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5T4U

Crystal structure of the bromodomain of human BRPF1 in complex with a quinolinone ligand

5T4U の概要
エントリーDOI10.2210/pdb5t4u/pdb
分子名称Peregrin, NITRATE ION, 1-METHYLQUINOLIN-2(1H)-ONE, ... (4 entities in total)
機能のキーワードtranscription, structural genomics, psi-2, protein structure initiative, structural genomics consortium, sgc
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13924.89
構造登録者
主引用文献Igoe, N.,Bayle, E.D.,Fedorov, O.,Tallant, C.,Savitsky, P.,Rogers, C.,Owen, D.R.,Deb, G.,Somervaille, T.C.,Andrews, D.M.,Jones, N.,Cheasty, A.,Ryder, H.,Brennan, P.E.,Muller, S.,Knapp, S.,Fish, P.V.
Design of a Biased Potent Small Molecule Inhibitor of the Bromodomain and PHD Finger-Containing (BRPF) Proteins Suitable for Cellular and in Vivo Studies.
J. Med. Chem., 60:668-680, 2017
Cited by
PubMed Abstract: The BRPF (bromodomain and PHD finger-containing) family are scaffolding proteins important for the recruitment of histone acetyltransferases of the MYST family to chromatin. Evaluation of the BRPF family as a potential drug target is at an early stage although there is an emerging understanding of a role in acute myeloid leukemia (AML). We report the optimization of fragment hit 5b to 13-d as a biased, potent inhibitor of the BRD of the BRPFs with excellent selectivity over nonclass IV BRD proteins. Evaluation of 13-d in a panel of cancer cell lines showed a selective inhibition of proliferation of a subset of AML lines. Pharmacokinetic studies established that 13-d had properties compatible with oral dosing in mouse models of disease (F 49%). We propose that NI-42 (13-d) is a new chemical probe for the BRPFs suitable for cellular and in vivo studies to explore the fundamental biology of these proteins.
PubMed: 28068087
DOI: 10.1021/acs.jmedchem.6b01583
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.5 Å)
構造検証レポート
Validation report summary of 5t4u
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2024-11-06に公開中

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