9mrs
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Crystal structure of human MMACHC in complex with MMADHC and B12
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Structural highlights
DiseaseMMAC_HUMAN Methylmalonic acidemia with homocystinuria, type cblC. The disease is caused by mutations affecting the gene represented in this entry. FunctionMMAC_HUMAN May be involved in the binding and intracellular trafficking of cobalamin (vitamin B12). Contents | ||||||||||||||||||
This page was last modified 07:35, 19 March 2026.