ⓘ MTHFD1L

                                     

ⓘ MTHFD1L

Monofunctional C1-tetrahydrofolate synthase, mitochondrial also known as formyltetrahydrofolate synthetase, is an enzyme that in humans is encoded by the MTHFD1L gene 1-like).

                                     
  • MTHFD 2 and to the N - terminal dehydrogenase cyclohydrolase domains of cytoplasmic and mitochondrial C 1 - THF synthases MTHFD 1 and MTHFD1L respectively
  • MTHFD 1 is a gene located in humans on chromosome 14 that encodes for a protein with three distinct enzymatic activities. C - 1 - tetrahydrofolate synthase
  • dehydrogenase cyclohydrolase, mitochondrial is an enzyme that in humans is encoded by the MTHFD 2 gene. This gene encodes a nuclear - encoded mitochondrial bifunctional enzyme
  • during glycolysis and in mitochondria either during the Krebs cycle or by MTHFD1L EC 6.3.4.3 an enzyme interconverting ADP phosphate 10 - formyltetrahydrofolate
  • include: MTHFD 1 cytoplasmic MTHFD1L mitochondrial As of late 2007, 3 structures have been solved for this class of enzymes, with PDB accession codes 1 EG7
  • MIR1269A: microRNA 1269a MLF 1 IP: Centromere protein U MMAA: methylmalonic aciduria cobalamin deficiency cblA type MTHFD 2 L NAD - dependent methylenetetrahydrofolate
  • MSH2: mutS homolog 2, colon cancer, nonpolyposis type 1 E. coli MSH6: mutS homolog 6 E. coli MTHFD 2: Bifunctional methylenetetrahydrofolate dehydrogenase cyclohydrolase
  • and pyridoxal. A second enzyme, methylenetetrahydrofolate dehydrogenase MTHFD 2 oxidizes 5, 10 - methylenetetrahydrofolate to an iminium cation which in
  • syndrome Hennekam lymphangiectasia - lymphedema syndrome Kabuki syndrome MTHFD 1 deficiency STAT5b deficiency IKAROS deficiency In certain conditions, the