8A5B
Crystal structure of human cathepsin L in complex with covalently bound MG-101
Summary for 8A5B
Entry DOI | 10.2210/pdb8a5b/pdb |
Related | 7QKD 7ZS7 7ZVF |
Related PRD ID | PRD_002460 |
Descriptor | Cathepsin L, Calpain Inhibitor I, TRIETHYLENE GLYCOL, ... (6 entities in total) |
Functional Keywords | cystein protease, drug target, lysosome, virus cell entry, hydrolase |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 8 |
Total formula weight | 98749.37 |
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 citation | Falke, 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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