PPARD
Peroxisome proliferator-activated receptor delta
Also known as: FAAR, NR1C2, NUC1, NUCII, PPARB, PPARD_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q03181
- Gene
- PPARD
- Ensembl
- ENSG00000112033
- Chromosome
- 6
- Canonical length
- 441 aa
- Protein class
- FDA approved drug targets, Nuclear receptors, Predicted intracellular proteins, Transcription factors
OverviewNCBI Gene
This gene encodes a member of the peroxisome proliferator-activated receptor (PPAR) family. The encoded protein is thought to function as an integrator of transcriptional repression and nuclear receptor signaling. It may inhibit the ligand-induced transcriptional activity of peroxisome proliferator activated receptors alpha and gamma, though evidence for this effect is inconsistent. Expression of this gene in colorectal cancer cells may be variable but is typically relatively low. Knockout studies in mice suggested a role for this protein in myelination of the corpus callosum, lipid metabolism, differentiation, and epidermal cell proliferation. Alternative splicing results in multiple transcript variants encoding distinct protein isoforms. [provided by RefSeq, Aug 2017]
Canonical amino-acid sequenceUniProt
441 residues, UniProt reviewed canonical sequence.
>Q03181|PPARD
1 MEQPQEEAPE VREEEEKEEV AEAEGAPELN GGPQHALPSS SYTDLSRSSS PPSLLDQLQM
61 GCDGASCGSL NMECRVCGDK ASGFHYGVHA CEGCKGFFRR TIRMKLEYEK CERSCKIQKK
121 NRNKCQYCRF QKCLALGMSH NAIRFGRMPE AEKRKLVAGL TANEGSQYNP QVADLKAFSK
181 HIYNAYLKNF NMTKKKARSI LTGKASHTAP FVIHDIETLW QAEKGLVWKQ LVNGLPPYKE
241 ISVHVFYRCQ CTTVETVREL TEFAKSIPSF SSLFLNDQVT LLKYGVHEAI FAMLASIVNK
301 DGLLVANGSG FVTREFLRSL RKPFSDIIEP KFEFAVKFNA LELDDSDLAL FIAAIILCGD
361 RPGLMNVPRV EAIQDTILRA LEFHLQANHP DAQYLFPKLL QKMADLRQLV TEHAQMMQRI
421 KKTETETSLH PLLQEIYKDM YLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PPARD can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 45 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 45 nTPM
- thyroid gland: 39 nTPM
- hippocampal formation: 35 nTPM
- cerebral cortex: 33 nTPM
- vagina: 33 nTPM
- liver: 32 nTPM
Single-cell type
- syncytiotrophoblasts: 371 nCPM
- pancreatic acinar cells: 320 nCPM
- urothelial cells: 282 nCPM
- esophageal apical cells: 278 nCPM
- mast cells: 268 nCPM
- monocytes: 246 nCPM
Immune cell
- eosinophil: 3.3 nTPM
- neutrophil: 2.3 nTPM
- naive CD4 T-cell: 2.1 nTPM
- naive CD8 T-cell: 2.1 nTPM
- naive B-cell: 1.6 nTPM
- classical monocyte: 1.5 nTPM
Brain region
- thalamus: 61 nTPM
- hippocampal formation: 58 nTPM
- cerebral cortex: 55 nTPM
- amygdala: 51 nTPM
- midbrain: 50 nTPM
- pons: 49 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.19
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 2.48
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adipose tissue development
- apoptotic process
- apoptotic signaling pathway
- axon ensheathment
- cell differentiation
- cell population proliferation
- cell-substrate adhesion
- cellular response to hypoxia
- cellular response to lipopolysaccharide
- cellular response to nutrient levels
- cholesterol metabolic process
- D-glucose transmembrane transport
- decidualization
- embryo implantation
- energy homeostasis
- fat cell proliferation
- fatty acid beta-oxidation
- fatty acid catabolic process
- fatty acid metabolic process
- fatty acid transport
- generation of precursor metabolites and energy
- glucose metabolic process
- heart development
- hormone-mediated signaling pathway
- intracellular receptor signaling pathway
- keratinocyte migration
- keratinocyte proliferation
- lipid metabolic process
- negative regulation of apoptotic process
- negative regulation of cell growth
- negative regulation of cholesterol storage
- negative regulation of collagen biosynthetic process
- negative regulation of DNA-templated transcription
- negative regulation of epithelial cell proliferation
- negative regulation of inflammatory response
- negative regulation of miRNA transcription
- negative regulation of myoblast differentiation
- negative regulation of smooth muscle cell migration
- negative regulation of smooth muscle cell proliferation
- negative regulation of transcription by RNA polymerase II
- phosphatidylinositol 3-kinase/protein kinase B signal transduction
- phospholipid biosynthetic process
- positive regulation of DNA-templated transcription
- positive regulation of epidermis development
- positive regulation of fat cell differentiation
- positive regulation of fat cell proliferation
- positive regulation of fatty acid metabolic process
- positive regulation of fatty acid oxidation
- positive regulation of gene expression
- positive regulation of insulin secretion involved in cellular response to glucose stimulus
- positive regulation of myoblast proliferation
- positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- positive regulation of skeletal muscle tissue regeneration
- positive regulation of transcription by RNA polymerase II
- proteoglycan metabolic process
- regulation of skeletal muscle satellite cell proliferation
- regulation of transcription by RNA polymerase II
- response to activity
- response to glucose
- response to vitamin A
- vasodilation
- wound healing
Molecular functions
- DNA binding
- DNA-binding transcription factor activity
- DNA-binding transcription factor activity, RNA polymerase II-specific
- DNA-binding transcription repressor activity, RNA polymerase II-specific
- lipid binding
- NF-kappaB binding
- nuclear receptor activity
- nuclear steroid receptor activity
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- sequence-specific double-stranded DNA binding
- transcription coactivator binding
- zinc ion binding
- linoleic acid binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Nuclear hormone receptor, ligand-binding domain
- Zinc finger, nuclear hormone receptor-type
- Nuclear hormone receptor
- Peroxisome proliferator-activated receptor
- Zinc finger, NHR/GATA-type
- Nuclear hormone receptor-like domain superfamily
- Nuclear hormone receptor family NR1 subfamily
- Ligand-binding domain of nuclear hormone receptor
- Double treble clef zinc finger, C4 type
- Peroxisome proliferator-activated receptor, beta
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PPARD in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PPARD as an antibody target. Whether an autoantibody or antibody against PPARD could matter depends on whether native PPARD is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PPARD is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label PPARD as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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