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6MHF

Galphai3 co-crystallized with GIV/Girdin

Summary for 6MHF
Entry DOI10.2210/pdb6mhf/pdb
DescriptorGuanine nucleotide-binding protein G(k) subunit alpha, Girdin, GUANOSINE-5'-DIPHOSPHATE, ... (5 entities in total)
Functional Keywordsexchange, modulator, gpcr, inhibitory, signaling protein
Biological sourceRattus norvegicus (Rat)
More
Total number of polymer chains2
Total formula weight43914.37
Authors
Rees, S.D.,Kalogriopoulos, N.A.,Ngo, T.,Kopcho, N.,Ilatovskiy, A.,Sun, N.,Komives, E.,Chang, G.,Ghosh, P.,Kufareva, I. (deposition date: 2018-09-17, release date: 2019-07-31, Last modification date: 2023-10-11)
Primary citationKalogriopoulos, N.A.,Rees, S.D.,Ngo, T.,Kopcho, N.J.,Ilatovskiy, A.V.,Sun, N.,Komives, E.A.,Chang, G.,Ghosh, P.,Kufareva, I.
Structural basis for GPCR-independent activation of heterotrimeric Gi proteins.
Proc.Natl.Acad.Sci.USA, 116:16394-16403, 2019
Cited by
PubMed Abstract: Heterotrimeric G proteins are key molecular switches that control cell behavior. The canonical activation of G proteins by agonist-occupied G protein-coupled receptors (GPCRs) has recently been elucidated from the structural perspective. In contrast, the structural basis for GPCR-independent G protein activation by a novel family of guanine-nucleotide exchange modulators (GEMs) remains unknown. Here, we present a 2.0-Å crystal structure of Gαi in complex with the GEM motif of GIV/Girdin. Nucleotide exchange assays, molecular dynamics simulations, and hydrogen-deuterium exchange experiments demonstrate that GEM binding to the conformational switch II causes structural changes that allosterically propagate to the hydrophobic core of the Gαi GTPase domain. Rearrangement of the hydrophobic core appears to be a common mechanism by which GPCRs and GEMs activate G proteins, although with different efficiency. Atomic-level insights presented here will aid structure-based efforts to selectively target the noncanonical G protein activation.
PubMed: 31363053
DOI: 10.1073/pnas.1906658116
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

226707

數據於2024-10-30公開中

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