Methylmalonic aciduria and homocystinuria type D protein, mitochondrial also known as MMADHC is a
protein that in humans is encoded by the MMADHCgene.[5]
Function
This gene encodes a protein localized in cytosol and mitochondria that is involved in an early step of
vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans.[6]
PDBe-KB provides an overview of all the structure information available in the PDB for Human Methylmalonic aciduria and homocystinuria type D protein, mitochondrial (MMADHC)
Methylmalonic aciduria and homocystinuria type D protein, mitochondrial also known as MMADHC is a
protein that in humans is encoded by the MMADHCgene.[5]
Function
This gene encodes a protein localized in cytosol and mitochondria that is involved in an early step of
vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans.[6]
PDBe-KB provides an overview of all the structure information available in the PDB for Human Methylmalonic aciduria and homocystinuria type D protein, mitochondrial (MMADHC)