6nyy

Structural highlights

Disease

[AFG32_HUMAN] Spinocerebellar ataxia type 28;Early-onset spastic ataxia-neuropathy syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.

Function

[AFG32_HUMAN] ATP-dependent protease which is essential for axonal development (By similarity).