5DSG

Structure of the M4 muscarinic acetylcholine receptor (M4-mT4L) bound to tiotropium

5DSG の概要

• エントリーDOI: 10.2210/pdb5dsg/pdb
• 分子名称: Muscarinic acetylcholine receptor M4,Endolysin,Endolysin,Muscarinic acetylcholine receptor M4, (1R,2R,4S,5S,7S)-7-{[hydroxy(dithiophen-2-yl)acetyl]oxy}-9,9-dimethyl-3-oxa-9-azoniatricyclo[3.3.1.0~2,4~]nonane, OLEIC ACID, ... (8 entities in total)
• 機能のキーワード: membrane, gpcr, signaling, antagonist, membrane protein
• 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: 100704.59

構造登録者

Thal, D.M.,Kobilka, B.K.,Sexton, P.M.,Christopoulos, A. (登録日: 2015-09-17, 公開日: 2016-03-16, 最終更新日: 2024-11-20)

主引用文献

Thal, D.M.,Sun, B.,Feng, D.,Nawaratne, V.,Leach, K.,Felder, C.C.,Bures, M.G.,Evans, D.A.,Weis, W.I.,Bachhawat, P.,Kobilka, T.S.,Sexton, P.M.,Kobilka, B.K.,Christopoulos, A.
Crystal structures of the M1 and M4 muscarinic acetylcholine receptors.
Nature, 531:335-340, 2016

PubMed Abstract: Muscarinic M1-M5 acetylcholine receptors are G-protein-coupled receptors that regulate many vital functions of the central and peripheral nervous systems. In particular, the M1 and M4 receptor subtypes have emerged as attractive drug targets for treatments of neurological disorders, such as Alzheimer's disease and schizophrenia, but the high conservation of the acetylcholine-binding pocket has spurred current research into targeting allosteric sites on these receptors. Here we report the crystal structures of the M1 and M4 muscarinic receptors bound to the inverse agonist, tiotropium. Comparison of these structures with each other, as well as with the previously reported M2 and M3 receptor structures, reveals differences in the orthosteric and allosteric binding sites that contribute to a role in drug selectivity at this important receptor family. We also report identification of a cluster of residues that form a network linking the orthosteric and allosteric sites of the M4 receptor, which provides new insight into how allosteric modulation may be transmitted between the two spatially distinct domains.

PubMed: 26958838
DOI: 10.1038/nature17188

実験手法

X-RAY DIFFRACTION (2.6 Å)