5AD3
Bivalent binding to BET bromodomains
5AD3 の概要
| エントリーDOI | 10.2210/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 | Waring, M.J.,Chen, H.,Rabow, A.A.,Walker, G.,Bobby, R.,Boiko, S.,Bradbury, R.H.,Callis, R.,Dale, I.,Daniels, D.,Flavell, L.,Holdgate, G.,Jowitt, T.A.,Kikhney, A.,McAlister, M.,Ogg, D.,Patel, J.,Petteruti, P.,Robb, G.R.,Robers, M.,Stratton, N.,Svergun, D.I.,Wang, W.,Whittaker, D. (登録日: 2015-08-19, 公開日: 2016-09-28, 最終更新日: 2024-01-10) |
| 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: 27775716DOI: 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) |
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