6DDE
Mu Opioid Receptor-Gi Protein Complex
Summary for 6DDE
Entry DOI | 10.2210/pdb6dde/pdb |
Related | 6DDF |
EMDB information | 7868 7869 |
Related PRD ID | PRD_002308 |
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 | complex, transmembrane, membrane protein |
Biological source | Homo sapiens (Human) More |
Total number of polymer chains | 6 |
Total formula weight | 154240.86 |
Authors | Koehl, A.,Hu, H.,Maeda, S.,Manglik, A.,Zhang, Y.,Kobilka, B.K.,Skiniotis, G.,Weis, W.I. (deposition date: 2018-05-10, release date: 2018-06-13, Last modification date: 2024-10-30) |
Primary citation | Koehl, A.,Hu, H.,Maeda, S.,Zhang, Y.,Qu, Q.,Paggi, J.M.,Latorraca, N.R.,Hilger, D.,Dawson, R.,Matile, H.,Schertler, G.F.X.,Granier, S.,Weis, W.I.,Dror, R.O.,Manglik, A.,Skiniotis, G.,Kobilka, B.K. Structure of the mu-opioid receptor-Giprotein complex. Nature, 558:547-552, 2018 Cited by PubMed Abstract: The μ-opioid receptor (μOR) is a G-protein-coupled receptor (GPCR) and the target of most clinically and recreationally used opioids. The induced positive effects of analgesia and euphoria are mediated by μOR signalling through the adenylyl cyclase-inhibiting heterotrimeric G protein G. Here we present the 3.5 Å resolution cryo-electron microscopy structure of the μOR bound to the agonist peptide DAMGO and nucleotide-free G. DAMGO occupies the morphinan ligand pocket, with its N terminus interacting with conserved receptor residues and its C terminus engaging regions important for opioid-ligand selectivity. Comparison of the μOR-G complex to previously determined structures of other GPCRs bound to the stimulatory G protein G reveals differences in the position of transmembrane receptor helix 6 and in the interactions between the G protein α-subunit and the receptor core. Together, these results shed light on the structural features that contribute to the G protein-coupling specificity of the µOR. PubMed: 29899455DOI: 10.1038/s41586-018-0219-7 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (3.5 Å) |
Structure validation
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