Target type: molecularfunction
Enables the transfer of folic acid (pteroylglutamic acid) from one side of a membrane to the other. Folic acid is widely distributed as a member of the vitamin B complex and is essential for the synthesis of purine and pyrimidines. [GOC:ai]
Folic acid transmembrane transporter activity refers to the movement of folic acid across cellular membranes. This process is crucial for maintaining adequate intracellular levels of folate, an essential vitamin vital for various cellular functions, including DNA synthesis, repair, and methylation.
The transport of folic acid is mediated by specific membrane-bound proteins, known as folate transporters. These transporters exhibit high affinity for folate and utilize various mechanisms to facilitate its uptake into cells. Some transporters employ passive diffusion, driven by the concentration gradient, while others utilize active transport mechanisms, requiring energy to move folate against its concentration gradient.
The primary function of folate transporters is to ensure the efficient delivery of folate into cells, where it is converted into tetrahydrofolic acid (THF), the active form of the vitamin. THF serves as a cofactor for numerous metabolic enzymes involved in crucial cellular processes, such as DNA synthesis, repair, and methylation.
Deficiency in folate uptake can lead to various health issues, including megaloblastic anemia, neural tube defects, and cardiovascular disease. Therefore, maintaining adequate folate levels through efficient transmembrane transport is essential for overall health and well-being.'
"
Protein | Definition | Taxonomy |
---|---|---|
Proton-coupled folate transporter | A proton-coupled folate transporter that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q96NT5] | Homo sapiens (human) |
Reduced folate transporter | A reduced folate transporter that is encoded in the genome of human. [PRO:DNx, UniProtKB:P41440] | Homo sapiens (human) |
Proton-coupled folate transporter | A proton-coupled folate transporter that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q96NT5] | Homo sapiens (human) |
Reduced folate transporter | A reduced folate transporter that is encoded in the genome of human. [PRO:DNx, UniProtKB:P41440] | Homo sapiens (human) |
Thiamine transporter 1 | A thiamine transporter 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:O60779] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
methotrexate | dicarboxylic acid; monocarboxylic acid amide; pteridines | abortifacient; antimetabolite; antineoplastic agent; antirheumatic drug; dermatologic drug; DNA synthesis inhibitor; EC 1.5.1.3 (dihydrofolate reductase) inhibitor; immunosuppressive agent | |
10-propargyl-10-deazaaminopterin | 10-propargyl-10-deazaaminopterin: structure in first source pralatrexate : A pteridine that is the N-4-[1-(2,4-diaminopteridin-6-yl)pent-4-yn-2-yl]benzoyl derivative of L-glutamic acid. Used for treatment of Peripheral T-Cell Lymphoma, an aggressive form of non-Hodgkins lymphoma. | N-acyl-L-glutamic acid; pteridines; terminal acetylenic compound | antimetabolite; antineoplastic agent; EC 1.5.1.3 (dihydrofolate reductase) inhibitor |
thiorphan | |||
raltitrexed | N-acyl-amino acid | ||
pemetrexed | pemetrexed disodium : An organic sodium salt that is the disodium salt of N-{4-[2-(2-amino-4-oxo-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl]benzoyl}-L-glutamic acid. Inhibits thymidylate synthase (TS), 421 dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT). | N-acyl-L-glutamic acid; pyrrolopyrimidine | antimetabolite; antineoplastic agent; EC 1.5.1.3 (dihydrofolate reductase) inhibitor; EC 2.1.1.45 (thymidylate synthase) inhibitor; EC 2.1.2.2 (phosphoribosylglycinamide formyltransferase) inhibitor |