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6P9F

Crystal structure of RAR-related orphan receptor C (NHIS-RORGT(244-487)-L6-SRC1(678-692)) in complex with a phenyl (3-phenylpyrrolidin-3-yl)sulfone inhibitor

6P9F の概要
エントリーDOI10.2210/pdb6p9f/pdb
分子名称Nuclear receptor ROR-gamma, Nuclear receptor coactivator 1 chimera, trans-4-{(3R)-3-[(4-fluorophenyl)sulfonyl]-3-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]pyrrolidine-1-carbonyl}cyclohexane-1-carboxylic acid (3 entities in total)
機能のキーワードrorgt, nuclear hormone receptor, ligand-binding domain, inve agonist, transferase-transferase inhibitor complex, transferase/transferase inhibitor
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67028.93
構造登録者
Sack, J. (登録日: 2019-06-10, 公開日: 2019-07-17, 最終更新日: 2023-10-11)
主引用文献Lu, Z.,Duan, J.J.,Xiao, H.,Neels, J.,Wu, D.R.,Weigelt, C.A.,Sack, J.S.,Khan, J.,Ruzanov, M.,An, Y.,Yarde, M.,Karmakar, A.,Vishwakrishnan, S.,Baratam, V.,Shankarappa, H.,Vanteru, S.,Babu, V.,Basha, M.,Kumar Gupta, A.,Kumaravel, S.,Mathur, A.,Zhao, Q.,Salter-Cid, L.M.,Carter, P.H.,Murali Dhar, T.G.
Identification of potent, selective and orally bioavailable phenyl ((R)-3-phenylpyrrolidin-3-yl)sulfone analogues as ROR gamma t inverse agonists.
Bioorg.Med.Chem.Lett., 29:2265-2269, 2019
Cited by
PubMed: 31257087
DOI: 10.1016/j.bmcl.2019.06.036
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.8 Å)
構造検証レポート
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2024-10-16に公開中

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