Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10048681HBVENSG00000139684.15protein_codingESDNoNo2098A0A140VJJ2
P10768
TVIS10048682HBVENSG00000139684.15protein_codingESDNoNo2098A0A140VJJ2
P10768
TVIS30006343HIVENSG00000139684.15protein_codingESDNoNo2098A0A140VJJ2
P10768
TVIS30035087HIVENSG00000139684.15protein_codingESDNoNo2098A0A140VJJ2
P10768
TVIS30035088HIVENSG00000139684.15protein_codingESDNoNo2098A0A140VJJ2
P10768
TVIS30035089HIVENSG00000139684.15protein_codingESDNoNo2098A0A140VJJ2
P10768
TVIS20009155HPVENSG00000139684.15protein_codingESDNoNo2098A0A140VJJ2
P10768
TVIS20009156HPVENSG00000139684.15protein_codingESDNoNo2098A0A140VJJ2
P10768
TVIS20024345HPVENSG00000139684.15protein_codingESDNoNo2098A0A140VJJ2
P10768
TVIS44034393HTLV-1ENSG00000139684.15protein_codingESDNoNo2098A0A140VJJ2
P10768
TCGA Plot Options
Drug Information
GeneESD
DrugBank IDDB00143
Drug NameGlutathione
Target IDBE0002283
UniProt IDP10768
Regulation Type
PubMed IDs17139284; 17016423; 12904537; 7397203; 2554783
CitationsOverington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6.@@Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34.@@Yurimoto H, Lee B, Yano T, Sakai Y, Kato N: Physiological role of S-formylglutathione hydrolase in C(1) metabolism of the methylotrophic yeast Candida boidinii. Microbiology. 2003 Aug;149(Pt 8):1971-9.@@Neben I, Sahm H, Kula MR: Studies on an enzyme, S-formylglutathione hydrolase, of the dissimilatory pathway of methanol in Candida boidinii. Biochim Biophys Acta. 1980 Jul 10;614(1):81-91.@@Sabatier L, Hoffschir F, al Achkar WA, Turleau C, de Grouchy J, Dutrillaux B: The decrease of catalase or esterase D activity in patients with microdeletions of 11p or 13q does not increase their radiosensitivity. Ann Genet. 1989;32(3):144-8.
GroupsApproved; Investigational; Nutraceutical
Direct ClassificationPeptides
SMILESN[C@@H](CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O)C(O)=O
PathwaysArachidonic Acid Metabolism; Flurbiprofen Action Pathway; 4-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency; Oxaprozin Action Pathway; Rofecoxib Action Pathway; Pyruvate Kinase Deficiency; Acetaminophen Metabolism Pathway; Mefenamic Acid Action Pathway; Bromfenac Action Pathway; 5-Oxoprolinuria; gamma-Glutamyltransferase Deficiency; Naproxen Action Pathway; Sulindac Action Pathway; Glutathione Synthetase Deficiency; Piroxicam Action Pathway; Nabumetone Action Pathway; 2-Hydroxyglutric Aciduria (D and L Form); Meloxicam Action Pathway; Cyclophosphamide Action Pathway; Succinic Semialdehyde Dehydrogenase Deficiency; Valdecoxib Action Pathway; Ketorolac Action Pathway; 5-Oxoprolinase Deficiency; Acetylsalicylic Acid Action Pathway; Antipyrine Action Pathway; Glutathione Metabolism; Diclofenac Action Pathway; Homocarnosinosis; Cyclophosphamide Metabolism Pathway; Nepafenac Action Pathway
PharmGKBPA449780
ChEMBLCHEMBL1543