Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS20001972HPVENSG00000130948.10protein_codingHSD17B3NoNo3293P37058
Q6FH62
TVIS20063402HPVENSG00000130948.10protein_codingHSD17B3NoNo3293P37058
Q6FH62
TVIS20020615HPVENSG00000130948.10protein_codingHSD17B3NoNo3293P37058
Q6FH62
TVIS20020616HPVENSG00000130948.10protein_codingHSD17B3NoNo3293P37058
Q6FH62
TVIS20020617HPVENSG00000130948.10protein_codingHSD17B3NoNo3293P37058
Q6FH62
TVIS44012794HTLV-1ENSG00000130948.10protein_codingHSD17B3NoNo3293P37058
Q6FH62
TVIS44029979HTLV-1ENSG00000130948.10protein_codingHSD17B3NoNo3293P37058
Q6FH62
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Drug Information
GeneHSD17B3
DrugBank IDDB00157
Drug NameNADH
Target IDBE0000336
UniProt IDP37058
Regulation Type
PubMed IDs17139284; 17016423; 237755
CitationsOverington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6.@@Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34.@@Inano H, Tamaoki B: Relationship between steroids and pyridine nucleotides in the oxido-reduction catalyzed by the 17 beta-hydroxysteroid dehydrogenase purified from the porcine testicular microsomal fraction. Eur J Biochem. 1975 May 6;53(2):319-26.
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