MMAA

Methylmalonic aciduria type A protein, mitochondrial also known as MMAA is a protein that in humans is encoded by the MMAA gene. ^[1]

6 relations: Adenosylcobalamin, Gene, Methylmalonic acidemia, Methylmalonyl-CoA mutase, Mitochondrion, Protein.

Adenosylcobalamin

Adenosylcobalamin (AdoCbl), which is also known as cobamamide and dibencozide, is, along with methylcobalamin (MeCbl), one of the active forms of vitamin B12.

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Gene

In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.

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Methylmalonic acidemia

Methylmalonic acidemia (MMA), also called methylmalonic aciduria, is an autosomal recessive metabolic disorder.

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Methylmalonyl-CoA mutase

Methylmalonyl-CoA mutase (MCM), mitochondrial, also known as methylmalonyl-CoA isomerase, is a protein that in humans is encoded by the MUT gene.

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Mitochondrion

The mitochondrion (plural mitochondria) is a double-membrane-bound organelle found in most eukaryotic organisms.

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Protein

Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.

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Redirects here:

MMAA (gene).

References

[1] https://en.wikipedia.org/wiki/MMAA

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