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9LMO

Cryo-EM structure of human apo inactive GPR4

9LMO の概要
エントリーDOI10.2210/pdb9lmo/pdb
EMDBエントリー39864 63219
分子名称Heavy chain of anti-Bril Fab, anti-Fab Nanobody, Light chain of anti-Bril Fab, ... (4 entities in total)
機能のキーワードgpcr, class a, gpr4, cryo-em, protein sensing, inactive state, membrane protein/immune system, membrane protein-immune system complex
由来する生物種Homo sapiens
詳細
タンパク質・核酸の鎖数4
化学式量合計114766.63
構造登録者
主引用文献Chen, L.N.,Zhou, H.,Xi, K.,Cheng, S.,Liu, Y.,Fu, Y.,Ma, X.,Xu, P.,Ji, S.Y.,Wang, W.W.,Shen, D.D.,Zhang, H.,Shen, Q.,Chai, R.,Zhang, M.,Yang, L.,Han, F.,Mao, C.,Cai, X.,Zhang, Y.
Proton perception and activation of a proton-sensing GPCR.
Mol.Cell, 85:1640-1657.e8, 2025
Cited by
PubMed Abstract: Maintaining pH at cellular, tissular, and systemic levels is essential for human health. Proton-sensing GPCRs regulate physiological and pathological processes by sensing the extracellular acidity. However, the molecular mechanism of proton sensing and activation of these receptors remains elusive. Here, we present cryoelectron microscopy (cryo-EM) structures of human GPR4, a prototypical proton-sensing GPCR, in its inactive and active states. Our studies reveal that three extracellular histidine residues are crucial for proton sensing of human GPR4. The binding of protons induces substantial conformational changes in GPR4's ECLs, particularly in ECL2, which transforms from a helix-loop to a β-turn-β configuration. This transformation leads to the rearrangements of H-bond network and hydrophobic packing, relayed by non-canonical motifs to accommodate G proteins. Furthermore, the antagonist NE52-QQ57 hinders human GPR4 activation by preventing hydrophobic stacking rearrangement. Our findings provide a molecular framework for understanding the activation mechanism of a human proton-sensing GPCR, aiding future drug discovery.
PubMed: 40215960
DOI: 10.1016/j.molcel.2025.02.030
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3.2 Å)
構造検証レポート
Validation report summary of 9lmo
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-02-04に公開中

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