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5NAH

Pseudomonas fluorescens kynurenine 3-monooxygenase (KMO) in complex with 3-{5-chloro-6-[(1R)-1-(6-methylpyridazin-3-yl)ethoxy]-1,2-benzoxazol-3-yl}propanoic acid

5NAH の概要
エントリーDOI10.2210/pdb5nah/pdb
分子名称Kynurenine 3-monooxygenase, FLAVIN-ADENINE DINUCLEOTIDE, 3-[5-chloranyl-6-[(1~{R})-1-(6-methylpyridazin-3-yl)ethoxy]-1,2-benzoxazol-3-yl]propanoic acid, ... (4 entities in total)
機能のキーワードkmo, oxidoreductase
由来する生物種Pseudomonas fluorescens
タンパク質・核酸の鎖数2
化学式量合計103869.69
構造登録者
Rowland, P. (登録日: 2017-02-27, 公開日: 2017-06-21, 最終更新日: 2025-04-09)
主引用文献Hutchinson, J.P.,Rowland, P.,Taylor, M.R.D.,Christodoulou, E.M.,Haslam, C.,Hobbs, C.I.,Holmes, D.S.,Homes, P.,Liddle, J.,Mole, D.J.,Uings, I.,Walker, A.L.,Webster, S.P.,Mowat, C.G.,Chung, C.W.
Structural and mechanistic basis of differentiated inhibitors of the acute pancreatitis target kynurenine-3-monooxygenase.
Nat Commun, 8:15827-15827, 2017
Cited by
PubMed Abstract: Kynurenine-3-monooxygenase (KMO) is a key FAD-dependent enzyme of tryptophan metabolism. In animal models, KMO inhibition has shown benefit in neurodegenerative diseases such as Huntington's and Alzheimer's. Most recently it has been identified as a target for acute pancreatitis multiple organ dysfunction syndrome (AP-MODS); a devastating inflammatory condition with a mortality rate in excess of 20%. Here we report and dissect the molecular mechanism of action of three classes of KMO inhibitors with differentiated binding modes and kinetics. Two novel inhibitor classes trap the catalytic flavin in a previously unobserved tilting conformation. This correlates with picomolar affinities, increased residence times and an absence of the peroxide production seen with previous substrate site inhibitors. These structural and mechanistic insights culminated in GSK065(C1) and GSK366(C2), molecules suitable for preclinical evaluation. Moreover, revising the repertoire of flavin dynamics in this enzyme class offers exciting new opportunities for inhibitor design.
PubMed: 28604669
DOI: 10.1038/ncomms15827
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.75 Å)
構造検証レポート
Validation report summary of 5nah
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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