Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10060391HBVENSG00000084110.11protein_codingHALNoNo3034P42357
TVIS44005306HTLV-1ENSG00000084110.11protein_codingHALNoNo3034P42357
TCGA Plot Options
Drug Information
GeneHAL
DrugBank IDDB00117
Drug NameHistidine
Target IDBE0000086
UniProt IDP42357
Regulation Type
PubMed IDs17191848; 17536021; 17185227; 17193285
CitationsViergutz S, Retey J: Kinetic analysis of the reactions catalyzed by histidine and phenylalanine ammonia lyases. Chem Biodivers. 2004 Feb;1(2):296-302.@@Lambrecht NW, Yakubov I, Sachs G: Fasting-induced changes in ECL cell gene expression. Physiol Genomics. 2007 Oct 22;31(2):183-92. Epub 2007 May 29.@@Watts KT, Mijts BN, Lee PC, Manning AJ, Schmidt-Dannert C: Discovery of a substrate selectivity switch in tyrosine ammonia-lyase, a member of the aromatic amino acid lyase family. Chem Biol. 2006 Dec;13(12):1317-26.@@Katona A, Tosa MI, Paizs C, Retey J: Inhibition of histidine ammonia lyase by heteroaryl-alanines and acrylates. Chem Biodivers. 2006 May;3(5):502-8.
GroupsInvestigational; Nutraceutical
Direct ClassificationHistidine and derivatives
SMILESN[C@@H](CC1=CNC=N1)C(O)=O
PathwaysClomocycline Action Pathway; Histidinemia; Rolitetracycline Action Pathway; Demeclocycline Action Pathway; Josamycin Action Pathway; Kanamycin Action Pathway; Gentamicin Action Pathway; Tobramycin Action Pathway; Carnosinuria, Carnosinemia; Azithromycin Action Pathway; Methylhistidine Metabolism; Clarithromycin Action Pathway; Minocycline Action Pathway; Troleandomycin Action Pathway; Amikacin Action Pathway; Streptomycin Action Pathway; Oxytetracycline Action Pathway; Tetracycline Action Pathway; Spectinomycin Action Pathway; Erythromycin Action Pathway; Netilmicin Action Pathway; beta-Alanine Metabolism; Doxycycline Action Pathway; Ammonia Recycling; Histidine Metabolism; Telithromycin Action Pathway; Neomycin Action Pathway; Roxithromycin Action Pathway; Arbekacin Action Pathway; Clindamycin Action Pathway
PharmGKBPA449882
ChEMBLCHEMBL17962