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8X83

The cryo-EM structure of insect gustatory receptor Gr43a I418A from Drosophila melanogaster in complex with fructose

Summary for 8X83
Entry DOI10.2210/pdb8x83/pdb
EMDB information38134
DescriptorGustatory receptor for sugar taste 43a, SODIUM ION, beta-D-fructofuranose, ... (4 entities in total)
Functional Keywordsgustatory receptor, ligand-gated ion channel, gr43a, fructose, membrane protein
Biological sourceDrosophila melanogaster (fruit fly)
Total number of polymer chains4
Total formula weight197835.85
Authors
Ma, D.,Guo, J. (deposition date: 2023-11-27, release date: 2024-02-07, Last modification date: 2024-03-06)
Primary citationMa, D.,Hu, M.,Yang, X.,Liu, Q.,Ye, F.,Cai, W.,Wang, Y.,Xu, X.,Chang, S.,Wang, R.,Yang, W.,Ye, S.,Su, N.,Fan, M.,Xu, H.,Guo, J.
Structural basis for sugar perception by Drosophila gustatory receptors.
Science, 383:eadj2609-eadj2609, 2024
Cited by
PubMed Abstract: Insects rely on a family of seven transmembrane proteins called gustatory receptors (GRs) to encode different taste modalities, such as sweet and bitter. We report structures of sweet taste receptors GR43a and GR64a in the apo and sugar-bound states. Both GRs form tetrameric sugar-gated cation channels composed of one central pore domain (PD) and four peripheral ligand-binding domains (LBDs). Whereas GR43a is specifically activated by the monosaccharide fructose that binds to a narrow pocket in LBDs, disaccharides sucrose and maltose selectively activate GR64a by binding to a larger and flatter pocket in LBDs. Sugar binding to LBDs induces local conformational changes, which are subsequently transferred to the PD to cause channel opening. Our studies reveal a structural basis for sugar recognition and activation of GRs.
PubMed: 38305684
DOI: 10.1126/science.adj2609
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.8 Å)
Structure validation

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