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This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found. Protein function: Adenosyltransferase involved in intracellular vitamin B12 metabolism. Generates adenosylcobalamin (AdoCbl) and directly delivers the cofactor to MUT in a transfer taht is stimulated by ATP-binding to MMAB and gated by MMAA. [The UniProt Consortium]
Keywords:
Anti-MMAB, EC=2.5.1.17, Anti-Corrinoid adenosyltransferase, Anti-Cob(II)alamin adenosyltransferase, Anti-Methylmalonic aciduria type B protein, Anti-Cobinamide/cobalamin adenosyltransferase, Anti-Cob(II)yrinic acid a,c-diamide adenosyltransferase, MMAB Po
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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