Target intelligence / Profile preview

Enzymes involved in folate metabolism and DNA synthesis

Molecular classification
Enzyme, Methyltransferase (for specific members), Transferase (for specific members)
01

Overview

Enzymes involved in folate metabolism and DNA synthesis comprise a group of metabolic proteins essential for generating nucleotides required for both de novo purine and thymidylate biosynthesis. Key examples include phosphoribosylglycinamide formyltransferase, phosphoribosylaminoimidazolecarboxamide formyltransferase, 5-methyltetrahydrofolate-homocysteine S-methyltransferase, methionine adenosyl transferase, and others. These enzymes support the production of adenine and guanine precursors as well as thymidine monophosphate—critical building blocks for DNA replication and repair. They also generate S‐adenosylmethionine, which is vital for methylation reactions including epigenetic regulation via DNA methylation. Disruption or inhibition of these pathways can lead to genome instability, increased cancer risk, birth defects such as neural tube defects, and other diseases related to one-carbon metabolism. Note: This entry refers collectively to a group rather than a single molecular entity; it is not standard practice to treat "enzymes involved in folate metabolism and DNA synthesis" as one canonical target but rather as several distinct targets with overlapping functions. For structured data purposes or drug development efforts, it is preferable to specify individual enzyme names such as "Dihydrofolate reductase," "Thymidylate synthase," etc., each with their own unique properties.

Other names
Folate pathway enzymesOne-carbon metabolism enzymesThymidylate synthesis enzymesPurine biosynthesis enzymes
02

Mechanism of action

Inhibition of nucleotide biosynthesis by blocking folate-dependent enzymatic steps, leading to impaired DNA replication and cell division.

03

Biological functions

DNA synthesisDNA repairEpigenetic modification (DNA methylation)Cell proliferation
04

Disease associations

CancerNeural tube defectsOther folate/vitamin B12–associated pathologies
05

Safety considerations

Myelosuppression from antifolate drugs due to inhibition of normal cell proliferation.Teratogenicity with folic acid deficiency or antifolate exposure during pregnancy.
06

Interacting drugs

Methotrexate (inhibits dihydrofolate reductase, a key enzyme in this pathway)

1 more in the full profile.

07

Biomarkers

Homocysteine levels (reflecting functional status of the pathway)Folate levelsUracil misincorporation into DNA as a marker of impaired thymidylate synthesis

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