8JBG
Neurokinin B bound to active human neurokinin 3 receptor in complex with Gq
This is a non-PDB format compatible entry.
Summary for 8JBG
| Entry DOI | 10.2210/pdb8jbg/pdb |
| EMDB information | 36145 |
| Descriptor | Neuromedin-K receptor (NK3R-pFastbac1), Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ScFv16 nanobody, ... (6 entities in total) |
| Functional Keywords | g protein coupled receptor, neurokinin, cryo-em, peptide agonists, membrane protein |
| Biological source | Homo sapiens (human) More |
| Total number of polymer chains | 6 |
| Total formula weight | 282621.72 |
| Authors | Sun, W.J.,Yang, F.,Zhang, H.H.,Yuan, Q.N.,Yin, W.C.,Shi, P.,Eric, X.,Tian, C.L. (deposition date: 2023-05-08, release date: 2024-02-07) |
| Primary citation | Sun, W.,Yang, F.,Zhang, H.,Yuan, Q.,Ling, S.,Wang, Y.,Lv, P.,Li, Z.,Luo, Y.,Liu, D.,Yin, W.,Shi, P.,Xu, H.E.,Tian, C. Structural insights into neurokinin 3 receptor activation by endogenous and analogue peptide agonists. Cell Discov, 9:66-66, 2023 Cited by PubMed Abstract: Neurokinin 3 receptor (NK3R) is a tachykinin receptor essential for the hypothalamic-pituitary-gonadal axis. The endogenous peptide agonist neurokinin B (NKB) preferentially activates NK3R, while substance P (SP) binds preferentially to NK1R. In addition, the SP analogue senktide more potently activates NK3R than NKB and SP. However, the mechanisms of preferential binding of peptide and NK3R activation remain elusive. Herein, we determined the cryogenic electron microscopy (cryo-EM) structures of the NK3R-G complex bound to NKB, SP and senktide. The three NK3R-G/peptide complexes utilize a class of noncanonical receptor activation mechanisms. Combining the structural analysis and functional assay illustrated that the consensus C-termini of the three peptide agonists share a conserved binding mode to NK3R, while the divergent N-termini of the peptides confer the preferential binding of the agonist to NK3R. In addition, the specific interactions between the N-terminus of senktide and the N-terminus and extracellular loops (ECL2 and ECL3) of NK3R lead to the improved activation displayed by senktide compared to SP and NKB. These findings pave the way to understand tachykinin receptor subtype selectivity and provide ideas to rationally develop drugs targeting NK3R. PubMed: 37391393DOI: 10.1038/s41421-023-00564-w PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (2.8 Å) |
Structure validation
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