7k3y
From Proteopedia
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[7k3y]] is a 2 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=7K3Y OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7K3Y FirstGlance]. <br> | <table><tr><td colspan='2'>[[7k3y]] is a 2 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=7K3Y OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7K3Y FirstGlance]. <br> | ||
| - | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7k3y FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7k3y OCA], [https://pdbe.org/7k3y PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7k3y RCSB], [https://www.ebi.ac.uk/pdbsum/7k3y PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7k3y ProSAT]</span></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.1Å</td></tr> |
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7k3y FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7k3y OCA], [https://pdbe.org/7k3y PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7k3y RCSB], [https://www.ebi.ac.uk/pdbsum/7k3y PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7k3y ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | + | [https://www.uniprot.org/uniprot/K2C8_HUMAN K2C8_HUMAN] The disease is caused by variants affecting the gene represented in this entry. | |
== Function == | == Function == | ||
| - | + | [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> | |
== References == | == References == | ||
<references/> | <references/> | ||
Current revision
GGYAGAS segment 52-58 from Keratin-8
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