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7RMH

Substance P bound to active human neurokinin 1 receptor in complex with miniGs399

Summary for 7RMH
Entry DOI10.2210/pdb7rmh/pdb
EMDB information24570
DescriptorGuanine nucleotide-binding protein G(s) subunit alpha isoforms short, 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 Keywordssubstance p, g protein, gpcr, neurokinin, tachykinin, signaling protein, signaling protein-membrane protein complex, signaling protein/membrane protein
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains6
Total formula weight141547.57
Authors
Harris, J.A.,Faust, B.,Gondin, A.B.,Daemgen, M.A.,Suomivuori, C.M.,Veldhuis, N.A.,Cheng, Y.,Dror, R.O.,Thal, D.,Manglik, A. (deposition date: 2021-07-27, release date: 2021-11-03, Last modification date: 2024-11-20)
Primary citationHarris, J.A.,Faust, B.,Gondin, A.B.,Damgen, M.A.,Suomivuori, C.M.,Veldhuis, N.A.,Cheng, Y.,Dror, R.O.,Thal, D.M.,Manglik, A.
Selective G protein signaling driven by substance P-neurokinin receptor dynamics.
Nat.Chem.Biol., 18:109-115, 2022
Cited by
PubMed Abstract: The neuropeptide substance P (SP) is important in pain and inflammation. SP activates the neurokinin-1 receptor (NK1R) to signal via G and G proteins. Neurokinin A also activates NK1R, but leads to selective G signaling. How two stimuli yield distinct G protein signaling at the same G protein-coupled receptor remains unclear. We determined cryogenic-electron microscopy structures of active NK1R bound to SP or the G-biased peptide SP6-11. Peptide interactions deep within NK1R are critical for receptor activation. Conversely, interactions between SP and NK1R extracellular loops are required for potent G signaling but not G signaling. Molecular dynamics simulations showed that these superficial contacts restrict SP flexibility. SP6-11, which lacks these interactions, is dynamic while bound to NK1R. Structural dynamics of NK1R agonists therefore depend on interactions with the receptor extracellular loops and regulate G protein signaling selectivity. Similar interactions between other neuropeptides and their cognate receptors may tune intracellular signaling.
PubMed: 34711980
DOI: 10.1038/s41589-021-00890-8
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.1 Å)
Structure validation

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건을2025-06-18부터공개중

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