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7QKC

Crystal structure of human Cathepsin L after incubation with Sulfo-Calpeptin

Summary for 7QKC
Entry DOI10.2210/pdb7qkc/pdb
Related7QKA 7QKB
Related PRD IDPRD_002386
DescriptorCathepsin L, DI(HYDROXYETHYL)ETHER, Calpeptin, ... (4 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 weight98847.46
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 (1.69 Å)
Structure validation

221051

數據於2024-06-12公開中

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