Page last updated: 2024-10-24

cyclic-GMP-AMP transmembrane transporter activity

Definition

Target type: molecularfunction

Enables the transfer of cyclic-GMP-AMP from one side of a membrane to the other. [PMID:31126740]

Cyclic-GMP-AMP (cGAMP) transmembrane transporter activity is a crucial molecular function involved in the innate immune response. cGAMP, a second messenger produced by the enzyme cGAS upon detection of foreign DNA, plays a critical role in activating the STING pathway. This pathway ultimately triggers the production of type I interferons (IFNs), potent antiviral cytokines.

cGAMP transmembrane transporters, also known as cGAMP importers, facilitate the transport of cGAMP across cellular membranes. This process is essential for the activation of STING in the cytoplasm, where the receptor is localized.

The precise mechanism of cGAMP transport remains under investigation, but it likely involves a facilitated diffusion process driven by the concentration gradient of cGAMP. The transporter protein likely interacts with cGAMP through specific binding sites, facilitating its movement across the membrane.

Overall, cGAMP transmembrane transporter activity is a vital component of the innate immune system. It enables the efficient transfer of cGAMP from the cytoplasm to the STING receptor, thereby triggering the activation of the antiviral signaling pathway. This function plays a critical role in the host's defense against viral infections.'
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Proteins (1)

ProteinDefinitionTaxonomy
Reduced folate transporterA reduced folate transporter that is encoded in the genome of human. [PRO:DNx, UniProtKB:P41440]Homo sapiens (human)

Compounds (4)

CompoundDefinitionClassesRoles
methotrexatedicarboxylic 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-deazaaminopterin10-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
raltitrexedN-acyl-amino acid
pemetrexedpemetrexed 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