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7S8O

CryoEM structure of Gi-coupled MRGPRX2 with small molecule agonist (R)-Zinc-3573

Summary for 7S8O
Entry DOI10.2210/pdb7s8o/pdb
EMDB information24899
DescriptorSoluble cytochrome b562,Mas-related G-protein coupled receptor member X2 chimera, Guanine nucleotide-binding protein G(i) subunit alpha-1, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ... (6 entities in total)
Functional Keywordsgpcr, signaling protein
Biological sourceEscherichia coli
More
Total number of polymer chains5
Total formula weight170724.22
Authors
Cao, C.,Fay, J.F.,Gumpper, R.H.,Roth, B.L. (deposition date: 2021-09-18, release date: 2021-11-17, Last modification date: 2025-05-28)
Primary citationCao, C.,Kang, H.J.,Singh, I.,Chen, H.,Zhang, C.,Ye, W.,Hayes, B.W.,Liu, J.,Gumpper, R.H.,Bender, B.J.,Slocum, S.T.,Krumm, B.E.,Lansu, K.,McCorvy, J.D.,Kroeze, W.K.,English, J.G.,DiBerto, J.F.,Olsen, R.H.J.,Huang, X.P.,Zhang, S.,Liu, Y.,Kim, K.,Karpiak, J.,Jan, L.Y.,Abraham, S.N.,Jin, J.,Shoichet, B.K.,Fay, J.F.,Roth, B.L.
Structure, function and pharmacology of human itch GPCRs.
Nature, 600:170-175, 2021
Cited by
PubMed Abstract: The MRGPRX family of receptors (MRGPRX1-4) is a family of mas-related G-protein-coupled receptors that have evolved relatively recently. Of these, MRGPRX2 and MRGPRX4 are key physiological and pathological mediators of itch and related mast cell-mediated hypersensitivity reactions. MRGPRX2 couples to both G and G in mast cells. Here we describe agonist-stabilized structures of MRGPRX2 coupled to G and G in ternary complexes with the endogenous peptide cortistatin-14 and with a synthetic agonist probe, respectively, and the development of potent antagonist probes for MRGPRX2. We also describe a specific MRGPRX4 agonist and the structure of this agonist in a complex with MRGPRX4 and G. Together, these findings should accelerate the structure-guided discovery of therapeutic agents for pain, itch and mast cell-mediated hypersensitivity.
PubMed: 34789874
DOI: 10.1038/s41586-021-04126-6
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.58 Å)
Structure validation

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