6BR2
Structure of RORgt in complex with a novel isoquinoline inverse agonist.
6BR2 の概要
エントリーDOI | 10.2210/pdb6br2/pdb |
分子名称 | Nuclear receptor ROR-gamma, (4S)-2-METHYL-2,4-PENTANEDIOL, (1R)-N-(4-tert-butyl-3-fluorophenyl)-6-methoxy-2-[(3-oxo-2,3-dihydro-1,2-oxazol-5-yl)acetyl]-1,2,3,4-tetrahydroisoquinoline-1-carboxamide, ... (4 entities in total) |
機能のキーワード | nuclear hormone receptor, inverse agonist, complex, transcription-agonist complex, transcription/agonist |
由来する生物種 | Homo sapiens (Human) |
細胞内の位置 | Nucleus : P51449 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 51201.21 |
構造登録者 | |
主引用文献 | Kono, M.,Ochida, A.,Oda, T.,Imada, T.,Banno, Y.,Taya, N.,Masada, S.,Kawamoto, T.,Yonemori, K.,Nara, Y.,Fukase, Y.,Yukawa, T.,Tokuhara, H.,Skene, R.,Sang, B.C.,Hoffman, I.D.,Snell, G.P.,Uga, K.,Shibata, A.,Igaki, K.,Nakamura, Y.,Nakagawa, H.,Tsuchimori, N.,Yamasaki, M.,Shirai, J.,Yamamoto, S. Discovery of [ cis-3-({(5 R)-5-[(7-Fluoro-1,1-dimethyl-2,3-dihydro-1 H-inden-5-yl)carbamoyl]-2-methoxy-7,8-dihydro-1,6-naphthyridin-6(5 H)-yl}carbonyl)cyclobutyl]acetic Acid (TAK-828F) as a Potent, Selective, and Orally Available Novel Retinoic Acid Receptor-Related Orphan Receptor gamma t Inverse Agonist. J. Med. Chem., 61:2973-2988, 2018 Cited by PubMed: 29510038DOI: 10.1021/acs.jmedchem.8b00061 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (3.18 Å) |
構造検証レポート
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