1nb5:C (SER69) to (VAL212) CRYSTAL STRUCTURE OF STEFIN A IN COMPLEX WITH CATHEPSIN H | CYSTEINE PROTEINASE, AMINOPEPTIDASE, CYSTATIN, ENZYME-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1nb5:D (PRO68) to (VAL212) CRYSTAL STRUCTURE OF STEFIN A IN COMPLEX WITH CATHEPSIN H | CYSTEINE PROTEINASE, AMINOPEPTIDASE, CYSTATIN, ENZYME-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2aux:A (MET68) to (MET215) CATHEPSIN K COMPLEXED WITH A SEMICARBAZONE INHIBITOR | CATK, CYSTEINE PROTEASE, HYDROLASE
1nl6:B (MET68) to (MET215) CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT AZEPANONE INHIBITOR | HYDROLASE, SULFHYDRYL PROTEINASE
2b1m:A (TYR70) to (LYS226) CRYSTAL STRUCTURE OF A PAPAIN-FOLD PROTEIN WITHOUT THE CATALYTIC CYSTEINE FROM SEEDS OF PACHYRHIZUS EROSUS | PAPAIN-LIKE, SUGAR BINDING PROTEIN
2b1n:A (TYR70) to (GLU225) CRYSTAL STRUCTURE OF A PAPAIN-FOLD PROTEIN WITHOUT THE CATALYTIC CYSTEINE FROM SEEDS OF PACHYRHIZUS EROSUS | PAPAIN-LIKE, PEPTIDE FRAGMENT, SUGAR BINDING PROTEIN
1npz:B (MET321) to (ILE467) CRYSTAL STRUCTURES OF CATHEPSIN S INHIBITOR COMPLEXES | ANTIGEN PRESENTATION, BINDING SPECIFICITY, CYSTEINE PROTEASES, INHIBITOR COMPLEXES, STRUCTURE-BASED DESIGN, STRUCTURAL PLASTICITY, HYDROLASE
1au0:A (MET68) to (MET215) CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT SYMMETRIC DIACYLAMINOMETHYL KETONE INHIBITOR | HYDROLASE, SULFHYDRYL PROTEINASE
2oz2:C (LEU67) to (ALA212) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO VINYL SULFONE DERIVED INHIBITOR (K11777) | CYSTEINE PROTEASE, COVALENT INHIBITOR, VINYL SULFONEAMIDE DERIVED, HYDROLASE
1o0e:A (PHE68) to (PRO205) 1.9 ANGSTROM CRYSTAL STRUCTURE OF A PLANT CYSTEINE PROTEASE ERVATAMIN C | PLANT CYSTEINE PROTEASE, TWO DOMAIN, STABLE AT PH 2-12, HYDROLASE
1o0e:B (PHE68) to (PRO205) 1.9 ANGSTROM CRYSTAL STRUCTURE OF A PLANT CYSTEINE PROTEASE ERVATAMIN C | PLANT CYSTEINE PROTEASE, TWO DOMAIN, STABLE AT PH 2-12, HYDROLASE
4x6j:A (MET68) to (MET215) DEVELOPMENT OF N-(FUNCTIONALIZED BENZOYL)-HOMOCYCLOLEUCYL- GLYCINONITRILES AS POTENT CATHEPSIN K INHIBITORS. | CATHEPSIN K, INHIBITOR, HYDROLASE
3f75:A (MET76) to (PRO222) ACTIVATED TOXOPLASMA GONDII CATHEPSIN L (TGCPL) IN COMPLEX WITH ITS PROPEPTIDE | MEDICAL STRUCTURAL GENOMICS OF PATHOGENIC PROTOZOA, MSGPP, CYSTEINE PROTEASE, PARASITE, PROTOZOA, HYDROLASE, THIOL PROTEASE
2pns:A (PHE68) to (PRO205) 1.9 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF A PLANT CYSTEINE PROTEASE ERVATAMIN-C REFINEMENT WITH CDNA DERIVED AMINO ACID SEQUENCE | PAPAIN-LIKE FOLD, THERMOSTABLE, PLANT CYSTEINE PROTEASE, ERVATAMIN, HYDROLASE
1cs8:A (MET70) to (VAL220) CRYSTAL STRUCTURE OF PROCATHEPSIN L | PROSEGMENT, PROPEPTIDE, INHIBITION, HYDROLASE
1ppo:A (PRO68) to (PRO213) DETERMINATION OF THE STRUCTURE OF PAPAYA PROTEASE OMEGA | HYDROLASE(THIOL PROTEASE)
1f2c:A (LEU67) to (ALA209) CRYSTAL STRUCTURE ANALYSIS OF CRYZAIN BOUND TO VINYL SULFONE DERIVED INHIBITOR (IV) | CYSTEINE PROTEASE, COVALENT INHIBITOR, VINYL SULFONAMIDE DERIVED, P1' POCKET, HYDROLASE
3h6s:B (MET70) to (VAL221) STRUCURE OF CLITOCYPIN - CATHEPSIN V COMPLEX | CATHEPSIN, CLITOCYPIN, KUNITZ INHIBITOR, CYSTEINE PROTEASE, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
3h6s:C (PHE69) to (VAL221) STRUCURE OF CLITOCYPIN - CATHEPSIN V COMPLEX | CATHEPSIN, CLITOCYPIN, KUNITZ INHIBITOR, CYSTEINE PROTEASE, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
3u8e:A (ALA68) to (PRO217) CRYSTAL STRUCTURE OF CYSTEINE PROTEASE FROM BULBS OF CROCUS SATIVUS AT 1.3 A RESOLUTION | PAPAIN-LIKE CYSTEINE PEPTIDASE, PEPTIDASE_C1A, HYDROLASE, INACTIVE FORM
3hha:A (MET70) to (VAL220) CRYSTAL STRUCTURE OF CATHEPSIN L IN COMPLEX WITH AZ12878478 | PROTEROS BIOSTRUCTURES GMBH, CATHEPSIN L, INHIBITORS, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN
3hha:B (ASP71) to (VAL220) CRYSTAL STRUCTURE OF CATHEPSIN L IN COMPLEX WITH AZ12878478 | PROTEROS BIOSTRUCTURES GMBH, CATHEPSIN L, INHIBITORS, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN
3hha:C (MET70) to (VAL220) CRYSTAL STRUCTURE OF CATHEPSIN L IN COMPLEX WITH AZ12878478 | PROTEROS BIOSTRUCTURES GMBH, CATHEPSIN L, INHIBITORS, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN
3hha:D (MET70) to (VAL220) CRYSTAL STRUCTURE OF CATHEPSIN L IN COMPLEX WITH AZ12878478 | PROTEROS BIOSTRUCTURES GMBH, CATHEPSIN L, INHIBITORS, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN
1fh0:A (PHE69) to (VAL220) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN V COMPLEXED WITH AN IRREVERSIBLE VINYL SULFONE INHIBITOR | CATHEPSIN, PAPAIN, PROTEASE, CANCER, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1fh0:B (MET2070) to (VAL2220) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN V COMPLEXED WITH AN IRREVERSIBLE VINYL SULFONE INHIBITOR | CATHEPSIN, PAPAIN, PROTEASE, CANCER, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2f1g:B (MET71) to (ILE217) CATHEPSIN S IN COMPLEX WITH NON-COVALENT 2-(BENZOXAZOL-2-YLAMINO)- ACETAMIDE | CATHEPSIN S, NONCOVALENT, INHIBITION, 2-(BENZOOXAZOL-2-YLAMINO) ACETAMIDES, HYDROLASE
4yva:A (MET68) to (MET215) CATHEPSIN K CO-CRYSTALLIZED WITH ACTINOMYCETES EXTRACT | CATHEPSIN K, ACTINOMYCETES, HYDROLASE
4yyr:A (MET70) to (PRO216) FICIN B CRYSTAL FORM I | CYSTEINE PROTEASE, HYDROLASE
2vhs:A (LEU69) to (VAL220) CATHSILICATEIN, A CHIMERA | ZYMOGEN, PROTEASE, LYSOSOME, HYDROLASE, GLYCOPROTEIN, THIOL PROTEASE, SILICA CONDENSATION
2vhs:B (LEU69) to (VAL220) CATHSILICATEIN, A CHIMERA | ZYMOGEN, PROTEASE, LYSOSOME, HYDROLASE, GLYCOPROTEIN, THIOL PROTEASE, SILICA CONDENSATION
3hwn:D (LEU69) to (VAL220) CATHEPSIN L WITH AZ13010160 | CATHEPSIN L, DRUG DESIGN, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN
3iv2:A (MET70) to (VAL220) CRYSTAL STRUCTURE OF MATURE APO-CATHEPSIN L C25A MUTANT | PROTEASE, MUTANT, APO, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, THIOL PROTEASE, ZYMOGEN
1tu6:B (MET182) to (MET329) CATHEPSIN K COMPLEXED WITH A KETOAMIDE INHIBITOR | CATK, CYSTEINE PROTEASE, HYDROLASE
2hhn:B (PHE70) to (ILE217) CATHEPSIN S IN COMPLEX WITH NON COVALENT ARYLAMINOETHYL AMIDE. | CATHEPSIN S, NONCOVALENT, INHIBITION, ARYLAMINOETHYL AMIDE, PROTEASE, HYDROLASE
2hxz:A (PHE70) to (ILE217) CRYSTAL STRUCTURE OF CATHEPSIN S IN COMPLEX WITH A NONPEPTIDIC INHIBITOR (HEXAGONAL SPACEGROUP) | CATHEPSIN S, NONPEPTIDIC, CHLOROMETHYLKETONE, SUBSTRATE ACTIVITY SCREENING, HYDROLASE
2hxz:C (PHE70) to (ILE217) CRYSTAL STRUCTURE OF CATHEPSIN S IN COMPLEX WITH A NONPEPTIDIC INHIBITOR (HEXAGONAL SPACEGROUP) | CATHEPSIN S, NONPEPTIDIC, CHLOROMETHYLKETONE, SUBSTRATE ACTIVITY SCREENING, HYDROLASE
4mzo:D (TYR193) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND (3S,4S)-N-[(2E)-2-IMINOETHYL]- 4-(MORPHOLIN-4-YLCARBONYL)-1-(PHENYLSULFONYL)PYRROLIDINE-3- CARBOXAMIDE | HYDROLASE, CYSTEINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4mzo:E (TYR193) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND (3S,4S)-N-[(2E)-2-IMINOETHYL]- 4-(MORPHOLIN-4-YLCARBONYL)-1-(PHENYLSULFONYL)PYRROLIDINE-3- CARBOXAMIDE | HYDROLASE, CYSTEINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4mzo:F (TYR193) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND (3S,4S)-N-[(2E)-2-IMINOETHYL]- 4-(MORPHOLIN-4-YLCARBONYL)-1-(PHENYLSULFONYL)PYRROLIDINE-3- CARBOXAMIDE | HYDROLASE, CYSTEINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2xu1:A (MET70) to (VAL220) CATHEPSIN L WITH A NITRILE INHIBITOR | HYDROLASE, DRUG DESIGN, THIOL PROTEASE
2xu1:B (MET70) to (VAL220) CATHEPSIN L WITH A NITRILE INHIBITOR | HYDROLASE, DRUG DESIGN, THIOL PROTEASE
2xu4:A (ASP71) to (VAL220) CATHEPSIN L WITH A NITRILE INHIBITOR | HYDROLASE, DRUG DESIGN, THIOL PROTEASE
2yj9:A (MET70) to (VAL220) CATHEPSIN L WITH A NITRILE INHIBITOR | HYDROLASE, DRUG DESIGN, THIOL PROTEASE
2yjc:A (MET70) to (VAL220) CATHEPSIN L WITH A NITRILE INHIBITOR | HYDROLASE, INHIBITOR, DRUG DESIGN, THIOL PROTEASE
2nqd:B (MET70) to (VAL220) CRYSTAL STRUCTURE OF CYSTEINE PROTEASE INHIBITOR, CHAGASIN, IN COMPLEX WITH HUMAN CATHEPSIN L | CHAGASIN-CATHEPSIN L COMPLEX, THREE PRONG INHIBITION MODE, HYDROLASE INHIBITOR-HYDROLASE COMPLEX
3k24:A (LEU69) to (VAL220) CRYSTAL STRUCTURE OF MATURE APO-CATHEPSIN L C25A MUTANT IN COMPLEX WITH GLN-LEU-ALA PEPTIDE | CO-CRYSTAL, SUBSTRATE, PROTEASE, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, HYDROLASE
1m6d:A (PRO68) to (ALA209) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN F | PAPAIN FAMILY CYSTEINE PROTEASE, HYDROLASE
1meg:A (PRO68) to (ASN216) CRYSTAL STRUCTURE OF A CARICAIN D158E MUTANT IN COMPLEX WITH E-64 | CYSTEINE PROTEINASE, THIOL PROTEASE, HYDROLASE
3kku:A (MET68) to (ALA212) CRUZAIN IN COMPLEX WITH A NON-COVALENT LIGAND | AUTOCATALYTIC CLEAVAGE, GLYCOPROTEIN, PROTEASE, THIOL PROTEASE, ZYMOGEN, HYDROLASE
4pi3:B (MET68) to (ALA212) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO VINYL SULFONE ANALOG OF WRR-483 (WRR-666) | CYSTEIN PROTEASE, CRUZAIN, CHAGAS DISEASE, COVALENT INHIBITOR, VINYL SULFONE DERIVATIVE, ANALOGE OF WRR-483, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4axm:B (MET70) to (VAL220) TRIAZINE CATHEPSIN INHIBITOR COMPLEX | HYDROLASE
4axm:I (LEU69) to (VAL220) TRIAZINE CATHEPSIN INHIBITOR COMPLEX | HYDROLASE
3lxs:C (LEU67) to (ALA212) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO VINYL SULFONE DERIVED INHIBITOR (WRR483) | CYSTEINE PROTEASE, COVALENT INHIBITOR, VINYL SULFONAMIDE, HYDROLASE
5ef4:A (MET198) to (ASN346) 2.05 A CRYSTAL STRUCTURE OF THE AMB A 11 CYSTEINE PROTEASE, A MAJOR RAGWEED POLLEN ALLERGEN, IN ITS PROFORM | ALLERGEN, RAGWEED, CYSTEINE PROTEASE, PROPEPTIDE
5ef4:B (MET198) to (PRO343) 2.05 A CRYSTAL STRUCTURE OF THE AMB A 11 CYSTEINE PROTEASE, A MAJOR RAGWEED POLLEN ALLERGEN, IN ITS PROFORM | ALLERGEN, RAGWEED, CYSTEINE PROTEASE, PROPEPTIDE
4qh6:C (LEU67) to (ALA212) CRYSTAL STRUCTURE OF CRUZAIN WITH NITRILE INHIBITOR N-(2-AMINOETHYL)- NALPHA-BENZOYL-L-PHENYLALANINAMIDE | THIOL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4qh6:D (MET68) to (ALA212) CRYSTAL STRUCTURE OF CRUZAIN WITH NITRILE INHIBITOR N-(2-AMINOETHYL)- NALPHA-BENZOYL-L-PHENYLALANINAMIDE | THIOL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3bcn:B (TYR67) to (PRO205) CRYSTAL STRUCTURE OF A PAPAIN-LIKE CYSTEINE PROTEASE ERVATAMIN-A COMPLEXED WITH IRREVERSIBLE INHIBITOR E-64 | PROTEASE-INHIBITOR COMPLEX, PAPAIN-LIKE FOLD, PLANT CYSTEINE PROTEASE, ERVATAMIN, HYDROLASE, THIOL PROTEASE
5f02:A (MET70) to (VAL220) CATHEPSIN L IN COMPLEX WITH (2S,4R)-4-(2-CHLORO-4-METHOXY- BENZENESULFONYL)-1-[3-(5-CHLORO-PYRIDIN-2-YL)-AZETIDINE-3-CARBONYL]- PYRROLIDINE-2-CARBOXYLIC ACID (1-CYANO-CYCLOPROPYL)-AMIDE | PROTEASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASE
4bpv:C (TYR193) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE, COVALENT LIGAND
4bpv:E (TYR193) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE, COVALENT LIGAND
4bqv:A (TYR193) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE
4bqv:D (TYR193) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE
4bqv:F (MET194) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE
4bqv:H (MET194) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE
4bs6:A (TYR193) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE, COVALENT LIGAND
4bsq:A (TYR193) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE
3n3g:A (MET71) to (ILE217) 4-(3-TRIFLUOROMETHYLPHENYL)-PYRIMIDINE-2-CARBONITRILE AS CATHEPSIN S INHIBITORS: N3, NOT N1 IS CRITICALLY IMPORTANT | CATHEPSIN S, COVALENT INHIBITOR, HYDROLASE
3n4c:A (MET71) to (ILE217) 6-PHENYL-1H-IMIDAZO[4,5-C]PYRIDINE-4-CARBONITRILE AS CATHEPSIN S INHIBITORS | CATHEPSIN S, COVALENT INHIBITOR, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4dmy:A (MET68) to (MET215) CATHEPSIN K INHIBITOR | CATHEPSIN K INHIBITOR, OSTEOARTHRITIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2bdz:A (TYR67) to (GLY212) MEXICAIN FROM JACARATIA MEXICANA | MEXICAIN, CYSTEINE PROTEASE, PEPTIDASE_C1, PAPAIN-LIKE, HYDROLASE
1ewo:A (LEU67) to (GLY212) THE CYSTEINE PROTEASE CRUZAIN BOUND TO WRR-204 | CYSTEINE PROTEASE, DRUG DESIGN, COVALENT INHIBITOR, CRUZIPAIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3h89:C (MET70) to (VAL220) A COMBINED CRYSTALLOGRAPHIC AND MOLECULAR DYNAMICS STUDY OF CATHEPSIN- L RETRO-BINDING INHIBITORS(COMPOUND 4) | CYSTEINE PROTEASES, CATHEPSIN L, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN
4klb:C (LEU67) to (ALA212) CRYSTAL STRUCTURE OF CRUZAIN IN COMPLEX WITH THE NON-COVALENT INHIBITOR NEQUIMED176 | HYDROLASE, PROTEASE, THIOL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4klb:E (LEU67) to (ALA212) CRYSTAL STRUCTURE OF CRUZAIN IN COMPLEX WITH THE NON-COVALENT INHIBITOR NEQUIMED176 | HYDROLASE, PROTEASE, THIOL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2ftd:A (MET68) to (MET215) CRYSTAL STRUCTURE OF CATHEPSIN K COMPLEXED WITH 7-METHYL- SUBSTITUTED AZEPAN-3-ONE COMPOUND | HYDROLASE, SULFHYDRYL PROTEINASE
4mzs:A (TYR193) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND (3S,4S)-1-[(2-CHLOROPHENYL) SULFONYL]-N-[(2E)-2-IMINOETHYL]-4-(MORPHOLIN-4-YLCARBONYL) PYRROLIDINE-3-CARBOXAMIDE | HYDROLASE, CYSTEINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4mzs:B (TYR193) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND (3S,4S)-1-[(2-CHLOROPHENYL) SULFONYL]-N-[(2E)-2-IMINOETHYL]-4-(MORPHOLIN-4-YLCARBONYL) PYRROLIDINE-3-CARBOXAMIDE | HYDROLASE, CYSTEINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2yj2:A (MET70) to (VAL220) CATHEPSIN L WITH A NITRILE INHIBITOR | HYDROLASE, DRUG DESIGN, THIOL PROTEASE
3kfq:A (MET70) to (VAL221) UNREDUCED CATHEPSIN V IN COMPLEX WITH STEFIN A | PAPAIN-LIKE CYSTEINE PROTEASE, CATHEPSIN, PROTEASE-INHIBITOR COMPLEX, HYDROLASE, LYSOSOME, PROTEASE, THIOL PROTEASE, ZYMOGEN, PROTEASE INHIBITOR, THIOL PROTEASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5egw:A (MET198) to (PRO343) 2.70 A CRYSTAL STRUCTURE OF THE AMB A 11 CYSTEINE PROTEASE, A MAJOR RAGWEED POLLEN ALLERGEN, IN ITS PROFORM | ALLERGEN, RAGWEED, CYSTEINE PROTEASE, PROPEPTIDE
5egw:B (MET198) to (PRO343) 2.70 A CRYSTAL STRUCTURE OF THE AMB A 11 CYSTEINE PROTEASE, A MAJOR RAGWEED POLLEN ALLERGEN, IN ITS PROFORM | ALLERGEN, RAGWEED, CYSTEINE PROTEASE, PROPEPTIDE
3of9:A (MET71) to (VAL221) STRUCTURAL BASIS FOR IRREVERSIBLE INHIBITION OF HUMAN CATHEPSIN L BY A DIAZOMETHYLKETONE INHIBITOR | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ovx:A (PHE70) to (ILE217) CATHEPSIN S IN COMPLEX WITH A COVALENT INHIBITOR WITH AN ALDEHYDE WARHEAD | CATHEPSIN S, HYDROLASE, COVALENT INHIBITOR, ALDEHYDE WARHEAD, LIGAND IS COVALENTLY BOUND TO CYS25, LYSOSOMEAL PROTEIN, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4w5b:A (LEU67) to (GLY215) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN WITH FRAGMENT 1 (N-(1H- BENZIMIDAZOL-2-YL)-1,3-DIMETHYL-PYRAZOLE-4-CARBOXAMIDE) | CYSTEINE PROTEASE, CRUZAIN, FRAGMENTS-BASED DRUG DISCOVERY, MUTAGENESIS, SPR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4w5b:B (MET68) to (GLY215) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN WITH FRAGMENT 1 (N-(1H- BENZIMIDAZOL-2-YL)-1,3-DIMETHYL-PYRAZOLE-4-CARBOXAMIDE) | CYSTEINE PROTEASE, CRUZAIN, FRAGMENTS-BASED DRUG DISCOVERY, MUTAGENESIS, SPR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4w5b:C (LEU67) to (GLY215) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN WITH FRAGMENT 1 (N-(1H- BENZIMIDAZOL-2-YL)-1,3-DIMETHYL-PYRAZOLE-4-CARBOXAMIDE) | CYSTEINE PROTEASE, CRUZAIN, FRAGMENTS-BASED DRUG DISCOVERY, MUTAGENESIS, SPR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5ja7:A (MET68) to (MET215) HUMAN CATHEPSIN K MUTANT C25S IN COMPLEX WITH THE ALLOSTERIC EFFECTOR NSC94914 | ALLOSTERY CYSTEINE PEPTIDASE PROTEOLYSIS ENZYME REGULATION COLLAGENASE, HYDROLASE