6nyy | pdb_00006nyy
From Proteopedia
human m-AAA protease AFG3L2, substrate-bound
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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). Contents | ||||||||||||||||||
This page was last modified 06:53, 23 May 2019.