4ASK

CRYSTAL STRUCTURE OF JMJD3 WITH GSK-J1

4ASK の概要

• エントリーDOI: 10.2210/pdb4ask/pdb
• 関連するPDBエントリー: 2XUE 2XXZ
• 分子名称: LYSINE-SPECIFIC DEMETHYLASE 6B, ZINC ION, 3-[[2-pyridin-2-yl-6-(1,2,4,5-tetrahydro-3-benzazepin-3-yl)pyrimidin-4-yl]amino]propanoic acid, ... (5 entities in total)
• 機能のキーワード: oxidoreductase, kdm6b, gsk-j1, inhibitor, lysine specific histone demethylase
• 由来する生物種: HOMO SAPIENS
• 細胞内の位置: Nucleus (Probable): O15054
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 117128.15

構造登録者

Chung, C.,Mosley, J.,Liddle, J. (登録日: 2012-05-01, 公開日: 2012-07-25, 最終更新日: 2023-12-20)

主引用文献

Kruidenier, L.,Chung, C.,Cheng, Z.,Liddle, J.,Che, K.,Joberty, G.,Bantscheff, M.,Bountra, C.,Bridges, A.,Diallo, H.,Eberhard, D.,Hutchinson, S.,Jones, E.,Katso, R.,Leveridge, M.,Mander, P.K.,Mosley, J.,Ramirez-Molina, C.,Rowland, P.,Schofield, C.J.,Sheppard, R.J.,Smith, J.E.,Swales, C.,Tanner, R.,Thomas, P.,Tumber, A.,Drewes, G.,Oppermann, U.,Patel, D.J.,Lee, K.,Wilson, D.M.
A Selective Jumonji H3K27 Demethylase Inhibitor Modulates the Proinflammatory Macrophage Response
Nature, 488:404-, 2012

PubMed Abstract: The jumonji (JMJ) family of histone demethylases are Fe2+- and α-ketoglutarate-dependent oxygenases that are essential components of regulatory transcriptional chromatin complexes. These enzymes demethylate lysine residues in histones in a methylation-state and sequence-specific context. Considerable effort has been devoted to gaining a mechanistic understanding of the roles of histone lysine demethylases in eukaryotic transcription, genome integrity and epigenetic inheritance, as well as in development, physiology and disease. However, because of the absence of any selective inhibitors, the relevance of the demethylase activity of JMJ enzymes in regulating cellular responses remains poorly understood. Here we present a structure-guided small-molecule and chemoproteomics approach to elucidating the functional role of the H3K27me3-specific demethylase subfamily (KDM6 subfamily members JMJD3 and UTX). The liganded structures of human and mouse JMJD3 provide novel insight into the specificity determinants for cofactor, substrate and inhibitor recognition by the KDM6 subfamily of demethylases. We exploited these structural features to generate the first small-molecule catalytic site inhibitor that is selective for the H3K27me3-specific JMJ subfamily. We demonstrate that this inhibitor binds in a novel manner and reduces lipopolysaccharide-induced proinflammatory cytokine production by human primary macrophages, a process that depends on both JMJD3 and UTX. Our results resolve the ambiguity associated with the catalytic function of H3K27-specific JMJs in regulating disease-relevant inflammatory responses and provide encouragement for designing small-molecule inhibitors to allow selective pharmacological intervention across the JMJ family.

PubMed: 22842901
DOI: 10.1038/NATURE11262

実験手法

X-RAY DIFFRACTION (1.86 Å)