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7CMU

Dopamine Receptor D3R-Gi-Pramipexole complex

7CMU の概要
エントリーDOI10.2210/pdb7cmu/pdb
EMDBエントリー30410
分子名称Guanine nucleotide-binding protein G(i) subunit alpha-1, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, ... (6 entities in total)
機能のキーワードg protein-coupled receptor, dopamine receptor, 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173685.30
構造登録者
主引用文献Xu, P.,Huang, S.,Mao, C.,Krumm, B.E.,Zhou, X.E.,Tan, Y.,Huang, X.P.,Liu, Y.,Shen, D.D.,Jiang, Y.,Yu, X.,Jiang, H.,Melcher, K.,Roth, B.L.,Cheng, X.,Zhang, Y.,Xu, H.E.
Structures of the human dopamine D3 receptor-G i complexes.
Mol.Cell, 81:1147-, 2021
Cited by
PubMed Abstract: The dopamine system, including five dopamine receptors (D1R-D5R), plays essential roles in the central nervous system (CNS), and ligands that activate dopamine receptors have been used to treat many neuropsychiatric disorders. Here, we report two cryo-EM structures of human D3R in complex with an inhibitory G protein and bound to the D3R-selective agonists PD128907 and pramipexole, the latter of which is used to treat patients with Parkinson's disease. The structures reveal agonist binding modes distinct from the antagonist-bound D3R structure and conformational signatures for ligand-induced receptor activation. Mutagenesis and homology modeling illuminate determinants of ligand specificity across dopamine receptors and the mechanisms for G protein coupling. Collectively our work reveals the basis of agonist binding and ligand-induced receptor activation and provides structural templates for designing specific ligands to treat CNS diseases targeting the dopaminergic system.
PubMed: 33548201
DOI: 10.1016/j.molcel.2021.01.003
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3 Å)
構造検証レポート
Validation report summary of 7cmu
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2025-10-15に公開中

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