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8HQF

Crystal structure of SARS-Cov-2 main protease G15S mutant in complex with inhibitor YH-53

8HQF の概要
エントリーDOI10.2210/pdb8hqf/pdb
分子名称Non-structural protein 7, N-[(2S)-1-[[(2S)-1-(1,3-benzothiazol-2-yl)-1-oxidanylidene-3-[(3S)-2-oxidanylidenepyrrolidin-3-yl]propan-2-yl]amino]-4-methyl-1-oxidanylidene-pentan-2-yl]-4-methoxy-1H-indole-2-carboxamide (3 entities in total)
機能のキーワードviral protein-inhibitor complex, viral protein/inhibitor
由来する生物種Severe acute respiratory syndrome coronavirus 2
タンパク質・核酸の鎖数2
化学式量合計67509.07
構造登録者
Zeng, P.,Zhang, J.,Li, J. (登録日: 2022-12-13, 公開日: 2024-01-31, 最終更新日: 2025-01-01)
主引用文献Luo, J.,Wang, W.,Jiang, H.,Li, W.,Zeng, P.,Wang, J.,Zhou, X.,Zou, X.,Chen, S.,Wang, Q.,Zhang, J.,Li, J.
Crystal structures of main proteases of SARS-CoV-2 variants bound to a benzothiazole-based inhibitor.
Acta Biochim.Biophys.Sin., 55:1257-1264, 2023
Cited by
PubMed Abstract: Main protease (M ) serves as an indispensable factor in the life cycle of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) as well as its constantly emerging variants and is therefore considered an attractive target for antiviral drug development. Benzothiazole-based inhibitors targeting M have recently been investigated by several groups and proven to be promising leads for coronaviral drug development. In the present study, we determine the crystal structures of a benzothiazole-based inhibitor, YH-53, bound to M mutants from SARS-CoV-2 variants of concern (VOCs) or variants of interest (VOIs), including K90R (Beta, B.1.351), G15S (Lambda, C.37), Y54C (Delta, AY.4), M49I (Omicron, BA.5) and P132H (Omicron, B.1.1.529). The structures show that the benzothiazole group in YH-53 forms a C-S covalent bond with the sulfur atom of catalytic residue Cys145 in SARS-CoV-2 M mutants. Structural analysis reveals the key molecular determinants necessary for interaction and illustrates the binding mode of YH-53 to these mutant M s. In conclusion, structural insights from this study offer more information to develop benzothiazole-based drugs that are broader spectrum, more effective and safer.
PubMed: 37357528
DOI: 10.3724/abbs.2023053
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.51 Å)
構造検証レポート
Validation report summary of 8hqf
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2025-06-11に公開中

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