9vhf: Difference between revisions

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'''Unreleased structure'''


The entry 9vhf is ON HOLD until Paper Publication
==Keratin 14 120 - 144 peptide fragment (R125G)==
 
<StructureSection load='9vhf' size='340' side='right'caption='[[9vhf]]' scene=''>
Authors:  
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9vhf]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9VHF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9VHF FirstGlance]. <br>
Description:  
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR,  models</td></tr>
[[Category: Unreleased Structures]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9vhf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9vhf OCA], [https://pdbe.org/9vhf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9vhf RCSB], [https://www.ebi.ac.uk/pdbsum/9vhf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9vhf ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/K1C14_HUMAN K1C14_HUMAN] Epidermolysis bullosa simplex, Dowling-Meara type;Localized epidermolysis bullosa simplex;Dermatopathia pigmentosa reticularis;Naegeli-Franceschetti-Jadassohn syndrome;Epidermolysis bullosa simplex with mottled pigmentation;Generalized epidermolysis bullosa simplex, non-Dowling-Meara type;KRT14-related epidermolysis bullosa simplex. The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/K1C14_HUMAN K1C14_HUMAN] The nonhelical tail domain is involved in promoting KRT5-KRT14 filaments to self-organize into large bundles and enhances the mechanical properties involved in resilience of keratin intermediate filaments in vitro.<ref>PMID:11724817</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Li HW]]
[[Category: Li ZY]]
[[Category: Wang CX]]
[[Category: Zhang WB]]
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