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CRYSTAL STRUCTURE OF HUMAN PROCATHEPSIN X: A CYSTEINE PROTEASE WITH THE PROREGION COVALENTLY LINKED TO THE ACTIVE SITE CYSTEINE[HYDROLASE]
View in iCn3D Similar StructuresPubMedProteinsConserved Domains
CRYSTAL STRUCTURE OF HUMAN CATHEPSIN X[HYDROLASE]
dipeptidyl peptidase I (cathepsin C), a tetrameric cysteine protease of the papain family[HYDROLASE]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
CRYSTAL STRUCTURES OF RECOMBINANT RAT CATHEPSIN B AND A CATHEPSIN B-INHIBITOR COMPLEX: IMPLICATIONS FOR STRUCTURE-BASED INHIBITOR DESIGN[THIOL PROTEASE]
Crystal structure of a papain-fold protein without the catalytic cysteine from seeds of Pachyrhizus erosus[SUGAR BINDING PROTEIN]
Mutant Human Cathepsin S with irreversible inhibitor CRA-14013[HYDROLASE]
View in iCn3D Similar StructuresProteinsConserved DomainsPubChem Compound
Human cathepsin S mutant with vinyl sulfone inhibitor CRA-14009[HYDROLASE]
Crystal structures of Cathepsin S inhibitor complexes[HYDROLASE]
X-RAY CRYSTAL STRUCTURE OF BOVINE CATHEPSIN B-CA074 COMPLEX[HYDROLASE]
6-Phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitors[HYDROLASE/HYDROLASE INHIBITOR]
Cathepsin S in complex with a covalent inhibitor with an aldehyde warhead[HYDROLASE/HYDROLASE INHIBITOR]
4-(3-Trifluoromethylphenyl)-Pyrimidine-2-Carbonitrile As Cathepsin S Inhibitors: N3, Not N1 Is Critically Important[Hydrolase, EC: 3.4.22.27]
The structure of cathepsin S with a novel 2-arylphenoxyacetaldehyde inhibitor derived by the Substrate Activity Screening (SAS) method[HYDROLASE]
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Crystal Structure of Cathepsin S in complex with a Nonpeptidic Inhibitor (Hexagonal spacegroup)[HYDROLASE]
Crystal Structure of Cathepsin S in complex with a Nonpeptidic Inhibitor[HYDROLASE]
Crystal Structure of Cathepsin S in complex with a Zinc mediated non-covalent arylaminoethyl amide[HYDROLASE]
Human Cathepsin S with inhibitor CRA-16981[HYDROLASE]
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