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6AFJ

DJ-1 with compound 13

6AFJ の概要
エントリーDOI10.2210/pdb6afj/pdb
分子名称Protein/nucleic acid deglycase DJ-1, butyl 2-[2,3-bis(oxidanylidene)indol-1-yl]ethanoate, CHLORIDE ION, ... (4 entities in total)
機能のキーワードdj-1, parkinson's disease, drug discovery, fragment-based drug discovery, hydrolase
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数1
化学式量合計20213.78
構造登録者
Caaveiro, J.M.M.,Tashiro, S.,Tsumoto, K. (登録日: 2018-08-08, 公開日: 2018-08-29, 最終更新日: 2023-11-22)
主引用文献Tashiro, S.,Caaveiro, J.M.M.,Nakakido, M.,Tanabe, A.,Nagatoishi, S.,Tamura, Y.,Matsuda, N.,Liu, D.,Hoang, Q.Q.,Tsumoto, K.
Discovery and Optimization of Inhibitors of the Parkinson's Disease Associated Protein DJ-1.
ACS Chem. Biol., 13:2783-2793, 2018
Cited by
PubMed Abstract: DJ-1 is a Parkinson's disease associated protein endowed with enzymatic, redox sensing, regulatory, chaperoning, and neuroprotective activities. Although DJ-1 has been vigorously studied for the past decade and a half, its exact role in the progression of the disease remains uncertain. In addition, little is known about the spatiotemporal regulation of DJ-1, or the biochemical basis explaining its numerous biological functions. Progress has been hampered by the lack of inhibitors with precisely known mechanisms of action. Herein, we have employed biophysical methodologies and X-ray crystallography to identify and to optimize a family of compounds inactivating the critical Cys106 residue of human DJ-1. We demonstrate these compounds are potent inhibitors of various activities of DJ-1 in vitro and in cell-based assays. This study reports a new family of DJ-1 inhibitors with a defined mechanism of action, and contributes toward the understanding of the biological function of DJ-1.
PubMed: 30063823
DOI: 10.1021/acschembio.8b00701
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.48 Å)
構造検証レポート
Validation report summary of 6afj
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2024-10-30に公開中

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