7klj
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Crystal structure of the WD-repeat domain of human KIF21A
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Structural highlights
DiseaseKI21A_HUMAN Congenital fibrosis of extraocular muscles. The disease is caused by mutations affecting the gene represented in this entry. FunctionKI21A_HUMAN Microtubule-binding motor protein probably involved in neuronal axonal transport. In vitro, has a plus-end directed motor activity (By similarity). See Also | ||||||||||||||||||||
This page was last modified 14:57, 6 March 2024.