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与混合谱系白血病蛋白-1肽结合的WDR5的结构。

Structure of WDR5 bound to mixed lineage leukemia protein-1 peptide.

作者信息

Patel Anamika, Dharmarajan Venkatasubramanian, Cosgrove Michael S

机构信息

Department of Biology, Syracuse University, Syracuse, New York 13244, USA.

出版信息

J Biol Chem. 2008 Nov 21;283(47):32158-61. doi: 10.1074/jbc.C800164200. Epub 2008 Oct 1.

Abstract

The mixed lineage leukemia protein-1 (MLL1) catalyzes histone H3 lysine 4 methylation and is regulated by interaction with WDR5 (WD-repeat protein-5), RbBP5 (retinoblastoma-binding protein-5), and the Ash2L (absent, small, homeotic discs-2-like) oncoprotein. In the accompanying investigation, we describe the identification of a conserved arginine containing motif, called the "Win" or WDR5 interaction motif, that is essential for the assembly and H3K4 dimethylation activity of the MLL1 core complex. Here we present a 1.7-A crystal structure of WDR5 bound to a peptide derived from the MLL1 Win motif. Our results show that Arg-3765 of MLL1 is bound in the same arginine binding pocket on WDR5 that was previously suggested to bind histone H3. Thermodynamic binding experiments show that the MLL1 Win peptide is preferentially recognized by WDR5. These results are consistent with a model in which WDR5 recognizes Arg-3765 of MLL1, which is essential for the assembly and enzymatic activity of the MLL1 core complex.

摘要

混合谱系白血病蛋白-1(MLL1)催化组蛋白H3赖氨酸4甲基化,并通过与WDR5(WD重复蛋白-5)、RbBP5(视网膜母细胞瘤结合蛋白-5)和Ash2L(缺失、小、同源异型盘-2样)癌蛋白相互作用来调节。在随附的研究中,我们描述了一种保守的含精氨酸基序的鉴定,该基序称为“Win”或WDR5相互作用基序,对MLL1核心复合物的组装和H3K4二甲基化活性至关重要。在此,我们展示了与源自MLL1 Win基序的肽结合的WDR5的1.7埃晶体结构。我们的结果表明,MLL1的Arg-3765结合在WDR5上先前被认为结合组蛋白H3的相同精氨酸结合口袋中。热力学结合实验表明,MLL1 Win肽优先被WDR5识别。这些结果与一个模型一致,即WDR5识别MLL1的Arg-3765,这对MLL1核心复合物的组装和酶活性至关重要。

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