Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS30018591HIVENSG00000161533.12protein_codingACOX1NoNo51Q15067
TVIS30019502HIVENSG00000161533.12protein_codingACOX1NoNo51Q15067
TVIS30045083HIVENSG00000161533.12protein_codingACOX1NoNo51Q15067
TVIS30045084HIVENSG00000161533.12protein_codingACOX1NoNo51Q15067
TVIS30045085HIVENSG00000161533.12protein_codingACOX1NoNo51Q15067
TVIS30045086HIVENSG00000161533.12protein_codingACOX1NoNo51Q15067
TVIS30045087HIVENSG00000161533.12protein_codingACOX1NoNo51Q15067
TVIS30045088HIVENSG00000161533.12protein_codingACOX1NoNo51Q15067
TVIS30045089HIVENSG00000161533.12protein_codingACOX1NoNo51Q15067
TVIS30045090HIVENSG00000161533.12protein_codingACOX1NoNo51Q15067
TCGA Plot Options
Drug Information
GeneACOX1
DrugBank IDDB03147
Drug NameFlavin adenine dinucleotide
Target IDBE0004135
UniProt IDQ15067
Regulation Type
PubMed IDs10592235
CitationsBerman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42.
GroupsApproved
Direct ClassificationFlavin nucleotides
SMILESCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC3=C1N=CN=C3N)C1=NC(=O)NC(=O)C1=N2
PathwaysCerivastatin Action Pathway; Ethylmalonic Encephalopathy; 3-Methylglutaconic Aciduria Type III; Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency); Caffeine Metabolism; Isovaleric Aciduria; Lysine Degradation; Riboflavin Metabolism; 5-Oxoprolinuria; Methylmalonic Aciduria Due to Cobalamin-Related Disorders; Glycerol Phosphate Shuttle; Propionic Acidemia; Hypercholesterolemia; Xanthine Dehydrogenase Deficiency (Xanthinuria); S-Adenosylhomocysteine (SAH) Hydrolase Deficiency; Tryptophan Metabolism; Glutaric Aciduria Type I; 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I; Phenylketonuria; Glycine N-Methyltransferase Deficiency; Dimethylglycine Dehydrogenase Deficiency; Lovastatin Action Pathway; 3-Methylglutaconic Aciduria Type IV; Dihydropyrimidine Dehydrogenase Deficiency (DHPD); Glutathione Metabolism; Folate Metabolism; Valine, Leucine, and Isoleucine Degradation; Maple Syrup Urine Disease; Glycerol Kinase Deficiency; Adenylosuccinate Lyase Deficiency
PharmGKB
ChEMBLCHEMBL1232653