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6E69

Ortho-substituted phenyl sulfonyl fluoride and fluorosulfate as potent elastase inhibitory fragments

6E69 の概要
エントリーDOI10.2210/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
Wolan, D.W.,Woehl, J.L.,Kitamura, S. (登録日: 2018-07-24, 公開日: 2019-07-24, 最終更新日: 2024-10-16)
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: 31484779
DOI: 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
Validation report summary of 6e69
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2024-11-13に公開中

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