Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10017816HBVENSG00000160282.15protein_codingFTCDNoNo10841O95954
TVIS10007942HBVENSG00000160282.15protein_codingFTCDNoNo10841O95954
TVIS10017853HBVENSG00000160282.15protein_codingFTCDNoNo10841O95954
TVIS10013906HBVENSG00000160282.15protein_codingFTCDNoNo10841O95954
TVIS10005985HBVENSG00000160282.15protein_codingFTCDNoNo10841O95954
TVIS10033585HBVENSG00000160282.15protein_codingFTCDNoNo10841O95954
TVIS10047015HBVENSG00000160282.15protein_codingFTCDNoNo10841O95954
TVIS10059084HBVENSG00000160282.15protein_codingFTCDNoNo10841O95954
TVIS10059097HBVENSG00000160282.15protein_codingFTCDNoNo10841O95954
TVIS10059098HBVENSG00000160282.15protein_codingFTCDNoNo10841O95954
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Drug Information
GeneFTCD
DrugBank IDDB00116
Drug NameTetrahydrofolic acid
Target IDBE0000822
UniProt IDO95954
Regulation Typecofactor
PubMed IDs9677387; 11488596; 10329787; 10673422
CitationsBashour AM, Bloom GS: 58K, a microtubule-binding Golgi protein, is a formiminotransferase cyclodeaminase. J Biol Chem. 1998 Jul 31;273(31):19612-7.@@Cook RJ: Disruption of histidine catabolism in NEUT2 mice. Arch Biochem Biophys. 2001 Aug 15;392(2):226-32.@@Kohls D, Croteau N, Mejia N, MacKenzie RE, Vrielink A: Crystallization and preliminary X-ray analysis of the formiminotransferase domain from the bifunctional enzyme formiminotransferase-cyclodeaminase. Acta Crystallogr D Biol Crystallogr. 1999 Jun;55(Pt 6):1206-8.@@Kohls D, Sulea T, Purisima EO, MacKenzie RE, Vrielink A: The crystal structure of the formiminotransferase domain of formiminotransferase-cyclodeaminase: implications for substrate channeling in a bifunctional enzyme. Structure. 2000 Jan 15;8(1):35-46.
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