cob(I)alamin adenosyltransferase
- cob(I)alamin adenosyltransferase
- co·b(I)al·a·min ad·e·no·syl·trans·fer·ase (ko-balґə-min ə-den″o-səl-transґfər-ās) a mitochondrial enzyme of the transferase class that catalyzes the transfer of an adenosyl group to cobalamin from ATP, forming the coenzyme adenosylcobalamin. Deficiency of the enzyme, an autosomal recessive trait (CblB), leads to deficiency of methylmalonyl-CoA mutase activity and results in methylmalonicacidemia. In official nomenclature, called cob(I)yrinic acid a,c-diamide adenosyltransferase [EC 2.5.1.17].
Medical dictionary.
2011.
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Cob(I)yrinic acid a,c-diamide adenosyltransferase — ATP:corrinoid adenosyltransferase the three dimensional structure of atp:corrinoid adenosyltransferase from salmonella typhimurium. apo atp form Identifiers Symbol CobA CobO BtuR … Wikipedia
cob(I)yrinic acid ac-diamide adenosyltransferase — co·b(I)y·rin·ic ac·id a,c di·a·mide ad·e·no·syl·trans·fer·ase (ko″bə rinґik asґid di amґīd ə den″o səl transґfər ās) [EC 2.5.1.17] official nomenclature for cob(I)alamin adenosyltransferase … Medical dictionary
MMAB — Methylmalonic aciduria (cobalamin deficiency) cblB type, also known as MMAB, is a human gene.cite web | title = Entrez Gene: MMAB methylmalonic aciduria (cobalamin deficiency) cblB type| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
MTRR (gene) — 5 methyltetrahydrofolate homocysteine methyltransferase reductase, also known as MTRR, is a human gene.cite web | title = Entrez Gene: MTRR 5 methyltetrahydrofolate homocysteine methyltransferase reductase| url =… … Wikipedia
methylmalonicacidemia — meth·yl·ma·lon·ic·ac·i·de·mia (meth″əl mə lon″ik as″ĭ deґme ə) 1. a genetically heterogeneous, autosomal recessive aminoacidopathy characterized by an 2. excess of methylmalonic acid in the blood and urine,… … Medical dictionary
