Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10025563HBVENSG00000131069.20protein_codingACSS2NoNo55902Q4G0E8
Q6DKJ3
Q96FY7
Q9NR19
TVIS30053433HIVENSG00000131069.20protein_codingACSS2NoNo55902Q4G0E8
Q6DKJ3
Q96FY7
Q9NR19
TVIS30053434HIVENSG00000131069.20protein_codingACSS2NoNo55902Q4G0E8
Q6DKJ3
Q96FY7
Q9NR19
TVIS20005833HPVENSG00000131069.20protein_codingACSS2NoNo55902Q4G0E8
Q6DKJ3
Q96FY7
Q9NR19
TVIS20043403HPVENSG00000131069.20protein_codingACSS2NoNo55902Q4G0E8
Q6DKJ3
Q96FY7
Q9NR19
TVIS44021380HTLV-1ENSG00000131069.20protein_codingACSS2NoNo55902Q4G0E8
Q6DKJ3
Q96FY7
Q9NR19
TCGA Plot Options
Drug Information
GeneACSS2
DrugBank IDDB00131
Drug NameAdenosine phosphate
Target IDBE0000350
UniProt IDQ9NR19
Regulation Typeproduct of
PubMed IDs17350930; 17303131; 16981708; 17497934
CitationsIngram-Smith C, Smith KS: AMP-forming acetyl-CoA synthetases in Archaea show unexpected diversity in substrate utilization. Archaea. 2007 May;2(2):95-107.@@Linne U, Schafer A, Stubbs MT, Marahiel MA: Aminoacyl-coenzyme A synthesis catalyzed by adenylation domains. FEBS Lett. 2007 Mar 6;581(5):905-10. Epub 2007 Feb 7.@@Ingram-Smith C, Woods BI, Smith KS: Characterization of the acyl substrate binding pocket of acetyl-CoA synthetase. Biochemistry. 2006 Sep 26;45(38):11482-90.@@Reger AS, Carney JM, Gulick AM: Biochemical and crystallographic analysis of substrate binding and conformational changes in acetyl-CoA synthetase. Biochemistry. 2007 Jun 5;46(22):6536-46. Epub 2007 May 12.
GroupsApproved; Investigational; Nutraceutical; Withdrawn
Direct ClassificationPurine ribonucleoside monophosphates
SMILESNC1=C2N=CN([C@@H]3O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]3O)C2=NC=N1
PathwaysLeigh Syndrome; Histidinemia; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); Fatty Acid Metabolism; Gentamicin Action Pathway; Pyruvate Dehydrogenase Complex Deficiency; Purine Nucleoside Phosphorylase Deficiency; Hyperprolinemia Type II; Glutamate Metabolism; Clarithromycin Action Pathway; Argininosuccinic Aciduria; Pyruvate Decarboxylase E1 Component Deficiency (PDHE1 Deficiency); Hyperinsulinism-Hyperammonemia Syndrome; Butyrate Metabolism; Pyruvate Metabolism; Pentose Phosphate Pathway; Propanoate Metabolism; Glycine and Serine Metabolism; Selenoamino Acid Metabolism; Thiamine Metabolism; Oxytetracycline Action Pathway; Tetracycline Action Pathway; Carbamoyl Phosphate Synthetase Deficiency; Hyperprolinemia Type I; Histidine Metabolism; Cystathionine beta-Synthase Deficiency; Arginine and Proline Metabolism; Roxithromycin Action Pathway; Purine Metabolism; Ammonia Recycling
PharmGKBPA164744376
ChEMBLCHEMBL752