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9KT9

Cryo-EM structure of HCA1-Gi complex with 3,5-DHBA

Summary for 9KT9
Entry DOI10.2210/pdb9kt9/pdb
EMDB information62560
DescriptorGuanine 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 Keywordsg-protein-coupled receptors; hydroxycarboxylic acid receptors, cryo-em; signaling protein, signaling protein/immune system, signaling protein-immune system complex
Biological sourceHomo sapiens (human)
More
Total number of polymer chains5
Total formula weight153866.45
Authors
Wu, S. (deposition date: 2024-12-02, release date: 2025-12-10)
Primary citationWang, J.,Qian, Y.,Han, Z.,Wang, Y.,Liu, Y.,Li, J.,Duanmu, Q.,Ye, S.,Qiao, A.,Wu, S.
Insights into the Activation Mechanism of HCA1, HCA2, and HCA3.
J.Med.Chem., 68:4527-4539, 2025
Cited by
PubMed Abstract: Hydroxy-carboxylic acid receptors HCA1, HCA2, and HCA3 can be activated by important intermediates of energy metabolism. Despite the research focusing on HCA2, its clinical application has been limited by adverse effects. Therefore, the role of HCA1 as a promising target for the treatment of lipolysis warrants further exploration. As HCAs exhibit high similarity when activated with diverse selective agonists, a conserved yet unique activation mechanism for HCAs remains undisclosed. Herein, we unveil the cryo-electron microscopy structures of the 3,5-DHBA-HCA1-Gi signaling complex, the acifran- and MK6892-bound HCA2-Gi signaling complexes, and the acifran-HCA3-Gi signaling complex. Comparative analysis across HCAs reveals key residues in HCA1 contributing to the stabilization of the ligand-binding pocket. Furthermore, chimeric complexes and mutational analyses identify residues that are pivotal for HCA2 and HCA3 selectivity. Our findings elucidate critical structural insights into the mechanisms of ligand recognition and activation within HCA1 and broaden our comprehension of ligand specificity binding across the HCA family.
PubMed: 39936872
DOI: 10.1021/acs.jmedchem.4c02567
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.7 Å)
Structure validation

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