8A4X

Crystal structure of human Cathepsin L with covalently bound Calpain inhibitor III

8A4X の概要

• エントリーDOI: 10.2210/pdb8a4x/pdb
• 関連するPDBエントリー: 7ZS7 7ZVF 7ZXA 8A4U 8A4V 8A4W
• 分子名称: Cathepsin L, (phenylmethyl) N-[(2S)-3-methyl-1-oxidanylidene-1-[[(2S)-1-oxidanyl-3-phenyl-propan-2-yl]amino]butan-2-yl]carbamate, DI(HYDROXYETHYL)ETHER, ... (7 entities in total)
• 機能のキーワード: cystein protease, drug target, lysosome, virus cell entry, 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: 99836.48

構造登録者

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. (登録日: 2022-06-13, 公開日: 2023-07-05, 最終更新日: 2024-05-22)

• 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., 67:7048-7067, 2024; PubMed: 38630165; DOI: 10.1021/acs.jmedchem.3c02351

実験手法

X-RAY DIFFRACTION (1.8 Å)