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Protein Page:
PPAR-gamma (human)
p Phosphorylation
ac Acetylation
me Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
ub Ubiquitylation
sm Sumoylation
ne Neddylation
gl O-GlcNAc
ga O-GalNAc
pa Palmitoylation
ad Adenylation
sn S-Nitrosylation
ca Caspase cleavage
sc Succinylation

Overview
PPAR-gamma a transcription factor, member of the nuclear hormone receptor superfamily. Receptor for hypolipidemic drugs and fatty acids. Preferentially expressed in adipocytes as well as in vascular smooth muscle cells and macrophage. Regulator of adipogenesis and lipid metabolism, modulates insulin sensitivity, cell proliferation and inflammation. Phosphorylated and inhibited by MAP kinase. Heterodimerizes with the retinoid X receptor. Interacts with NCOA6 coactivator, leading to a strong increase in transcription of target genes. Two splice-variant isoforms have been described. Note: This description may include information from UniProtKB.
Protein type: DNA-binding; Nuclear receptor
Chromosomal Location of Human Ortholog: 3p25
Cellular Component: cytosol; Golgi apparatus; intracellular membrane-bound organelle; nucleoplasm; nucleus
Molecular Function: alpha-actinin binding; arachidonic acid binding; chromatin binding; DNA binding; drug binding; enzyme binding; identical protein binding; ligand-dependent nuclear receptor activity; ligand-dependent nuclear receptor transcription coactivator activity; prostaglandin receptor activity; protein binding; retinoid X receptor binding; sequence-specific DNA binding; transcription activator binding; transcription factor activity
Biological Process: caspase activation; cell fate commitment; cell maturation; cellular response to insulin stimulus; epithelial cell differentiation; glucose homeostasis; innate immune response; lipid homeostasis; lipid metabolic process; lipoprotein transport; long-chain fatty acid transport; low-density lipoprotein receptor biosynthetic process; monocyte differentiation; negative regulation of smooth muscle cell proliferation; negative regulation of transcription from RNA polymerase II promoter; negative regulation of transcription, DNA-dependent; placenta development; positive regulation of fat cell differentiation; positive regulation of transcription factor activity; positive regulation of transcription from RNA polymerase II promoter; positive regulation of transcription, DNA-dependent; regulation of blood pressure; regulation of circadian rhythm; response to lipid; response to low density lipoprotein stimulus; response to nutrient; response to retinoic acid; signal transduction; transcription initiation from RNA polymerase II promoter; white fat cell differentiation
Disease: Carotid Intimal Medial Thickness 1; Diabetes Mellitus, Noninsulin-dependent; Lipodystrophy, Familial Partial, Type 3; Obesity
Reference #:  P37231 (UniProtKB)
Alt. Names/Synonyms: CIMT1; GLM1; NR1C3; Nuclear receptor subfamily 1 group C member 3; peroxisome proliferative activated receptor gamma; Peroxisome proliferator-activated receptor gamma; peroxisome proliferator-activated receptor gamma 1; PPAR gamma; PPAR-gamma; PPARG; PPARG1; PPARG2; PPARgamma
Gene Symbols: PPARG
Molecular weight: 57,620 Da
Basal Isoelectric point: 5.61  Predict pI for various phosphorylation states
CST Pathways:  Growth And Differentiation Control by MAPKs  |  mTOR Signaling
Protein-Specific Antibodies or siRNAs from Cell Signaling Technology® Total Proteins
Select Structure to View Below

PPAR-gamma

Protein Structure Not Found.
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Download ChimeraX Script


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Sites Implicated In
cell differentiation, altered: S112‑p
cell growth, altered: S112‑p
transcription, altered: S112‑p
transcription, induced: S273‑p
transcription, inhibited: S112‑p, S273‑p
protein degradation: S112‑p

Modification Sites and Domains Show Modification Legend
Click here to view phosphorylation modifications only

Modification Sites in Parent Protein, Orthologs, and Isoforms Show Modification Legend
 

Show Multiple Sequence Alignment



 LTP 

LTP: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 HTP 

HTP: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

► Hide Isoforms
 
1 0 S46 WPTNFGISSVDLSVM
1 0 S51 GISSVDLSVMEDHSH
2 0 K63 HSHSFDIKPFTTVDF
2 1 Y78‑p SSISTPHyEDIPFTR
1 0 K94 DPVVADYKyDLKLQE
0 1 Y95‑p PVVADYKyDLKLQEy
1 0 K98 ADYKyDLKLQEyQSA
2 1 Y102‑p yDLKLQEyQSAIkVE
10 0 K107‑sm QEyQSAIkVEPAsPP
21 4 S112‑p AIkVEPAsPPYYSEK
1 1 S133 PHEEPSNSLMAIECR
0 1 Y173 TIRLKLIYDRCDLNC
1 0 K184‑ub DLNCRIHkkSRNKCQ
1 0 K185‑ub LNCRIHkkSRNKCQY
1 1 K268 ARAILTGKtTDKsPF
0 1 T269‑p RAILTGKtTDKsPFV
8 2 S273‑p TGKtTDKsPFVIYDM
1 1 K293 GEDKIKFKHITPLQE
1 1 T296 KIKFKHITPLQEQSK
0 1 S317 FQGCQFRSVEAVQEI
4 0 K395‑sm FGDFMEPkFEFAVKF
1 0 K462 ESSQLFAKLLQKMTD
  PPAR-gamma iso2  
S18 WPTNFGISSVDLSVM
S23 GISSVDLSVMEDHSH
K35 HSHSFDIKPFTTVDF
Y50 SSISTPHYEDIPFTR
K66 DPVVADYKYDLKLQE
Y67 PVVADYKYDLKLQEy
K70 ADYKYDLKLQEyQSA
Y74‑p YDLKLQEyQSAIkVE
K79‑sm QEyQSAIkVEPASPP
S84 AIkVEPASPPYYSEK
S105 PHEEPSNSLMAIECR
Y145 TIRLKLIYDRCDLNC
K156 DLNCRIHKKSRNKCQ
K157 LNCRIHKKSRNKCQY
K240 ARAILTGKTTDKsPF
T241 RAILTGKTTDKsPFV
S245‑p TGKTTDKsPFVIYDM
K265 GEDKIKFKHITPLQE
T268 KIKFKHITPLQEQSK
S289 FQGCQFRSVEAVQEI
K367‑sm FGDFMEPkFEFAVKF
K434 ESSQLFAKLLQKMTD
  PPAR-gamma iso3  
S18 WPTNFGISSVDLSVM
S23 GISSVDLSVMEDHSH
K35 HSHSFDIKPFTTVDF
Y50 SSISTPHYEDIPFTR
K66 DPVVADYKYDLKLQE
Y67 PVVADYKYDLKLQEY
K70 ADYKYDLKLQEYQSA
Y74 YDLKLQEYQSAIKVE
K79 QEYQSAIKVEPAsPP
S84‑p AIKVEPAsPPYYSEK
S105 PHEEPSNSLMAIECR
Y145 TIRLKLIYDRCDLNC
K156 DLNCRIHKKSRNKCQ
K157 LNCRIHKKSRNKCQY
- gap
- gap
- gap
- gap
- gap
- gap
- gap
- gap
  mouse

► Hide Isoforms
 
S46 WPTNFGISSVDLSVM
S51 GISSVDLSVMEDHSH
K63‑sm HSHSFDIkPFTTVDF
Y78‑p SSISAPHyEDIPFTR
K94 DPMVADYKYDLKLQE
Y95 PMVADYKYDLKLQEY
K98 ADYKYDLKLQEYQSA
Y102 YDLKLQEYQSAIkVE
K107‑sm QEYQSAIkVEPAsPP
S112‑p AIkVEPAsPPYYSEK
S133‑p PHEEPSNsLMAIECR
Y173‑p TIRLKLIyDRCDLNC
K184 DLNCRIHKKSRNKCQ
K185 LNCRIHKKSRNKCQY
K268‑ac ARAILTGkTTDKsPF
T269 RAILTGkTTDKsPFV
S273‑p TGkTTDKsPFVIYDM
K293‑ac GEDKIKFkHItPLQE
T296‑p KIKFkHItPLQEQSK
S317‑p FQGCQFRsVEAVQEI
K395 FGDFMEPKFEFAVKF
K462 ESSQLFAKVLQKMTD
  PPAR-gamma iso2  
S16‑p WPTNFGIsSVDLsVM
S21‑p GIsSVDLsVMEDHSH
K33‑sm HSHSFDIkPFTTVDF
Y48 SSISAPHYEDIPFTR
K64‑sm DPMVADYkYDLkLQE
Y65 PMVADYkYDLkLQEY
K68‑sm ADYkYDLkLQEYQSA
Y72 YDLkLQEYQSAIkVE
K77‑sm QEYQSAIkVEPAsPP
S82‑p AIkVEPAsPPYYSEK
S103 PHEEPSNSLMAIECR
Y143 TIRLKLIYDRCDLNC
K154 DLNCRIHKKSRNKCQ
K155 LNCRIHKKSRNKCQY
K238 ARAILTGKTTDKSPF
T239 RAILTGKTTDKSPFV
S243 TGKTTDKSPFVIYDM
K263 GEDKIKFKHITPLQE
T266 KIKFKHITPLQEQSK
S287 FQGCQFRSVEAVQEI
K365‑sm FGDFMEPkFEFAVKF
K432‑ub ESSQLFAkVLQKMTD
  rat

 
S46 WPTNFGISSVDLSVM
S51 GISSVDLSVMDDHSH
K63 HSHSFDIKPFTTVDF
Y78 SSISAPHYEDIPFTR
K94 DPMVADYKYDLKLQE
Y95 PMVADYKYDLKLQEY
K98 ADYKYDLKLQEYQSA
Y102 YDLKLQEYQSAIKVE
K107 QEYQSAIKVEPASPP
S112 AIKVEPASPPYYSEK
S133 PHEEPSNSLMAIECR
Y173 TIRLKLIYDRCDLNC
K184 DLNCRIHKKSRNKCQ
K185 LNCRIHKKSRNKCQY
K268 ARAILTGKTTDKSPF
T269 RAILTGKTTDKSPFV
S273 TGKTTDKSPFVIYDM
K293 GEDKIKFKHITPLQE
T296 KIKFKHITPLQEQSK
S317 FQGCQFRSVEAVQEI
K395 FGDFMEPKFEFAVKF
K462 ESSQLFAKVLQKMTD
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