7epc

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Current revision (13:33, 6 November 2024) (edit) (undo)
 
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<StructureSection load='7epc' size='340' side='right'caption='[[7epc]], [[Resolution|resolution]] 4.00&Aring;' scene=''>
<StructureSection load='7epc' size='340' side='right'caption='[[7epc]], [[Resolution|resolution]] 4.00&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[7epc]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7EPC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7EPC FirstGlance]. <br>
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7EPC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7EPC FirstGlance]. <br>
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</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">GRM7, GPRC1G, MGLUR7 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 4&#8491;</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7epc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7epc OCA], [https://pdbe.org/7epc PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7epc RCSB], [https://www.ebi.ac.uk/pdbsum/7epc PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7epc ProSAT]</span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7epc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7epc OCA], [https://pdbe.org/7epc PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7epc RCSB], [https://www.ebi.ac.uk/pdbsum/7epc PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7epc ProSAT]</span></td></tr>
</table>
</table>
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<div style="background-color:#fffaf0;">
 
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== Publication Abstract from PubMed ==
 
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The metabotropic glutamate receptors (mGlus) are involved in the modulation of synaptic transmission and neuronal excitability in the central nervous system(1). These receptors probably exist as both homo- and heterodimers that have unique pharmacological and functional properties(2-4). Here we report four cryo-electron microscopy structures of the human mGlu subtypes mGlu2 and mGlu7, including inactive mGlu2 and mGlu7 homodimers; mGlu2 homodimer bound to an agonist and a positive allosteric modulator; and inactive mGlu2-mGlu7 heterodimer. We observed a subtype-dependent dimerization mode for these mGlus, as a unique dimer interface that is mediated by helix IV (and that is important for limiting receptor activity) exists only in the inactive mGlu2 structure. The structures provide molecular details of the inter- and intra-subunit conformational changes that are required for receptor activation, which distinguish class C G-protein-coupled receptors from those in classes A and B. Furthermore, our structure and functional studies of the mGlu2-mGlu7 heterodimer suggest that the mGlu7 subunit has a dominant role in controlling dimeric association and G-protein activation in the heterodimer. These insights into mGlu homo- and heterodimers highlight the complex landscape of mGlu dimerization and activation.
 
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Structures of human mGlu2 and mGlu7 homo- and heterodimers.,Du J, Wang D, Fan H, Xu C, Tai L, Lin S, Han S, Tan Q, Wang X, Xu T, Zhang H, Chu X, Yi C, Liu P, Wang X, Zhou Y, Pin JP, Rondard P, Liu H, Liu J, Sun F, Wu B, Zhao Q Nature. 2021 Jun;594(7864):589-593. doi: 10.1038/s41586-021-03641-w. Epub 2021, Jun 16. PMID:34135509<ref>PMID:34135509</ref>
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==See Also==
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*[[Metabotropic glutamate receptor 3D structures|Metabotropic glutamate receptor 3D structures]]
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 7epc" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Human]]
 
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Du, J]]
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[[Category: Du J]]
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[[Category: Fan, H]]
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[[Category: Fan H]]
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[[Category: Han, S]]
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[[Category: Han S]]
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[[Category: Lin, S]]
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[[Category: Lin S]]
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[[Category: Sun, F]]
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[[Category: Sun F]]
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[[Category: Tai, L]]
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[[Category: Tai L]]
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[[Category: Wang, D]]
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[[Category: Wang D]]
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[[Category: Wu, B]]
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[[Category: Wu B]]
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[[Category: Zhao, Q]]
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[[Category: Zhao Q]]
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[[Category: Cryo-em structure]]
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[[Category: Gpcr]]
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[[Category: Membrane protein]]
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Current revision

Cryo-EM structure of inactive mGlu7 homodimer

PDB ID 7epc

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