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9ASB

Structure of human calcium-sensing receptor in complex with chimeric Gq (miniGisq) protein in nanodiscs

これはPDB形式変換不可エントリーです。
9ASB の概要
エントリーDOI10.2210/pdb9asb/pdb
EMDBエントリー43811
分子名称Isoform 1 of Extracellular calcium-sensing receptor, 3-(2-chlorophenyl)-N-[(1R)-1-(3-methoxyphenyl)ethyl]propan-1-amine, CHOLESTEROL HEMISUCCINATE, ... (12 entities in total)
機能のキーワードcalcium-sensing receptor, g-protein-coupled receptor, g protein, signal transduction, 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286041.54
構造登録者
主引用文献Zuo, H.,Park, J.,Frangaj, A.,Ye, J.,Lu, G.,Manning, J.J.,Asher, W.B.,Lu, Z.,Hu, G.B.,Wang, L.,Mendez, J.,Eng, E.,Zhang, Z.,Lin, X.,Grassucci, R.,Hendrickson, W.A.,Clarke, O.B.,Javitch, J.A.,Conigrave, A.D.,Fan, Q.R.
Promiscuous G-protein activation by the calcium-sensing receptor.
Nature, 629:481-488, 2024
Cited by
PubMed Abstract: The human calcium-sensing receptor (CaSR) detects fluctuations in the extracellular Ca concentration and maintains Ca homeostasis. It also mediates diverse cellular processes not associated with Ca balance. The functional pleiotropy of CaSR arises in part from its ability to signal through several G-protein subtypes. We determined structures of CaSR in complex with G proteins from three different subfamilies: G, G and G. We found that the homodimeric CaSR of each complex couples to a single G protein through a common mode. This involves the C-terminal helix of each Gα subunit binding to a shallow pocket that is formed in one CaSR subunit by all three intracellular loops (ICL1-ICL3), an extended transmembrane helix 3 and an ordered C-terminal region. G-protein binding expands the transmembrane dimer interface, which is further stabilized by phospholipid. The restraint imposed by the receptor dimer, in combination with ICL2, enables G-protein activation by facilitating conformational transition of Gα. We identified a single Gα residue that determines G and G versus G selectivity. The length and flexibility of ICL2 allows CaSR to bind all three Gα subtypes, thereby conferring capacity for promiscuous G-protein coupling.
PubMed: 38632411
DOI: 10.1038/s41586-024-07331-1
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3.4 Å)
構造検証レポート
Validation report summary of 9asb
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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