1npz:A (ALA107) to (ILE217) CRYSTAL STRUCTURES OF CATHEPSIN S INHIBITOR COMPLEXES | ANTIGEN PRESENTATION, BINDING SPECIFICITY, CYSTEINE PROTEASES, INHIBITOR COMPLEXES, STRUCTURE-BASED DESIGN, STRUCTURAL PLASTICITY, HYDROLASE
2oul:A (TYR106) to (PRO221) THE STRUCTURE OF CHAGASIN IN COMPLEX WITH A CYSTEINE PROTEASE CLARIFIES THE BINDING MODE AND EVOLUTION OF A NEW INHIBITOR FAMILY | CYSTEINE PROTEASE, INHIBITOR, MACROMOLECULAR INTERACTION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3s3r:B (LYS219) to (ARG321) STRUCTURE OF CATHEPSIN B1 FROM SCHISTOSOMA MANSONI IN COMPLEX WITH K11777 INHIBITOR | PEPTIDASE, DIGESTIVE TRACT, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2pbh:A (TYR148) to (ILE250) CRYSTAL STRUCTURE OF HUMAN PROCATHEPSIN B AT 3.3 ANGSTROM RESOLUTION | THIOL PROTEASE, CATHEPSIN B, CYSTEINE PROTEASE, PROENZYME, CRYSTAL STRUCTURE, PAPAIN
4i07:A (LYS219) to (ARG321) STRUCTURE OF MATURE FORM OF CATHEPSIN B1 FROM SCHISTOSOMA MANSONI | PEPTIDASE, DIGESTIVE TRACT, HYDROLASE
1pci:A (GLY109) to (PRO213) PROCARICAIN | ZYMOGEN, HYDROLASE, THIOL PROTEASE
1pci:B (GLY109) to (PRO213) PROCARICAIN | ZYMOGEN, HYDROLASE, THIOL PROTEASE
1pci:C (GLY109) to (PRO213) PROCARICAIN | ZYMOGEN, HYDROLASE, THIOL PROTEASE
4xui:A (ALA110) to (ALA212) CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO THE NO-COVALENT ANALOG OF WRR-483 (WRR-669) | CRUZAIN, CYSTEINE PROTEASE, COVALENT REVERSIBLE INHIBITOR, CHAGAS DISEASE, TRYPANOSOMA CRUZI, VINYL SULFONE ANALOG, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3tnx:A (ALA211) to (PRO316) STRUCTURE OF THE PRECURSOR OF A THERMOSTABLE VARIANT OF PAPAIN AT 2.6 ANGSTROEM RESOLUTION | HYDROLASE, CYTOPLASM FOR RECOMBINANT EXPRESSION
3tnx:C (ALA211) to (PRO316) STRUCTURE OF THE PRECURSOR OF A THERMOSTABLE VARIANT OF PAPAIN AT 2.6 ANGSTROEM RESOLUTION | HYDROLASE, CYTOPLASM FOR RECOMBINANT EXPRESSION
4yyw:A (VAL107) to (ALA219) FICIN D2 | CYSTEIN PROTEASE, HYDROLASE
2frq:A (ALA107) to (ILE218) HUMAN CATHEPSIN S WITH INHIBITOR CRA-26871 | PAPAIN, CYSTEINE PROTEASE, PROTEINASE, 26871, HYDROLASE
2fye:A (ALA103) to (ILE211) MUTANT HUMAN CATHEPSIN S WITH IRREVERSIBLE INHIBITOR CRA- 14013 | PAPAIN, CYSTEINE PROTEASE, DRUG DESIGN, 14013, HYDROLASE
2g6d:A (ALA103) to (ILE211) HUMAN CATHEPSIN S MUTANT WITH VINYL SULFONE INHIBITOR CRA- 14009 | PAPAIN, CYSTEINE PROTEASE, PROTEINASE, 14009, HYDROLASE
2ghu:A (LYS122) to (ILE240) CRYSTAL STRUCTURE OF FALCIPAIN-2 FROM PLASMODIUM FALCIPARUM | PAPAIN-LIKE CYSTEINE PROTEASE, L-DOMAIN, R-DOMAIN, ALPHA HELIX, RANDOM COIL, TWISTED ANTIPARALLEL BETA-SHEET, HYDROLASE
2ghu:B (LYS122) to (ILE240) CRYSTAL STRUCTURE OF FALCIPAIN-2 FROM PLASMODIUM FALCIPARUM | PAPAIN-LIKE CYSTEINE PROTEASE, L-DOMAIN, R-DOMAIN, ALPHA HELIX, RANDOM COIL, TWISTED ANTIPARALLEL BETA-SHEET, HYDROLASE
1u9w:A (ALA104) to (MET215) CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH THE COVALENT INHIBITOR NVP-ABI491 | HYDROLASE, SULFHYDRYL PROTEINASE
1jqp:A (SER318) to (ILE433) DIPEPTIDYL PEPTIDASE I (CATHEPSIN C), A TETRAMERIC CYSTEINE PROTEASE OF THE PAPAIN FAMILY | CATHEPSIN C, DPP I, PAPAIN, TETRAMER, CHLORIDE, CYSTEINE PROTEASE, HYDROLASE
4mzo:C (ALA230) 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:G (ALA230) 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
4p6g:C (ALA107) to (ILE217) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN S BOUND TO A NON-COVALENT INHIBITOR. | CATHESPSIN S, NON-COVALENT INHIBITOR, CYSTEINE PROTEASE
1yvb:A (ASN108) to (GLU212) THE PLASMODIUM FALCIPARUM CYSTEINE PROTEASE FALCIPAIN-2 | CYSTEINE PROTEASE-INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ai8:B (TYR148) to (ILE250) CATHEPSIN B IN COMPLEX WITH THE NITROXOLINE | CATHEPSIN B, REVERSIBLE INHIBITOR, NITROXOLINE, 8-HYDROXY-5- NITROQUINOLINE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ai8:A (TYR148) to (ILE250) CATHEPSIN B IN COMPLEX WITH THE NITROXOLINE | CATHEPSIN B, REVERSIBLE INHIBITOR, NITROXOLINE, 8-HYDROXY-5- NITROQUINOLINE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4axm:A (VAL106) to (VAL220) TRIAZINE CATHEPSIN INHIBITOR COMPLEX | HYDROLASE
3bcn:A (VAL102) 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
3mpe:A (ALA107) to (ILE217) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN-S C25S MUTANT WITH BOUND DRUG | CATS, CATHEPSIN S, DIAZINONES, PYRAZOLE, P3, HYDROLASE
4bqv:B (ALA230) to (ILE340) MOUSE CATHEPSIN S WITH COVALENT LIGAND | HYDROLASE, CYSTEINE PROTEASE
3bwk:B (SER136) to (PRO247) CRYSTAL STRUCTURE OF FALCIPAIN-3 WITH ITS INHIBITOR, K11017 | FALCIPAIN, MALARIA, CYSTEINE PROTEASE, HYDROLASE
3qsd:A (LYS219) to (ARG321) STRUCTURE OF CATHEPSIN B1 FROM SCHISTOSOMA MANSONI IN COMPLEX WITH CA074 INHIBITOR | CYSTEINE PEPTIDASE, DIGESTIVE TRACT, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
8pch:A (ILE104) to (PRO211) CRYSTAL STRUCTURE OF PORCINE CATHEPSIN H DETERMINED AT 2.1 ANGSTROM RESOLUTION: LOCATION OF THE MINI-CHAIN C-TERMINAL CARBOXYL GROUP DEFINES CATHEPSIN H AMINOPEPTIDASE FUNCTION | HYDROLASE, PROTEASE, CYSTEINE PROTEINASE, AMINOPEPTIDASE
2op3:B (ALA107) to (ILE217) THE STRUCTURE OF CATHEPSIN S WITH A NOVEL 2- ARYLPHENOXYACETALDEHYDE INHIBITOR DERIVED BY THE SUBSTRATE ACTIVITY SCREENING (SAS) METHOD | CATHEPSIN S, NONPEPTIDIC, SUBSTRATE ACTIVITY SCREENING, HYDROLASE
3s3q:A (LYS219) to (ILE322) STRUCTURE OF CATHEPSIN B1 FROM SCHISTOSOMA MANSONI IN COMPLEX WITH K11017 INHIBITOR | PEPTIDASE, DIGESTIVE TRACT, HYDROLASE-HYDROLASE INHIBITOR COMPLEX