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2H60

Solution Structure of Human Brg1 Bromodomain

2H60 の概要
エントリーDOI10.2210/pdb2h60/pdb
分子名称Probable global transcription activator SNF2L4 (1 entity in total)
機能のキーワードalfa helix, transcription
由来する生物種Homo sapiens (human)
細胞内の位置Nucleus: P51532
タンパク質・核酸の鎖数1
化学式量合計15188.44
構造登録者
Shen, W.,Xu, C.,Zhang, J.,Wu, J.,Shi, Y. (登録日: 2006-05-30, 公開日: 2007-02-13, 最終更新日: 2024-05-29)
主引用文献Shen, W.,Xu, C.,Huang, W.,Zhang, J.,Carlson, J.E.,Tu, X.,Wu, J.,Shi, Y.
Solution structure of human Brg1 bromodomain and its specific binding to acetylated histone tails
Biochemistry, 46:2100-2110, 2007
Cited by
PubMed Abstract: Human brahma-related gene 1 (Brg1) is a core protein in human SWI/SNF chromatin-remodeling complex which regulates gene expression. Brg1 contains a bromodomain that has been shown to anchor the entire complex to promoter nucleosomes by interacting with histones that are acetylated at specific lysine residues. The Brg1 bromodomain belongs to an important subclass of the bromodomain family for which no structural information is known. Here we report the solution structure of the Brg1 bromodomain determined by NMR. The Brg1 bromodomain conserves the left-handed, four-helix bundle topology found in other bromodomain structures. However, the alphaZ helix of Brg1 bromodomain is about 4 residues shorter relative to previously published bromodomain structures. Using NMR perturbation studies, we demonstrate the Brg1 bromodomain binds acetyllysine in the context of histone tails, with no comparable affinity for unacetylated peptides. The estimated dissociation constants (KD) for acetylated histone peptides H4-AcK8 and H4-AcK12 are 4.0 and 3.6 mM, respectively. In this study the dominant substrate was H3-AcK14 (KD approximately 1.2 mM). Mutagenesis analysis reveals several residues important for the binding specificity. Using molecular dynamics simulations, we present a model of the Brg1 bromodomain in complex with H3-AcK14 and discuss the potential interactions which provide the selectivity of the Brg1 bromodomain for histone H3-AcK14.
PubMed: 17274598
DOI: 10.1021/bi0611208
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 2h60
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2026-02-11に公開中

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