7C7S
Cryo-EM structure of the CGP54626-bound human GABA(B) receptor in inactive state.
7C7S の概要
| エントリーDOI | 10.2210/pdb7c7s/pdb |
| EMDBエントリー | 30301 |
| 分子名称 | Gamma-aminobutyric acid type B receptor subunit 1, Gamma-aminobutyric acid type B receptor subunit 2, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total) |
| 機能のキーワード | gabab, cryo-em, gpcr, 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 | 199513.71 |
| 構造登録者 | |
| 主引用文献 | Mao, C.,Shen, C.,Li, C.,Shen, D.D.,Xu, C.,Zhang, S.,Zhou, R.,Shen, Q.,Chen, L.N.,Jiang, Z.,Liu, J.,Zhang, Y. Cryo-EM structures of inactive and active GABABreceptor. Cell Res., 30:564-573, 2020 Cited by PubMed Abstract: Metabotropic GABA G protein-coupled receptor functions as a mandatory heterodimer of GB1 and GB2 subunits and mediates inhibitory neurotransmission in the central nervous system. Each subunit is composed of the extracellular Venus flytrap (VFT) domain and transmembrane (TM) domain. Here we present cryo-EM structures of full-length human heterodimeric GABA receptor in the antagonist-bound inactive state and in the active state complexed with an agonist and a positive allosteric modulator in the presence of G protein at a resolution range of 2.8-3.0 Å. Our structures reveal that agonist binding stabilizes the closure of GB1 VFT, which in turn triggers a rearrangement of TM interfaces between the two subunits from TM3-TM5/TM3-TM5 in the inactive state to TM6/TM6 in the active state and finally induces the opening of intracellular loop 3 and synergistic shifting of TM3, 4 and 5 helices in GB2 TM domain to accommodate the α5-helix of G. We also observed that the positive allosteric modulator anchors at the dimeric interface of TM domains. These results provide a structural framework for understanding class C GPCR activation and a rational template for allosteric modulator design targeting the dimeric interface of GABA receptor. PubMed: 32494023DOI: 10.1038/s41422-020-0350-5 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (2.9 Å) |
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