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9LKD

Cryo-EM structure of the receptor of PL45-Olfr110-Gs complex

This is a non-PDB format compatible entry.
Summary for 9LKD
Entry DOI10.2210/pdb9lkd/pdb
EMDB information63175
DescriptorOlfactory receptor, methyl (9R,10E,12E)-9-methoxyoctadeca-10,12-dienoate (2 entities in total)
Functional Keywordsolfr110, receptor, membrane protein
Biological sourceMus musculus (house mouse)
Total number of polymer chains1
Total formula weight36112.67
Authors
Rong, N.K.,Zhang, M.H.,Yang, F.,Sun, J.P. (deposition date: 2025-01-16, release date: 2026-01-21, Last modification date: 2026-02-18)
Primary citationHan, X.,Zhang, M.H.,Rong, N.K.,Zhu, K.K.,Pei, Y.,Ge, X.Y.,Liu, Q.,Lu, H.,Liu, J.,Zhang, L.J.,Bao, H.Q.,Pi, J.H.,Fan, L.,Fu, Y.,Shao, X.H.,Yan, W.Q.,Gao, X.H.,Zhang, M.Y.,Guo, L.L.,Lu, Y.,Ning, S.L.,Zhang, H.,Xu, Y.F.,Feng, X.Y.,Cheng, J.,Xia, M.,Li, Q.,Yu, X.,Yang, F.,Sun, J.P.
Mechanistic insights into fatty acid odor detection mediated by class II olfactory receptors.
Cell, 2026
Cited by
PubMed Abstract: Smell is one of the fundamental senses mediated by thousands of odorant receptors (ORs). How hydrophobic and volatile odor molecules are recognized by class II ORs remains elusive. Here, we present cryo-electron microscopy (cryo-EM) structures of class II OR Olfr110 complexed with the unsaturated fatty acid metabolite (UFAM) PL45, Gs, and cons-OR5. The structural study revealed an unusually large hydrophobic pocket accommodating PL45 and the endogenous agonist 12(S)-hydroxyeicosapentaenoic acid (12(S)-HEPE). This pocket is decorated with polar residues and aromatic residue arrays, constituting polar networks and π-π interactions with the natural agonist PL45, respectively. Conserved motifs in the type II OR5 subfamily responsible for ligand recognition are characterized. The inward movement of extracellular loop 3 (ECL3) and an unconventional activation mechanism underlie Olfr110 activation. At the G protein interface, Olfr110 displays common and unique interactions. Overall, we revealed the structural basis of odor recognition and the activation mechanism of class II ORs, which may facilitate drug development targeting these receptors.
PubMed: 41570821
DOI: 10.1016/j.cell.2025.12.018
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.6 Å)
Structure validation

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PDB entries from 2026-03-04

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