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7pov

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'''Unreleased structure'''
 
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The entry 7pov is ON HOLD until Paper Publication
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==MUC2 Tubules of D1D2D3 domains==
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<StructureSection load='7pov' size='340' side='right'caption='[[7pov]], [[Resolution|resolution]] 3.80&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7pov]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7POV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7POV FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></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=7pov FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7pov OCA], [https://pdbe.org/7pov PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7pov RCSB], [https://www.ebi.ac.uk/pdbsum/7pov PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7pov ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The glycoprotein von Willebrand factor (VWF) contributes to hemostasis by stanching injuries in blood vessel walls. A distinctive feature of VWF is its assembly into long, helical tubules in endothelial cells prior to secretion. When VWF is released into the bloodstream, these tubules unfurl to release linear polymers that bind subendothelial collagen at wound sites, recruit platelets, and initiate the clotting cascade. VWF evolved from gel-forming mucins, the polymeric glycoproteins that coat and protect exposed epithelia. Despite the divergent function of VWF in blood vessel repair, sequence conservation and shared domain organization imply that VWF retained key aspects of the mucin bioassembly mechanism. Here, we show using cryo-electron microscopy that the ability to form tubules, a property hitherto thought to have arisen as a VWF adaptation to the vasculature, is a feature of the amino-terminal region of mucin. This segment of the human intestinal gel-forming mucin (MUC2) was found to self-assemble into tubules with a striking resemblance to those of VWF itself. To facilitate a comparison, we determined the residue-resolution structure of tubules formed by the homologous segment of VWF. The structures of the MUC2 and VWF tubules revealed the flexible joints and the intermolecular interactions required for tubule formation. Steric constraints in full-length MUC2 suggest that linear filaments, a previously observed supramolecular assembly form, are more likely than tubules to be the physiological mucin storage intermediate. Nevertheless, MUC2 tubules indicate a possible evolutionary origin for VWF tubules and elucidate design principles present in mucins and VWF.
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Authors: Javitt, G., Fass, D.
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Helical self-assembly of a mucin segment suggests an evolutionary origin for von Willebrand factor tubules.,Javitt G, Fass D Proc Natl Acad Sci U S A. 2022 Apr 12;119(15):e2116790119. doi:, 10.1073/pnas.2116790119. Epub 2022 Apr 4. PMID:35377815<ref>PMID:35377815</ref>
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Description: MUC2 Tubules of D1D2D3 domains
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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 7pov" 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]]
[[Category: Fass, D]]
[[Category: Fass, D]]
[[Category: Javitt, G]]
[[Category: Javitt, G]]
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[[Category: 2-start]]
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[[Category: Antimicrobial protein]]
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[[Category: Helix]]
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[[Category: Muc2]]
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[[Category: Mucin]]
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[[Category: Tubule]]

Current revision

MUC2 Tubules of D1D2D3 domains

PDB ID 7pov

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