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7Z58

Crystal structure of human Cathepsin L in complex with covalently bound Calpeptin

Summary for 7Z58
Entry DOI10.2210/pdb7z58/pdb
Related7QGW 7QKA 7QKB 7QKC 7QKD 7Z2K 7Z3T 7Z3U
DescriptorCathepsin L, DI(HYDROXYETHYL)ETHER, TRIETHYLENE GLYCOL, ... (7 entities in total)
Functional Keywordscathepsin, cystein protease, drug development, drug target, peptide-like inhibitor, lysosome, protein degradation, sars-cov-2, covid-19, spike protein maturation, hydrolase
Biological sourceHomo sapiens (human)
Total number of polymer chains4
Total formula weight100046.92
Authors
Primary citationReinke, P.Y.A.,de Souza, E.E.,Gunther, S.,Falke, S.,Lieske, J.,Ewert, W.,Loboda, J.,Herrmann, A.,Rahmani Mashhour, A.,Karnicar, K.,Usenik, A.,Lindic, N.,Sekirnik, A.,Botosso, V.F.,Santelli, G.M.M.,Kapronezai, J.,de Araujo, M.V.,Silva-Pereira, T.T.,Filho, A.F.S.,Tavares, M.S.,Florez-Alvarez, L.,de Oliveira, D.B.L.,Durigon, E.L.,Giaretta, P.R.,Heinemann, M.B.,Hauser, M.,Seychell, B.,Bohler, H.,Rut, W.,Drag, M.,Beck, T.,Cox, R.,Chapman, H.N.,Betzel, C.,Brehm, W.,Hinrichs, W.,Ebert, G.,Latham, S.L.,Guimaraes, A.M.S.,Turk, D.,Wrenger, C.,Meents, A.
Calpeptin is a potent cathepsin inhibitor and drug candidate for SARS-CoV-2 infections.
Commun Biol, 6:1058-1058, 2023
Cited by
PubMed: 37853179
DOI: 10.1038/s42003-023-05317-9
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.35 Å)
Structure validation

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