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2R9M

Cathepsin S complexed with Compound 15

Summary for 2R9M
Entry DOI10.2210/pdb2r9m/pdb
Related2R9N 2R9O
DescriptorCathepsin S, N-[(1S)-2-[(4-cyano-1-methylpiperidin-4-yl)amino]-1-(cyclohexylmethyl)-2-oxoethyl]morpholine-4-carboxamide (3 entities in total)
Functional Keywordshydrolase, cathepsin, protease, glycoprotein, lysosome, polymorphism, thiol protease, zymogen
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight50206.41
Authors
Primary citationWard, Y.D.,Emmanuel, M.J.,Thomson, D.S.,Liu, W.,Bekkali, Y.,Frye, L.L.,Girardot, M.,Morwick, T.,Young, E.R.R.,Zindell, R.,Hrapchak, M.,DeTuri, M.,White, A.,Crane, K.M.,White, D.M.,Wang, Y.,Hao, M.-H.,Grygon, C.A.,Labadia, M.E.,Wildeson, J.,Freeman, D.,Nelson, R.,Capolino, A.,Peterson, J.D.,Raymond, E.L.,Brown, M.L.,Spero, D.M.
Design and Synthesis of Reversible Inhibitors of Cathepsin S: alpha,alpha-Disubstitution at the P1 Residue Provides Potent Inhibitors in Cellular Assays and In Vivo Models of Antigen Presentation
To be Published,
Experimental method
X-RAY DIFFRACTION (1.97 Å)
Structure validation

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PDB entries from 2024-04-17

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