Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS42000826EBVENSG00000128609.16protein_codingNDUFA5NoNo4698A0A087WXR5
A0A087X1G1
Q16718
TVIS30067882HIVENSG00000128609.16protein_codingNDUFA5NoNo4698A0A087WXR5
A0A087X1G1
Q16718
TVIS44036016HTLV-1ENSG00000128609.16protein_codingNDUFA5NoNo4698A0A087WXR5
A0A087X1G1
Q16718
TCGA Plot Options
Drug Information
GeneNDUFA5
DrugBank IDDB00157
Drug NameNADH
Target IDBE0000473
UniProt IDQ16718
Regulation Type
PubMed IDs17444656; 17209562
CitationsChen CL, Zhang L, Yeh A, Chen CA, Green-Church KB, Zweier JL, Chen YR: Site-specific S-glutathiolation of mitochondrial NADH ubiquinone reductase. Biochemistry. 2007 May 15;46(19):5754-65. Epub 2007 Apr 20.@@Belevich G, Euro L, Wikstrom M, Verkhovskaya M: Role of the conserved arginine 274 and histidine 224 and 228 residues in the NuoCD subunit of complex I from Escherichia coli. Biochemistry. 2007 Jan 16;46(2):526-33.
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