6akf

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'''Unreleased structure'''
 
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The entry 6akf is ON HOLD until Paper Publication
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==Crystal structure of mouse claudin-3 P134A mutant in complex with C-terminal fragment of Clostridium perfringens enterotoxin==
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<StructureSection load='6akf' size='340' side='right'caption='[[6akf]], [[Resolution|resolution]] 3.90&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6akf]] is a 8 chain structure with sequence from [https://en.wikipedia.org/wiki/Clostridium_perfringens Clostridium perfringens] and [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6AKF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6AKF 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]] 3.9&#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=6akf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6akf OCA], [https://pdbe.org/6akf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6akf RCSB], [https://www.ebi.ac.uk/pdbsum/6akf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6akf ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/CLD3_MOUSE CLD3_MOUSE] Plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity.<ref>PMID:10508613</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Tight junction is a cell adhesion apparatus functioning as barrier and/or channel in the paracellular spaces of epithelia. Claudin is the major component of tight junction and polymerizes to form tight junction strands with various morphologies that may correlate with their functions. Here we present the crystal structure of mammalian claudin-3 at 3.6 A resolution. The third transmembrane helix of claudin-3 is clearly bent compared with that of other subtypes. Structural analysis of additional two mutants with a single mutation representing other subtypes in the third helix indicates that this helix takes a bent or straight structure depending on the residue. The presence or absence of the helix bending changes the positions of residues related to claudin-claudin interactions and affects the morphology and adhesiveness of the tight junction strands. These results evoke a model for tight junction strand formation with different morphologies - straight or curvy strands - observed in native epithelia.
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Authors: Nakamura, S., Irie, K., Fujiyoshi, Y.
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Morphologic determinant of tight junctions revealed by claudin-3 structures.,Nakamura S, Irie K, Tanaka H, Nishikawa K, Suzuki H, Saitoh Y, Tamura A, Tsukita S, Fujiyoshi Y Nat Commun. 2019 Feb 18;10(1):816. doi: 10.1038/s41467-019-08760-7. PMID:30778075<ref>PMID:30778075</ref>
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Description: Crystal structure of mouse claudin-3 P134A mutant in complex with C-terminal fragment of Clostridium perfringens enterotoxin
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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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[[Category: Fujiyoshi, Y]]
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<div class="pdbe-citations 6akf" style="background-color:#fffaf0;"></div>
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[[Category: Irie, K]]
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== References ==
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[[Category: Nakamura, S]]
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Clostridium perfringens]]
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[[Category: Large Structures]]
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[[Category: Mus musculus]]
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[[Category: Fujiyoshi Y]]
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[[Category: Irie K]]
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[[Category: Nakamura S]]

Current revision

Crystal structure of mouse claudin-3 P134A mutant in complex with C-terminal fragment of Clostridium perfringens enterotoxin

PDB ID 6akf

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