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9AXF

Structure of human calcium-sensing receptor in complex with chimeric Gq (miniGisq) protein in detergent

Summary for 9AXF
Entry DOI10.2210/pdb9axf/pdb
EMDB information43966
DescriptorExtracellular calcium-sensing receptor, PHOSPHATE ION, CALCIUM ION, ... (15 entities in total)
Functional Keywordscalcium-sensing receptor, g-protein-coupled receptor, g protein, signal transduction, membrane protein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains7
Total formula weight340556.71
Authors
Primary citationZuo, H.,Park, J.,Frangaj, A.,Ye, J.,Lu, G.,Manning, J.J.,Asher, W.B.,Lu, Z.,Hu, G.B.,Wang, L.,Mendez, J.,Eng, E.,Zhang, Z.,Lin, X.,Grassucci, R.,Hendrickson, W.A.,Clarke, O.B.,Javitch, J.A.,Conigrave, A.D.,Fan, Q.R.
Promiscuous G-protein activation by the calcium-sensing receptor.
Nature, 629:481-488, 2024
Cited by
PubMed Abstract: The human calcium-sensing receptor (CaSR) detects fluctuations in the extracellular Ca concentration and maintains Ca homeostasis. It also mediates diverse cellular processes not associated with Ca balance. The functional pleiotropy of CaSR arises in part from its ability to signal through several G-protein subtypes. We determined structures of CaSR in complex with G proteins from three different subfamilies: G, G and G. We found that the homodimeric CaSR of each complex couples to a single G protein through a common mode. This involves the C-terminal helix of each Gα subunit binding to a shallow pocket that is formed in one CaSR subunit by all three intracellular loops (ICL1-ICL3), an extended transmembrane helix 3 and an ordered C-terminal region. G-protein binding expands the transmembrane dimer interface, which is further stabilized by phospholipid. The restraint imposed by the receptor dimer, in combination with ICL2, enables G-protein activation by facilitating conformational transition of Gα. We identified a single Gα residue that determines G and G versus G selectivity. The length and flexibility of ICL2 allows CaSR to bind all three Gα subtypes, thereby conferring capacity for promiscuous G-protein coupling.
PubMed: 38632411
DOI: 10.1038/s41586-024-07331-1
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.5 Å)
Structure validation

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