8vsb

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Current revision (06:07, 11 September 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8vsb is ON HOLD until Paper Publication
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==L-TGF-b3/GARP==
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<StructureSection load='8vsb' size='340' side='right'caption='[[8vsb]], [[Resolution|resolution]] 2.93&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8vsb]] is a 3 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=8VSB OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8VSB FirstGlance]. <br>
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Description:
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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]] 2.93&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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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=8vsb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8vsb OCA], [https://pdbe.org/8vsb PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8vsb RCSB], [https://www.ebi.ac.uk/pdbsum/8vsb PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8vsb ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/TGFB3_HUMAN TGFB3_HUMAN] Defects in TGFB3 are a cause of familial arrhythmogenic right ventricular dysplasia type 1 (ARVD1) [MIM:[https://omim.org/entry/107970 107970]; also known as arrhythmogenic right ventricular cardiomyopathy 1 (ARVC1). ARVD is an autosomal dominant disease characterized by partial degeneration of the myocardium of the right ventricle, electrical instability, and sudden death. It is clinically defined by electrocardiographic and angiographic criteria; pathologic findings, replacement of ventricular myocardium with fatty and fibrous elements, preferentially involve the right ventricular free wall.<ref>PMID:15639475</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/TGFB3_HUMAN TGFB3_HUMAN] Involved in embryogenesis and cell differentiation.
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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: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Cheng Y]]
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[[Category: Jin M]]
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[[Category: Nishimura SL]]

Current revision

L-TGF-b3/GARP

PDB ID 8vsb

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