7QKD

Crystal structure of human Cathepsin L in complex with covalently bound MG132

7QKD の概要

• エントリーDOI: 10.2210/pdb7qkd/pdb
• 関連するPDBエントリー: 7QKB 7QKC
• 関連するBIRD辞書のPRD_ID: PRD_001210
• 分子名称: Cathepsin L, N-[(benzyloxy)carbonyl]-L-leucyl-N-[(2S)-1-hydroxy-4-methylpentan-2-yl]-L-leucinamide, DI(HYDROXYETHYL)ETHER, ... (5 entities in total)
• 機能のキーワード: cathepsin, cystein protease, drug development, drug target, peptide-like inhibitor, lysosome, protein degradation, sars-cov-2, covid-19, spike protein maturation, hydrolase
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 99359.14

構造登録者

Reinke, P.Y.A.,Falke, S.,Lieske, J.,Ewert, W.,Loboda, J.,Rahmani Mashhour, A.,Hauser, M.,Karnicar, K.,Usenik, A.,Lindic, N.,Lach, M.,Boehler, H.,Beck, T.,Cox, R.,Chapman, H.N.,Hinrichs, W.,Turk, D.,Guenther, S.,Meents, A. (登録日: 2021-12-17, 公開日: 2022-12-28, 最終更新日: 2024-05-15)

• 主引用文献: Falke, S.,Lieske, J.,Herrmann, A.,Loboda, J.,Karnicar, K.,Gunther, S.,Reinke, P.Y.A.,Ewert, W.,Usenik, A.,Lindic, N.,Sekirnik, A.,Dretnik, K.,Tsuge, H.,Turk, V.,Chapman, H.N.,Hinrichs, W.,Ebert, G.,Turk, D.,Meents, A.; Structural Elucidation and Antiviral Activity of Covalent Cathepsin L Inhibitors.; J.Med.Chem., 2024; PubMed: 38630165; DOI: 10.1021/acs.jmedchem.3c02351

実験手法

X-RAY DIFFRACTION (1.5 Å)