3som | pdb_00003som
From Proteopedia
crystal structure of human MMACHC
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Structural highlights
Disease[MMAC_HUMAN] Methylmalonic acidemia with homocystinuria, type cblC. The disease is caused by mutations affecting the gene represented in this entry. Function[MMAC_HUMAN] May be involved in the binding and intracellular trafficking of cobalamin (vitamin B12). Contents | ||||||||||||||||||||||
This page was last modified 13:09, 9 December 2014.