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- Table of Contents
Facts about Methylmalonic aciduria type A homolog, mitochondrial.
Functions as a G-protein chaperone that assists AdoCbl cofactor delivery from MMAB into the methylmalonyl-CoA mutase (MUT) and reactivation of the enzyme during catalysis. .
| Mouse | |
|---|---|
| Gene Name: | Mmaa |
| Uniprot: | Q8C7H1 |
| Entrez: | 109136 |

| Belongs to: |
|---|
| SIMIBI class G3E GTPase family |

cblA; EC 3.6; methylmalonic aciduria (cobalamin deficiency) cblA type; methylmalonic aciduria (cobalamin deficiency) type A; MGC120011; MGC120012; MGC120013; mitochondrial
Mass (kDA):
45.932 kDA

| Mouse | |
|---|---|
| Location: | 8|8 C1 |
| Sequence: | 8; |



PMID: 16141072 by Carninci P., et al. The transcriptional landscape of the mammalian genome.
PMID: 21183079 by Huttlin E.L., et al. A tissue-specific atlas of mouse protein phosphorylation and expression.