3fb2
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Crystal structure of the human brain alpha spectrin repeats 15 and 16. Northeast Structural Genomics Consortium target HR5563a.
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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 09:32, 6 December 2023.