5nfd | pdb_00005nfd
From Proteopedia
Antiparallel monomeric coiled coil of Kif21A
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Structural highlights
Disease[KI21A_HUMAN] Congenital fibrosis of extraocular muscles. The disease is caused by mutations affecting the gene represented in this entry. Function[KI21A_HUMAN] Microtubule-binding motor protein probably involved in neuronal axonal transport. In vitro, has a plus-end directed motor activity (By similarity). Contents | ||||||||||||||||
This page was last modified 07:56, 2 May 2018.