7mfw

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'''Unreleased structure'''
 
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The entry 7mfw is ON HOLD until Paper Publication
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==Drosophila melanogaster Canoe PDZ domain in complex with Echinoid C-terminal region==
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<StructureSection load='7mfw' size='340' side='right'caption='[[7mfw]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7mfw]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Drosophila_melanogaster Drosophila melanogaster]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7MFW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7MFW FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.104&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7mfw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7mfw OCA], [https://pdbe.org/7mfw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7mfw RCSB], [https://www.ebi.ac.uk/pdbsum/7mfw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7mfw ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/Q9VN82_DROME Q9VN82_DROME] [https://www.uniprot.org/uniprot/Q9BN17_DROME Q9BN17_DROME]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Embryogenesis requires cells to change shape and move without disrupting epithelial integrity. This requires robust, responsive linkage between adherens junctions and the actomyosin cytoskeleton. Using Drosophila morphogenesis, we define molecular mechanisms mediating junction-cytoskeletal linkage and explore the role of mechanosensing. We focus on the junction-cytoskeletal linker Canoe, a multidomain protein. We engineered the canoe locus to define how its domains mediate its mechanism of action. To our surprise, the PDZ and FAB domains, which we thought connected junctions and F-actin, are not required for viability or mechanosensitive recruitment to junctions under tension. The FAB domain stabilizes junctions experiencing elevated force, but in its absence, most cells recover, suggesting redundant interactions. In contrast, the Rap1-binding RA domains are critical for all Cno functions and enrichment at junctions under tension. This supports a model in which junctional robustness derives from a large protein network assembled via multivalent interactions, with proteins at network nodes and some node connections more critical than others.
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Authors:
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Multivalent interactions make adherens junction-cytoskeletal linkage robust during morphogenesis.,Perez-Vale KZ, Yow KD, Johnson RI, Byrnes AE, Finegan TM, Slep KC, Peifer M J Cell Biol. 2021 Dec 6;220(12). pii: 212790. doi: 10.1083/jcb.202104087. Epub, 2021 Nov 11. PMID:34762121<ref>PMID:34762121</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 7mfw" 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: Drosophila melanogaster]]
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[[Category: Large Structures]]
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[[Category: Byrnes AE]]
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[[Category: Peifer M]]
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[[Category: Slep KC]]

Current revision

Drosophila melanogaster Canoe PDZ domain in complex with Echinoid C-terminal region

PDB ID 7mfw

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