5fwc | pdb_00005fwc
From Proteopedia
Human Spectrin SH3 domain D48G, E7A, K60A
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Structural highlights
Disease[SPTN1_HUMAN] West syndrome. The disease is caused by mutations affecting the gene represented in this entry. Function[SPTN1_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 07:40, 6 May 2020.