3JSX

X-ray Crystal structure of NAD(P)H: Quinone Oxidoreductase-1 (NQO1) bound to the coumarin-based inhibitor AS1

3JSX の概要

• エントリーDOI: 10.2210/pdb3jsx/pdb
• 分子名称: NAD(P)H dehydrogenase [quinone] 1, FLAVIN-ADENINE DINUCLEOTIDE, 4-hydroxy-6,7-dimethyl-3-(naphthalen-1-ylmethyl)-2H-chromen-2-one, ... (4 entities in total)
• 機能のキーワード: coumarin-based inhibitors, nq01, fad, flavoprotein, nad, nadp, oxidoreductase
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Cytoplasm: P15559
• タンパク質・核酸の鎖数: 8
• 化学式量合計: 255138.71

構造登録者

Dunstan, M.S.,Levy, C.,Leys, D. (登録日: 2009-09-11, 公開日: 2010-01-12, 最終更新日: 2023-11-01)

主引用文献

Nolan, K.A.,Doncaster, J.R.,Dunstan, M.S.,Scott, K.A.,Frenkel, A.D.,Siegel, D.,Ross, D.,Barnes, J.,Levy, C.,Leys, D.,Whitehead, R.C.,Stratford, I.J.,Bryce, R.A.
Synthesis and biological evaluation of coumarin-based inhibitors of NAD(P)H: quinone oxidoreductase-1 (NQO1).
J.Med.Chem., 52:7142-7156, 2009

PubMed Abstract: The synthesis is reported here of two novel series of inhibitors of human NAD(P)H quinone oxidoreductase-1 (NQO1), an enzyme overexpressed in several types of tumor cell. The first series comprises substituted symmetric dicoumarol analogues; the second series contains hybrid compounds where one 4-hydroxycoumarin system is replaced by a different aromatic moiety. Several compounds show equivalent or improved NQO1 inhibition over dicoumarol, both in the presence and in the absence of added protein. Further, correlation is demonstrated between the ability of these agents to inhibit NQO1 and computed binding affinity. We have solved the crystal structure of NQO1 complexed to a hybrid compound and find good agreement with the in silico model. For both MIA PaCa-2 pancreatic tumor cells and HCT116 colon cancer cells, dicoumarol shows the greatest toxicity of all compounds. Thus, we provide a computational, synthetic, and biological platform to generate competitive NQO1 inhibitors with superior pharmacological properties to dicoumarol. This will allow a more definitive study of NQO1 activity in cells, in particular, its drug activating/detoxifying properties and ability to modulate oncoprotein stability.

PubMed: 19877692
DOI: 10.1021/jm9011609

実験手法

X-RAY DIFFRACTION (2.45 Å)