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7QKB

Crystal structure of human Cathepsin L in complex with covalently bound GC376

Summary for 7QKB
Entry DOI10.2210/pdb7qkb/pdb
Related7QKA
Related PRD IDPRD_002495
DescriptorCathepsin L, DI(HYDROXYETHYL)ETHER, SODIUM ION, ... (9 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 weight99915.81
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 (1.8 Å)
Structure validation

221051

건을2024-06-12부터공개중

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