Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS30007896HIVENSG00000138363.15protein_codingATICYesNo471P31939
TVIS30052334HIVENSG00000138363.15protein_codingATICYesNo471P31939
TVIS30052335HIVENSG00000138363.15protein_codingATICYesNo471P31939
TVIS44037937HTLV-1ENSG00000138363.15protein_codingATICYesNo471P31939
TVIS44037738HTLV-1ENSG00000138363.15protein_codingATICYesNo471P31939
TVIS44037936HTLV-1ENSG00000138363.15protein_codingATICYesNo471P31939
TVIS44044411HTLV-1ENSG00000138363.15protein_codingATICYesNo471P31939
TVIS44037935HTLV-1ENSG00000138363.15protein_codingATICYesNo471P31939
TCGA Plot Options
Drug Information
GeneATIC
DrugBank IDDB00116
Drug NameTetrahydrofolic acid
Target IDBE0001240
UniProt IDP31939
Regulation Typecofactor
PubMed IDs12974624; 11948179
CitationsWolan DW, Greasley SE, Wall MJ, Benkovic SJ, Wilson IA: Structure of avian AICAR transformylase with a multisubstrate adduct inhibitor beta-DADF identifies the folate binding site. Biochemistry. 2003 Sep 23;42(37):10904-14.@@Bulock KG, Beardsley GP, Anderson KS: The kinetic mechanism of the human bifunctional enzyme ATIC (5-amino-4-imidazolecarboxamide ribonucleotide transformylase/inosine 5'-monophosphate cyclohydrolase). A surprising lack of substrate channeling. J Biol Chem. 2002 Jun 21;277(25):22168-74. Epub 2002 Apr 10.
GroupsNutraceutical
Direct ClassificationGlutamic acid and derivatives
SMILESNC1=NC(=O)C2=C(NCC(CNC3=CC=C(C=C3)C(=O)N[C@@H](CCC(O)=O)C(O)=O)N2)N1
PathwaysHistidinemia; Lesch-Nyhan Syndrome (LNS); Molybdenum Cofactor Deficiency; Azathioprine Action Pathway; AICA-Ribosiduria; Purine Nucleoside Phosphorylase Deficiency; Methionine Adenosyltransferase Deficiency; Folate Malabsorption, Hereditary; Adenine Phosphoribosyltransferase Deficiency (APRT); Thioguanine Action Pathway; Mercaptopurine Action Pathway; Non-Ketotic Hyperglycinemia; Methotrexate Action Pathway; Betaine Metabolism; S-Adenosylhomocysteine (SAH) Hydrolase Deficiency; Glycine and Serine Metabolism; Adenosine Deaminase Deficiency; Xanthinuria Type II; Methionine Metabolism; Dihydropyrimidine Dehydrogenase Deficiency (DHPD); Histidine Metabolism; Cystathionine beta-Synthase Deficiency; Folate Metabolism; Sarcosine Oncometabolite Pathway; Sarcosinemia; Methylenetetrahydrofolate Reductase Deficiency (MTHFRD); Purine Metabolism; Gout or Kelley-Seegmiller Syndrome; Adenylosuccinate Lyase Deficiency; Ammonia Recycling
PharmGKBPA164745110
ChEMBLCHEMBL2021342