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7k3x

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(New page: '''Unreleased structure''' The entry 7k3x is ON HOLD Authors: Murray, K.A., Sawaya, M.R., Eisenberg, D.S. Description: SGMGCIT segment 58-64 from Keratin-8 with G62C mutation [[Categor...)
Current revision (07:17, 3 April 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 7k3x is ON HOLD
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==SGMGCIT segment 58-64 from Keratin-8 with G62C mutation==
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<StructureSection load='7k3x' size='340' side='right'caption='[[7k3x]], [[Resolution|resolution]] 1.71&Aring;' scene=''>
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Authors: Murray, K.A., Sawaya, M.R., Eisenberg, D.S.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7k3x]] 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=7K3X OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7K3X FirstGlance]. <br>
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Description: SGMGCIT segment 58-64 from Keratin-8 with G62C mutation
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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]] 1.705&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=IPA:ISOPROPYL+ALCOHOL'>IPA</scene></td></tr>
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[[Category: Sawaya, M.R]]
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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=7k3x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7k3x OCA], [https://pdbe.org/7k3x PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7k3x RCSB], [https://www.ebi.ac.uk/pdbsum/7k3x PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7k3x ProSAT]</span></td></tr>
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[[Category: Murray, K.A]]
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</table>
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[[Category: Eisenberg, D.S]]
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== Disease ==
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[https://www.uniprot.org/uniprot/K2C8_HUMAN K2C8_HUMAN] The disease is caused by variants affecting the gene represented in this entry.
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== Function ==
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[https://www.uniprot.org/uniprot/K2C8_HUMAN K2C8_HUMAN] Together with KRT19, helps to link the contractile apparatus to dystrophin at the costameres of striated muscle.<ref>PMID:16000376</ref>
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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: Eisenberg DS]]
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[[Category: Murray KA]]
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[[Category: Sawaya MR]]

Current revision

SGMGCIT segment 58-64 from Keratin-8 with G62C mutation

PDB ID 7k3x

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