MMAA 蛋白
(Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria. [provided by RefSeq, Jul 2008].
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3 results
MMAA
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliases for MMAA 蛋白
methylmalonic aciduria (cobalamin deficiency) type A (Mmaa) 蛋白methylmalonic aciduria (cobalamin deficiency) cblA type (MMAA) 蛋白
methylmalonic aciduria (cobalamin deficiency) cblA type (Mmaa) 蛋白
2810018E08Rik 蛋白
AI840684 蛋白
cblA 蛋白
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