5d3a
KIF21A regulatory coiled coilKIF21A regulatory coiled coil
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 |
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