4ZJ8
Structures of the human OX1 orexin receptor bound to selective and dual antagonists
4ZJ8 の概要
エントリーDOI | 10.2210/pdb4zj8/pdb |
関連するPDBエントリー | 4ZJC |
分子名称 | human OX1R fusion protein to P.abysii glycogen synthase, [(7R)-4-(5-chloro-1,3-benzoxazol-2-yl)-7-methyl-1,4-diazepan-1-yl][5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl]methanone, OLEIC ACID, ... (4 entities in total) |
機能のキーワード | orexin, suvorexant, sb674042, signaling protein |
由来する生物種 | Homo sapiens (Human) 詳細 |
細胞内の位置 | Cell membrane; Multi-pass membrane protein: O43613 |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 64830.72 |
構造登録者 | Yin, J.,Brautigam, C.A.,Shao, Z.,Clark, L.,Harrell, C.M.,Gotter, A.L.,Coleman, P.,Renger, J.J.,Rosenbaum, D.M. (登録日: 2015-04-29, 公開日: 2016-03-09, 最終更新日: 2024-10-23) |
主引用文献 | Yin, J.,Babaoglu, K.,Brautigam, C.A.,Clark, L.,Shao, Z.,Scheuermann, T.H.,Harrell, C.M.,Gotter, A.L.,Roecker, A.J.,Winrow, C.J.,Renger, J.J.,Coleman, P.J.,Rosenbaum, D.M. Structure and ligand-binding mechanism of the human OX1 and OX2 orexin receptors. Nat.Struct.Mol.Biol., 23:293-299, 2016 Cited by PubMed Abstract: The orexin (also known as hypocretin) G protein-coupled receptors (GPCRs) regulate sleep and other behavioral functions in mammals, and are therapeutic targets for sleep and wake disorders. The human receptors hOX1R and hOX2R, which are 64% identical in sequence, have overlapping but distinct physiological functions and potential therapeutic profiles. We determined structures of hOX1R bound to the OX1R-selective antagonist SB-674042 and the dual antagonist suvorexant at 2.8-Å and 2.75-Å resolution, respectively, and used molecular modeling to illuminate mechanisms of antagonist subtype selectivity between hOX1R and hOX2R. The hOX1R structures also reveal a conserved amphipathic α-helix, in the extracellular N-terminal region, that interacts with orexin-A and is essential for high-potency neuropeptide activation at both receptors. The orexin-receptor crystal structures are valuable tools for the design and development of selective orexin-receptor antagonists and agonists. PubMed: 26950369DOI: 10.1038/nsmb.3183 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.751 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
