7JST
Crystal structure of SARS-CoV-2 3CL in apo form
7JST の概要
| エントリーDOI | 10.2210/pdb7jst/pdb |
| 分子名称 | 3C-like proteinase, PHOSPHATE ION (3 entities in total) |
| 機能のキーワード | 3cl main protease, viral protein, hydrolase |
| 由来する生物種 | Severe acute respiratory syndrome coronavirus 2 (2019-nCoV, SARS-CoV-2, COVID-19 virus) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 33920.52 |
| 構造登録者 | Iketani, S.,Forouhar, F.,Liu, H.,Hong, S.J.,Lin, F.-Y.,Nair, M.S.,Zask, A.,Huang, Y.,Xing, L.,Stockwell, B.R.,Chavez, A.,Ho, D.D. (登録日: 2020-08-16, 公開日: 2021-03-03, 最終更新日: 2023-10-18) |
| 主引用文献 | Iketani, S.,Forouhar, F.,Liu, H.,Hong, S.J.,Lin, F.Y.,Nair, M.S.,Zask, A.,Huang, Y.,Xing, L.,Stockwell, B.R.,Chavez, A.,Ho, D.D. Lead compounds for the development of SARS-CoV-2 3CL protease inhibitors. Nat Commun, 12:2016-2016, 2021 Cited by PubMed Abstract: We report the identification of three structurally diverse compounds - compound 4, GC376, and MAC-5576 - as inhibitors of the SARS-CoV-2 3CL protease. Structures of each of these compounds in complex with the protease revealed strategies for further development, as well as general principles for designing SARS-CoV-2 3CL protease inhibitors. These compounds may therefore serve as leads for the basis of building effective SARS-CoV-2 3CL protease inhibitors. PubMed: 33795671DOI: 10.1038/s41467-021-22362-2 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.85 Å) |
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