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6ukt

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Current revision (07:29, 11 March 2020) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 6ukt is ON HOLD until Paper Publication
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==Cryo-EM structure of mammalian Ric-8A:Galpha(i):nanobody complex==
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<StructureSection load='6ukt' size='340' side='right'caption='[[6ukt]], [[Resolution|resolution]] 3.87&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6ukt]] is a 6 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6UKT OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6UKT FirstGlance]. <br>
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</td></tr><tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=SEP:PHOSPHOSERINE'>SEP</scene>, <scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6ukt FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ukt OCA], [http://pdbe.org/6ukt PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6ukt RCSB], [http://www.ebi.ac.uk/pdbsum/6ukt PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6ukt ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/GNAI1_RAT GNAI1_RAT]] Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems. The G(i) proteins are involved in hormonal regulation of adenylate cyclase: they inhibit the cyclase in response to beta-adrenergic stimuli. The inactive GDP-bound form prevents the association of RGS14 with centrosomes and is required for the translocation of RGS14 from the cytoplasm to the plasma membrane. May play a role in cell division.<ref>PMID:16870394</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Ric-8A is a cytosolic Guanine Nucleotide exchange Factor (GEF) that activates heterotrimeric G protein alpha subunits (Galpha) and serves as an essential Galpha chaperone. Mechanisms by which Ric-8A catalyzes these activities, which are stimulated by Casein Kinase II phosphorylation, are unknown. We report the structure of the nanobody-stabilized complex of nucleotide-free Galpha bound to phosphorylated Ric-8A at near atomic resolution by cryo-electron microscopy and X-ray crystallography. The mechanism of Ric-8A GEF activity differs considerably from that employed by G protein-coupled receptors at the plasma membrane. Ric-8A engages a specific conformation of Galpha at multiple interfaces to form a complex that is stabilized by phosphorylation within a Ric-8A segment that connects two Galpha binding sites. The C-terminus of Galpha is ejected from its beta sheet core, thereby dismantling the GDP binding site. Ric-8A binds to the exposed Galpha beta sheet and switch II to stabilize the nucleotide-free state of Galpha.
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Authors:
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Structure of the G protein chaperone and guanine nucleotide exchange factor Ric-8A bound to Galphai1.,McClelland LJ, Zhang K, Mou TC, Johnston J, Yates-Hansen C, Li S, Thomas CJ, Doukov TI, Triest S, Wohlkonig A, Tall GG, Steyaert J, Chiu W, Sprang SR Nat Commun. 2020 Feb 26;11(1):1077. doi: 10.1038/s41467-020-14943-4. PMID:32103024<ref>PMID:32103024</ref>
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Description:
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 6ukt" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Chiu, W]]
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[[Category: Johnston, J D]]
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[[Category: Mou, T C]]
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[[Category: Sprang, S R]]
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[[Category: Zhang, K]]
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[[Category: G protein]]
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[[Category: Gef]]
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[[Category: Ric-8a]]
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[[Category: Signaling protein]]

Current revision

Cryo-EM structure of mammalian Ric-8A:Galpha(i):nanobody complex

PDB ID 6ukt

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