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7MMB

Crystal structure of HCV NS3/4A D168A protease in complex with NR01-127

7MMB の概要
エントリーDOI10.2210/pdb7mmb/pdb
分子名称NS3 protease, cyclobutyl {(2R,4S,6S,12Z,13aS,14aR,16aS)-2-[(7-methoxy-3-methylquinoxalin-2-yl)oxy]-14a-[(1-methylcyclopropane-1-sulfonyl)carbamoyl]-5,16-dioxo-1,2,3,5,6,7,8,9,10,11,13a,14,14a,15,16,16a-hexadecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecin-6-yl}carbamate, 1,2-ETHANEDIOL, ... (6 entities in total)
機能のキーワードns3/4a protease, hepatitis c virus, drug resistance, protease inhibitor, hydrolase-hydrolase inhibitor complex, hydrolase, hydrolase-inhibitor complex, viral protein, hydrolase/inhibitor
由来する生物種Hepacivirus C
タンパク質・核酸の鎖数1
化学式量合計22528.70
構造登録者
Zephyr, J.,Schiffer, C.A. (登録日: 2021-04-29, 公開日: 2022-03-16, 最終更新日: 2023-10-18)
主引用文献Zephyr, J.,Nageswara Rao, D.,Vo, S.V.,Henes, M.,Kosovrasti, K.,Matthew, A.N.,Hedger, A.K.,Timm, J.,Chan, E.T.,Ali, A.,Kurt Yilmaz, N.,Schiffer, C.A.
Deciphering the Molecular Mechanism of HCV Protease Inhibitor Fluorination as a General Approach to Avoid Drug Resistance.
J.Mol.Biol., 434:167503-167503, 2022
Cited by
PubMed: 35183560
DOI: 10.1016/j.jmb.2022.167503
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.99 Å)
構造検証レポート
Validation report summary of 7mmb
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-05-15に公開中

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