6PB0
Cryo-EM structure of Urocortin 1-bound Corticotropin-releasing factor 1 receptor in complex with Gs protein and Nb35
Summary for 6PB0
Entry DOI | 10.2210/pdb6pb0/pdb |
EMDB information | 20284 |
Descriptor | Corticotropin-releasing factor receptor 1, Urocortin, Guanine nucleotide-binding protein G(s) subunit alpha isoforms short,Guanine nucleotide-binding protein G(i) subunit alpha-1,Guanine nucleotide-binding protein G(s) subunit alpha isoforms short, ... (8 entities in total) |
Functional Keywords | corticotropin-releasing factor 1 receptor, urocortins1, gs protein, gpcr, signaling protein |
Biological source | Homo sapiens (Human) More |
Total number of polymer chains | 6 |
Total formula weight | 156958.67 |
Authors | Ma, S.,Shen, Q.,Zhao, L.-H.,Mao, C.,Zhou, X.E.,Shen, D.-D.,de Waal, P.W.,Bi, P.,Li, C.,Jiang, Y.,Wang, M.-W.,Sexton, P.M.,Wootten, D.,Melcher, K.,Zhang, Y.,Xu, H.E. (deposition date: 2019-06-12, release date: 2020-02-12, Last modification date: 2024-10-23) |
Primary citation | Ma, S.,Shen, Q.,Zhao, L.H.,Mao, C.,Zhou, X.E.,Shen, D.D.,de Waal, P.W.,Bi, P.,Li, C.,Jiang, Y.,Wang, M.W.,Sexton, P.M.,Wootten, D.,Melcher, K.,Zhang, Y.,Xu, H.E. Molecular Basis for Hormone Recognition and Activation of Corticotropin-Releasing Factor Receptors. Mol.Cell, 77:669-, 2020 Cited by PubMed Abstract: Corticotropin-releasing factor (CRF) and the three related peptides urocortins 1-3 (UCN1-UCN3) are endocrine hormones that control the stress responses by activating CRF1R and CRF2R, two members of class B G-protein-coupled receptors (GPCRs). Here, we present two cryoelectron microscopy (cryo-EM) structures of UCN1-bound CRF1R and CRF2R with the stimulatory G protein. In both structures, UCN1 adopts a single straight helix with its N terminus dipped into the receptor transmembrane bundle. Although the peptide-binding residues in CRF1R and CRF2R are different from other members of class B GPCRs, the residues involved in receptor activation and G protein coupling are conserved. In addition, both structures reveal bound cholesterol molecules to the receptor transmembrane helices. Our structures define the basis of ligand-binding specificity in the CRF receptor-hormone system, establish a common mechanism of class B GPCR activation and G protein coupling, and provide a paradigm for studying membrane protein-lipid interactions for class B GPCRs. PubMed: 32004470DOI: 10.1016/j.molcel.2020.01.013 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (3 Å) |
Structure validation
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