6nyy
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human m-AAA protease AFG3L2, substrate-bound
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Structural highlights
DiseaseAFG32_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. FunctionAFG32_HUMAN ATP-dependent protease which is essential for axonal development (By similarity). Contents | ||||||||||||||||
This page was last modified 09:22, 20 March 2024.