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7CX2

Cryo-EM structure of the PGE2-bound EP2-Gs complex

7CX2 の概要
エントリーDOI10.2210/pdb7cx2/pdb
EMDBエントリー30489
分子名称Prostaglandin E2 receptor EP2 subtype, Guanine nucleotide-binding protein G(s) subunit alpha isoforms short, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ... (7 entities in total)
機能のキーワードgpcr, ep2, complex, pge2, 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147072.07
構造登録者
主引用文献Qu, C.,Mao, C.,Xiao, P.,Shen, Q.,Zhong, Y.N.,Yang, F.,Shen, D.D.,Tao, X.,Zhang, H.,Yan, X.,Zhao, R.J.,He, J.,Guan, Y.,Zhang, C.,Hou, G.,Zhang, P.J.,Hou, G.,Li, Z.,Yu, X.,Chai, R.J.,Guan, Y.F.,Sun, J.P.,Zhang, Y.
Ligand recognition, unconventional activation, and G protein coupling of the prostaglandin E 2 receptor EP2 subtype.
Sci Adv, 7:-, 2021
Cited by
PubMed Abstract: Selective modulation of the heterotrimeric G protein α S subunit-coupled prostaglandin E (PGE) receptor EP2 subtype is a promising therapeutic strategy for osteoporosis, ocular hypertension, neurodegenerative diseases, and cardiovascular disorders. Here, we report the cryo-electron microscopy structure of the EP2-G complex with its endogenous agonist PGE and two synthesized agonists, taprenepag and evatanepag (CP-533536). These structures revealed distinct features of EP2 within the EP receptor family in terms of its unconventional receptor activation and G protein coupling mechanisms, including activation in the absence of a typical W "toggle switch" and coupling to G via helix 8. Moreover, inspection of the agonist-bound EP2 structures uncovered key motifs governing ligand selectivity. Our study provides important knowledge for agonist recognition and activation mechanisms of EP2 and will facilitate the rational design of drugs targeting the PGE signaling system.
PubMed: 33811074
DOI: 10.1126/sciadv.abf1268
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.8 Å)
構造検証レポート
Validation report summary of 7cx2
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2024-11-20に公開中

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