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5D7X

Crystal structure of the human BRPF1 bromodomain in complex with XZ08

5D7X の概要
エントリーDOI10.2210/pdb5d7x/pdb
分子名称Peregrin, NITRATE ION, 4-(1-acetyl-1H-indol-3-yl)-5-methyl-1,2-dihydro-3H-pyrazol-3-one, ... (4 entities in total)
機能のキーワードbromodomain and phd finger-containing protein 1(brpf1), monocytic leukemia zinc-finger (moz), inhibitor, dna binding protein
由来する生物種Homo sapiens (Human)
細胞内の位置Nucleus : P55201
タンパク質・核酸の鎖数1
化学式量合計14020.98
構造登録者
Zhu, J.,Caflisch, A. (登録日: 2015-08-14, 公開日: 2016-05-25, 最終更新日: 2024-01-10)
主引用文献Unzue, A.,Zhao, H.,Lolli, G.,Dong, J.,Zhu, J.,Zechner, M.,Dolbois, A.,Caflisch, A.,Nevado, C.
The "Gatekeeper" Residue Influences the Mode of Binding of Acetyl Indoles to Bromodomains.
J.Med.Chem., 59:3087-3097, 2016
Cited by
PubMed Abstract: Small-molecule hits for the bromodomains of CREBBP and BAZ2B have been identified by scaffold hopping followed by docking of a set of ∼200 compounds containing the acetyl indole scaffold. Chemical synthesis of nearly 30 derivatives has resulted in ligands of representatives of three subfamilies of human bromodomains with favorable ligand efficiency. The X-ray crystal structures of three different bromodomains (CREBBP, BAZ2B, and BRPF1b) in complex with acetyl indole derivatives reveal the influence of the gatekeeper residue on the orientation of small-molecule ligands in the acetyl lysine binding site.
PubMed: 26982797
DOI: 10.1021/acs.jmedchem.5b01757
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.35 Å)
構造検証レポート
Validation report summary of 5d7x
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2026-02-04に公開中

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