8D8I
Crystal structure of Reverb alpha in complex with synthetic agonist
8D8I の概要
| エントリーDOI | 10.2210/pdb8d8i/pdb |
| 分子名称 | Nuclear receptor subfamily 1 group D member 1, Nuclear receptor corepressor 1, (4S)-6-[([1,1'-biphenyl]-2-yl)oxy]-3-chloro[1,2,4]triazolo[4,3-b]pyridazine, ... (4 entities in total) |
| 機能のキーワード | rev-erb, nuclear receptor, agonist, transcription |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 29093.50 |
| 構造登録者 | Ronin, C.,Ciesielski, F.,Hegazy, L.,Burris, P.T. (登録日: 2022-06-08, 公開日: 2022-12-14, 最終更新日: 2024-04-03) |
| 主引用文献 | Murray, M.H.,Valfort, A.C.,Koelblen, T.,Ronin, C.,Ciesielski, F.,Chatterjee, A.,Veerakanellore, G.B.,Elgendy, B.,Walker, J.K.,Hegazy, L.,Burris, T.P. Structural basis of synthetic agonist activation of the nuclear receptor REV-ERB. Nat Commun, 13:7131-7131, 2022 Cited by PubMed Abstract: The nuclear receptor REV-ERB plays an important role in a range of physiological processes. REV-ERB behaves as a ligand-dependent transcriptional repressor and heme has been identified as a physiological agonist. Our current understanding of how ligands bind to and regulate transcriptional repression by REV-ERB is based on the structure of heme bound to REV-ERB. However, porphyrin (heme) analogues have been avoided as a source of synthetic agonists due to the wide range of heme binding proteins and potential pleotropic effects. How non-porphyrin synthetic agonists bind to and regulate REV-ERB has not yet been defined. Here, we characterize a high affinity synthetic REV-ERB agonist, STL1267, and describe its mechanism of binding to REV-ERB as well as the method by which it recruits transcriptional corepressor both of which are unique and distinct from that of heme-bound REV-ERB. PubMed: 36414641DOI: 10.1038/s41467-022-34892-4 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.504 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






