4K5Y
Crystal structure of human corticotropin-releasing factor receptor 1 (CRF1R) in complex with the antagonist CP-376395
4K5Y の概要
エントリーDOI | 10.2210/pdb4k5y/pdb |
関連するPDBエントリー | 3EHS 3EHT 3EHU |
分子名称 | Corticotropin-releasing factor receptor 1, T4-Lysozyme chimeric construct, 3,6-dimethyl-N-(pentan-3-yl)-2-(2,4,6-trimethylphenoxy)pyridin-4-amine, OLEIC ACID, ... (8 entities in total) |
機能のキーワード | 7tm, gpcr, family b, signalling protein, g-protein, membrane, membrane protein, receptor |
由来する生物種 | HOMO SAPIENS (human) 詳細 |
細胞内の位置 | Cell membrane; Multi-pass membrane protein: P34998 |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 156772.32 |
構造登録者 | Hollenstein, K.,Kean, J.,Bortolato, A.,Cheng, R.K.Y.,Dore, A.S.,Jazayeri, A.,Cooke, R.M.,Weir, M.,Marshall, F.H. (登録日: 2013-04-15, 公開日: 2013-07-17, 最終更新日: 2023-09-20) |
主引用文献 | Hollenstein, K.,Kean, J.,Bortolato, A.,Cheng, R.K.,Dore, A.S.,Jazayeri, A.,Cooke, R.M.,Weir, M.,Marshall, F.H. Structure of class B GPCR corticotropin-releasing factor receptor 1. Nature, 499:438-443, 2013 Cited by PubMed Abstract: Structural analysis of class B G-protein-coupled receptors (GPCRs), cell-surface proteins that respond to peptide hormones, has been restricted to the amino-terminal extracellular domain, thus providing little understanding of the membrane-spanning signal transduction domain. The corticotropin-releasing factor receptor type 1 is a class B receptor which mediates the response to stress and has been considered a drug target for depression and anxiety. Here we report the crystal structure of the transmembrane domain of the human corticotropin-releasing factor receptor type 1 in complex with the small-molecule antagonist CP-376395. The structure provides detailed insight into the architecture of class B receptors. Atomic details of the interactions of the receptor with the non-peptide ligand that binds deep within the receptor are described. This structure provides a model for all class B GPCRs and may aid in the design of new small-molecule drugs for diseases of brain and metabolism. PubMed: 23863939DOI: 10.1038/nature12357 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.977 Å) |
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