VIS ID | Virus | Ensembl ID | Gene Type | Target Gene | Oncogene | Tumor Suppressor Gene | NCBI ID | Uniprot ID |
---|---|---|---|---|---|---|---|---|
TVIS20050388 | HPV | ENSG00000089250.20 | protein_coding | NOS1 | No | No | 4842 | A0PJJ7 B3VK56 P29475 |
TVIS20050392 | HPV | ENSG00000089250.20 | protein_coding | NOS1 | No | No | 4842 | A0PJJ7 B3VK56 P29475 |
TVIS20021051 | HPV | ENSG00000089250.20 | protein_coding | NOS1 | No | No | 4842 | A0PJJ7 B3VK56 P29475 |
TVIS44034700 | HTLV-1 | ENSG00000089250.20 | protein_coding | NOS1 | No | No | 4842 | A0PJJ7 B3VK56 P29475 |
Target Gene Table
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TCGA Plot Options
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Drug Information
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Gene | NOS1 |
---|---|
DrugBank ID | DB00155 |
Drug Name | Citrulline |
Target ID | BE0000067 |
UniProt ID | P29475 |
Regulation Type | |
PubMed IDs | 10502685; 10681601; 10799481; 10945985; 10962148 |
Citations | Kominami S, Yamazaki T, Koga T, Hori H: EPR studies on the photo-induced intermediates of ferric NO complexes of rat neuronal nitric oxide synthase trapped at low temperature. J Biochem. 1999 Oct;126(4):756-61.@@Giraldi-Guimaraes A, Tenorio F, Bruning G, Mayer B, Mendez-Otero R, Cavalcante LA: Nitric oxide synthase expression in the opossum superior colliculus: a histochemical, immunohistochemical and biochemical study. Brain Behav Evol. 1999 Dec;54(6):303-13.@@Perry JM, Zhao Y, Marletta MA: Cu2+ and Zn2+ inhibit nitric-oxide synthase through an interaction with the reductase domain. J Biol Chem. 2000 May 12;275(19):14070-6.@@Adak S, Wang Q, Stuehr DJ: Arginine conversion to nitroxide by tetrahydrobiopterin-free neuronal nitric-oxide synthase. Implications for mechanism. J Biol Chem. 2000 Oct 27;275(43):33554-61.@@Yu W, Juang S, Lee J, Liu T, Cheng J: Decrease of neuronal nitric oxide synthase in the cerebellum of aged rats. Neurosci Lett. 2000 Sep 8;291(1):37-40. |
Groups | Investigational; Nutraceutical |
Direct Classification | L-alpha-amino acids |
SMILES | N[C@@H](CCCNC(N)=O)C(O)=O |
Pathways | Citrullinemia Type I; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); Argininemia; Hyperornithinemia with Gyrate Atrophy (HOGA); Canavan Disease; Hypoacetylaspartia; Hyperprolinemia Type II; Argininosuccinic Aciduria; L-Arginine:Glycine Amidinotransferase Deficiency; Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome]; Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency); Prolidase Deficiency (PD); Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency; Carbamoyl Phosphate Synthetase Deficiency; Ornithine Aminotransferase Deficiency (OAT Deficiency); Hyperprolinemia Type I; Aspartate Metabolism; Nitric Oxide Signaling Pathway; Arginine and Proline Metabolism; Ornithine Transcarbamylase Deficiency (OTC Deficiency); Prolinemia Type II; Urea Cycle |
PharmGKB | PA164747225 |
ChEMBL | CHEMBL444814 |