Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10017304HBVENSG00000160209.19protein_codingPDXKNoNo8566F2Z2Y4
O00764
TVIS30054773HIVENSG00000160209.19protein_codingPDXKNoNo8566F2Z2Y4
O00764
TVIS20002225HPVENSG00000160209.19protein_codingPDXKNoNo8566F2Z2Y4
O00764
TVIS20068127HPVENSG00000160209.19protein_codingPDXKNoNo8566F2Z2Y4
O00764
TVIS20045247HPVENSG00000160209.19protein_codingPDXKNoNo8566F2Z2Y4
O00764
TVIS44042877HTLV-1ENSG00000160209.19protein_codingPDXKNoNo8566F2Z2Y4
O00764
TVIS44042961HTLV-1ENSG00000160209.19protein_codingPDXKNoNo8566F2Z2Y4
O00764
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Drug Information
GenePDXK
DrugBank IDDB00147
Drug NamePyridoxal
Target IDBE0000042
UniProt IDO00764
Regulation Type
PubMed IDs15985434; 16494569; 16978644
CitationsTang L, Li MH, Cao P, Wang F, Chang WR, Bach S, Reinhardt J, Ferandin Y, Galons H, Wan Y, Gray N, Meijer L, Jiang T, Liang DC: Crystal structure of pyridoxal kinase in complex with roscovitine and derivatives. J Biol Chem. 2005 Sep 2;280(35):31220-9. Epub 2005 Jun 28.@@Adams JB, George F, Audhya T: Abnormally high plasma levels of vitamin B6 in children with autism not taking supplements compared to controls not taking supplements. J Altern Complement Med. 2006 Jan-Feb;12(1):59-63.@@Newman JA, Das SK, Sedelnikova SE, Rice DW: The crystal structure of an ADP complex of Bacillus subtilis pyridoxal kinase provides evidence for the parallel emergence of enzyme activity during evolution. J Mol Biol. 2006 Oct 20;363(2):520-30. Epub 2006 Aug 12.
GroupsExperimental; Nutraceutical
Direct ClassificationPyridoxals and derivatives
SMILESCC1=NC=C(CO)C(C=O)=C1O
Pathways3-Methylglutaconic Aciduria Type III; 3-Methylglutaconic Aciduria Type I; beta-Ketothiolase Deficiency; Isovaleric Aciduria; Isobutyryl-CoA Dehydrogenase Deficiency; Propionic Acidemia; 3-Hydroxyisobutyric Aciduria; 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency; Hypophosphatasia; Vitamin B6 Metabolism; 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency; 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I; 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency; Methylmalonic Aciduria; 3-Methylglutaconic Aciduria Type IV; Methylmalonate Semialdehyde Dehydrogenase Deficiency; Valine, Leucine, and Isoleucine Degradation; Maple Syrup Urine Disease; Isovaleric Acidemia
PharmGKBPA164749166
ChEMBLCHEMBL102970