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Description for Protein PPARG

peroxisome proliferator-activated receptor gamma
57 total interacting proteins; 21 platelet interacting proteins
Icon Book Platelet Evidence (proteome studies/others : 0/1)
(undefined: 1)
Summary:
This gene encodes a member of the peroxisome proliferator-activated receptor (PPAR) subfamily of nuclear receptors. PPARs form heterodimers with retinoid X receptors (RXRs) and these heterodimers regulate transcription of various genes. Three subtypes of PPARs are known: PPAR-alpha, PPAR-delta, and PPAR-gamma. The protein encoded by this gene is PPAR-gamma and is a regulator of adipocyte differentiation. Additionally, PPAR-gamma has been implicated in the pathology of numerous diseases including obesity, diabetes, atherosclerosis and cancer. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq] (PubMed Links)
Domains and Motifs:
  • ZnF_C4: c4 zinc finger in nuclear hormone receptors
  • HOLI: Ligand binding domain of hormone receptors

  • Gene Ontology:
    Gene Ontology Annotations

    KEGG - Enzyme ID(s):
    None Available
    KEGG - Orthology:
    K08530
    KEGG - Pathway(s):
    hsa03320; hsa05016; hsa05200; hsa05216
    (The yellow boxes represents platelet proteins)
    Nomenclature / Alternative Names:
    PPARG1; PPARG2; PPARG3; PAX8/PPARG fusion gene; NR1C3; HUMPPARG; PPAR gamma; PPAR gamma2; Peroxisome proliferative activated receptor gamma isoform 2; Peroxisome proliferative activated receptor gamma isoform 1
    Approved Symbol:
    PPARG
    (De-) Phosphorylations:
    Total (de-) phosphorylation sites: 6
    Human (de-) phosphorylation sites: 6; No platelet phosphorylation sites

    Phosphorylation Targets:
    Total phosphorylation targets: 0
    Human phosphorylation targets: 0;Predicted platelet targets: 0
    Protein Characteristics:
    Isoform-specific Information
    Icon DrugsAssociated Drugs (DrugBank Accession):

  • (2S)-2-(4-chlorophenoxy)-3-phenylpropanoic acid(db);
  • (2S)-2-(4-ethylphenoxy)-3-phenylpropanoic acid(db);
  • (2S)-2-(biphenyl-4-yloxy)-3-phenylpropanoic acid(db);
  • (2S)-2-ETHOXY-3-[4-(2-{4-[(METHYLSULFONYL)OXY]PHENYL}ETHOXY)PHENYL]PROPANOIC ACID(db);
  • (2S)-2-ETHOXY-3-{4-[2-(10H-PHENOXAZIN-10-YL)ETHOXY]PHENYL}PROPANOIC ACID(db);
  • (2S)-2-methoxy-3-{4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1-benzothiophen-7-yl}propanoic acid(db);
  • (2S)-3-(1-{[2-(2-CHLOROPHENYL)-5-METHYL-1,3-OXAZOL-4-YL]METHYL}-1H-INDOL-5-YL)-2-ETHOXYPROPANOIC ACID(db);
  • (4S,5E,7Z,10Z,13Z,16Z,19Z)-4-hydroxydocosa-5,7,10,13,16,19-hexaenoic acid(db);
  • (5E,14E)-11-oxoprosta-5,9,12,14-tetraen-1-oic acid(db);
  • (5R,6E,8Z,11Z,14Z,17Z)-5-hydroxyicosa-6,8,11,14,17-pentaenoic acid(db);
  • (8E,10S,12Z)-10-hydroxy-6-oxooctadeca-8,12-dienoic acid(db);
  • (8R,9Z,12Z)-8-hydroxy-6-oxooctadeca-9,12-dienoic acid(db);
  • (9S,10E,12Z)-9-hydroxyoctadeca-10,12-dienoic acid(db);
  • (9Z,11E,13S)-13-hydroxyoctadeca-9,11-dienoic acid(db);
  • (S)-3-(4-(2-Carbazol-9-Yl-Ethoxy)-Phenyl)-2-Ethoxy-Propionic Acid(db);
  • 2-chloro-5-nitro-N-phenylbenzamide(db);
  • 2-[(2,4-DICHLOROBENZOYL)AMINO]-5-(PYRIMIDIN-2-YLOXY)BENZOIC ACID(db);
  • 2-{5-[3-(6-BENZOYL-1-PROPYLNAPHTHALEN-2-YLOXY)PROPOXY]INDOL-1-YL}ETHANOIC ACID(db);
  • 2-{5-[3-(7-PROPYL-3-TRIFLUOROMETHYLBENZO[D]ISOXAZOL-6-YLOXY)PROPOXY]INDOL-1-YL}ETHANOIC ACID(db);
  • 3-(5-methoxy-1H-indol-3-yl)propanoic acid(db);
  • 3-FLUORO-N-[1-(4-FLUOROPHENYL)-3-(2-THIENYL)-1H-PYRAZOL-5-YL]BENZENESULFONAMIDE(db);
  • 3-[5-(2-nitropent-1-en-1-yl)furan-2-yl]benzoic acid(db);
  • 3-{5-methoxy-1-[(4-methoxyphenyl)sulfonyl]-1H-indol-3-yl}propanoic acid(db);
  • Balsalazide(db);
  • Bezafibrate(db);
  • difluoro(5-{2-[(5-octyl-1H-pyrrol-2-yl-kappaN)methylidene]-2H-pyrrol-5-yl-kappaN}pentanoato)boron(db);
  • Glipizide(db);
  • Icosapent(db);
  • Indomethacin(db);
  • Mesalazine(db);
  • Mitiglinide(db);
  • Nateglinide(db);
  • Pioglitazone(db);
  • Repaglinide(db);
  • Rosiglitazone(db);
  • Sulfasalazine(db);
  • Telmisartan(db);
  • Troglitazone(db)


    Associated Genetic Diseases:

  • Colon cancer, somatic(Pd);
  • Diabetes mellitus, type II, modifier of(Pd);
  • Glioblastoma, susceptibility to(Pd);
  • Insulin resistance, digenic(Pd);
  • Lipodystrophy, familial partial, type 3(Pd);
  • Obesity, severe(Pd);
  • Pparg polymorphism c/t(Pd)
  • Predicted Transmembrane Domains:
  • Isoform 4 : 0
  • Isoform 3 : 0
  • Isoform 2 : 0
  • Isoform 1 : 0
  • Additional Identifiers:

    HPRD: 03288 Entrez Gene ID: 5468 OMIM ID: 601487 Swissprot Accession: P37231D2KUA6