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9F9M

Crystal structure of MUS81-EME1 bound by compound 21.

これはPDB形式変換不可エントリーです。
9F9M の概要
エントリーDOI10.2210/pdb9f9m/pdb
関連するPDBエントリー9F98 9F99 9F9A 9F9K 9F9L
分子名称Crossover junction endonuclease MUS81, Crossover junction endonuclease EME1, MAGNESIUM ION, ... (4 entities in total)
機能のキーワードendonuclease, fragment, drug discovery, hydrolase
由来する生物種Homo sapiens (human)
詳細
タンパク質・核酸の鎖数4
化学式量合計141336.04
構造登録者
Collie, G.W. (登録日: 2024-05-08, 公開日: 2024-06-19, 最終更新日: 2024-07-31)
主引用文献Collie, G.W.,Borjesson, U.,Chen, Y.,Dong, Z.,Di Fruscia, P.,Gohlke, A.,Hoyle, A.,Hunt, T.A.,Jesani, M.H.,Luo, H.,Luptak, J.,Milbradt, A.G.,Narasimhan, P.,Packer, M.,Patel, S.,Qiao, J.,Storer, R.I.,Stubbs, C.J.,Tart, J.,Truman, C.,Wang, A.T.,Wheeler, M.G.,Winter-Holt, J.
Fragment-Based Discovery of Novel MUS81 Inhibitors.
Acs Med.Chem.Lett., 15:1151-1158, 2024
Cited by
PubMed Abstract: MUS81 is a structure-selective endonuclease that cleaves various branched DNA structures arising from natural physiological processes such as homologous recombination and mitosis. Due to this, MUS81 is able to relieve replication stress, and its function has been reported to be critical to the survival of many cancers, particularly those with dysfunctional DNA-repair machinery. There is therefore interest in MUS81 as a cancer drug target, yet there are currently few small molecule inhibitors of this enzyme reported, and no liganded crystal structures are available to guide hit optimization. Here we report the fragment-based discovery of novel small molecule MUS81 inhibitors with sub-μM biochemical activity. These inhibitors were used to develop a novel crystal system, providing the first structural insight into the inhibition of MUS81 with small molecules.
PubMed: 39015284
DOI: 10.1021/acsmedchemlett.3c00453
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.469 Å)
構造検証レポート
Validation report summary of 9f9m
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2026-02-04に公開中

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