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8X9S

Identification, structure and agonist design of an androgen membrane receptor.

Summary for 8X9S
Entry DOI10.2210/pdb8x9s/pdb
EMDB information38183
DescriptorGuanine 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, Adhesion G-protein coupled receptor D1, ... (5 entities in total)
Functional Keywordscomplex, agonist, gpcr, membrane protein
Biological sourceRattus norvegicus (Norway rat)
More
Total number of polymer chains4
Total formula weight153504.18
Authors
Ping, Y.Q.,Yang, Z. (deposition date: 2023-12-01, release date: 2025-02-12, Last modification date: 2025-04-09)
Primary citationYang, Z.,Ping, Y.Q.,Wang, M.W.,Zhang, C.,Zhou, S.H.,Xi, Y.T.,Zhu, K.K.,Ding, W.,Zhang, Q.Y.,Song, Z.C.,Zhao, R.J.,He, Z.L.,Wang, M.X.,Qi, L.,Ullmann, C.,Ricken, A.,Schoneberg, T.,Gan, Z.J.,Yu, X.,Xiao, P.,Yi, F.,Liebscher, I.,Sun, J.P.
Identification, structure, and agonist design of an androgen membrane receptor.
Cell, 188:1589-, 2025
Cited by
PubMed Abstract: Androgens, such as 5α-dihydrotestosterone (5α-DHT), regulate numerous functions by binding to nuclear androgen receptors (ARs) and potential unknown membrane receptors. Here, we report that the androgen 5α-DHT activates membrane receptor GPR133 in muscle cells, thereby increasing intracellular cyclic AMP (cAMP) levels and enhancing muscle strength. Further cryoelectron microscopy (cryo-EM) structural analysis of GPR133-Gs in complex with 5α-DHT or its derivative methenolone (MET) reveals the structural basis for androgen recognition. Notably, the presence of the "Φ(F/L)-F-W" and the "F××N/D" motifs, which recognize the hydrophobic steroid core and polar groups, respectively, are common in adhesion GPCRs (aGPCRs), suggesting that many aGPCRs may recognize different steroid hormones. Finally, we exploited in silico screening methods to identify a small molecule, AP503, which activates GPR133 and separates the beneficial muscle-strengthening effects from side effects mediated by AR. Thus, GPR133 represents an androgen membrane receptor that contributes to normal androgen physiology and has important therapeutic potentials.
PubMed: 39884271
DOI: 10.1016/j.cell.2025.01.006
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.49 Å)
Structure validation

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