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5AD3

Bivalent binding to BET bromodomains

5AD3 の概要
エントリーDOI10.2210/pdb5ad3/pdb
関連するPDBエントリー5AD2
分子名称BROMODOMAIN-CONTAINING PROTEIN 4, 3-methoxy-N-[2-[4-[1-(3-methoxy-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)-4-piperidyl]phenoxy]ethyl]-N-methyl-[1,2,4]triazolo[4,3-b]pyridazin-6-amine (3 entities in total)
機能のキーワードtranscription
由来する生物種HOMO SAPIENS (HUMAN)
細胞内の位置Nucleus: O60885
タンパク質・核酸の鎖数2
化学式量合計30729.34
構造登録者
主引用文献Waring, M.J.,Chen, H.,Rabow, A.A.,Walker, G.,Bobby, R.,Boiko, S.,Bradbury, R.H.,Callis, R.,Clark, E.,Dale, I.,Daniels, D.L.,Dulak, A.,Flavell, L.,Holdgate, G.,Jowitt, T.A.,Kikhney, A.,Mcalister, M.,Ogg, D.,Patel, J.,Petteruti, P.,Robb, G.R.,Robers, M.B.,Saif, S.,Stratton, N.,Svergun, D.I.,Wang, W.,Whittaker, D.,Wilson, D.M.,Yao, Y.
Potent and Selective Bivalent Inhibitors of Bet Bromodomains
Nat.Chem.Biol., 12:1097-, 2016
Cited by
PubMed Abstract: Proteins of the bromodomain and extraterminal (BET) family, in particular bromodomain-containing protein 4 (BRD4), are of great interest as biological targets. BET proteins contain two separate bromodomains, and existing inhibitors bind to them monovalently. Here we describe the discovery and characterization of probe compound biBET, capable of engaging both bromodomains simultaneously in a bivalent, in cis binding mode. The evidence provided here was obtained in a variety of biophysical and cellular experiments. The bivalent binding results in very high cellular potency for BRD4 binding and pharmacological responses such as disruption of BRD4-mediator complex subunit 1 foci with an EC of 100 pM. These compounds will be of considerable utility as BET/BRD4 chemical probes. This work illustrates a novel concept in ligand design-simultaneous targeting of two separate domains with a drug-like small molecule-providing precedent for a potentially more effective paradigm for developing ligands for other multi-domain proteins.
PubMed: 27775716
DOI: 10.1038/NCHEMBIO.2210
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.49 Å)
構造検証レポート
Validation report summary of 5ad3
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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