Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10050536HBVENSG00000228716.7protein_codingDHFRNoNo1719B4DM58
P00374
TVIS10049990HBVENSG00000228716.7protein_codingDHFRNoNo1719B4DM58
P00374
TVIS30008799HIVENSG00000228716.7protein_codingDHFRNoNo1719B4DM58
P00374
TVIS20012134HPVENSG00000228716.7protein_codingDHFRNoNo1719B4DM58
P00374
TVIS20024726HPVENSG00000228716.7protein_codingDHFRNoNo1719B4DM58
P00374
TVIS44004386HTLV-1ENSG00000228716.7protein_codingDHFRNoNo1719B4DM58
P00374
TVIS44038861HTLV-1ENSG00000228716.7protein_codingDHFRNoNo1719B4DM58
P00374
TVIS44038892HTLV-1ENSG00000228716.7protein_codingDHFRNoNo1719B4DM58
P00374
TVIS44038891HTLV-1ENSG00000228716.7protein_codingDHFRNoNo1719B4DM58
P00374
TVIS44045060HTLV-1ENSG00000228716.7protein_codingDHFRNoNo1719B4DM58
P00374
TCGA Plot Options
Drug Information
GeneDHFR
DrugBank IDDB00157
Drug NameNADH
Target IDBE0000330
UniProt IDP00374
Regulation Type
PubMed IDs17115689; 17032644
CitationsArgyrou A, Jin L, Siconilfi-Baez L, Angeletti RH, Blanchard JS: Proteome-wide profiling of isoniazid targets in Mycobacterium tuberculosis. Biochemistry. 2006 Nov 28;45(47):13947-53.@@Vickers TJ, Orsomando G, de la Garza RD, Scott DA, Kang SO, Hanson AD, Beverley SM: Biochemical and genetic analysis of methylenetetrahydrofolate reductase in Leishmania metabolism and virulence. J Biol Chem. 2006 Dec 15;281(50):38150-8. Epub 2006 Oct 10.
GroupsApproved; Nutraceutical
Direct Classification(5'->5')-dinucleotides
SMILESNC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C(N)N=CN=C23)[C@@H](O)[C@H]1O
PathwaysEthylmalonic Encephalopathy; 3-Methylglutaconic Aciduria Type III; Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency); Caffeine Metabolism; Fructose and Mannose Degradation; Isovaleric Aciduria; Lysine Degradation; Methylmalonic Aciduria Due to Cobalamin-Related Disorders; Glycerol Phosphate Shuttle; Zellweger Syndrome; Propionic Acidemia; Glycolysis; Xanthine Dehydrogenase Deficiency (Xanthinuria); S-Adenosylhomocysteine (SAH) Hydrolase Deficiency; Tryptophan Metabolism; Glutaric Aciduria Type I; 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I; Glycine N-Methyltransferase Deficiency; Dimethylglycine Dehydrogenase Deficiency; Androgen and Estrogen Metabolism; Nucleotide Sugars Metabolism; 3-Methylglutaconic Aciduria Type IV; Dihydropyrimidine Dehydrogenase Deficiency (DHPD); Malate-Aspartate Shuttle; Folate Metabolism; Valine, Leucine, and Isoleucine Degradation; Maple Syrup Urine Disease; Glycerol Kinase Deficiency; Adenylosuccinate Lyase Deficiency; Cysteine Metabolism
PharmGKBPA164755085
ChEMBLCHEMBL1234616