Folic acid: nutritional biochemistry, molecular biology, and role in disease processes

M Lucock - Molecular genetics and metabolism, 2000 - Elsevier
This paper reviews the chemistry, metabolism, and molecular biology of folic acid, with a
particular emphasis on how it is, or may be, involved in many disease processes. Folic acid …

Folate‐mediated one‐carbon metabolism

JT Fox, PJ Stover - Vitamins & hormones, 2008 - Elsevier
Tetrahydrofolate (THF) polyglutamates are a family of cofactors that carry and chemically
activate one‐carbon units for biosynthesis. THF‐mediated one‐carbon metabolism is a …

Methylenetetrahydrofolate reductase and methionine synthase: biochemistry and molecular biology

RG Matthews, C Sheppard, C Goulding - European journal of pediatrics, 1998 - Springer
Methylenetetrahydrofolate reductase and cobalamin-dependent methionine synthase
catalyze the penultimate and ultimate steps in the biosynthesis of methionine in prokaryotes …

[HTML][HTML] Gene Identification for the cblD Defect of Vitamin B12 Metabolism

D Coelho, T Suormala, M Stucki… - … England Journal of …, 2008 - Mass Medical Soc
Background Vitamin B12 (cobalamin) is an essential cofactor in several metabolic pathways.
Intracellular conversion of cobalamin to its two coenzymes, adenosylcobalamin in …

The regulation of folate and methionine metabolism

HA Krebs, R Hems, B Tyler - Biochemical Journal, 1976 - portlandpress.com
1. The isolated perfused rat liver and suspensions of isolated rat hepatocytes fail to form
glucose from histidine, in contrast with the liver in vivo. Both rat liver preparations readily …

The clinical presentation of cobalamin‐related disorders: from acquired deficiencies to inborn errors of absorption and intracellular pathways

M Huemer, MR Baumgartner - Journal of inherited metabolic …, 2019 - Wiley Online Library
This review gives an overview of clinical characteristics, treatment and outcome of nutritional
and acquired cobalamin (Cbl; synonym: vitamin B12) deficiencies, inborn errors of Cbl …

Mutations in the B12-Binding Region of Methionine Synthase:  How the Protein Controls Methylcobalamin Reactivity

JT Jarrett, M Amaratunga, CL Drennan, JD Scholten… - Biochemistry, 1996 - ACS Publications
Vitamin B12-dependent methionine synthase catalyzes the transfer of a methyl group from
methyltetrahydrofolate to homocysteine via the enzyme-bound cofactor methylcobalamin. To …

[HTML][HTML] MeaB is a component of the methylmalonyl-CoA mutase complex required for protection of the enzyme from inactivation

N Korotkova, ME Lidstrom - Journal of Biological Chemistry, 2004 - ASBMB
Adenosylcobalamin-dependent methylmalonyl-CoA mutase catalyzes the interconversion of
methylmalonyl-CoA and succinyl-CoA. In humans, deficiencies in the mutase lead to …

Methionine synthase supports tumour tetrahydrofolate pools

JM Ghergurovich, X Xu, JZ Wang, L Yang… - Nature …, 2021 - nature.com
Mammalian cells require activated folates to generate nucleotides for growth and division.
The most abundant circulating folate species is 5-methyl tetrahydrofolate (5-methyl-THF) …

[HTML][HTML] Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency

M Huemer, D Diodato, B Schwahn, M Schiff… - Journal of inherited …, 2017 - Springer
Background Remethylation defects are rare inherited disorders in which impaired
remethylation of homocysteine to methionine leads to accumulation of homocysteine and …