Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS42000264EBVENSG00000169567.13protein_codingHINT1NoNo3094P49773
TVIS30063496HIVENSG00000169567.13protein_codingHINT1NoNo3094P49773
TVIS30063497HIVENSG00000169567.13protein_codingHINT1NoNo3094P49773
TVIS30063498HIVENSG00000169567.13protein_codingHINT1NoNo3094P49773
TVIS30063499HIVENSG00000169567.13protein_codingHINT1NoNo3094P49773
TVIS30063500HIVENSG00000169567.13protein_codingHINT1NoNo3094P49773
TVIS20040727HPVENSG00000169567.13protein_codingHINT1NoNo3094P49773
TCGA Plot Options
Drug Information
GeneHINT1
DrugBank IDDB00131
Drug NameAdenosine phosphate
Target IDBE0001473
UniProt IDP49773
Regulation Typeproduct of
PubMed IDs17337452; 17158446; 17217311
CitationsChou TF, Tikh IB, Horta BA, Ghosh B, De Alencastro RB, Wagner CR: Engineered monomeric human histidine triad nucleotide-binding protein 1 hydrolyzes fluorogenic acyl-adenylate and lysyl-tRNA synthetase-generated lysyl-adenylate. J Biol Chem. 2007 May 18;282(20):15137-47. Epub 2007 Mar 2.@@Chou TF, Wagner CR: Lysyl-tRNA synthetase-generated lysyl-adenylate is a substrate for histidine triad nucleotide binding proteins. J Biol Chem. 2007 Feb 16;282(7):4719-27. Epub 2006 Dec 8.@@Chou TF, Baraniak J, Kaczmarek R, Zhou X, Cheng J, Ghosh B, Wagner CR: Phosphoramidate pronucleotides: a comparison of the phosphoramidase substrate specificity of human and Escherichia coli histidine triad nucleotide binding proteins. Mol Pharm. 2007 Mar-Apr;4(2):208-17. Epub 2007 Jan 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GroupsApproved; Investigational; Nutraceutical; Withdrawn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