETHYL]-4-SULFAMOYLBENZAMIDE | LYASE-LYASE INHIBITOR COMPLEX
3vbd:A (ALA1115) to (LEU1212) COMPLEX OF HUMAN CARBONIC ANHYDRASE II WITH 4-(6-METHOXY-3,4- DIHYDROISOQUINOLIN-1-YL)BENZENESULFONAMIDE | LYASE-LYASE INHIBITOR COMPLEX
4kuv:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE 5-(3-(4-CHLOROPHENYLSULFONYL)UREIDO)PYRIDINE-2-SULFONAMIDE INHIBITOR | LYASE, LYASE-LYASE INHIBITOR COMPLEX
4kuw:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE 5-(3-(4-FLUOROPHENYLSULFONYL)UREIDO)PYRIDINE-2-SULFONAMIDE INHIBITOR | LYASE, LYASE-LYASE INHIBITOR COMPLEX
4kv0:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE 5-(3-TOSYLUREIDO)PYRIDINE-2-SULFONAMIDE INHIBITOR | LYASE, LYASE-LYASE INHIBITOR COMPLEX
2vva:X (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE IN COMPLEX WITH CO2 | METAL-BINDING, CARBON DIOXIDE, DISEASE MUTATION, SUBSTRATE BINDING, CARBONIC ANHYDRASE, ZINC, LYASE, CYTOPLASM, ACETYLATION, POLYMORPHISM
2vvb:X (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH BICARBONATE | POLYMORPHISM, METAL-BINDING, DISEASE MUTATION, ZINC, LYASE, CYTOPLASM, ACETYLATION, BICARBONATE, SUBSTRATE BINDING, CARBONIC ANHYDRASE
2gd8:A (ALA115) to (LEU212) CRYSTAL STRUCTURE ANALYSIS OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A 2-SUBSTITUTED ESTRADIOL BIS-SULFAMATE | PROTEIN-INHIBITOR COMPLEXES, LYASE
3ibi:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH AN ALIPHATIC SULFAMATE INHIBITOR | CARBONIC ANHYDRASE II, PROTEIN-INHIBITOR COMPLEX, ALIPHATIC SULFAMATE INHIBITOR, DISEASE MUTATION, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3ibn:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH AN ALIPHATIC BIS-SULFAMATE INHIBITOR | CARBONIC ANHYDRASE II, PROTEIN-INHIBITOR COMPLEX, ALIPHATIC BIS- SULFAMATE INHIBITOR, DISEASE MUTATION, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3ibu:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH AN ALIPHATIC SULFAMATE INHIBITOR | CARBONIC ANHYDRASE II, PROTEIN-INHIBITOR COMPLEX, ALIPHATIC SULFAMATE INHIBITOR, DISEASE MUTATION, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4l5u:A (ALA115) to (LEU212) THE STRUCTURAL IMPLICATIONS OF THE SECONDARY CO2 BINDING POCKET IN HUMAN CARBONIC ANHYDRASE II | ALLOSTERIC REGULATION, THERMOSTABILITY, LYASE
4l5v:A (ALA115) to (LEU212) THE STRUCTURAL IMPLICATIONS OF THE SECONDARY CO2 BINDING POCKET IN HUMAN CARBONIC ANHYDRASE II | ALLOSTERIC REGULATION, THERMOSTABILITY, LYASE
1h4n:A (ALA115) to (LEU212) H94N CARBONIC ANHYDRASE II COMPLEXED WITH TRIS | LYASE, OXO-ACID, ACETYLATION
3ieo:A (ALA115) to (LEU212) THE COUMARIN-BINDING SITE IN CARBONIC ANHYDRASE: THE ANTIEPILEPTIC LACOSAMIDE AS AN EXAMPLE | CARBONIC ANHYDRASE, ANTIEPILECTIC, DISEASE MUTATION, LYASE, METAL- BINDING, LYASE-LYASE INHIBITOR COMPLEX
3igp:A (ALA115) to (LEU212) STRUCTURE OF INHIBITOR BINDING TO CARBONIC ANHYDRASE II | CARBONIC ANHYDRASE INHIBITORS, ISOQUINOLINES, LYASE, ACETYLATION, CYTOPLASM, DISEASE MUTATION, METAL-BINDING, POLYMORPHISM, ZINC
1t9n:A (ALA115) to (LEU212) EFFECT OF SHUTTLE LOCATION AND PH ENVIRONMENT ON H+ TRANSFER IN HUMAN CARBONIC ANHYDRASE II | PROTON SHUTTLE, CARBONIC ANHYDRASE, METALLOENZYME, LYASE
1h9q:A (ALA115) to (LEU212) H119Q CARBONIC ANHYDRASE II | LYASE, OXO-ACID, ACETYLATION
1tb0:X (ALA115) to (LEU212) EFFECT OF SHUTTLE LOCATION AND PH ENVIRONMENT ON H+ TRANSFER IN HUMAN CARBONIC ANHYDRASE II | PROTON SHUTTLE CARBONIC ANHYDRASE METALLOENZYME, LYASE
1tbt:X (ALA115) to (LEU212) EFFECT OF SHUTTLE LOCATION AND PH ENVIRONMENT ON H+ TRANSFER IN HUMAN CARBONIC ANHYDRASE II | PROTON SHUTTLE CARBONIC ANHYDRASE METALLOENZYME, LYASE
1te3:X (ALA115) to (LEU212) EFFECT OF SHUTTLE LOCATION AND PH ENVIRONMENT ON H+ TRANSFER IN HUMAN CARBONIC ANHYDRASE II | PROTON SHUTTLE CARBONIC ANHYDRASE METALLOENZYME, LYASE
1teq:X (ALA115) to (LEU212) EFFECT OF SHUTTLE LOCATION AND PH ENVIRONMENT ON H+ TRANSFER IN HUMAN CARBONIC ANHYDRASE II | PROTON SHUTTLE CARBONIC ANHYDRASE METALLOENZYME, LYASE
1teu:X (ALA115) to (LEU212) EFFECT OF SHUTTLE LOCATION AND PH ENVIRONMENT ON H+ TRANSFER IN HUMAN CARBONIC ANHYDRASE II | PROTON SHUTTLE CARBONIC ANHYDRASE METALLOENZYME, LYASE
1hca:A (ALA115) to (LEU212) UNEXPECTED PH-DEPENDENT CONFORMATION OF HIS-64, THE PROTON SHUTTLE OF CARBONIC ANHYDRASE II. | LYASE(OXO-ACID)
1hcb:A (SER115) to (CYS212) ENZYME-SUBSTRATE INTERACTIONS: STRUCTURE OF HUMAN CARBONIC ANHYDRASE I COMPLEXED WITH BICARBONATE | LYASE(OXO-ACID)
1tg9:A (ALA115) to (LEU212) EFFECT OF SHUTTLE LOCATION AND PH ENVIRONMENT ON H+ TRANSFER IN HUMAN CARBONIC ANHYDRASE II | PROTON SHUTTLE CARBONIC ANHYDRASE METALLOENZYME, LYASE
1heb:A (ALA115) to (LEU212) STRUCTURAL CONSEQUENCES OF HYDROPHILIC AMINO-ACID SUBSTITUTIONS IN THE HYDROPHOBIC POCKET OF HUMAN CARBONIC ANHYDRASE II | LYASE(OXO-ACID)
1th9:A (ALA115) to (LEU212) EFFECT OF SHUTTLE LOCATION AND PH ENVIRONMENT ON H+ TRANSFER IN HUMAN CARBONIC ANHYDRASE II | PROTON SHUTTLE CARBONIC ANHYDRASE METALLOENZYME, LYASE
1thk:A (ALA115) to (LEU212) EFFECT OF SHUTTLE LOCATION AND PH ENVIRONMENT ON H+ TRANSFER IN HUMAN CARBONIC ANHYDRASE II | PROTON SHUTTLE CARBONIC ANHYDRASE METALLOENZYME, LYASE
4lhi:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 5- (PHENYLSULFONYL)THIOPHENE-2-SULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
2h4n:A (ALA115) to (LEU212) H94N CARBONIC ANHYDRASE II COMPLEXED WITH ACETAZOLAMIDE | LYASE, OXO-ACID, ACETYLATION
4zwy:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A GLUCOSYL SULFAMATE INHIBITOR | CARBONIC ANHYDRASE II, GLUCOSYL SULFAMATE, INHIBITOR COMPLEX., LYASE- LYASE INHIBITOR COMPLEX
4zwz:A (ALA115) to (LEU212) ENGINEERED CARBONIC ANHYDRASE IX MIMIC IN COMPLEX WITH A GLUCOSYL SULFAMATE INHIBITOR | CARBONIC ANHYDRASE IX MIMIC, GLUCOSYL SULFAMATE, INHIBITOR COMPLEX., LYASE-LYASE INHIBITOR COMPLEX
4zx0:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A GLUCOSYL SULFAMATE INHIBITOR | CARBONIC ANHYDRASE II, GLUCOSYL SULFAMATE, INHIBITOR COMPLEX., LYASE- LYASE INHIBITOR COMPLEX
2wd3:A (ALA115) to (LEU211) HIGHLY POTENT FIRST EXAMPLES OF DUAL AROMATASE-STEROID SULFATASE INHIBITORS BASED ON A BIPHENYL TEMPLATE | HUMAN CARBONIC ANHYDRASE INHIBITOR, LYASE, CANCER, BIPHENYL, TRIAZOLE, DUAL AROMATASE-STEROID SULFATASE INHIBITOR, SULFAMATE, METAL-BINDING
2hd6:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A HYPOXIA-ACTIVATABLE SULFONAMIDE. | PROTEIN-INHIBITOR COMPLEX, LYASE
2weg:A (ALA115) to (LEU212) THERMODYNAMIC OPTIMISATION OF CARBONIC ANHYDRASE FRAGMENT INHIBITORS | METAL-BINDING, DISEASE MUTATION, LYASE, ZINC, CYTOPLASM, ACETYLATION, POLYMORPHISM
2weh:A (ALA115) to (LEU212) THERMODYNAMIC OPTIMISATION OF CARBONIC ANHYDRASE FRAGMENT INHIBITORS | METAL-BINDING, DISEASE MUTATION, LYASE, ZINC, CYTOPLASM, ACETYLATION, POLYMORPHISM
2wej:A (ALA115) to (LEU212) THERMODYNAMIC OPTIMISATION OF CARBONIC ANHYDRASE FRAGMENT INHIBITORS | METAL-BINDING, DISEASE MUTATION, ZINC, LYASE, CYTOPLASM, ACETYLATION, POLYMORPHISM
2weo:A (ALA115) to (LEU212) THERMODYNAMIC OPTIMISATION OF CARBONIC ANHYDRASE FRAGMENT INHIBITORS | METAL-BINDING, DISEASE MUTATION, ZINC, LYASE, CYTOPLASM, ACETYLATION, POLYMORPHISM
1ttm:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH 667-COUMATE | CANCER, HUMAN CARBONIC ANHYDRASE INHIBITORS, 667-COUMATE, OBESITY, STEROID SULFATASE INHIBITOR, LYASE
2hkk:A (ALA115) to (LEU211) CARBONIC ANHYDRASE ACTIVATORS: SOLUTION AND X-RAY CRYSTALLOGRAPHY FOR THE INTERACTION OF ANDRENALINE WITH VARIOUS CARBONIC ANHYDRASE ISOFORMS | CARBONIC ANHYDRASE, ACTIVATORS, LYASE
2hl4:A (ALA115) to (LEU212) CRYSTAL STRUCTURE ANALYSIS OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A BENZENESULFONAMIDE DERIVATIVE | PROTEIN-INHIBITOR COMPLEX, LYASE
1hug:A (SER115) to (CYS212) DIFFERENCES IN ANIONIC INHIBITION OF HUMAN CARBONIC ANHYDRASE I REVEALED FROM THE STRUCTURES OF IODIDE AND GOLD CYANIDE INHIBITOR COMPLEXES | LYASE(OXO-ACID)
2hoc:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE 5-(4-AMINO-3-CHLORO-5-FLUOROPHENYLSULFONAMIDO)-1,3,4-THIADIAZOLE- 2-SULFONAMIDE INHIBITOR | PROTEIN-INHIBITOR COMPLEX, LYASE
5a25:A (ALA115) to (LEU211) RATIONAL ENGINEERING OF A MESOPHILIC CARBONIC ANHYDRASE TO AN EXTREME HALOTOLERANT BIOCATALYST | LYASE, PROTEIN ENGINEERING, BIOCATALYSIS
5a25:B (ALA115) to (LEU211) RATIONAL ENGINEERING OF A MESOPHILIC CARBONIC ANHYDRASE TO AN EXTREME HALOTOLERANT BIOCATALYST | LYASE, PROTEIN ENGINEERING, BIOCATALYSIS
1i90:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH AL-8520 2H-THIENO[3,2- E]-1,2-THIAZINE-6-SULFONAMIDE, 4-AMINO-3,4-DIHYDRO-2-(3- METHOXYPROPYL)-, 1,1-DIOXIDE, (R) | CARBONIC ANHYDRASE II, AL-8520, LYASE
1i91:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH AL-6619 2H-THIENO[3,2- E]-1,2-THIAZINE-6-SULFONAMIDE, 2-(3-HYDROXYPHENYL)-3-(4- MORPHOLINYL)-, 1,1-DIOXIDE | CARBONIC ANHYDRASE II, AL-6619, LYASE
1i9l:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) COMPLEXED WITH 4- (AMINOSULFONYL)-N-[(4-FLUOROPHENYL)METHYL]-BENZAMIDE | HUMAN CARBONIC ANHYDRASE II, 4-(AMINOSULFONYL)-N-[(4- FLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1i9m:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) COMPLEXED WITH 4- (AMINOSULFONYL)-N-[(2,4-DIFLUOROPHENYL)METHYL]-BENZAMIDE | HUMAN CARBONIC ANHYDRASE II, 4-(AMINOSULFONYL)-N-[(2,4- DIFLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1i9n:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) COMPLEXED WITH 4- (AMINOSULFONYL)-N-[(2,5-DIFLUOROPHENYL)METHYL]-BENZAMIDE | HUMAN CARBONIC ANHYDRASE II, 4-(AMINOSULFONYL)-N-[(2,5- DIFLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1i9o:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) COMPLEXED WITH 4- (AMINOSULFONYL)-N-[(2,3,4-TRIFLUOROPHENYL)METHYL]-BENZAMIDE | HUMAN CARBONIC ANHYDRASE II, 4-(AMINOSULFONYL)-N-[(2,3,4- TRIFLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1i9p:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) COMPLEXED WITH 4- (AMINOSULFONYL)-N-[(2,4,6-TRIFLUOROPHENYL)METHYL]-BENZAMIDE | HUMAN CARBONIC ANHYDRASE II, 4-(AMINOSULFONYL)-N-[(2,4,6- TRIFLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1i9q:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) COMPLEXED WITH 4- (AMINOSULFONYL)-N-[(3,4,5-TRIFLUOROPHENYL)METHYL]-BENZAMIDE | HUMAN CARBONIC ANHYDRASE II, 4-(AMINOSULFONYL)-N-[(3,4,5- TRIFLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1if4:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH 4- FLUOROBENZENESULFONAMIDE | CARBONIC ANHYDRASE II, 4-FLUOROBENZENESULFONAMIDE, LYASE
1if5:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH 2,6- DIFLUOROBENZENESULFONAMIDE | CARBONIC ANHYDRASE II, 2,6-DIFLUOROBENZENESULFONAMIDE, LYASE
1if6:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH 3,5- DIFLUOROBENZENESULFONAMIDE | CARBONIC ANHYDRASE II, 3,5-DIFLUOROBENZENESULFONAMIDE, LYASE
1if7:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH (R)-N-(3-INDOL-1-YL-2- METHYL-PROPYL)-4-SULFAMOYL-BENZAMIDE | CARBONIC ANHYDRASE II, (R)-N-(3-INDOL-1-YL-2-METHYL-PROPYL)- 4-SULFAMOYL-BENZAMIDE, LYASE
1if8:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH (S)-N-(3-INDOL-1-YL-2- METHYL-PROPYL)-4-SULFAMOYL-BENZAMIDE | CARBONIC ANHYDRASE II, (S)-N-(3-INDOL-1-YL-2-METHYL-PROPYL)- 4-SULFAMOYL-BENZAMIDE, LYASE
1if9:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH N-[2-(1H-INDOL-5-YL)- BUTYL]-4-SULFAMOYL-BENZAMIDE | CARBONIC ANHYDRASE II, N-[2-(1H-INDOL-5-YL)-BUTYL]-4- SULFAMOYL-BENZAMIDE, LYASE
1uga:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II[HCAII] (E.C.4.2.1.1) MUTANT WITH ALA 65 REPLACED BY PHE (A65F) | LYASE (OXO-ACID), ACETYLATION, ZINC, POLYMORPHISM, DISEASE MUTATION
1ugc:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II [HCAII] (E.C.4.2.1.1) MUTANT WITH ALA 65 REPLACED BY HIS (A65H) | LYASE, ACETYLATION, ZINC, POLYMORPHISM, DISEASE MUTATION
1ugd:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II[HCAII] (E.C.4.2.1.1) MUTANT WITH ALA 65 REPLACED BY SER (A65S) | LYASE (OXO-ACID), ACETYLATION, ZINC, POLYMORPHISM, DISEASE MUTATION
1uge:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II [HCAII] (E.C.4.2.1.1) MUTANT WITH ALA 65 REPLACED BY LEU (A65L) | LYASE, ACETYLATION, ZINC, POLYMORPHISM, DISEASE MUTATION
1ugf:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II [HCAII] (E.C.4.2.1.1) MUTANT WITH ALA 65 REPLACED BY THR (A65T) | LYASE, ACETYLATION, ZINC, POLYMORPHISM, DISEASE MUTATION
1ugg:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II[HCAII] (E.C.4.2.1.1) MUTANT WITH ALA 65 REPLACED BY SER (A65S)-ORTHORHOMBIC FORM | LYASE (OXO-ACID), ACETYLATION, ZINC, POLYMORPHISM, DISEASE MUTATION
5a6h:A (ALA115) to (LEU212) SYNTHESIS, CARBONIC ANHYDRASE INHIBITION AND PROTEIN X-RAY STRUCTURE OF THE UNUSUAL NATURAL PRODUCT PRIMARY SULFONAMIDE PSAMMAPLIN C | LYASE, CARBONIC ANHYDRASE INHIBITOR, NATURAL PRODUCT
4m2r:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH BRINZOLAMIDE | LYASE-LYASE INHIBITOR COMPLEX
4m2v:A (ALA115) to (LEU212) GENETICALLY ENGINEERED CARBONIC ANHYDRASE IX IN COMPLEX WITH BRINZOLAMIDE | CARBONIC ANHYDRASE IX MIMIC, LYASE-LYASE INHIBITOR COMPLEX
4m2w:A (ALA115) to (LEU212) GENETICALLY ENGINEERED CARBONIC ANHYDRASE IX IN COMPLEX WITH DORZOLAMIDE | CARBONIC ANHYDRASE IX MIMIC, LYASE-LYASE INHIBITOR COMPLEX
1urt:A (PRO115) to (GLN212) MURINE CARBONIC ANHYDRASE V | LYASE, ZINC, MITOCHONDRION, TRANSIT PEPTIDE
4mdg:A (ALA115) to (LEU212) CLOSO CARBORANE CARBONIC ANHYDRASE INHIBITOR | CARBONIC ANHYDRASE INHIBITOR COMPLEX, LYASE-LYASE INHIBITOR COMPLEX
4mdm:A (ALA115) to (LEU212) NIDO-CARBORANE CARBONIC ANHYDRASE INHIBITOR | CARBONIC ANHYDRASE INHIBITOR COMPLEX, LYASE-LYASE INHIBITOR COMPLEX
2ili:A (ALA115) to (LEU212) REFINE ATOMIC STRUCTURE OF HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER, PROTON SHUTTLE, CARBONIC ANHYDRASE, LYASE
2it4:A (SER115) to (CYS212) X RAY STRUCTURE OF THE COMPLEX BETWEEN CARBONIC ANHYDRASE I AND THE PHOSPHONATE ANTIVIRAL DRUG FOSCARNET | CARBONIC ANHYDRASE, ANTIVIRAL, CRYSTAL STUCTURE, LYASE
5amd:A (ALA115) to (LEU212) THREE DIMENSIONAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 2-((2-PHENYLETHYL)SULFAMOYL)-4-SULFAMOYLBENZOIC ACID | LYASE, CA II, CA 2
5amg:A (ALA115) to (LEU212) THREE DIMENSIONAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 2-(PENTYLSULFAMOYL)-4-SULFAMOYLBENZOIC ACID | LYASE, CA II, CA 2
5aml:A (ALA115) to (LEU212) THREE DIMENSIONAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 2-(BUT-2-YN-1-YLSULFAMOYL)-4-SULFAMOYLBENZOIC ACID | LYASE, CA II, CA 2
4mlt:A (ALA115) to (LEU212) STRUCTURE OF A MONODENTATE 3-HYDROXY-4H-PYRAN-4-THIONE LIGAND BOUND TO HCAII | LYASE
4mlx:A (ALA115) to (LEU212) STRUCTURE OF A BIDENTATE 3-HYDROXY-4H-PYRAN-4-THIONE LIGAND BOUND TO HCAII | LYASE
1v9i:C (ALA116) to (LEU212) CRYSTAL STRUCTURE ANALYSIS OF THE SITE SPECIFIC MUTANT (Q253C) OF BOVINE CARBONIC ANHYDRASE II | BETA SHEET, ZINC METALLOENZYME, LYASE
4mo8:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH N-[2-(2-METHYL-5-NITRO-1H-IMIDAZOL-1-YL)ETHYL]SULFAMIDE | SULFAMIDE, ZINC BINDING, LYASE-LYASE INHIBITOR COMPLEX
4mty:A (ALA115) to (LEU211) STRUCTURE AT 2.1 A REOLUTION OF A HELICAL AROMATIC FOLDAMER-PROTEIN COMPLEX. | MIXED ALPHA BETA, LYASE-LYASE INHIBITOR COMPLEX
4n0x:B (ALA115) to (LEU212) ROOM TEMPERATURE CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THIOPHENE-2-SULFONAMIDE | MIXED ALPHA/BETA, CARBONATE DEHYDRATASE, CYTOSOLIC, LYASE
4n16:A (ALA115) to (LEU212) STRUCTURE OF CHOLATE BOUND TO HUMAN CARBONIC ANHYDRASE II | CHOLATE, CHOLIC ACID, LYASE
5bnl:A (ALA115) to (LEU212) DECIPHERING THE MECHANISM OF CARBONIC ANHYDRASE INHIBITION WITH COUMARINS AND THIOCOUMARINS | HCA2, COUMARIN, INHIBITORS, LYASE
5bru:A (ALA115) to (LEU211) CATALYTIC IMPROVEMENT OF AN ARTIFICIAL METALLOENZYME BY COMPUTATIONAL DESIGN | ARTIFICIAL METALLOENZYME, OXIDOREDUCTASE
5brv:A (ALA115) to (LEU211) CATALYTIC IMPROVEMENT OF AN ARTIFICIAL METALLOENZYME BY COMPUTATIONAL DESIGN | ARTIFICIAL METALLOENZYME, OXIDOREDUCTASE
5brw:A (ALA115) to (LEU211) CATALYTIC IMPROVEMENT OF AN ARTIFICIAL METALLOENZYME BY COMPUTATIONAL DESIGN | ARTIFICIAL METALLOENZYME, LYASE, IMINE REDUCTASE, TRANSFER HYDROGENASE, OXIDOREDUCTASE
5byi:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II WITH AN AZOBENZENE INHIBITOR (1D) | CARBONIC ANHYDRASE, SULFONAMIDE, PHOTOPHARMACOLOGY, INHIBITOR, LYASE
1keq:A (PRO115) to (GLN212) CRYSTAL STRUCTURE OF F65A/Y131C CARBONIC ANHYDRASE V, COVALENTLY MODIFIED WITH 4-CHLOROMETHYLIMIDAZOLE | PROTON TRANSFER, ENGINEERED RESIDUE, LYASE
1keq:B (PRO115) to (GLN212) CRYSTAL STRUCTURE OF F65A/Y131C CARBONIC ANHYDRASE V, COVALENTLY MODIFIED WITH 4-CHLOROMETHYLIMIDAZOLE | PROTON TRANSFER, ENGINEERED RESIDUE, LYASE
3zp9:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II AS A SCAFFOLD FOR AN ARTIFICIAL TRANSFER HYDROGENASE | ARTIFICIAL METALLOENZYME, LYASE, INHIBITOR, IRIDIUM PENTAMETHYLCYCLOPENTADIENYL, PIANO STOOL COMPLEX
1kwq:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH INHIBITOR 2000-07 | LYASE, ZINC, INHIBITOR
1kwr:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH INHIBITOR 0134-36 | LYASE, ZINC, INHIBITOR
5c8i:A (ALA115) to (LEU212) JOINT X-RAY/NEUTRON STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH METHAZOLAMIDE | METHAZOLAMIDE, ACETAZOLAMIDE, WATER DISPLACEMENT, LYASE
2nmx:A (SER115) to (CYS212) STRUCTURE OF INHIBITOR BINDING TO CARBONIC ANHYDRASE I | METALLOENZYME, HYDRO LYASE, LYASE
2nn1:A (SER115) to (CYS212) STRUCTURE OF INHIBITOR BINDING TO CARBONIC ANHYDRASE I | ZINC METALLOENZYME, LYASE
2nn1:B (SER115) to (CYS212) STRUCTURE OF INHIBITOR BINDING TO CARBONIC ANHYDRASE I | ZINC METALLOENZYME, LYASE
2nn7:A (SER115) to (CYS212) STRUCTURE OF INHIBITOR BINDING TO CARBONIC ANHYDRASE I | ZINC METALLOENZYME, LYASE
2nn7:B (SER115) to (CYS212) STRUCTURE OF INHIBITOR BINDING TO CARBONIC ANHYDRASE I | ZINC METALLOENZYME, LYASE
2nng:A (ALA115) to (LEU212) STRUCTURE OF INHIBITOR BINDING TO CARBONIC ANHYDRASE II | ZINC METALLOENZYME, SULFONAMIDE, LYASE
2nno:A (ALA115) to (LEU212) STRUCTURE OF INHIBITOR BINDING TO CARBONIC ANHYDRASE II | ZINC METALLOENZYME, SULFONAMIDE, LYASE
2nns:A (ALA115) to (LEU212) STRUCTURE OF INHIBITOR BINDING TO CARBONIC ANHYDRASE II | ZINC METALLOENZYME, SULFONAMIDE, LYASE
1xev:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN A NEW CRYSTAL FORM | HUMAN CARBONIC ANHYDRASE II, TRANSLATIONAL SYMMETRY, X-RAY STRUCTURE, LYASE
1xev:C (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN A NEW CRYSTAL FORM | HUMAN CARBONIC ANHYDRASE II, TRANSLATIONAL SYMMETRY, X-RAY STRUCTURE, LYASE
1xev:D (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN A NEW CRYSTAL FORM | HUMAN CARBONIC ANHYDRASE II, TRANSLATIONAL SYMMETRY, X-RAY STRUCTURE, LYASE
5ca2:A (ALA115) to (LEU212) CONFORMATIONAL MOBILITY OF HIS-64 IN THE THR-200 (RIGHT ARROW) SER MUTANT OF HUMAN CARBONIC ANHYDRASE II | LYASE(OXO-ACID)
5cac:A (ALA115) to (LEU212) REFINED STRUCTURE OF HUMAN CARBONIC ANHYDRASE II AT 2.0 ANGSTROMS RESOLUTION | LYASE(OXO-ACID)
3jxh:C (PRO171) to (PHE270) CA-LIKE DOMAIN OF HUMAN PTPRG | CA-LIKE DOMAIN, ALTERNATIVE SPLICING, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN PHOSPHATASE, TRANSMEMBRANE, CELL ADHESION
2nwo:A (ALA115) to (LEU212) STRUCTURAL AND KINETIC EFFECT OF HYDROPHOBIC MUTATIONS IN THE ACTIVE SITE OF HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER, HISTIDINE 64, CARBONIC ANHYDRASE, LYASE
2nwp:A (ALA115) to (LEU212) STRUCTURAL AND KINETIC EFFECTS OF HYDROPHOBIC MUTATIONS IN THE ACTIVE SITE OF HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER, HISTIDINE 64, CARBONIC ANHYDRASE, LYASE
2nwz:A (ALA115) to (LEU212) STRUCTURAL AND KINETIC EFFECTS OF HYDROPHOBIC MUTATIONS ON THE ACTIVE SITE OF HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER, HISTIDINE 64, CARBONIC ANHYDRASE, LYASE
2nxr:A (ALA115) to (LEU212) STRUCTURAL EFFECTS OF HYDROPHOBIC MUTATIONS ON THE ACTIVE SITE OF HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER, HISTIDINE 64, CARBONIC ANHYDRASE, LYASE
2nxs:A (ALA115) to (LEU212) STRUCTURAL AND KINETIC EFFECTS OF HYDROPHOBIC MUTATIONS IN THE ACTIVE SITE OF HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER, HISTIDINE 64, CARBONIC ANHYDRASE, LYASE
2nxt:A (ALA115) to (LEU211) STRUCTURAL AND KINETIC EFFECTS OF HYDROPHOBIC MUTATIONS IN THE ACTIVE SITE OF HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER, HISTIDINE 64, CARBONIC ANHYDRASE, LYASE
5cjl:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A HETEROARYL-PYRAZOLE CARBOXYLIC ACID DERIVATIVE. | HUMAN CARBONIC ANHYDRASE II, INHIBITOR COMPLEX, CARBOXYLIC ACID., LYASE-LYASE INHIBITOR COMPLEX
1lg5:A (ALA115) to (LEU212) CRYSTAL STRUCTURE ANALYSIS OF THE HCA II MUTANT T199P IN COMPLEX WITH BETA-MERCAPTOETHANOL | HCAII MUTANT T199P-BME COMPLEX, LYASE
1lgd:A (ALA115) to (LEU212) CRYSTAL STRUCTURE ANALYSIS OF HCA II MUTANT T199P IN COMPLEX WITH BICARBONATE | HCAII MUTANT T199P-BCT COMPLEX, LYASE
3k2f:A (ALA115) to (LEU212) NITRIC OXIDE-DONATING CARBONIC ANHYDRASE INHIBITORS FOR THE TREATMENT OF OPEN-ANGLE GLAUCOMA | CARBONIC ANHYDRASE, NO-DONATING AGENT, ANTIGLAUCOMA DRUG, SULFONAMIDE, XRAY CRYSTALLOGRAPHY, LYASE, ACETYLATION, CYTOPLASM, DISEASE MUTATION, METAL-BINDING, POLYMORPHISM, ZINC
5clu:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE COMPLEX OF HCAII WITH A SACCHARINE DERIVATIVE | CARBONIC ANHYDRASE II, LYASE
2o4z:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE CARBONIC ANHYDRASE II COMPLEXED WITH HYDROXYSULFAMIDE INHIBITOR | CARBONIC ANHYDRASE, INHIBITORS, CRYSTAL STRUCTURE, LYASE
1lug:A (ALA115) to (LEU211) FULL MATRIX ERROR ANALYSIS OF CARBONIC ANHYDRASE | ERROR ANALYSIS, FULL-MATRIX, METALLOENZYME, LYASE
1lzv:A (ALA115) to (LEU212) SITE-SPECIFIC MUTANT (TYR7 REPLACED WITH HIS) OF HUMAN CARBONIC ANHYDRASE II | TWISTED BETA SHEET, ZINC METALLOENZYME, LYASE
1xpz:A (ALA115) to (LEU212) STRUCTURE OF HUMAN CARBONIC ANHYDRASE II WITH 4-[4-O- SULFAMOYLBENZYL)(4-CYANOPHENYL)AMINO]-4H-[1,2,4]-TRIAZOLE | CARBONIC ANHYDRASE, DUAL AROMATASE-STEROID SULFATASE INHIBITOR (DASI), ANTI-CANCER DRUG DELIVERY, LYASE
1xq0:A (ALA115) to (LEU212) STRUCTURE OF HUMAN CARBONIC ANHYDRASE II WITH 4-[(3-BROMO-4- O-SULFAMOYLBENZYL)(4-CYANOPHENYL)AMINO]-4H-[1,2,4]-TRIAZOLE | CARBONIC ANHYDRASE, DUAL AROMATASE-STEROID SULFATASE INHIBITOR (DASI), ANTI-CANCER DRUG DELIVERY, LYASE
3kig:A (ALA115) to (LEU211) MUTANT CARBONIC ANHYDRASE II IN COMPLEX WITH AN AZIDE AND AN ALKYNE | 10 STRANDED, TWISTED BETA-SHEETS, LYASE, DISEASE MUTATION, METAL- BINDING
3kkx:A (ALA115) to (LEU212) NEUTRON STRUCTURE OF HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER, NEUTRON, HCA II, CYTOPLASM, LYASE, METAL- BINDING, ZINC
3kne:A (ALA115) to (LEU211) CARBONIC ANHYDRASE II H64C MUTANT IN COMPLEX WITH AN IN SITU FORMED TRIAZOLE | 10 STRANDED; TWISTED BETA-SHEETS; LYASE; ACETYLATION, METAL-BINDING, CLICK-CHEMISTRY, AZIDE, ALKYNE, LYASE
3koi:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF COBALT (III) HUMAN CARBONIC ANHYDRASE II AT PH 6.0 | CARBONIC ANHYDRASE, METALLOENZYME, COBALT SUBSTITUTION, CRYSTAL PH, LYASE
3kok:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF COBALT (II) HUMAN CARBONIC ANHYDRASE II AT PH 8.5 | CARBONIC ANHYDRASE, METALLOENZYME, COBALT SUBSTITUTION, CRYSTAL PH, LYASE
3kon:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF COBALT (II) HUMAN CARBONIC ANHYDRASE II AT PH 11.0 | CARBONIC ANHYDRASE, METALLOENZYME, COBALT SUBSTITUTION, CRYSTAL PH, LYASE
1moo:A (ALA115) to (LEU212) SITE SPECIFIC MUTANT (H64A) OF HUMAN CARBONIC ANHYDRASE II AT HIGH RESOLUTION | HIGH-RESOLUTION, 4-METHYLIMIDAZOLE, TWISTED BETA SHEET, ZINC METALLOENZYME, LYASE
1yda:A (ALA115) to (LEU212) STRUCTURAL BASIS OF INHIBITOR AFFINITY TO VARIANTS OF HUMAN CARBONIC ANHYDRASE II | HYDRO-LYASE
1ydb:A (ALA115) to (LEU212) STRUCTURAL BASIS OF INHIBITOR AFFINITY TO VARIANTS OF HUMAN CARBONIC ANHYDRASE II | HYDRO-LYASE
1mua:A (ALA115) to (LEU212) STRUCTURE AND ENERGETICS OF A NON-PROLINE CIS-PEPTIDYL LINKAGE IN AN ENGINEERED PROTEIN | LYASE(OXO-ACID)
3ks3:A (ALA115) to (LEU212) HIGH RESOLUTION STRUCTURE OF HUMAN CARBONIC ANHYDRASE II AT 0.9 A | HIGH RESOLUTION, CARBONIC ANHYDRASE, SHORT HYDROGEN BOND
3kwa:A (ALA115) to (LEU212) POLYAMINES INHIBIT CARBONIC ANHYDRASES | POLYAMINES, CARBONIC ANHYDRASE II, INHIBITION, LYASE
1yo2:A (ALA115) to (LEU212) PROTON TRANSFER FROM HIS200 IN HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER HUMAN CARBONIC ANHYDRASE, LYASE
5dog:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 2- (BENZYLAMINO)-3,5,6-TRIFLUORO-4-[(2-PHENYLETHYL)THIO]BENZENE- SULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
5doh:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 2-[(1S)- 2,3-DIHYDRO-1H-INDEN-1-YLAMINO]-3,5,6-TRIFLUORO-4-[(2-HYDROXYETHYL) THIO]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
5doh:B (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 2-[(1S)- 2,3-DIHYDRO-1H-INDEN-1-YLAMINO]-3,5,6-TRIFLUORO-4-[(2-HYDROXYETHYL) THIO]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
4pq7:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A SULFAMIDE INHIBITOR | SULFAMIDE, ZINC BINDING, LYASE-LYASE INHIBITOR COMPLEX
1z97:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE III: STRUCTURAL AND KINETIC STUDY OF CATALYSIS AND PROTON TRANSFER. | CARBONIC ANHYDRASE, PROTON WIRE, CHEMICAL RESCUE, LYASE
1z9y:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH FUROSEMIDE AS SULFONAMIDE INHIBITOR | 10 STRANDED, TWISTED BETA-SHEETS, LYASE, LYASE-LYASE INHIBITOR COMPLEX
5drs:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASEISOZYME II WITH 3-[(1S)- 2,3-DIHYDRO-1H-INDEN-1-YLAMINO]-2,5,6-TRIFLUORO-4-[(2-HYDROXYETHYL) SULFONYL]BENZENESULFONAMIDE | LYASE, DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL- BINDING, LYASE-LYASE INHIBITOR COMPLEX
5dsi:A (ALA115) to (LEU212) STRUCTURE OF CO2 BOUND HOLO-FORM OF HUMAN CARBONIC ANHYDRASE II WITH 0 SEC (NO) WARMING | CARBONIC ANHYDRASE II, CO2 RELEASE, INTERMEDIATE STATES, LYASE
5dsk:A (ALA115) to (LEU212) STRUCTURE OF CO2 RELEASED HOLO-FORM OF HUMAN CARBONIC ANHYDRASE II WITH 3 MIN WARMING | CARBONIC ANHYDRASE II, CO2 RELEASE, INTERMEDIATE STATES, LYASE
5dsl:A (ALA115) to (LEU212) STRUCTURE OF CO2 RELEASED HOLO-FORM OF HUMAN CARBONIC ANHYDRASE II WITH 10 MIN WARMING | CARBONIC ANHYDRASE II, CO2 RELEASE, INTERMEDIATE STATES, LYASE
5dsm:A (ALA115) to (LEU212) STRUCTURE OF CO2 RELEASED HOLO-FORM OF HUMAN CARBONIC ANHYDRASE II WITH 25 MIN WARMING | CARBONIC ANHYDRASE II, CO2 RELEASE, INTERMEDIATE STATES, LYASE
5dsn:A (ALA115) to (LEU212) STRUCTURE OF CO2 RELEASED HOLO-FORM OF HUMAN CARBONIC ANHYDRASE II WITH 1 HR WARMING | CARBONIC ANHYDRASE II, CO2 RELEASE, INTERMEDIATE STATES, LYASE
5dso:A (ALA115) to (LEU212) STRUCTURE OF CO2 BOUND APO-FORM OF HUMAN CARBONIC ANHYDRASE II WITH 0 SEC (NO) WARMING | CARBONIC ANHYDRASE II, CO2 RELEASE, INTERMEDIATE STATES, LYASE
5dsp:A (ALA115) to (LEU212) STRUCTURE OF CO2 RELEASED APO-FORM OF HUMAN CARBONIC ANHYDRASE II WITH 40 SEC WARMING | CARBONIC ANHYDRASE II, CO2 RELEASE, INTERMEDIATE STATES, LYASE
5dsq:A (ALA115) to (LEU212) STRUCTURE OF CO2 RELEASED APO-FORM OF HUMAN CARBONIC ANHYDRASE II WITH 3 MIN WARMING | CARBONIC ANHYDRASE II, CO2 RELEASE, INTERMEDIATE STATES, LYASE
5dsr:A (ALA115) to (LEU212) STRUCTURE OF CO2 RELEASED APO-FORM OF HUMAN CARBONIC ANHYDRASE II WITH 10 MIN WARMING | CARBONIC ANHYDRASE II, CO2 RELEASE, INTERMEDIATE STATES, LYASE
1zfk:A (ALA1115) to (LEU1212) CARBONIC ANHYDRASE II IN COMPLEX WITH N-4-SULFONAMIDPHENYL-N'-4- METHYLBENZOSULFONYLUREASE AS SULFONAMIDE INHIBITOR | 10 STRANDED, TWISTED BETA-SHEETS, LYASE
1zfq:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH ETHOXZOLAMIDPHENOLE AS SULFONAMIDE INHIBITOR | 10 STRANDED, TWISTED BETA-SHEETS, LYASE
1zge:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH P-SULFONAMIDO-O,O'- DICHLOROANILINE AS SULFONAMIDE INHIBITOR | 10 STRANDED, TWISTED BETA-SHEETS, LYASE
1zgf:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH TRICHLOROMETHIAZIDE AS SULFONAMIDE INHIBITOR | 10 STRANDED, TWISTED BETA-SHEETS, LYASE
1zh9:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH N-4-METHYL-1- PIPERAZINYL-N'-(P-SULFONAMIDE)PHENYLTHIOUREA AS SULFONAMIDE INHIBITOR | 10 STRANDED, TWISTED BETA-SHEETS, LYASE
4pyx:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4pyy:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4pzh:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 2,3,5,6- TETRAFLUORO-4[(2-HYDROXYETHYL)SULFONYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4q06:A (ALA115) to (LEU211) CRYSTAL STRUCTURE OF CHIMERIC CARBONIC ANHYDRASE IX WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4q09:A (ALA115) to (LEU211) CRYSTAL STRUCTURE OF CHIMERIC CARBONIC ANHYDRASE XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4q49:A (ALA115) to (LEU212) ROOM TEMPERATURE NEUTRON CRYSTAL STRUCTURE OF APO HUMAN CARBONIC ANHYDRASE AT PH 7.5 | MIXED ALPHA BETA, PROTON TRANSFER, CYTOSOLIC, LYASE
1zsa:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II MUTANT E117Q, APO FORM | LYASE, OXO-ACID, ACETYLATION, ZINC, POLYMORPHISM, LYASE (OXO-ACID)
1zsb:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II MUTANT E117Q, TRANSITION STATE ANALOGUE ACETAZOLAMIDE | LYASE, OXO-ACID, ACETYLATION, ZINC, POLYMORPHISM, LYASE (OXO-ACID)
1zsc:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II MUTANT E117Q, HOLO FORM | LYASE, OXO-ACID, ACETYLATION, ZINC, POLYMORPHISM, LYASE (OXO-ACID)
5e28:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE 4-(4-AMINOPHENYL)BENZENESULFONAMIDE INHIBITOR | LYASE
5e2k:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE 4-(3-AMINOPHENYL)BENZENESULFONAMIDE INHIBITOR | LYASE
5e2m:A (SER115) to (CYS212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME I WITH 3- (CYCLOOCTYLAMINO)-2,5,6-TRIFLUORO-4-[(2-HYDROXYETHYL) SULFONYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
5e2m:B (SER115) to (CYS212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME I WITH 3- (CYCLOOCTYLAMINO)-2,5,6-TRIFLUORO-4-[(2-HYDROXYETHYL) SULFONYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
5e2n:A (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH 3- (CYCLOOCTYLAMINO)-2,5,6-TRIFLUORO-4-[(2-HYDROXYETHYL) SULFONYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
5e2n:B (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH 3- (CYCLOOCTYLAMINO)-2,5,6-TRIFLUORO-4-[(2-HYDROXYETHYL) SULFONYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
5e2r:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A 1,1'-BIPHENYL-4-SULFONAMIDE INHIBITOR | 1'-BIPHENYL-4-SULFONAMIDE, LYASE, COMPLEX, INHIBITOR
5e2s:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE 4-(2-ISO-PROPYLPHENYL)BENZENESULFONAMIDE INHIBITOR | LYASE
4q6d:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-[(Z)- AZEPAN-1-YLDIAZENYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4q6e:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-{[3- (3,5-DIMETHYL-1H-PYRAZOL-1-YL)-3-OXOPROPYL]AMINO}BENZENE-1- SULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
5e5r:C (PRO171) to (PHE270) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN CARBONIC ANHYDRASE-LIKE DOMAIN OF PTPRG AND IMMUNOGLOBULIN DOMAINS 2-3 OF CNTN3 | NEURAL CELL ADHESION MOLECULE, RECEPTOR-TYPE PROTEIN TYROSINE PHOSPHATASE, IMMUNOGLOBULIN DOMAINS, CARBONIC ANHYDRASE-LIKE DOMAIN, HYDROLASE-CELL ADHESION COMPLEX
5e5u:A (PRO171) to (PHE270) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN CARBONIC ANHYDRASE-LIKE DOMAIN OF PTPRG AND IMMUNOGLOBULIN DOMAINS 2-3 OF CNTN6 | NEURAL CELL ADHESION MOLECULE, RECEPTOR-TYPE PROTEIN TYROSINE PHOSPHATASE, IMMUNOGLOBULIN DOMAINS, CARBONIC ANHYDRASE-LIKE DOMAIN, CELL ADHESION-HYDROLASE COMPLEX
5e5u:C (PRO171) to (PHE270) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN CARBONIC ANHYDRASE-LIKE DOMAIN OF PTPRG AND IMMUNOGLOBULIN DOMAINS 2-3 OF CNTN6 | NEURAL CELL ADHESION MOLECULE, RECEPTOR-TYPE PROTEIN TYROSINE PHOSPHATASE, IMMUNOGLOBULIN DOMAINS, CARBONIC ANHYDRASE-LIKE DOMAIN, CELL ADHESION-HYDROLASE COMPLEX
4q7p:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 1-HYDROXY-3-METHYLPYRIDINE-2(1H)-THIONE BOUND TO HCAII | LYASE
4q7s:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 1-HYDROXY-4-METHYLPYRIDINE-2(1H)-THIONE BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
4q7v:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 1-HYDROXY-5-METHYLPYRIDINE-2(1H)-THIONE BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
4q7w:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 1-HYDROXY-6-METHYLPYRIDINE-2(1H)-THIONE BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
4q81:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 1-HYDROXY-4,6-DIMETHYLPYRIDINE-2(1H)-THIONE BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
4q83:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 1-HYDROXY-3-(TRIFLUOROMETHYL)PYRIDINE-2(1H)- THIONE BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
4q87:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 1-HYDROXY-4-(TRIFLUOROMETHYL)PYRIDINE-2(1H)- THIONE BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
3lxe:A (SER115) to (CYS212) HUMAN CARBONIC ANHYDRASE I IN COMPLEX WITH TOPIRAMATE | CARBONIC ANHYDRASE 1, TOPIRAMATE, ENZYME-INHIBITOR COMPLEX, LYASE
3lxe:B (SER115) to (CYS212) HUMAN CARBONIC ANHYDRASE I IN COMPLEX WITH TOPIRAMATE | CARBONIC ANHYDRASE 1, TOPIRAMATE, ENZYME-INHIBITOR COMPLEX, LYASE
4q8x:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 1-HYDROXY-5-(TRIFLUOROMETHYL)PYRIDINE-2(1H)- THIONE BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
4q8y:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 2-HYDROXYISOQUINOLINE-1(2H)-THIONE BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
4q8z:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 1-HYDROXY-4-METHYLPYRIDIN-2(1H)-ONE BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
4q90:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 4-METHYLPYRIDINE-2(1H)-THIONE BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
4q99:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 2-MERCAPTO-4-METHYLPHENOL BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
3m04:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH NOVEL SULFONAMIDE INHIBITOR | 10 STRANDED TWISTED BETA-SHEETS, LYASE, DISEASE MUTATION, METAL- BINDING, LYASE-LYASE INHIBITOR COMPLEX
4q9y:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF 3-METHYLTHIOPHENOL BOUND TO HUMAN CARBONIC ANHYDRASE II | LYASE
3m14:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH NOVEL SULFONAMIDE INHIBITOR | 10 STRANDED TWISTED BETA-SHEETS, LYASE, DISEASE MUTATION, METAL- BINDING, LYASE-LYASE INHIBITOR COMPLEX
3m1j:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF A NAMI A-CARBONIC ANHYDRASE II ADDUCT DISCLOSES THE MODE OF ACTION OF THIS NOVEL ANTICANCER METALLODRUG | RUTHENIUM COMPLEXES, NAMI-A, ANTIMETASTATIC AGENTS, CARBONIC ANHYDRASE, LYASE
3m1k:A (ALA115) to (LEU212) CARBONIC ANHYDRASE IN COMPLEX WITH FRAGMENT | 10 STRANDED TWISTED BETA-SHEETS, LYASE, DISEASE MUTATION, METAL- BINDING
3m1q:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II MUTANT W5C-H64C WITH OPENED DISULFIDE BOND | 10 STRANDED TWISTED BETA-SHEETS, LYASE, DISEASE MUTATION, METAL- BINDING
3m1w:A (ALA115) to (LEU212) CARBONIC ANHYRDASE II MUTANT W5CH64C WITH CLOSED DISULFIDE BOND IN COMPLEX WITH SULFATE | 10 STRANDED TWISTED BETA-SHEETS, LYASE, DISEASE MUTATION, METAL- BINDING
3m2n:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-{2-[N- (6-CHLORO-5-NITROPYRIMIDIN-4-YL)AMINO]ETHYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, SULFONAMIDE, LYASE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3m2x:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH NOVEL SULFONAMIDE INHIBITOR | 10 STRANDED TWISTED BETA-SHEETS, LYASE, DISEASE MUTATION, METAL- BINDING, LYASE-LYASE INHIBITOR COMPLEX
3m2y:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH NOVEL SULFONAMIDE INHIBITOR | 10 STRANDED TWISTED BETA-SHEETS, LYASE, DISEASE MUTATION, METAL- BINDING, LYASE-LYASE INHIBITOR COMPLEX
3m2z:A (ALA115) to (LEU212) FRAGMENT TETHERED TO CARBONIC ANHYDRASE II H64C MUTANT | 10 STRANDED TWISTED BETA-SHEETS, LYASE, DISEASE MUTATION, METAL- BINDING
4qef:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II V207I - CYANATE INHIBITOR COMPLEX | LYASE, PROTON TRANSFER, LYASE-LYASE INHIBITOR COMPLEX
3m3x:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-{2-[N- (6-METHOXY-5-NITROPYRIMIDIN-4-YL)AMINO]ETHYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, SULFONAMIDE, METAL-BINDING, LYASE- LYASE INHIBITOR COMPLEX
3m40:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-[N-(6- CHLORO-5-NITROPYRIMIDIN-4-YL)AMINO]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, SULFONAMIDE, METAL-BINDING, LYASE- LYASE INHIBITOR COMPLEX
3m5e:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-{[N- (6-CHLORO-5-FORMYL-2-METHYLTHIOPYRIMIDIN-4-YL) AMINO]METHYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, SULFONAMIDE, METAL-BINDING, LYASE- LYASE INHIBITOR COMPLEX
3m5s:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II MUTANT H64C IN COMPLEX WITH CARBONATE | STRANDED TWISTED BETA-SHEETS, LYASE, DISEASE MUTATION, METAL-BINDING
3m5t:A (ALA115) to (LEU212) FRAGMENT TETHERED TO CARBONIC ANHYDRASE II H64C MUTANT | STRANDED TWISTED BETA-SHEETS, LYASE, DISEASE MUTATION, METAL-BINDING
3m67:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 2- CHLORO-5-[(6,7-DIHYDRO-1H-[1,4]DIOXINO[2,3-F]BENZIMIDAZOL-2- YLSULFANYL)ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3m96:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 5-{[(5- BROMO-1H-BENZIMIDAZOL-2-YL)SULFANYL]ACETYL}-2- CHLOROBENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, LYASE
3m98:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 5-(1H- BENZIMIDAZOL-1-YLACETYL)-2-CHLOROBENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, LYASE
3b4f:A (ALA115) to (LEU212) CARBONIC ANHYDRASE INHIBITORS. INTERACTION OF 2- (HYDRAZINOCARBONYL)-3-PHENYL-1H-INDOLE-5-SULFONAMIDE WITH TWELVE MAMMALIAN ISOFORMS: KINETIC AND X-RAY CRYSTALLOGRAPHIC STUDIES | CARBONIC ANHYDRASE, INHIBITORS, CRYSTAL STRUCTURE, SULFONAMIDE, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC, LYASE(OXO-ACID)
5eh5:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH LIGAND | HUMAN CARBONIC ANHYDRASE, LIGAND, LYASE
5eh7:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH LIGAND | HUMAN CARBONIC ANHYDRASE, LYASE
5eh8:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH LIGAND | HUMAN CARBONIC ANHYDRASE, LYASE
5ehe:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 3- (BENZYLAMINO)-2,5,6-TRIFLUORO-4-[(2-HYDROXYETHYL) SULFONYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, LYASE
5ehv:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH LIGAND | HUMAN CARBONIC ANHYDRASE II, TRANSFERASE
2abe:A (ALA115) to (LEU212) CARBONIC ANHYDRASE ACTIVATORS: X-RAY CRYSTAL STRUCTURE OF THE ADDUCT OF HUMAN ISOZYME II WITH L-HISTIDINE AS A PLATFORM FOR THE DESIGN OF STRONGER ACTIVATORS | PROTEIN-ACTIVATOR COMPLEX, LYASE
5ehw:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH LIGAND | HUMAN CARBONIC ANHYDRASE II, TRANSFERASE
4qiz:A (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qiz:B (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
5eij:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH SULFONAMIDE INHIBITOR | SULFONAMIDE, INHIBITOR, LYASE-LYASE INHIBITOR COMPLEX
4qjm:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qjp:B (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qjp:A (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qjx:A (ALA117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qk1:A (ALA115) to (LEU212) STRUCTURAL AND CATALYTIC EFFECTS OF PROLINE SUBSTITUTION AND SURFACE LOOP DELETION IN THE EXTENDED ACTIVE SITE OF HUMAN CARBONIC ANHYDRASE II - K170P | LYASE
4qk2:A (ALA115) to (LEU212) STRUCTURAL AND CATALYTIC EFFECTS OF PROLINE SUBSTITUTION AND SURFACE LOOP DELETION IN THE EXTENDED ACTIVE SITE OF HUMAN CARBONIC ANHYDRASE II - E234P | LYASE
4qk3:A (ALA115) to (LEU212) STRUCTURAL AND CATALYTIC EFFECTS OF PROLINE SUBSTITUTION AND SURFACE LOOP DELETION IN THE EXTENDED ACTIVE SITE OF HUMAN CARBONIC ANHYDRASE II - [DELTA]230-240 | LYASE
4bcw:A (ALA115) to (LEU212) CARBONIC ANHYDRASE IX MIMIC IN COMPLEX WITH (E)-2-(5-BROMO- 2-HYDROXYPHENYL)ETHENESULFONIC ACID | LYASE, SULFOCOUMARIN
5ekh:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH A TWO-FACED GUEST | LYASE-LYASE INHIBITOR COMPLEX
5ekj:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH A TWO-FACED GUEST | LYASE-LYASE INHIBITOR COMPLEX
5ekm:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH A TWO-FACED GUEST | LYASE-LYASE INHIBITOR COMPLEX
3mhi:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-{[(5- NITRO-6-OXO-1,6-DIHYDRO-4-PYRIMIDINYL)AMINO]METHYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, SULFONAMIDE, LYASE-LYASE INHIBITOR COMPLEX
3mhm:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-{[N- (6-BENZYLAMINO-5-NITROPYRIMIDIN-4-YL)AMINO]METHYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, SULFONAMIDE, LYASE-LYASE INHIBITOR COMPLEX
3mho:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-[N-(6- CHLORO-5-FORMYL-2-METHYLTHIOPYRIMIDIN-4-YL)AMINO]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, SULFONAMIDE, LYASE-LYASE INHIBITOR COMPLEX
5eoi:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF COPPER BOUND HUMAN CARBONIC ANHYDRASE II | LYASE
4bf6:A (ALA115) to (LEU212) THREE DIMENSIONAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 5-(1-(3-CYANOPHENYL)-1H-1,2,3-TRIAZOL-4-YL) THIOPHENE-2-SULFONAMIDE | LYASE
4qsb:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 3-{[(4- METHYL-6-OXO-1,6-DIHYDROPYRIMIDIN-2-YL)THIO]ACETYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3mmf:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A 1, 3,5-TRIAZINE-SUBSTITUTED BENZENESULFONAMIDE INHIBITOR | ZINC METALLOENZYME, INHIBITOR, SULFONAMIDE, METAL-BINDING, TRIAZINE, LYASE, LYASE-LYASE INHIBITOR COMPLEX
4qsi:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 5-{[(4- TERT-BUTHYL-6-OXO-1,6-DIHYDROPYRIMIDIN-2-YL)THIO]ACETYL}-2- CHLOROBENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qsj:B (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH 2- CHLORO-4-{[(4-METHYL-6-OXO-1,6-DIHYDROPYRIMIDIN-2-YL) THIO]ACETYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qsj:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XIII WITH 2- CHLORO-4-{[(4-METHYL-6-OXO-1,6-DIHYDROPYRIMIDIN-2-YL) THIO]ACETYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3mna:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A 1,3,5-TRIAZINE-SUBSTITUTED BENZENESULFONAMIDE INHIBITOR | ZINC METALLOENZYME, INHIBITOR, SULFONAMIDE, LYASE, TRIAZINE, LYASE- LYASE INHIBITOR COMPLEX
3mni:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II MUTANT K170D | PROTON TRANSFER, METALLOENZYME, PROTON TRANSPORT
3mnj:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II MUTANT K170E | PROTON TRANSFER, METALLOENZYME, PROTON TRANSPORT
3mnk:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II MUTANT K170H | PROTON TRANSFER, METALLOENZYME, PROTON TRANSPORT
4qtl:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3bl0:A (ALA115) to (LEU212) CARBONIC ANHYDRASE INHIBITORS. INTERACTION OF 2-N,N- DIMETHYLAMINO-1,3,4-THIADIAZOLE-5-METHANESULFONAMIDE WITH TWELVE MAMMALIAN ISOFORMS: KINETIC AND X-RAY CRYSTALLOGRAPHIC STUDIES | CARBONIC ANHYDRASE, INHIBITORS, CRYSTAL STRUCTURE, SULFONAMIDE, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC, LYASE(OXO-ACID)
5ezt:X (ALA114) to (LEU210) PERACETYLATED BOVINE CARBONIC ANHYDRASE II | CARBONIC ANHYDRASE, PERACETYLATED, TRANSFERASE
3mwo:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN A DOUBLED MONOCLINIC CELL: A RE- DETERMINATION | DOUBLED UNIT CELL, LYASE, PSEUDOSYMMETRY, TRANSLATIONAL NCS
3mwo:B (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN A DOUBLED MONOCLINIC CELL: A RE- DETERMINATION | DOUBLED UNIT CELL, LYASE, PSEUDOSYMMETRY, TRANSLATIONAL NCS
3myq:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 2- CHLORO-5-[(1H-IMIDAZO[4,5-C]QUINOLIN-2-YLSULFANYL) ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, LYASE
3mzc:A (ALA115) to (LEU212) HUMAN CARBONIC AHYDRASE II IN COMPLEX WITH A BENZENESULFONAMIDE INHIBITOR | LYASE, BENZENESULFONAMIDE INHIBITOR, ZINC METALLOENZYME, ZINC COORDINATION, LYASE-LYASE INHIBITOR COMPLEX
3n0n:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A BENZENESULFONAMIDE INHIBITOR | ZINC METALLOENZYME LYASE, BENZENESULFONAMIDE INHIBITOR, ZINC LIGANDS, , LYASE, LYASE-LYASE INHIBITOR COMPLEX
3n2p:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A BENZENESULFONAMIDE INHIBITOR | LYASE, ZINC METALLOENZYME, ZINC LIGANDS, BENZENESULFONAMIDE, INHIBITOR., LYASE-LYASE INHIBITOR COMPLEX
5fdc:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE ANTICONVULSANT SULFAMIDE JNJ-26990990 AND ITS S,S-DIOXIDE ANALOG. | SULFAMIDE INHIBITOR, PROTEIN-INHIBITOR COMPLEX, LYASE
4r5a:A (ALA115) to (LEU212) A CARBONIC ANHYDRASE IX MIMIC IN COMPLEX WITH A CARBOHYDRATE-BASED SULFAMATE | CARBONIC ANHYDRASE IX MIMIC, LYASE
4r5b:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A CARBOHYDRATE-BASED SULFAMATE | CYTOSOL, LYASE
3c7p:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH STX237 | PROTEIN-INHIBITOR COMPLEX, DISEASE MUTATION, LYASE, METAL-BINDING
3ca2:A (ALA115) to (LEU212) CRYSTALLOGRAPHIC STUDIES OF INHIBITOR BINDING SITES IN HUMAN CARBONIC ANHYDRASE II. A PENTACOORDINATED BINDING OF THE SCN-ION TO THE ZINC AT HIGH P*H | LYASE(OXO-ACID)
3caj:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH ETHOXZOLAMIDE | PROTEIN-INHIBITOR COMPLEX, DISEASE MUTATION, LYASE, METAL-BINDING
4rfc:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH TERT-BUTYL 4-(4- SULFAMOYLPHENOXY)BUTYLCARBAMATE | SULFONAMIDE, CARBONIC ANHYDRASE, ANTIGLAUCOMA, O-(-AMINOALKYL)- BENZENESULFONAMIDES, LYASE
4rfd:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 4-(4-SULFAMOYL-PHENOXY)- BUTYLAMMONIUM | SULFONAMIDE, CARBONIC ANHYDRASE, ANTIGLAUCOMA, O-(-AMINOALKYL)- BENZENESULFONAMIDESS, LYASE
5flo:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, CARBONIC ANHYDRASE, METALLOPROTEIN
5flp:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, CARBONIC ANHYDRASE, METALLOPROTEIN
5flq:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, FRAGMENTS, CARBONIC ANHYDRASE, METALLOPROTEIN
4rh2:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 2-(6- HYDROXY-3-OXO-3H-XANTHEN-9-YL)-5-{3-1-(4-SULFAMOYL-PHENYL)-1H-[1,2, 3]TRIAZOL-4-YLMETHYL-THIOUREIDO}-BENZOIC ACID | LYASE
3nj9:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF CARBONIC ANHYDRASE II IN COMPLEX WITH A NIR INHIBITOR | CARBONIC ANHYDRASE, NIR MOIETY, INHIBITORS, LYASE-LYASE INHIBITOR COMPLEX
5fng:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, FRAGMENTS, CARBONIC ANHYDRASE, METALLOPROTEIN
5fnh:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, FRAGMENTS, CARBONIC ANHYDRASE, METALLOPROTEIN
5fnj:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, FRAGMENTS, CARBONIC ANHYDRASE, METALLOPROTEIN
5fnk:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, FRAGMENTS, CARBONIC ANHYDRASE, METALLOPROTEIN
5fnl:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, FRAGMENTS, CARBONIC ANHYDRASE, METALLOPROTEIN
5fnm:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, FRAGMENTS, CARBONIC ANHYDRASE, METALLOPROTEIN
4riu:A (ALA115) to (LEU212) A CARBONIC ANHYDRASE IX MIMIC IN COMPLEX WITH A SACCHARIN-BASED INHIBITOR | CARBONIC ANHYDRASE FOLD, REVERSIBLE HYDRATION OF CO2, ACTIVE SITE POINT MUTATIONS, CYTOSOLIC, LYASE-LYASE INHIBITOR COMPLEX
4riv:A (ALA115) to (LEU212) A CARBONIC ANHYDRASE IX MIMIC IN COMPLEX WITH SACCHARIN | CARBONIC ANHYDRASE FOLD, REVERSIBLE HYDRATION OF CO2, ACTIVE SITE POINT MUTATIONS, CYTOSOLIC, LYASE
4cac:A (ALA115) to (LEU212) REFINED STRUCTURE OF HUMAN CARBONIC ANHYDRASE II AT 2.0 ANGSTROMS RESOLUTION | LYASE(OXO-ACID)
4rn4:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASES II IN COMPLEX WITH A ACETAZOLAMIDE DERIVATIVE COMPRISING ONE HYDROPHOBIC AND ONE HYDROPHILIC TAIL MOIETY | CARBONIC ANHYDRASE, ACETAZOLAMIDE, LYASE-LYASE INHIBITOR COMPLEX
4rux:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 4- (ALLYLOXY)BENZENESULFONAMIDE | METALLOENZYME, ANALGESIC, LYASE
4ruy:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 4- PROPOXYBENZENESULFONAMIDE | METALLOENZYME, ANALGESIC, LYASE
4ruz:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 4- ETHOXYBENZENESULFONAMIDE | METALLOENZYME, ANALGESIC, LYASE
4cnv:A (ALA115) to (LEU211) SURFACE RESIDUE ENGINEERING OF BOVINE CARBONIC ANHYDRASE TO AN EXTREME HALOPHILIC ENZYME FOR POTENTIAL APPLICATION IN POSTCOMBUSTION CO2 CAPTURE | LYASE, PROTEIN ENGINEERING
4cnw:A (ALA115) to (LEU211) SURFACE RESIDUE ENGINEERING OF BOVINE CARBONIC ANHYDRASE TO AN EXTREME HALOPHILIC ENZYME FOR POTENTIAL APPLICATION IN POSTCOMBUSTION CO2 CAPTURE | LYASE, PROTEIN ENGINEERING, CO2 CAPTURE
4cnw:B (ALA115) to (LEU211) SURFACE RESIDUE ENGINEERING OF BOVINE CARBONIC ANHYDRASE TO AN EXTREME HALOPHILIC ENZYME FOR POTENTIAL APPLICATION IN POSTCOMBUSTION CO2 CAPTURE | LYASE, PROTEIN ENGINEERING, CO2 CAPTURE
4cnx:A (ALA115) to (LEU211) SURFACE RESIDUE ENGINEERING OF BOVINE CARBONIC ANHYDRASE TO AN EXTREME HALOPHILIC ENZYME FOR POTENTIAL APPLICATION IN POSTCOMBUSTION CO2 CAPTURE | LYASE, PROTEIN ENGINEERING, CO2 CAPTURE
5g01:A (ALA115) to (LEU212) AN UNUSUAL NATURAL PRODUCT PRIMARY SULFONAMIDE: SYNTHESIS, CARBONIC ANHYDRASE INHIBITION AND PROTEIN X-RAY STRUCTURE OF PSAMMAPLIN C | LYASE, NATURAL PRODUCT INHIBITOR, ENGINEERED PROTEINS, CARBONIC ANHYDRASE
5g03:A (ALA115) to (LEU212) AN UNUSUAL NATURAL PRODUCT PRIMARY SULFONAMIDE: SYNTHESIS, CARBONIC ANHYDRASE INHIBITION AND PROTEIN X-RAY STRUCTURE OF PSAMMAPLIN C | LYASE, NATURAL PRODUCT INHIBITOR, PROTEIN ENGINEERING, CARBONIC ANHYDRASE
3d0n:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE XIII | CARBONIC ANHYDRASE, LYASE, METAL-BINDING, METAL BINDING PROTEIN
4cq0:A (ALA115) to (LEU212) CYCLIC SECONDARY SULFONAMIDES: UNUSUALLY GOOD INHIBITORS OF CANCER-RELATED CARBONIC ANHYDRASE ENZYMES | LYASE, SACCHARIN, CLICK CHEMISTRY, DRUG DESIGN
5g0c:A (ALA115) to (LEU212) AN UNUSUAL NATURAL PRODUCT PRIMARY SULFONAMIDE: SYNTHESIS, CARBONIC ANHYDRASE INHIBITION AND PROTEIN X-RAY STRUCTURE OF PSAMMAPLIN C | LYASE, PROTEIN ENGINEERING, NATURAL PRODUCT INHIBITOR, CARBONIC ANHYDRASE
3d8w:A (ALA115) to (LEU212) USE OF A CARBONIC ANHYDRASE II, IX ACTIVE-SITE MIMIC, FOR THE PURPOSE OF SCREENING INHIBITORS FOR POSSIBLE ANTI- CANCER PROPERTIES | CARBONIC ANHYDRASE II, ANTI-CANCER, BENZOLAMIDE, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL- BINDING, POLYMORPHISM, ZINC
3d92:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II BOUND WITH SUBSTRATE CARBON DIOXIDE | ZINC METALLOENZYME, SUBSTRATE-BOUND, DISEASE MUTATION, LYASE, METAL- BINDING
3d93:A (ALA115) to (LEU212) APO HUMAN CARBONIC ANHYDRASE II BOUND WITH SUBSTRATE CARBON DIOXIDE | ZINC METALLOENZYME, SUBSTRATE-BOUND, DISEASE MUTATION, LYASE, METAL- BINDING
3d9z:A (ALA115) to (LEU212) USE OF CARBONIC ANHYDRASE II, IX ACTIVE-SITE MIMIC, FOR THE PURPOSE OF SCREENING INHIBITORS FOR POSSIBLE ANTI-CANCER PROPERTIES | CARBONIC ANHYDRASE II COMPLEX, CAIX MIMIC INHIBITORS, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL- BINDING, POLYMORPHISM, ZINC
3da2:B (ALA116) to (LEU213) X-RAY STRUCTURE OF HUMAN CARBONIC ANHYDRASE 13 IN COMPLEX WITH INHIBITOR | CARBONIC ANHYDRASE, SULFONAMIDE, SGC, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, LYASE, METAL-BINDING
3daz:A (ALA115) to (LEU212) USE OF CARBONIC ANHYDRASE II, IX ACTIVE-SITE MIMIC, FOR THE PURPOSE OF SCREENING INHIBITORS FOR POSSIBLE ANTI-CANCER PROPERTIES | CARBONIC ANHYDRASE II COMPLEX, CAIX MIMIC INHIBITORS, DISEASE MUTATION, LYASE, METAL-BINDING
3dbu:A (ALA115) to (LEU212) USE OF CARBONIC ANHYDRASE II, IX ACTIVE-SITE MIMIC, FOR THE PURPOSE OF SCREENING INHIBITORS FOR POSSIBLE ANTI-CANCER PROPERTIES | CARBONIC ANHYDRASE II COMPLEX, CAIX MIMIC INHIBITORS, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL- BINDING, POLYMORPHISM, ZINC
3dc9:A (ALA115) to (LEU212) USE OF CARBONIC ANHYDRASE II, IX ACTIVE-SITE MIMIC, FOR THE PURPOSE OF SCREENING INHIBITORS FOR POSSIBLE ANTI-CANCER PROPERTIES | CARBONIC ANHYDRASE II COMPLEX, CAIX MIMIC INHIBITORS, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL- BINDING, POLYMORPHISM, ZINC
3dcc:A (ALA115) to (LEU212) USE OF CARBONIC ANHYDRASE II, IX ACTIVE-SITE MIMIC, FOR THE PURPOSE OF SCREENING INHIBITORS FOR POSSIBLE ANTI-CANCER PROPERTIES | CARBONIC ANHYDRASE II COMPLEX, CAIX MIMIC INHIBITORS, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL- BINDING, POLYMORPHISM, ZINC
3dcs:A (ALA115) to (LEU212) USE OF CARBONIC ANHYDRASE II, IX ACTIVE-SITE MIMIC, FOR THE PURPOSE OF SCREENING INHIBITORS FOR POSSIBLE ANTI-CANCER PROPERTIES | CARBONIC ANHYDRASE II COMPLEX, CAIX MIMIC INHIBITORS, DISEASE MUTATION, LYASE, METAL-BINDING
3dcw:A (ALA115) to (LEU212) USE OF CARBONIC ANHYDRASE II, IX ACTIVE-SITE MIMIC, FOR THE PURPOSE OF SCREENING INHIBITORS FOR POSSIBLE ANTI-CANCER PROPERTIES | CARBONIC ANHYDRASE II COMPLEX, CAIX MIMIC INHIBITORS, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL- BINDING, POLYMORPHISM, ZINC
3oik:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II MUTANT A65S, N67Q (CA IX MIMIC) BOUND BY 2-ETHYLESTRADIOL 3,17-O,O-BIS-SULFAMATE | 2-ETHYLESTRONE, ESTRADIOL, SULFAMATE, MIXED ALPHA-BETA, CARBON DIOXIDE/BICARBONATE CONVERSION, LYASE
3oil:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II MUTANT A65S, N67Q (CA IX MIMIC) BOUND BY 2-ETHYLESTRADIOL 3-O-SULFAMATE | 2-ETHYLESTRONE, ESTRADIOL, SULFAMATE, MIXED ALPHA-BETA, CARBON DIOXIDE/BICARBONATE CONVERSION, LYASE
3oim:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II BOUND BY 2-ETHYLESTRADIOL 3-O-SULFAMATE | 2-ETHYLESTRONE, ESTRADIOL, SULFAMATE, MIXED ALPHA-BETA, CARBON DIOXIDE/BICARBONATE CONVERSION, LYASE
3oku:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 2-ETHYLESTRONE-3-O- SULFAMATE | MIXED ALPHA/BETA FOLD, REVERSIBLE HYDRATION OF CARBON DIOXIDE TO BICARBONATE, LYASE
3okv:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II A65S, N67Q (CA IX MIMIC) BOUND WITH 2- ETHYLESTRONE 3-O-SULFAMATE | MIXES ALPHA/BETA FOLD, REVERSIBLE HYDRATION OF CARBON DIOXIDE TO BICARBONATE, LYASE
3dvd:A (ALA115) to (LEU212) X-RAY CRYSTAL STRUCTURE OF MUTANT N62D OF HUMAN CARBONIC ANHYDRASE II | HUMAN CARBONIC ANHYDRASE II, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC
3oyq:A (ALA115) to (LEU212) STRUCTURE OF HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH 5,6-DIHYDRO- BENZO[H]CINNOLIN-3-YLAMINE | BENZENE SULPHONAMIDE INHIBITOR, DRUG INTERACTIONS, LYASE-LYASE INHIBITOR COMPLEX
3oys:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH 2-{[4-AMINO-3-(3- HYDROXYPROP-1-YN-1-YL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-1-YL]METHYL}-5- METHYL-3-(2-METHYLPHENYL)QUINAZOLIN-4(3H)-ONE | BENZENE SULPHONAMIDE INHIBITOR, DRUG INTERACTIONS, LYASE-LYASE INHIBITOR COMPLEX
3p3j:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH P-(5-RUTHENOCENYL-1H-1,2, 3-TRIAZOL-1-YL)BENZENESULFONAMIDE | CARBONIC ANHYDRASE ALPHA, LYASE, CYTOSOLIC
3p44:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH P-(4-RUTHENOCENYL-1H-1,2, 3-TRIAZOL-1-YL)BENZENESULFONAMIDE | CARBONIC ANHYDRASE ALPHA, LYASE, CYTOSOLIC
3p4v:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH (+)-XYLARIAMIDE A | CARBONIC ANHYDRASE, ALPHA TYPE, LYASE-LYASE INHIBITOR COMPLEX
3p55:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH P-(4-FERROCENYL-1H-1,2,3- TRIAZOL-1-YL)BENZENESULFONAMIDE | CARBONIC ANHYDRASE ALPHA, LYASE, CYTOSOLIC
3p58:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE IN COMPLEX WITH BENZYL (METHYL) CARBAMODITHOIC ACID | CARBOTHIOATES, HCAII INHIBITORS, LYASE-INHIBITOR COMPLEX
3p5a:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE COMPLEXED WITH SODIUM MORPHOLINOCARBODITHIOATE | CARBOTHIOATES, HCAII INHIBITORS, LYASE-INHIBITOR COMPLEX
3p5l:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE COMPLEXED WITH SODIUM 4-CYANO-4- PHENYLPIPERIDINE-1-CARBODITHIOATE | CARBOTHIOATES, HCAII INHIBITORS, LYASE-INHIBITOR COMPLEX
4dz7:A (ALA115) to (LEU212) HCA II IN COMPLEX WITH NOVEL SULFONAMIDE INHIBITORS SET D | MIXED A/B GLOBULAR PROTEIN, INTERCONVERSION OF CO2 AND BICARBONATE, LYASE-LYASE INHIBITOR COMPLEX
4dz9:A (ALA115) to (LEU212) HCA II IN COMPLEX WITH NOVEL SULFONAMIDE INHIBITORS SET D | MIXED A/B GLOBULAR PROTEIN, INTERCONVERSION OF CO2 AND BICARBONATE, LYASE-LYASE INHIBITOR COMPLEX
4e3d:A (ALA115) to (LEU212) NUCLEOPHILE RECOGNITION AS AN ALTERNATIVE INHIBITION MODE FOR BENZOIC ACID BASED CARBONIC ANHYDRASE INHIBITORS | CARBONATE DEHYDRATASE, LYASE-LYASE INHIBITOR COMPLEX
4e3f:A (ALA115) to (LEU212) NUCLEOPHILE RECOGNITION AS AN ALTERNATIVE INHIBITION MODE FOR BENZOIC ACID BASED CARBONIC ANHYDRASE INHIBITORS | CARBONATE DEHYDRATASE, INHIBITOR BINDING, LYASE-LYASE INHIBITOR COMPLEX
4e3g:A (ALA115) to (LEU212) NUCLEOPHILE RECOGNITION AS AN ALTERNATIVE INHIBITION MODE FOR BENZOIC ACID BASED CARBONIC ANHYDRASE INHIBITORS | CARBONATE DEHYDRATASE, INHIBITOR, LYASE-LYASE INHIBITOR COMPLEX
4e3h:A (ALA115) to (LEU212) NUCLEOPHILE RECOGNITION AS AN ALTERNATIVE INHIBITION MODE FOR BENZOIC ACID BASED CARBONIC ANHYDRASE INHIBITORS | CARBONATE DEHYDRATASE, INHIBITOR, LYASE-LYASE INHIBITOR COMPLEX
4e49:A (ALA115) to (LEU212) NUCLEOPHILE RECOGNITION AS AN ALTERNATIVE INHIBITION MODE FOR BENZOIC ACID BASED CARBONIC ANHYDRASE INHIBITORS | CARBONATE DEHYDRATASE, INHIBITOR, LYASE-LYASE INHIBITOR COMPLEX
4e4a:A (ALA115) to (LEU212) NUCLEOPHILE RECOGNITION AS AN ALTERNATIVE INHIBITION MODE FOR BENZOIC ACID BASED CARBONIC ANHYDRASE INHIBITORS | CARBONATE DEHYDRATASE, INHIBITOR, LYASE-LYASE INHIBITOR COMPLEX
4e5q:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH CYANATE | MIXED ALPHA BETA PROTEIN, ENZYME PROTON TRANSFER, LYASE
3pyk:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II AS HOST FOR PIANOSTOOL COMPLEXES BEARING A SULFONAMIDE ANCHOR | 10 STRANDED, TWISTED BETA-SHEETS, CARBONATE DEHYDRATASE ACTIVITY, PROTEIN BINDING, ZINC ION BINDING, LYASE ACTIVITY, METAL ION BINDING, CO2, BICARBONATE, SULFONAMIDES, METAL IONS, LYASE-LYASE INHIBITOR COMPLEX
4etq:X (SER88) to (THR187) VACCINIA VIRUS D8L IMV ENVELOPE PROTEIN IN COMPLEX WITH FAB OF MURINE IGG2A LA5 | VARIABLE DOMAIN, CONSTANT DOMAIN, IGG2A, IGG DOMAIN, CDR, HYPERVARIABLE REGION, NEUTRALIZING ANTIBODY, BETA SHEET, CARBONIC ANHYDRASE FOLD, LOOSE KNOT, CHONDROITIN-SULFATE BINDING SITE, DELTA 262, IMMUNE SYSTEM-VIRAL PROTEIN COMPLEX
4etq:C (SER88) to (THR187) VACCINIA VIRUS D8L IMV ENVELOPE PROTEIN IN COMPLEX WITH FAB OF MURINE IGG2A LA5 | VARIABLE DOMAIN, CONSTANT DOMAIN, IGG2A, IGG DOMAIN, CDR, HYPERVARIABLE REGION, NEUTRALIZING ANTIBODY, BETA SHEET, CARBONIC ANHYDRASE FOLD, LOOSE KNOT, CHONDROITIN-SULFATE BINDING SITE, DELTA 262, IMMUNE SYSTEM-VIRAL PROTEIN COMPLEX
3qyk:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH TRIPLE RING BENZENE SULFONAMIDE INHIBITOR | HYDRATION OF CO2, CO2, LYASE-LYASE INHIBITOR COMPLEX
4fik:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II H64A COMPLEXED WITH THIOXOLONE HYDROLYSIS PRODUCTS | CARBONIC ANHYDRASE II, HUMAN CARBONIC ANHYDRASE II, HCA II, HCA2, CA II, CA2, CARBONATE DEHYDRATASE II, CARBONIC ANHYDRASE C, THIOXOLONE, 4-MERCAPTOBENZENE-1,3-DIOL, 4-(2,4-DIHYDROXYPHENYL) DISULFANYLBENZENE-1,3-DIOL, DISEASE MUTATION, LYASE, METAL-BINDING
3r16:A (ALA115) to (LEU212) HUMAN CAII BOUND TO N-(4-SULFAMOYLPHENYL)-2-(THIOPHEN-2-YL) ACETAMIDE | REVERSIBLE HYDRATION OF CARBONDIOXIDE, LYASE
3r17:B (ALA115) to (LEU212) HCARBONIC ANHYDRASE II BOUND TO N-(2-FLUORO.4-SULFAMOYLPHENYL)-2- (THIOPHEN-2-YL) ACETAMIDE | REVERSIBLE HYDRATION OF CARBONDIOXIDE, LYASE
4fl7:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH N-(HYDROXY)-BENZAMIDE | LYASE
4fpt:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH ETHYL (2Z,4R)-2- (SULFAMOYLIMINO)-1,3-THIAZOLIDINE-4-CARBOXYLATE | 10 STRANDED TWISTED BETA-SHEETS, LYASE, LYASE-LYASE INHIBITOR COMPLEX
3rg3:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE W5E MUTANT OF HUMAN CARBONIC ANHYDRASE II | ZINC METALLOENZYME, W5E MUTATION, LYASE
3rg4:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE W5F MUTANT OF HUMAN CARBONIC ANHYDRASE II | ZINC METALLOENZYME, W5F MUTATION, LYASE
4frc:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH N'-SULFAMOYLPYRROLIDINE-1- CARBOXIMIDAMIDE | 10 STRANDED TWISTED BETA-SHEETS, LYASE, LYASE-LYASE INHIBITOR COMPLEX
4fu5:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH N-[(2Z)-1,3-OXAZOLIDIN-2- YLIDENE]SULFURIC DIAMIDE | 10 STRANDED TWISTED BETA-SHEETS, LYASE, LYASE-LYASE INHIBITOR COMPLEX
4fvo:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH N-[(2E)-3,4-DIHYDROQUINAZOLIN- 2(1H)-YLIDENE]SULFURIC DIAMIDE | 10 STRANDED TWISTED BETA-SHEETS, LYASE, LYASE-LYASE INHIBITOR COMPLEX
3rj7:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH ITS INHIBITOR RHENIUM(I) TRISCARBONYL-CYCLOPENTADIENYL-CARBOXY-4-AMINOMETHYLBENZENE- SULFONAMIDE | INHIBITOR, TRANSITION METAL COMPLEX, ANHYDRASE, CARBON DIOXIDE, LYASE-LYASE INHIBITOR COMPLEX
5jq0:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH BENZOXABOROLE AT PH=8.7 | BENZOXABOROLE, LYASE, BORON, ZINC, CARBONATE DEHYDRATASE
5jqt:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH BENZOXABOROLE AT PH 7.4 | BENZOXABOROLE, LYASE, BORON, ZINC, CARBONATE DEHYDRATASE
4g0c:A (ALA115) to (LEU212) NEUTRON STRUCTURE OF ACETAZOLAMIDE-BOUND HUMAN CARBONIC ANHYDRASE II REVEAL MOLECULAR DETAILS OF DRUG BINDING. | CARBONIC ANHYDRASE, ACETAZOLAMIDE, HYDROGEN BONDING, LYASE-LYASE INHIBITOR COMPLEX
4gl1:X (ALA115) to (LEU212) STRUCTURE OF H64A/N62L/N67L HUMAN CARBONIC ANHYDRASE II TRIPLE MUTANT | MIXED ALPA BETA, LYASE
5lmd:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF HCA II IN COMPLEX WITH A BENZOXABOROLE INHIBITOR | BENZOXABOROLE, ZINC ENZYME, INHIBITOR, LYASE
6ca2:A (ALA115) to (LEU212) ENGINEERING THE HYDROPHOBIC POCKET OF CARBONIC ANHYDRASE II | LYASE(OXO-ACID)
7ca2:A (ALA115) to (LEU212) ENGINEERING THE HYDROPHOBIC POCKET OF CARBONIC ANHYDRASE II | LYASE(OXO-ACID)
3ryy:A (ALA115) to (LEU212) FLUOROALKYL AND ALKYL CHAINS HAVE SIMILAR HYDROPHOBICITIES IN BINDING TO THE HYDROPHOBIC WALL OF CARBONIC ANHYDRASE | ALPHA BETA, LYASE
1avn:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH THE HISTAMINE ACTIVATOR | LYASE, OXO-ACID
1bic:A (ALA115) to (LEU212) CRYSTALLOGRAPHIC ANALYSIS OF THR-200-> HIS HUMAN CARBONIC ANHYDRASE II AND ITS COMPLEX WITH THE SUBSTRATE, HCO3- | LYASE(OXO-ACID)
3s71:B (ALA115) to (LEU212) THE ORIGIN OF THE HYDROPHOBIC EFFECT IN THE MOLECULAR RECOGNITION OF ARYLSULFONAMIDES BY CARBONIC ANHYDRASE | ALPHA BETA, LYASE
3s77:B (ALA115) to (LEU212) THE ORIGIN OF THE HYDROPHOBIC EFFECT IN THE MOLECULAR RECOGNITION OF ARYLSULFONAMIDES BY CARBONIC ANHYDRASE | ALPHA BETA, LYASE
1bzm:A (SER115) to (CYS212) DRUG-PROTEIN INTERACTIONS: STRUCTURE OF SULFONAMIDE DRUG COMPLEXED WITH HUMAN CARBONIC ANHYDRASE I | PROTEIN-DRUG INTERACTIONS, OXO-ACID LYASE, SULFONAMIDES, LYASE(OXO- ACID)
3ffp:X (ALA115) to (LEU212) X RAY STRUCTURE OF THE COMPLEX BETWEEN CARBONIC ANHYDRASE II AND LC INHIBITORS | CARBONIC ANHYDRASE, INHIBITORS, CRYSTAL STRUCTURE, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL- BINDING, POLYMORPHISM, ZINC
1ca2:A (ALA115) to (LEU212) REFINED STRUCTURE OF HUMAN CARBONIC ANHYDRASE II AT 2.0 ANGSTROMS RESOLUTION | LYASE(OXO-ACID)
1okn:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEX WITH THE 1OKN INHIBITOR 4- SULFONAMIDE-[1-(4-N-(5-FLUORESCEIN THIOUREA)BUTANE)] | LYASE (OXO-ACID), INHIBITOR
1cnb:A (ALA115) to (LEU212) COMPENSATORY PLASTIC EFFECTS IN THE REDESIGN OF PROTEIN- ZINC BINDING SITES | LYASE(OXO-ACID)
1cnx:A (ALA115) to (LEU212) SECONDARY INTERACTIONS SIGNIFICANTLY REMOVED FROM THE SULFONAMIDE BINDING POCKET OF CARBONIC ANHYDRASE II INFLUENCE BINDING CONSTANTS | LYASE (OXO-ACID)
2q38:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH SACCHARIN AT 1.95 ANGSTROM | TEN STRANDED TWISTED BETA SHEET, LYASE
1cva:A (ALA115) to (LEU212) STRUCTURAL AND FUNCTIONAL IMPORTANCE OF A CONSERVED HYDROGEN BOND NETWORK IN HUMAN CARBONIC ANHYDRASE II | LYASE(OXO-ACID)
1czm:A (SER115) to (CYS212) DRUG-PROTEIN INTERACTIONS: STRUCTURE OF SULFONAMIDE DRUG COMPLEXED WITH HUMAN CARBONIC ANHYDRASE I | PROTEIN-DRUG INTERACTIONS, OXO-ACID LYASE, SULFONAMIDES, LYASE(OXO-ACID)
4ilx:A (ALA115) to (LEU212) STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH AN ADAMANTYL SULFONAMIDE INHIBITOR | LYASE, REVERSIBLE HYDRATION OF CARBON DIOXIDE, CYTOSOLIC, LYASE-LYASE INHIBITOR COMPLEX
3t84:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH ACETYLATED CARBOHYDRATE SULFAMATES | ALPHA CARBONIC ANHYDRASE, LYASE-LYASE INHIBITOR COMPLEX
3u7c:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE V143I MUTANT OF HUMAN CARBONIC ANHYDRASE II | LYASE, CARBONIC ANYDRASE C, CAC, SUBSTRATE BOUND, PRODUCT BOUND, CO2 PRESSURIZED, PRIMARILY BETA
4z0q:A (ALA115) to (LEU212) CARBONIC ANHYDRASE INHIBITORS: DESIGN AND SYNTHESIS OF NEW HETEROARYL- N-CARBONYLBENZENESULFONAMIDES TARGETING DRUGGABLE HUMAN CARBONIC ANHYDRASE ISOFORMS (HCA VII, HCA IX, AND HCA XIV) | CARBONATE DEHYDRATASE II, CARBONIC ANHYDRASE C, CARBONIC ANHYDRASE II, CA-II, CARBONATE DEHYDRATASE II- INHIBITOR COMPLEX, LYASE
1g1d:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH 4-(AMINOSULFONYL)-N- [(2-FLUOROPHENYL)METHYL]-BENZAMIDE | CARBONIC ANHYDRASE II, 4-(AMINOSULFONYL)-N-[(2- FLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
4z1j:A (ALA115) to (LEU211) CARBONIC ANHYDRASE INHIBITORS: DESIGN AND SYNTHESIS OF NEW HETEROARYL- N-CARBONYLBENZENESULFONAMIDES TARGETING DRUGGABLE HUMAN CARBONIC ANHYDRASE ISOFORMS (HCA VII, HCA IX, AND HCA XIV) | CARBONATE DEHYDRATASE II, CARBONIC ANHYDRASE C, CARBONIC ANHYDRASE II, CA-II, CARBONATE DEHYDRATASE II- INHIBITOR COMPLEX, LYASE
1g46:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) COMPLEXED WITH 4- (AMINOSULFONYL)-N-[(2,3-DIFLUOROPHENYL)METHYL]-BENZAMIDE | CARBONIC ANHYDRASE II, F131V, 4-(AMINOSULFONYL)-N-[(2,3- DIFLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1g48:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) COMPLEXED WITH 4- (AMINOSULFONYL)-N-[(2,6-DIFLUOROPHENYL)METHYL]-BENZAMIDE | CARBONIC ANHYDRASE II, F131V, 4-(AMINOSULFONYL)-N-[(2,6- DIFLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1g4j:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (F131V) COMPLEXED WITH 4- (AMINOSULFONYL)-N-[(2,3,4,5,6-PENTAFLUOROPHENYL)METHYL]- BENZAMIDE | CARBONIC ANHYDRASE II, F131V, 4-(AMINOSULFONYL)-N-[(2,3,4,5, 6-PENTAFLUOROPHENYL)METHYL]-BENZAMIDE, LYASE
1rza:A (ALA115) to (LEU212) X-RAY ANALYSIS OF METAL SUBSTITUTED HUMAN CARBONIC ANHYDRASE II DERIVATIVES | LYASE(OXO-ACID)
4knj:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 2- CHLORO-4-[(PYRIMIDIN-2-YLSULFANYL)ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4kuy:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE 5-(3-(O-TOLYLSULFONYL)UREIDO)PYRIDINE-2-SULFONAMIDE INHIBITOR | LYASE, LYASE-LYASE INHIBITOR COMPLEX
3ibl:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH AN ALIPHATIC BIS-SULFAMATE INHIBITOR | CARBONIC ANHYDRASE II, PROTEIN-INHIBITOR COMPLEX, ALIPHATIC BIS- SULFAMATE INHIBITOR, DISEASE MUTATION, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4l5w:A (ALA115) to (LEU212) STRUCTURAL IMPLICATIONS OF THE SECONDARY CO2 BINDING POCKET IN HUMAN CARBONIC ANHYDRASE II | ALLOSTERIC REGULATION, THERMOSTABILITY, LYASE
1tg3:A (ALA115) to (LEU212) EFFECT OF SHUTTLE LOCATION AND PH ENVIRONMENT ON H+ TRANSFER IN HUMAN CARBONIC ANHYDRASE II | PROTON SHUTTLE CARBONIC ANHYDRASE METALLOENZYME, LYASE
1hea:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II (CARBONATE DEHYDRATASE) (HCA II) (E.C.4.2.1.1) MUTANT WITH LEU 198 REPLACED BY ARG (L198R) | LYASE(OXO-ACID)
1hec:A (ALA115) to (LEU212) STRUCTURAL CONSEQUENCES OF HYDROPHILIC AMINO-ACID SUBSTITUTIONS IN THE HYDROPHOBIC POCKET OF HUMAN CARBONIC ANHYDRASE II | LYASE(OXO-ACID)
4zwi:A (ALA115) to (LEU212) SURFACE LYSINE ACETYLATED HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A SULFAMATE-BASED INHIBITOR | ACETYLATED LYSINES, SULFAMATE-BASED INHIBITOR, LYASE-LYASE INHIBITOR COMPLEX
2hnc:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH THE 5-AMINO-1,3,4-THIADIAZOLE-2-SULFONAMIDE INHIBITOR. | PROTEIN-INHIBITOR COMPLEX, LYASE
1i8z:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II COMPLEXED WITH AL-6629 2H-THIENO[3,2- E]-1,2-THIAZINE-6-SULFONAMIDE, 2-(3-METHOXYPHENYL)-3-(4- MORPHOLINYL)-, 1,1-DIOXIDE | CARBONIC ANHYDRASE II, AL-6629, LYASE
1ugb:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II[HCAII] (E.C.4.2.1.1) MUTANT WITH ALA 65 REPLACED BY GLY (A65G) | LYASE (OXO-ACID), ACETYLATION, ZINC, POLYMORPHISM, DISEASE MUTATION
4m2u:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH DORZOLAMIDE | LYASE-LYASE INHIBITOR COMPLEX
4mdl:A (ALA115) to (LEU212) META CARBORANE CARBONIC ANHYDRASE INHIBITOR | CARBONIC ANHYDRASE INHIBITOR COMPLEX, LYASE-LYASE INHIBITOR COMPLEX
1j9w:A (SER115) to (CYS212) SOLUTION STRUCTURE OF THE CAI MICHIGAN 1 VARIANT | 10-STRANDED-BETA-SHEET, LYASE
1jv0:A (SER115) to (CYS212) THE CRYSTAL STRUCTURE OF THE ZINC(II) ADDUCT OF THE CAI MICHIGAN 1 VARIANT | 10-STRANDED-BETA-SHEET, LYASE
2nnv:A (ALA115) to (LEU212) STRUCTURE OF INHIBITOR BINDING TO CARBONIC ANHYDRASE II | ZINC METALLOENZYME, SULFONAMIDE, LYASE
3jxg:B (PRO171) to (ARG271) CA-LIKE DOMAIN OF MOUSE PTPRG | CA-LIKE DOMAIN, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PHOSPHOPROTEIN, PROTEIN PHOSPHATASE, TRANSMEMBRANE, CELL ADHESION
3jxg:D (PRO171) to (PHE270) CA-LIKE DOMAIN OF MOUSE PTPRG | CA-LIKE DOMAIN, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PHOSPHOPROTEIN, PROTEIN PHOSPHATASE, TRANSMEMBRANE, CELL ADHESION
3jxf:A (PRO150) to (PHE249) CA-LIKE DOMAIN OF HUMAN PTPRZ | CA-LIKE DOMAIN, ALTERNATIVE SPLICING, GLYCOPROTEIN, HYDROLASE, MEMBRANE, POLYMORPHISM, PROTEIN PHOSPHATASE, TRANSMEMBRANE, CELL ADHESION
3jxf:B (PRO150) to (PHE249) CA-LIKE DOMAIN OF HUMAN PTPRZ | CA-LIKE DOMAIN, ALTERNATIVE SPLICING, GLYCOPROTEIN, HYDROLASE, MEMBRANE, POLYMORPHISM, PROTEIN PHOSPHATASE, TRANSMEMBRANE, CELL ADHESION
2nwy:A (ALA115) to (LEU212) STRUCTURAL AND KINETIC EFFECTS OF HYDROPHOBIC MUTATIONS ON THE ACTIVE SITE OF HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER, HISTIDINE 64, CARBONIC ANHYDRASE, LYASE
3k34:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II WITH A SULFONAMIDE INHIBITOR | CARBONIC ANHYDRASE, ATOMIC RESOLUTION, SULFONAMIDE INHIBITOR, DISEASE MUTATION, LYASE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3k7k:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN CARBONIC ANHYDRASE II AND ANIONS | INORGANIC ANION, TRITHIOCARBONATE, X RAY, CARBONIC ANHYDRASE II
1ydc:A (ALA115) to (LEU212) STRUCTURAL BASIS OF INHIBITOR AFFINITY TO VARIANTS OF HUMAN CARBONIC ANHYDRASE II | HYDRO-LYASE
1yo0:A (ALA115) to (LEU211) PROTON TRANSFER FROM HIS200 IN HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER, HUMAN CARBONIC ANHYDRASE, LYASE
1yo1:A (ALA115) to (LEU211) PROTON TRANSFER FROM HIS200 IN HUMAN CARBONIC ANHYDRASE II | PROTON TRANSFER HUMAN CARBONIC ANHYDRASE, LYASE
3l14:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH ALTHIAZIDE | LYASE, CARBONIC ANHYDRASE II, ALTHIAZIDE, 6-CHLORO-3, 4-DIHYDRO-3- ((2-PROPENYLTHIO)METHYL)-2H-1, 2, 4-BENZOTHIADIAZINE-7-SULFONAMIDE, DISEASE MUTATION, METAL-BINDING
5dsj:A (ALA115) to (LEU212) STRUCTURE OF CO2 RELEASED HOLO-FORM OF HUMAN CARBONIC ANHYDRASE II WITH 50 SEC WARMING | CARBONIC ANHYDRASE II, CO2 RELEASE, INTERMEDIATE STATES, LYASE
1ze8:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH A MEMBRANE-IMPERMEANT SULFONAMIDE INHIBITOR | TWISTED BETA-SHEET, LYASE
4q78:A (ALA115) to (LEU212) STRUCTURE-ASSISTED DESIGN OF CARBORANE-BASED INHIBITORS OF CARBONIC ANHYDRASE | CARBONIC ANHYDRASE, LYASE-LYASE INHIBITOR COMPLEX
4qiy:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qiy:B (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qiy:C (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qiy:D (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3mdz:A (PRO117) to (LEU214) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE VII [ISOFORM 1], CA7 | CARBONIC ANHYDRASE VII, CA7, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, CYTOPLASM, LYASE, METAL-BINDING, ZINC
3mhc:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CABONIC ANHYDRASE II IN ADDUCT WITH AN ADAMANTYL ANALOGUE OF ACETAZOLAMIDE IN A NOVEL HYDROPHOBIC BINDING POCKET | CARBONIC ANHYDRASE INHIBITORS, ADAMANTYL, ACETAZOLAMIDE, LYASE
3mhl:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 4-{[N- (6-METHOXY-5-NITROPYRIMIDIN-4-YL)AMINO]METHYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, SULFONAMIDE, LYASE-LYASE INHIBITOR COMPLEX
3ml2:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDSASE II IN COMPLEX WITH AN ARYL SULFONAMIDE INHIBITOR | ZINC METALLOENZYME, METAL-BINDING, LYASE,SULFONAMIDE, ZINC LIGANDS, INHIBITOR, LYASE, LYASE-LYASE INHIBITOR COMPLEX
3ml5:A (PRO115) to (LEU212) CRYSTAL STRUCTURE OF THE C183S/C217S MUTANT OF HUMAN CA VII IN COMPLEX WITH ACETAZOLAMIDE | PROTEIN-INHIBITOR COMPLEX, LYASE
3bet:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH STX 641 AT 1.85 ANGSTROMS RESOLUTION | PROTEIN-INHIBITOR COMPLEX, DISEASE MUTATION, LYASE, METAL-BINDING
4bf1:A (ALA115) to (LEU212) THREE DIMENSIONAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 5-(1-NAPHTHALEN-1-YL-1,2,3-TRIAZOL-4-YL) THIOPHENE-2-SULFONAMIDE | LYASE
4qsa:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME II WITH 2- CHLORO-4-{[(4-METHYL-6-OXO-1,6-DIHYDROPYRIMIDIN-2-YL) THIO]ACETYL}BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3mnh:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II MUTANT K170A | PROTON TRANSFER, METALLOENZYME, PROTON TRANSPORT
3mnu:A (ALA115) to (LEU212) CARBONIC ANHYDRASE INHIBITORS: CRYSTALLOGRAPHIC AND SOLUTION BINDING STUDIES FOR THE INTERACTION OF A BORON CONTAINING AROMATIC SULFAMIDE WITH MAMMALIAN ISOFORMS I-XV | PROTEIN-INHIBITOR COMPLEX, LYASE
3bl1:A (ALA115) to (LEU212) CARBONIC ANHYDRASE INHIBITORS. SULFONAMIDE DIURETICS REVISITED OLD LEADS FOR NEW APPLICATIONS | CARBONIC ANHYDRASE, INHIBITORS, CRYSTAL STRUCTURE, DIURETICS, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC, LYASE(OXO-ACID)
4qy3:A (ALA115) to (LEU212) THE CRYSTAL STRUCTURE OF THE COMPLEX OF HCAII WITH AN ORTHO- SUBSTITUTED BENZOIC ACID | CARBONIC ANHYDRASE II, LYASE, LYASE-LYASE INHIBITOR COMPLEX
3n3j:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A BENZENESULFONAMIDE INHIBITOR | LYASE, METALLOENZYME, ZINC LIGANDS, BENZENESULFONAMIDE, INHIBITOR, GLYCEROL, LYASE-LYASE INHIBITOR COMPLEX
3n4b:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH A BENZENESULFONAMIDE INHIBITOR | LYASE, ZINC METALLOENZYME, ZINC LIGANDS, BENZENESULFONAMIDE, INHIBITOR, LYASE-LYASE INHIBITOR COMPLEX
5fdi:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II WITH THE ANTICONVULSANT SULFAMIDE JNJ-26990990 AND ITS S,S-DIOXIDE ANALOG. | SULFAMIDE INHIBITOR, PROTEIN-INHIBITOR COMPLEX, LYASE
3nb5:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH 2-(3-CHLORO-4- HYDROXYPHENYL)-N-(4-SULFAMOYLPHENETHYL)ACETAMIDE | DRUG DESIGN, NATURAL PRODUCT, SULFAMATE, LYASE-LYASE INHIBITOR COMPLEX
5flr:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, FRAGMENTS, METALLOPROTEIN
5fls:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, FRAGMENTS, METALLOPROTEIN
5flt:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, FRAGMENTS, CARBONIC ANHYDRASE, METALLOPROTEIN
5fni:A (ALA115) to (LEU212) NATIVE STATE MASS SPECTROMETRY, SURFACE PLASMON RESONANCE AND X-RAY CRYSTALLOGRAPHY CORRELATE STRONGLY AS A FRAGMENT SCREENING COMBINATION | LYASE, FRAGMENTS, CARBONIC ANHYDRASE, METALLOPROTEIN
4ca2:A (ALA115) to (LEU212) ENGINEERING THE HYDROPHOBIC POCKET OF CARBONIC ANHYDRASE II | LYASE(OXO-ACID)
4cnr:A (ALA115) to (LEU211) SURFACE RESIDUE ENGINEERING OF BOVINE CARBONIC ANHYDRASE TO AN EXTREME HALOPHILIC ENZYME FOR POTENTIAL APPLICATION IN POSTCOMBUSTION CO2 CAPTURE | LYASE, PROTEIN ENGINEERING, CO2 CAPTURE
4cnr:B (ALA115) to (LEU211) SURFACE RESIDUE ENGINEERING OF BOVINE CARBONIC ANHYDRASE TO AN EXTREME HALOPHILIC ENZYME FOR POTENTIAL APPLICATION IN POSTCOMBUSTION CO2 CAPTURE | LYASE, PROTEIN ENGINEERING, CO2 CAPTURE
4cnr:C (ALA115) to (LEU211) SURFACE RESIDUE ENGINEERING OF BOVINE CARBONIC ANHYDRASE TO AN EXTREME HALOPHILIC ENZYME FOR POTENTIAL APPLICATION IN POSTCOMBUSTION CO2 CAPTURE | LYASE, PROTEIN ENGINEERING, CO2 CAPTURE
4cnr:D (ALA115) to (LEU211) SURFACE RESIDUE ENGINEERING OF BOVINE CARBONIC ANHYDRASE TO AN EXTREME HALOPHILIC ENZYME FOR POTENTIAL APPLICATION IN POSTCOMBUSTION CO2 CAPTURE | LYASE, PROTEIN ENGINEERING, CO2 CAPTURE
5g0b:A (ALA115) to (LEU212) AN UNUSUAL NATURAL PRODUCT PRIMARY SULFONAMIDE: SYNTHESIS, CARBONIC ANHYDRASE INHIBITION AND PROTEIN X-RAY STRUCTURE OF PSAMMAPLIN C | LYASE, PROTEIN ENGINEERING, NATURAL PRODUCT INHIBITOR, CARBONIC ANHYDRASE
3dc3:A (ALA115) to (LEU212) USE OF CARBONIC ANHYDRASE II, IX ACTIVE-SITE MIMIC, FOR THE PURPOSE OF SCREENING INHIBITORS FOR POSSIBLE ANTI-CANCER PROPERTIES | CARBONIC ANHYDRASE II COMPLEX, CAIX MIMIC INHIBITORS, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL- BINDING, POLYMORPHISM, ZINC
3dd0:A (ALA115) to (LEU212) USE OF CARBONIC ANHYDRASE II, IX ACTIVE-SITE MIMIC, FOR THE PURPOSE OF SCREENING INHIBITORS FOR POSSIBLE ANTI-CANCER PROPERTIES | CARBONIC ANHYDRASE II COMPLEX, CAIX MIMIC INHIBITORS, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL- BINDING, POLYMORPHISM, ZINC
3dd8:A (ALA115) to (LEU212) CARBONIC ANHYDRASE INHIBITORS. INTERACTION OF THE ANTITUMOR SULFAMATE EMD-486019 WITH TWELVE MAMMALIAN ISOFORMS: KINETIC AND X-RAY CRYSTALLOGRAPHIC STUDIES | CARBONIC ANHYDRASE, INHIBITORS, CRYSTAL STRUCTURE, ANTIGLAUCOMA, OAO-ACID, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC
3dv7:A (ALA115) to (LEU212) ROLE OF HYDROPHILIC RESIDUES IN PROTON TRANSFER DURING CATALYSIS BY HUMAN CARBONIC ANHYDRASE II (N62A) | HCA II, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC
3dvb:A (ALA115) to (LEU212) X-RAY CRYSTAL STRUCTURE OF MUTANT N62V HUMAN CARBONIC ANHYDRASE II | HUMAN CARBONIC ANHYDRASE II, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC
3dvc:A (ALA115) to (LEU212) X-RAY CRYSTAL STRUCTURE OF MUTANT N62T OF HUMAN CARBONIC ANHYDRASE II | HUMAN CARBONIC ANHYDRASE, ACETYLATION, CYTOPLASM, DISEASE MUTATION, LYASE, METAL-BINDING, POLYMORPHISM, ZINC
3oy0:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH 1-(4-(4-(2- (ISOPROPYLSULFONYL)PHENYLAMINO)-1H-PYRROLO[2,3-B]PYRIDIN-6-YLAMINO)- 3-METHOXYPHENYL)PIPERIDIN-4-OL | BENZENE SULFONAMIDE, DRUG INTERACTION, LYASE-LYASE INHIBITOR COMPLEX
3p3h:A (ALA115) to (LEU211) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH P-(5-FERROCENYL-1H-1,2,3- TRIAZOL-1-YL)BENZENESULFONAMIDE | CARBONIC ANHYDRASE ALPHA, LYASE, CYTOSOLIC
3po6:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE II WITH 6,7-DIMETHOXY-1- METHYL-3,4-DIHYDROISOQUINOLINE-2(1H)-SULFONAMIDE | CARBONIC ANHYDRASE, LYASE-LYASE INHIBITOR COMPLEX
5j8z:A (ALA115) to (LEU212) HUMAN CARBONIC ANHYDRASE II IN COMPLEX WITH LIGAND | CYTOPLASM, LYASE, 2-THIO-6-OXO-1, 6-DIHYDROPYRIMIDINES, SULFONAMIDES
3rge:A (ALA115) to (LEU212) CRYSTAL STRUCTURE OF THE W5H MUTANT OF HUMAN CARBONIC ANHYDRASE II | ZINC METALLOENZYME, W5H MUTATION, LYASE
4fvn:A (ALA115) to (LEU212) CARBONIC ANHYDRASE II IN COMPLEX WITH N-(TETRAHYDROPYRIMIDIN-2(1H)- YLIDENE)SULFURIC DIAMIDE | 10 STRANDED TWISTED BETA-SHEETS, LYASE, LYASE-LYASE INHIBITOR COMPLEX
8ca2:A (ALA115) to (LEU212) ENGINEERING THE HYDROPHOBIC POCKET OF CARBONIC ANHYDRASE II | LYASE(OXO-ACID)