Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10040030HBVENSG00000151632.18protein_codingAKR1C2NoNo1646B4DK69
P52895
TVIS10059666HBVENSG00000151632.18protein_codingAKR1C2NoNo1646B4DK69
P52895
TVIS30027108HIVENSG00000151632.18protein_codingAKR1C2NoNo1646B4DK69
P52895
TVIS30027109HIVENSG00000151632.18protein_codingAKR1C2NoNo1646B4DK69
P52895
TVIS30027110HIVENSG00000151632.18protein_codingAKR1C2NoNo1646B4DK69
P52895
TCGA Plot Options
Drug Information
GeneAKR1C2
DrugBank IDDB01586
Drug NameUrsodeoxycholic acid
Target IDBE0000622
UniProt IDP52895
Regulation Typeinhibitor
PubMed IDs17139284; 17016423; 19747134; 18826220; 9973208; 24929818
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.@@Amaral JD, Sola S, Steer CJ, Rodrigues CM: Role of nuclear steroid receptors in apoptosis. Curr Med Chem. 2009;16(29):3886-902.@@Halim M, Yee DJ, Sames D: Imaging induction of cytoprotective enzymes in intact human cells: coumberone, a metabolic reporter for human AKR1C enzymes reveals activation by panaxytriol, an active component of red ginseng. J Am Chem Soc. 2008 Oct 29;130(43):14123-8. doi: 10.1021/ja801245y. Epub 2008 Oct 1.@@Burczynski ME, Lin HK, Penning TM: Isoform-specific induction of a human aldo-keto reductase by polycyclic aromatic hydrocarbons (PAHs), electrophiles, and oxidative stress: implications for the alternative pathway of PAH activation catalyzed by human dihydrodiol dehydrogenase. Cancer Res. 1999 Feb 1;59(3):607-14.@@Martin N, Salazar-Cardozo C, Vercamer C, Ott L, Marot G, Slijepcevic P, Abbadie C, Pluquet O: Identification of a gene signature of a pre-transformation process by senescence evasion in normal human epidermal keratinocytes. Mol Cancer. 2014 Jun 14;13:151. doi: 10.1186/1476-4598-13-151.
GroupsApproved; Investigational
Direct ClassificationDihydroxy bile acids, alcohols and derivatives
SMILES[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@@H](O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCC(O)=O
Pathways
PharmGKBPA451837
ChEMBLCHEMBL1551