6E69
Ortho-substituted phenyl sulfonyl fluoride and fluorosulfate as potent elastase inhibitory fragments
6E69 の概要
エントリーDOI | 10.2210/pdb6e69/pdb |
関連するPDBエントリー | 5ABW |
分子名称 | Neutrophil elastase, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (6 entities in total) |
機能のキーワード | neutrophil, elastase, fragment, inhibitor, sulfonyl fluoride, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
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 | 98013.42 |
構造登録者 | |
主引用文献 | Zheng, Q.,Woehl, J.L.,Kitamura, S.,Santos-Martins, D.,Smedley, C.J.,Li, G.,Forli, S.,Moses, J.E.,Wolan, D.W.,Sharpless, K.B. SuFEx-enabled, agnostic discovery of covalent inhibitors of human neutrophil elastase. Proc.Natl.Acad.Sci.USA, 116:18808-18814, 2019 Cited by PubMed Abstract: Sulfur fluoride exchange (SuFEx) has emerged as the new generation of click chemistry. We report here a SuFEx-enabled, agnostic approach for the discovery and optimization of covalent inhibitors of human neutrophil elastase (hNE). Evaluation of our ever-growing collection of SuFExable compounds toward various biological assays unexpectedly revealed a selective and covalent hNE inhibitor: benzene-1,2-disulfonyl fluoride. Synthetic derivatization of the initial hit led to a more potent agent, 2-(fluorosulfonyl)phenyl fluorosulfate with IC 0.24 μM and greater than 833-fold selectivity over the homologous neutrophil serine protease, cathepsin G. The optimized, yet simple benzenoid probe only modified active hNE and not its denatured form. PubMed: 31484779DOI: 10.1073/pnas.1909972116 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.33 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