7CMV
Dopamine Receptor D3R-Gi-PD128907 complex
Summary for 7CMV
Entry DOI | 10.2210/pdb7cmv/pdb |
EMDB information | 30411 |
Descriptor | 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) |
Functional Keywords | g protein-coupled receptor, dopamine receptor, membrane protein |
Biological source | Homo sapiens (Human) More |
Total number of polymer chains | 5 |
Total formula weight | 173723.28 |
Authors | |
Primary citation | 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: 33548201DOI: 10.1016/j.molcel.2021.01.003 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.7 Å) |
Structure validation
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