4F11

Crystal structure of the extracellular domain of human GABA(B) receptor GBR2

4F11 の概要

• エントリーDOI: 10.2210/pdb4f11/pdb
• 分子名称: Gamma-aminobutyric acid type B receptor subunit 2 (2 entities in total)
• 機能のキーワード: venus flytrap module, g-protein coupled receptor, signaling protein
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Cell membrane; Multi-pass membrane protein: O75899
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 49127.49

構造登録者

Geng, Y.,Xiong, D.,Mosyak, L.,Malito, D.L.,Kniazeff, J.,Chen, Y.,Burmakina, S.,Quick, M.,Bush, M.,Javitch, J.A.,Pin, J.-P.,Fan, Q.R. (登録日: 2012-05-05, 公開日: 2012-06-06, 最終更新日: 2024-11-20)

主引用文献

Geng, Y.,Xiong, D.,Mosyak, L.,Malito, D.L.,Kniazeff, J.,Chen, Y.,Burmakina, S.,Quick, M.,Bush, M.,Javitch, J.A.,Pin, J.P.,Fan, Q.R.
Structure and functional interaction of the extracellular domain of human GABA(B) receptor GBR2.
Nat.Neurosci., 15:970-978, 2012

PubMed Abstract: Inhibitory neurotransmission is mediated primarily by GABA. The metabotropic GABA(B) receptor is a G protein-coupled receptor central to mammalian brain function. Malfunction of GABA(B) receptor has been implicated in several neurological disorders. GABA(B) receptor functions as a heterodimeric assembly of GBR1 and GBR2 subunits, where GBR1 is responsible for ligand-binding and GBR2 is responsible for G protein coupling. Here we demonstrate that the GBR2 ectodomain directly interacts with the GBR1 ectodomain to increase agonist affinity by selectively stabilizing the agonist-bound conformation of GBR1. We present the crystal structure of the GBR2 ectodomain, which reveals a polar heterodimeric interface. We also identify specific heterodimer contacts from both subunits, and GBR1 residues involved in ligand recognition. Lastly, our structural and functional data indicate that the GBR2 ectodomain adopts a constitutively open conformation, suggesting a structural asymmetry in the active state of GABA(B) receptor that is unique to the GABAergic system.

PubMed: 22660477
DOI: 10.1038/nn.3133

実験手法

X-RAY DIFFRACTION (2.38 Å)