PMID:2407589
| Citation |
Banerjee, RV and Matthews, RG (1990) Cobalamin-dependent methionine synthase. FASEB J. 4:1450-9 |
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| Abstract |
Cobalamin-dependent methionine synthase catalyzes the transfer of a methyl group from N5-methyltetrahydrofolate to homocysteine, producing tetrahydrofolate and methionine. Insufficient availability of cobalamin, or inhibition of methionine synthase by exposure to nitrous oxide, leads to diminished activity of this enzyme. In humans, severe inhibition of methionine synthase results in the development of megaloblastic anemia, and eventually in subacute combined degeneration of the spinal cord. It also results in diminished intracellular folate levels and a redistribution of folate derivatives. In this review, we summarize recent progress in understanding the catalysis and regulation of this important enzyme from both bacterial and mammalian sources. Because inhibition of mammalian methionine synthase can restrict the incorporation of methyltetrahydrofolate from the blood into cellular folate pools that can be used for nucleotide biosynthesis, it is a potential chemotherapeutic target. The review emphasizes the mechanistic information that will be needed in order to design rational inhibitors of the enzyme. |
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| Keywords |
5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase/antagonists & inhibitors; 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase/genetics; 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase/metabolism; Amino Acid Sequence; Animals; Antineoplastic Agents/pharmacology; Base Sequence; Cloning, Molecular; Escherichia coli/enzymology; Folic Acid/metabolism; Humans; Methyltransferases/metabolism; Models, Chemical; Molecular Sequence Data; Nitrous Oxide/pharmacology; Vitamin B 12/metabolism; Vitamin B 12/physiology |
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