Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10011544HBVENSG00000115919.15protein_codingKYNUNoNo8942Q16719
TVIS10011545HBVENSG00000115919.15protein_codingKYNUNoNo8942Q16719
TVIS10003394HBVENSG00000115919.15protein_codingKYNUNoNo8942Q16719
TVIS10021827HBVENSG00000115919.15protein_codingKYNUNoNo8942Q16719
TVIS10028721HBVENSG00000115919.15protein_codingKYNUNoNo8942Q16719
TVIS20005639HPVENSG00000115919.15protein_codingKYNUNoNo8942Q16719
TVIS20017819HPVENSG00000115919.15protein_codingKYNUNoNo8942Q16719
TVIS44004105HTLV-1ENSG00000115919.15protein_codingKYNUNoNo8942Q16719
TCGA Plot Options
Drug Information
GeneKYNU
DrugBank IDDB00114
Drug NamePyridoxal phosphate
Target IDBE0000392
UniProt IDQ16719
Regulation Typecofactor
PubMed IDs14756555; 12204580; 17300176; 11985583
CitationsMomany C, Levdikov V, Blagova L, Lima S, Phillips RS: Three-dimensional structure of kynureninase from Pseudomonas fluorescens. Biochemistry. 2004 Feb 10;43(5):1193-203.@@Rooseboom M, Vermeulen NP, Groot EJ, Commandeur JN: Tissue distribution of cytosolic beta-elimination reactions of selenocysteine Se-conjugates in rat and human. Chem Biol Interact. 2002 Aug 15;140(3):243-64.@@Lima S, Khristoforov R, Momany C, Phillips RS: Crystal structure of Homo sapiens kynureninase. Biochemistry. 2007 Mar 13;46(10):2735-44. Epub 2007 Feb 15.@@Walsh HA, Botting NP: Purification and biochemical characterization of some of the properties of recombinant human kynureninase. Eur J Biochem. 2002 Apr;269(8):2069-74.
GroupsApproved; Investigational; Nutraceutical
Direct ClassificationPyridoxals and derivatives
SMILESCC1=NC=C(COP(O)(O)=O)C(C=O)=C1O
PathwaysHistidinemia; 3-Methylglutaconic Aciduria Type I; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); beta-Ketothiolase Deficiency; Tyrosine Metabolism; Disulfiram Action Pathway; Hyperprolinemia Type II; Glutamate Metabolism; Argininosuccinic Aciduria; Tyrosinemia Type I; Hyperinsulinism-Hyperammonemia Syndrome; Porphyrin Metabolism; 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency; Glutaric Aciduria Type I; Propanoate Metabolism; Taurine and Hypotaurine Metabolism; Catecholamine Biosynthesis; Glycine and Serine Metabolism; Carnitine Synthesis; Tyrosinemia Type 3 (TYRO3); Selenoamino Acid Metabolism; Carbamoyl Phosphate Synthetase Deficiency; Hyperprolinemia Type I; Saccharopinuria/Hyperlysinemia II; Histidine Metabolism; Cystathionine beta-Synthase Deficiency; Arginine and Proline Metabolism; Starch and Sucrose Metabolism; Globoid Cell Leukodystrophy; Ammonia Recycling
PharmGKBPA164749650
ChEMBLCHEMBL82202