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Crystal structure of stefin A in complex with cathepsin H[HYDROLASE/HYDROLASE INHIBITOR]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
Crystal structure of stefin A in complex with cathepsin H: N-terminal residues of inhibitors can adapt to the active sites of endo-and exopeptidases[HYDROLASE]
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]
Crystal Structure of ProCathepsin L1 from Fasciola hepatica[HYDROLASE]
View in iCn3D Similar StructuresPubMedProteinsConserved Domains
THE CRYSTAL STRUCTURE OF HUMAN PROCATHEPSIN K[HYDROLASE]
CRYSTAL STRUCTURE OF WILD TYPE HUMAN PROCATHEPSIN K[HYDROLASE]
CRYSTAL STRUCTURE OF A CYSTEINE PROTEASE PROFORM[HYDROLASE]
CRYSTAL STRUCTURE OF PROCATHEPSIN L[HYDROLASE]
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Crystal structure of a pyrrolopyrimidine inhibitor in complex with human Cathepsin K[HYDROLASE]
Crystal Structure of the Cysteine Protease Human Cathepsin K in Complex with the Covalent Inhibitor NVP-ABJ688[HYDROLASE]
Crystal Structure of the Cysteine Protease Human Cathepsin K in Complex with the Covalent Inhibitor NVP-ABI491[HYDROLASE]
Crystal Structure of the Cysteine Protease Human Cathepsin K in Complex with the Covalent Inhibitor NVP-ABE854[HYDROLASE]
Cathepsin K covalently bound to a cyano-pyrimidine inhibitor with improved selectivity over hERG[HYDROLASE/HYDROLASE INHIBITOR]
Cathepsin K covalently bound to a 2-cyano pyrimidine inhibitor with a benzyl P3 group[HYDROLASE]
Structure Of Catk Covalently Bound To A Dioxo-Triazine Inhibitor[Hydrolase, EC: 3.4.22.38]
Cathepsin K in complex with a selective 2-cyano-pyrimidine inhibitor[HYDROLASE]
Cathepsin K in complex with a non-selective 2-cyano-pyrimidine inhibitor[HYDROLASE]
X-ray structure of Cathepsin K covalently bound to a triazine ligand[HYDROLASE]
Crystal Structure Of The Cathepsin K : Chondroitin Sulfate Complex[Hydrolase, EC: 3.4.22.38]
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