Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10015168HBVENSG00000135423.13protein_codingGLS2NoNo27165A0A087X004
Q9UI32
TVIS10015169HBVENSG00000135423.13protein_codingGLS2NoNo27165A0A087X004
Q9UI32
TVIS10026882HBVENSG00000135423.13protein_codingGLS2NoNo27165A0A087X004
Q9UI32
TVIS10026883HBVENSG00000135423.13protein_codingGLS2NoNo27165A0A087X004
Q9UI32
TVIS10026884HBVENSG00000135423.13protein_codingGLS2NoNo27165A0A087X004
Q9UI32
TVIS10026885HBVENSG00000135423.13protein_codingGLS2NoNo27165A0A087X004
Q9UI32
TVIS10049961HBVENSG00000135423.13protein_codingGLS2NoNo27165A0A087X004
Q9UI32
TVIS30033215HIVENSG00000135423.13protein_codingGLS2NoNo27165A0A087X004
Q9UI32
TVIS20034424HPVENSG00000135423.13protein_codingGLS2NoNo27165A0A087X004
Q9UI32
TVIS44026809HTLV-1ENSG00000135423.13protein_codingGLS2NoNo27165A0A087X004
Q9UI32
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Drug Information
GeneGLS2
DrugBank IDDB00142
Drug NameGlutamic acid
Target IDBE0000003
UniProt IDQ9UI32
Regulation Type
PubMed IDs17373776; 17321558; 16793004
CitationsDossena L, Curti B, Vanoni MA: Activation and coupling of the glutaminase and synthase reaction of glutamate synthase is mediated by E1013 of the ferredoxin-dependent enzyme, belonging to loop 4 of the synthase domain. Biochemistry. 2007 Apr 17;46(15):4473-85. Epub 2007 Mar 21.@@Kita K, Suzuki T, Ochi T: Down-regulation of glutaminase C in human hepatocarcinoma cell by diphenylarsinic acid, a degradation product of chemical warfare agents. Toxicol Appl Pharmacol. 2007 May 1;220(3):262-70. Epub 2007 Jan 24.@@Yoshimune K, Shirakihara Y, Shiratori A, Wakayama M, Chantawannakul P, Moriguchi M: Crystal structure of a major fragment of the salt-tolerant glutaminase from Micrococcus luteus K-3. Biochem Biophys Res Commun. 2006 Aug 11;346(4):1118-24. Epub 2006 Jun 6.
GroupsApproved; Nutraceutical
Direct ClassificationGlutamic acid and derivatives
SMILESN[C@@H](CCC(O)=O)C(O)=O
PathwaysHistidinemia; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); 3-Methylglutaconic Aciduria Type I; beta-Ketothiolase Deficiency; Purine Nucleoside Phosphorylase Deficiency; Tyrosine Metabolism; Ketoprofen Action Pathway; Glutamate Metabolism; Argininosuccinic Aciduria; Salla Disease/Infantile Sialic Acid Storage Disease; Tyrosinemia Type I; Hyperinsulinism-Hyperammonemia Syndrome; 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency; Glutaric Aciduria Type I; Propanoate Metabolism; Celecoxib Action Pathway; Glycine and Serine Metabolism; Suprofen Action Pathway; Indomethacin Action Pathway; Carbamoyl Phosphate Synthetase Deficiency; Sialuria or French Type Sialuria; Ibuprofen Action Pathway; Saccharopinuria/Hyperlysinemia II; Histidine Metabolism; Arginine and Proline Metabolism; Purine Metabolism; Diflunisal Action Pathway; Etodolac Action Pathway; Ammonia Recycling
PharmGKBPA449776
ChEMBLCHEMBL575060