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8A5B

Crystal structure of human cathepsin L in complex with covalently bound MG-101

Summary for 8A5B
Entry DOI10.2210/pdb8a5b/pdb
Related7QKD 7ZS7 7ZVF
Related PRD IDPRD_002460
DescriptorCathepsin L, Calpain Inhibitor I, TRIETHYLENE GLYCOL, ... (6 entities in total)
Functional Keywordscystein protease, drug target, lysosome, virus cell entry, hydrolase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains8
Total formula weight98749.37
Authors
Falke, S.,Lieske, J.,Guenther, S.,Reinke, P.Y.A.,Ewert, W.,Loboda, J.,Karnicar, K.,Usenik, A.,Lindic, N.,Sekirnik, A.,Chapman, H.N.,Hinrichs, W.,Turk, D.,Meents, A. (deposition date: 2022-06-14, release date: 2023-07-05, Last modification date: 2024-02-07)
Primary citationFalke, S.,Lieske, J.,Herrmann, A.,Guenther, S.,Reinke, P.Y.A.,Ewert, W.,Loboda, J.,Karnicar, K.,Usenik, A.,Lindic, N.,Sekirnik, A.,Chapman, H.N.,Hinrichs, W.,Ebert, G.,Turk, D.,Meents, A.
Structural elucidation of antiviral cathepsin L inhibitors
To be published,
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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