Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10046614HBVENSG00000103415.12protein_codingHMOX2NoNo3163A0A087WT44
P30519
TVIS30012070HIVENSG00000103415.12protein_codingHMOX2NoNo3163A0A087WT44
P30519
TVIS30006748HIVENSG00000103415.12protein_codingHMOX2NoNo3163A0A087WT44
P30519
TVIS30012071HIVENSG00000103415.12protein_codingHMOX2NoNo3163A0A087WT44
P30519
TVIS30002419HIVENSG00000103415.12protein_codingHMOX2NoNo3163A0A087WT44
P30519
TVIS30012072HIVENSG00000103415.12protein_codingHMOX2NoNo3163A0A087WT44
P30519
TVIS30006749HIVENSG00000103415.12protein_codingHMOX2NoNo3163A0A087WT44
P30519
TVIS30006750HIVENSG00000103415.12protein_codingHMOX2NoNo3163A0A087WT44
P30519
TVIS30012073HIVENSG00000103415.12protein_codingHMOX2NoNo3163A0A087WT44
P30519
TVIS30002420HIVENSG00000103415.12protein_codingHMOX2NoNo3163A0A087WT44
P30519
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Drug Information
GeneHMOX2
DrugBank IDDB00157
Drug NameNADH
Target IDBE0000587
UniProt IDP30519
Regulation Type
PubMed IDs16986858; 17157188
CitationsTanaka M, Ohkubo K, Fukuzumi S: DNA cleavage by UVA irradiation of NADH with dioxygen via radical chain processes. J Phys Chem A. 2006 Sep 28;110(38):11214-8.@@Goldstone AB, Liochev SI, Fridovich I: Inactivation of copper, zinc superoxide dismutase by H2O2 : mechanism of protection. Free Radic Biol Med. 2006 Dec 15;41(12):1860-3. Epub 2006 Sep 19.
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