5fwc
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Human Spectrin SH3 domain D48G, E7A, K60A
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Structural highlights
DiseaseSPTN1_HUMAN West syndrome. The disease is caused by mutations affecting the gene represented in this entry. FunctionSPTN1_HUMAN Fodrin, which seems to be involved in secretion, interacts with calmodulin in a calcium-dependent manner and is thus candidate for the calcium-dependent movement of the cytoskeleton at the membrane. See Also | ||||||||||||||||||||
This page was last modified 13:29, 26 July 2023.