Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10005041HBVENSG00000155511.19protein_codingGRIA1NoNo2890P42261
TVIS10005042HBVENSG00000155511.19protein_codingGRIA1NoNo2890P42261
TVIS10034071HBVENSG00000155511.19protein_codingGRIA1NoNo2890P42261
TVIS10051034HBVENSG00000155511.19protein_codingGRIA1NoNo2890P42261
TVIS10050959HBVENSG00000155511.19protein_codingGRIA1NoNo2890P42261
TVIS30086592HIVENSG00000155511.19protein_codingGRIA1NoNo2890P42261
TVIS30086040HIVENSG00000155511.19protein_codingGRIA1NoNo2890P42261
TVIS30083783HIVENSG00000155511.19protein_codingGRIA1NoNo2890P42261
TVIS30063832HIVENSG00000155511.19protein_codingGRIA1NoNo2890P42261
TVIS30063833HIVENSG00000155511.19protein_codingGRIA1NoNo2890P42261
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Drug Information
GeneGRIA1
DrugBank IDDB00142
Drug NameGlutamic acid
Target IDBE0000640
UniProt IDP42261
Regulation Type
PubMed IDs17139284; 17016423; 1279377; 7679210; 7838123
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.@@Stein E, Cox JA, Seeburg PH, Verdoorn TA: Complex pharmacological properties of recombinant alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate receptor subtypes. Mol Pharmacol. 1992 Nov;42(5):864-71.@@Henley JM, Jenkins R, Hunt SP: Localisation of glutamate receptor binding sites and mRNAs to the dorsal horn of the rat spinal cord. Neuropharmacology. 1993 Jan;32(1):37-41.@@Li F, Owens N, Verdoorn TA: Functional effects of mutations in the putative agonist binding region of recombinant alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors. Mol Pharmacol. 1995 Jan;47(1):148-54.
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