8AXP
Neisseria gonorrhoeae peptidyl-tRNA hydrolase complexed with an XChem hit.
8AXP の概要
| エントリーDOI | 10.2210/pdb8axp/pdb |
| 分子名称 | Peptidyl-tRNA hydrolase, N-[4-(2-amino-1,3-thiazol-4-yl)phenyl]acetamide, SULFATE ION, ... (4 entities in total) |
| 機能のキーワード | inhibitor, complex, hydrolase |
| 由来する生物種 | Neisseria gonorrhoeae |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 44098.30 |
| 構造登録者 | |
| 主引用文献 | Hassell-Hart, S.,Speranzini, E.,Srikwanjai, S.,Hossack, E.,Roe, S.M.,Fearon, D.,Akinbosede, D.,Hare, S.,Spencer, J. Synthesis of a Thiazole Library via an Iridium-Catalyzed Sulfur Ylide Insertion Reaction. Org.Lett., 24:7924-7927, 2022 Cited by PubMed Abstract: A library of thiazoles and selenothiazoles were synthesized via Ir-catalyzed ylide insertion chemistry. This process is a functional group, particularly heterocycle-substituent tolerant. This was applied to the synthesis of fanetizole, an anti-inflammatory drug, and a thiazole-containing drug fragment that binds to the peptidyl-tRNA hydrolase (Pth) in Neisseria gonorrheae bacteria. PubMed: 36265082DOI: 10.1021/acs.orglett.2c02996 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.83 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






