6LI3
cryo-EM structure of GPR52-miniGs-NB35
6LI3 の概要
エントリーDOI | 10.2210/pdb6li3/pdb |
関連するPDBエントリー | 6LI2 |
EMDBエントリー | 0902 |
分子名称 | G-protein coupled receptor 52, Guanine nucleotide-binding protein G(s) subunit alpha isoforms short, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ... (5 entities in total) |
機能のキーワード | g-protein coupled receptor, orphan gpcr, self-activation, cryo-em, membrane protein |
由来する生物種 | Homo sapiens (Human) 詳細 |
タンパク質・核酸の鎖数 | 5 |
化学式量合計 | 129352.70 |
構造登録者 | |
主引用文献 | Lin, X.,Li, M.,Wang, N.,Wu, Y.,Luo, Z.,Guo, S.,Han, G.W.,Li, S.,Yue, Y.,Wei, X.,Xie, X.,Chen, Y.,Zhao, S.,Wu, J.,Lei, M.,Xu, F. Structural basis of ligand recognition and self-activation of orphan GPR52. Nature, 579:152-157, 2020 Cited by PubMed Abstract: GPR52 is a class-A orphan G-protein-coupled receptor that is highly expressed in the brain and represents a promising therapeutic target for the treatment of Huntington's disease and several psychiatric disorders. Pathological malfunction of GPR52 signalling occurs primarily through the heterotrimeric G protein, but it is unclear how GPR52 and G couple for signal transduction and whether a native ligand or other activating input is required. Here we present the high-resolution structures of human GPR52 in three states: a ligand-free state, a G-coupled self-activation state and a potential allosteric ligand-bound state. Together, our structures reveal that extracellular loop 2 occupies the orthosteric binding pocket and operates as a built-in agonist, conferring an intrinsically high level of basal activity to GPR52. A fully active state is achieved when G is coupled to GPR52 in the absence of an external agonist. The receptor also features a side pocket for ligand binding. These insights into the structure and function of GPR52 could improve our understanding of other self-activated GPCRs, enable the identification of endogenous and tool ligands, and guide drug discovery efforts that target GPR52. PubMed: 32076264DOI: 10.1038/s41586-020-2019-0 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (3.32 Å) |
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