3SMR

Crystal structure of human WD repeat domain 5 with compound

3SMR の概要

• エントリーDOI: 10.2210/pdb3smr/pdb
• 分子名称: WD repeat-containing protein 5, 2-chloro-N-[2-(4-methylpiperazin-1-yl)-5-nitrophenyl]benzamide, 1,2-ETHANEDIOL, ... (5 entities in total)
• 機能のキーワード: wdr5, sgc, structural genomics, structural genomics consortium, wd repeat domain 5, transcription
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Nucleus : P61964
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 140086.40

構造登録者

Dong, A.,Dombrovski, L.,Wasney, G.A.,Tempel, W.,Senisterra, G.,Bolshan, Y.,Smil, D.,Nguyen, K.T.,Hajian, T.,Poda, G.,Al-Awar, R.,Bountra, C.,Weigelt, J.,Edwards, A.M.,Brown, P.J.,Schapira, M.,Arrowsmith, C.H.,Vedadi, M.,Wu, H.,Structural Genomics Consortium (SGC) (登録日: 2011-06-28, 公開日: 2011-08-31, 最終更新日: 2023-09-13)

主引用文献

Senisterra, G.,Wu, H.,Allali-Hassani, A.,Wasney, G.A.,Barsyte-Lovejoy, D.,Dombrovski, L.,Dong, A.,Nguyen, K.T.,Smil, D.,Bolshan, Y.,Hajian, T.,He, H.,Seitova, A.,Chau, I.,Li, F.,Poda, G.,Couture, J.F.,Brown, P.J.,Al-Awar, R.,Schapira, M.,Arrowsmith, C.H.,Vedadi, M.
Small-molecule inhibition of MLL activity by disruption of its interaction with WDR5.
Biochem. J., 449:151-159, 2013

PubMed Abstract: WDR5 (WD40 repeat protein 5) is an essential component of the human trithorax-like family of SET1 [Su(var)3-9 enhancer-of-zeste trithorax 1] methyltransferase complexes that carry out trimethylation of histone 3 Lys4 (H3K4me3), play key roles in development and are abnormally expressed in many cancers. In the present study, we show that the interaction between WDR5 and peptides from the catalytic domain of MLL (mixed-lineage leukaemia protein) (KMT2) can be antagonized with a small molecule. Structural and biophysical analysis show that this antagonist binds in the WDR5 peptide-binding pocket with a Kd of 450 nM and inhibits the catalytic activity of the MLL core complex in vitro. The degree of inhibition was enhanced at lower protein concentrations consistent with a role for WDR5 in directly stabilizing the MLL multiprotein complex. Our data demonstrate inhibition of an important protein-protein interaction and form the basis for further development of inhibitors of WDR5-dependent enzymes implicated in MLL-rearranged leukaemias or other cancers.

PubMed: 22989411
DOI: 10.1042/BJ20121280

実験手法

X-RAY DIFFRACTION (1.82 Å)