5d3a | pdb_00005d3a
From Proteopedia
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 10:19, 21 June 2023.