Trifunctional purine biosynthetic protein adenosine-3
Also known as: GART, PGFT, PRGS
Function
Trifunctional enzyme that catalyzes three distinct reactions as part of the 'de novo' inosine monophosphate biosynthetic pathway.
Classification
- Family (Pfam)
- PF00586 AIRS, PF02769 AIRS_C, PF00551 Formyl_trans_N, PF01071 GARS_A, PF02843 GARS_C, PF02844 GARS_N
- InterPro
- ATP-grasp, ATP_grasp_subdomain_1, Formyl_transf_N, Formyl_transf_N_sf, GART, GART_AS, PreATP-grasp_dom_sf, PRibGlycinamid_synth_ATP-grasp, PRibGlycinamide_synth, PRibGlycinamide_synth_C-dom, PRibGlycinamide_synth_C_sf, PRibGlycinamide_synth_CS, PRibGlycinamide_synth_N, PurM-like_C_dom, PurM-like_C_sf, PurM-like_N, PurM-like_N_sf, PurM_cligase, Rudment_hybrid_motif
- Functional cluster
- DNA Glycosylases & Cofactor Biosynthesis Enzymes
Experimental structures · PDB · 40
- 1MEJ X-ray 2.00A
- 1MEN X-ray 2.23A
- 1MEO X-ray 1.72A
- 1NJS X-ray 1.98A
- 1RBM X-ray 2.30A
- 1RBQ X-ray 2.10A
- 1RBY X-ray 2.10A
- 1RBZ X-ray 2.10A
- 1RC0 X-ray 2.05A
- 1RC1 X-ray 2.25A
- 1ZLX X-ray 2.20A
- 1ZLY X-ray 2.07A
- … and 28 more
A predicted model is available from AlphaFold.
Gene Ontology · 17
- GO:0005829 cytosol
- GO:0070062 extracellular exosome
- GO:0005524 ATP binding
- GO:0046872 metal ion binding
- GO:0004637 phosphoribosylamine-glycine ligase activity
- GO:0004641 phosphoribosylformylglycinamidine cyclo-ligase activity
- GO:0004644 phosphoribosylglycinamide formyltransferase activity
- GO:0044208 'de novo' AMP biosynthetic process
- GO:0006189 'de novo' IMP biosynthetic process
- GO:0097294 'de novo' XMP biosynthetic process
- GO:0046084 adenine biosynthetic process
- GO:0003360 brainstem development
- GO:0021549 cerebellum development
- GO:0021987 cerebral cortex development
- GO:0006177 GMP biosynthetic process
- GO:0006164 purine nucleotide biosynthetic process
- GO:0009168 purine ribonucleoside monophosphate biosynthetic process
Drugs targeting this protein · 6
- PELITREXOL inhibitor
- PEMETREXED inhibitor
- PEMETREXED DISODIUM inhibitor
- PEMETREXED TROMETHAMINE inhibitor
- PEMETREXED MONOHYDRATE inhibitor
- PEMETREXED DIPOTASSIUM inhibitor
Related proteins · sequence + function similarity
- Trifunctional purine biosynthetic protein adenosine-3 0.97
- Trifunctional purine biosynthetic protein adenosine-3 0.97
- Trifunctional purine biosynthetic protein adenosine-3 0.97
- Trifunctional purine biosynthetic protein adenosine-3 0.79
- Trifunctional purine biosynthetic protein adenosine-3 0.75
- Bifunctional purine biosynthetic protein ADE1 0.71
- Bifunctional purine biosynthetic protein ADE5,7 0.70
- Bifunctional purine biosynthetic protein ADE5,7 0.69
- Phosphoribosylamine--glycine ligase, chloroplastic 0.68
- Bifunctional purine biosynthetic protein purD 0.65
- Phosphoribosylamine--glycine ligase 0.62
- Phosphoribosylamine--glycine ligase 0.62
Co-cited proteins · studied together in the literature
Literature · 16 cited papers
- An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome. J. Proteomics · 2014
- Toward a comprehensive characterization of a human cancer cell phosphoproteome. J. Proteome Res. · 2013
- Initial characterization of the human central proteome. BMC Syst. Biol. · 2011
- Structural studies of tri-functional human GART. Nucleic Acids Res. · 2010
- Lysine acetylation targets protein complexes and co-regulates major cellular functions. Science · 2009
- Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach. Anal. Chem. · 2009
- The apo and ternary complex structures of a chemotherapeutic target: human glycinamide ribonucleotide transformylase. Biochemistry · 2005
- Immunoaffinity profiling of tyrosine phosphorylation in cancer cells. Nat. Biotechnol. · 2005
- The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Genome Res. · 2004
- Complete sequencing and characterization of 21,243 full-length human cDNAs. Nat. Genet. · 2004
- Proteomic characterization of the human centrosome by protein correlation profiling. Nature · 2003
- Rational design, synthesis, evaluation, and crystal structure of a potent inhibitor of human GAR Tfase: 10-(trifluoroacetyl)-5,10-dideazaacyclic-5,6,7,8-tetrahydrofolic acid. Biochemistry · 2003
- … and 4 more in the literature graph
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