VIS ID | Virus | Ensembl ID | Gene Type | Target Gene | Oncogene | Tumor Suppressor Gene | NCBI ID | Uniprot ID |
---|---|---|---|---|---|---|---|---|
TVIS10060128 | HBV | ENSG00000091140.15 | protein_coding | DLD | No | No | 1738 | E9PEX6 P09622 |
TVIS30009389 | HIV | ENSG00000091140.15 | protein_coding | DLD | No | No | 1738 | E9PEX6 P09622 |
TVIS30011013 | HIV | ENSG00000091140.15 | protein_coding | DLD | No | No | 1738 | E9PEX6 P09622 |
TVIS30067751 | HIV | ENSG00000091140.15 | protein_coding | DLD | No | No | 1738 | E9PEX6 P09622 |
TVIS30067752 | HIV | ENSG00000091140.15 | protein_coding | DLD | No | No | 1738 | E9PEX6 P09622 |
TVIS20036188 | HPV | ENSG00000091140.15 | protein_coding | DLD | No | No | 1738 | E9PEX6 P09622 |
Target Gene Table
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TCGA Plot Options
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Drug Information
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Gene | DLD |
---|---|
DrugBank ID | DB00157 |
Drug Name | NADH |
Target ID | BE0000737 |
UniProt ID | P09622 |
Regulation Type | |
PubMed IDs | 17315258; 17017892; 17314104 |
Citations | Yan LJ, Yang SH, Shu H, Prokai L, Forster MJ: Histochemical staining and quantification of dihydrolipoamide dehydrogenase diaphorase activity using blue native PAGE. Electrophoresis. 2007 Apr;28(7):1036-45.@@Gutierrez-Correa J: Trypanosoma cruzi dihydrolipoamide dehydrogenase as target for phenothiazine cationic radicals. Effect of antioxidants. Curr Drug Targets. 2006 Sep;7(9):1155-79.@@Islam MM, Wallin R, Wynn RM, Conway M, Fujii H, Mobley JA, Chuang DT, Hutson SM: A novel branched-chain amino acid metabolon. Protein-protein interactions in a supramolecular complex. J Biol Chem. 2007 Apr 20;282(16):11893-903. Epub 2007 Feb 21. |
Groups | Approved; Nutraceutical |
Direct Classification | (5'->5')-dinucleotides |
SMILES | NC(=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 |
Pathways | Ethylmalonic 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 |
PharmGKB | PA164755085 |
ChEMBL | CHEMBL1234616 |