7k3c | pdb_00007k3c
From Proteopedia
SGMGGIT segment 58-64 from Keratin-8
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Structural highlights
Disease[K2C8_HUMAN] The disease is caused by variants affecting the gene represented in this entry. Function[K2C8_HUMAN] Together with KRT19, helps to link the contractile apparatus to dystrophin at the costameres of striated muscle.[1] References
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This page was last modified 07:16, 8 September 2022.