7qbi

Structure of the GPCR dimer Ste2 in the active-like state bound to agonist

spinqualitylabelsall models 7qbi, resolution 3.46Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 7qbi is a 4 chain structure with sequence from Saccharomyces cerevisiae. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: Electron Microscopy, Resolution 3.46Å Ligands: NAG, Y01 Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function STE2_YEAST Receptor for the peptide pheromone alpha factor, the mating factor of yeast. Publication Abstract from PubMed The fungal class D1 G-protein-coupled receptor (GPCR) Ste2 has a different arrangement of transmembrane helices compared with mammalian GPCRs and a distinct mode of coupling to the heterotrimeric G protein Gpa1-Ste2-Ste18(1). In addition, Ste2 lacks conserved sequence motifs such as DRY, PIF and NPXXY, which are associated with the activation of class A GPCRs(2). This suggested that the activation mechanism of Ste2 may also differ. Here we determined structures of Saccharomyces cerevisiae Ste2 in the absence of G protein in two different conformations bound to the native agonist alpha-factor, bound to an antagonist and without ligand. These structures revealed that Ste2 is indeed activated differently from other GPCRs. In the inactive state, the cytoplasmic end of transmembrane helix H7 is unstructured and packs between helices H1-H6, blocking the G protein coupling site. Agonist binding results in the outward movement of the extracellular ends of H6 and H7 by 6 A. On the intracellular surface, the G protein coupling site is formed by a 20 A outward movement of the unstructured region in H7 that unblocks the site, and a 12 A inward movement of H6. This is a distinct mechanism in GPCRs, in which the movement of H6 and H7 upon agonist binding facilitates G protein coupling. Activation mechanism of the class D fungal GPCR dimer Ste2.,Velazhahan V, Ma N, Vaidehi N, Tate CG Nature. 2022 Mar;603(7902):743-748. doi: 10.1038/s41586-022-04498-3. Epub 2022, Mar 16. PMID:35296853 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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