3g7c

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{{Seed}}
 
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[[Image:3g7c.jpg|left|200px]]
 
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==Structure of the Phosphorylation Mimetic of Occludin C-term Tail==
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The line below this paragraph, containing "STRUCTURE_3g7c", creates the "Structure Box" on the page.
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<StructureSection load='3g7c' size='340' side='right'caption='[[3g7c]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
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== Structural highlights ==
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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<table><tr><td colspan='2'>[[3g7c]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3G7C OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3G7C 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&#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=3g7c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3g7c OCA], [https://pdbe.org/3g7c PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3g7c RCSB], [https://www.ebi.ac.uk/pdbsum/3g7c PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3g7c ProSAT]</span></td></tr>
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{{STRUCTURE_3g7c| PDB=3g7c | SCENE= }}
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/OCLN_HUMAN OCLN_HUMAN] Defects in OCLN are the cause of band-like calcification with simplified gyration and polymicrogyria (BLCPMG) [MIM:[https://omim.org/entry/251290 251290]; also known as pseudo-TORCH syndrome. BLCPMG is a neurologic disorder with characteristic clinical and neuroradiologic features that mimic intrauterine TORCH infection in the absence of evidence of infection. Affected individuals have congenital microcephaly, intracranial calcifications, and severe developmental delay.<ref>PMID:20727516</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/OCLN_HUMAN OCLN_HUMAN] May play a role in the formation and regulation of the tight junction (TJ) paracellular permeability barrier. It is able to induce adhesion when expressed in cells lacking tight junctions.<ref>PMID:19114660</ref>
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== Evolutionary Conservation ==
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[[Image:Consurf_key_small.gif|200px|right]]
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Check<jmol>
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<jmolCheckbox>
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/g7/3g7c_consurf.spt"</scriptWhenChecked>
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
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<text>to colour the structure by Evolutionary Conservation</text>
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</jmolCheckbox>
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</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=3g7c ConSurf].
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<div style="clear:both"></div>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The molecular function of occludin, an integral membrane component of tight junctions, remains unclear. VEGF-induced phosphorylation sites were mapped on occludin by combining MS data analysis with bioinformatics. In vivo phosphorylation of Ser490 was validated and protein interaction studies combined with crystal structure analysis suggest that Ser490 phosphorylation attenuates the interaction between occludin and ZO-1. This study demonstrates that combining MS data and bioinformatics can successfully identify novel phosphorylation sites from limiting samples.
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===Structure of the Phosphorylation Mimetic of Occludin C-term Tail===
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Identification and analysis of occludin phosphosites: a combined mass spectrometry and bioinformatics approach.,Sundstrom JM, Tash BR, Murakami T, Flanagan JM, Bewley MC, Stanley BA, Gonsar KB, Antonetti DA J Proteome Res. 2009 Feb;8(2):808-17. PMID:19125584<ref>PMID:19125584</ref>
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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 3g7c" style="background-color:#fffaf0;"></div>
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(as it appears on PubMed at http://www.pubmed.gov), where 19125584 is the PubMed ID number.
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== References ==
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<references/>
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{{ABSTRACT_PUBMED_19125584}}
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__TOC__
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</StructureSection>
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==About this Structure==
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3G7C is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3G7C OCA].
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==Reference==
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<ref group="xtra">PMID:19125584</ref><references group="xtra"/>
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Antonetii, D A.]]
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[[Category: Large Structures]]
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[[Category: Bewley, M C.]]
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[[Category: Antonetii DA]]
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[[Category: Flanagan, J M.]]
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[[Category: Bewley MC]]
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[[Category: Murakami, T.]]
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[[Category: Flanagan JM]]
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[[Category: Sundstrom, J M.]]
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[[Category: Murakami T]]
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[[Category: Tash, B R.]]
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[[Category: Sundstrom JM]]
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[[Category: Adhesion]]
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[[Category: Tash BR]]
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[[Category: Cell adhesion]]
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[[Category: Cell junction]]
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[[Category: Coiled coil]]
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[[Category: Diabetic retinopathy]]
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[[Category: Membrane]]
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[[Category: Occludin]]
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[[Category: Phosphoprotein]]
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[[Category: Tight junction]]
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[[Category: Transmembrane]]
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[[Category: Zo-1]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed May 13 09:59:19 2009''
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Current revision

Structure of the Phosphorylation Mimetic of Occludin C-term Tail

PDB ID 3g7c

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