PREP
Prolyl endopeptidase
Also known as: PPCE_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P48147
- Gene
- PREP
- Ensembl
- ENSG00000085377
- Chromosome
- 6
- Canonical length
- 710 aa
- Protein class
- Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a cytosolic prolyl endopeptidase that cleaves peptide bonds on the C-terminal side of prolyl residues within peptides that are up to approximately 30 amino acids long. Prolyl endopeptidases have been reported to be involved in the maturation and degradation of peptide hormones and neuropeptides. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
710 residues, UniProt reviewed canonical sequence.
>P48147|PREP
1 MLSLQYPDVY RDETAVQDYH GHKICDPYAW LEDPDSEQTK AFVEAQNKIT VPFLEQCPIR
61 GLYKERMTEL YDYPKYSCHF KKGKRYFYFY NTGLQNQRVL YVQDSLEGEA RVFLDPNILS
121 DDGTVALRGY AFSEDGEYFA YGLSASGSDW VTIKFMKVDG AKELPDVLER VKFSCMAWTH
181 DGKGMFYNSY PQQDGKSDGT ETSTNLHQKL YYHVLGTDQS EDILCAEFPD EPKWMGGAEL
241 SDDGRYVLLS IREGCDPVNR LWYCDLQQES SGIAGILKWV KLIDNFEGEY DYVTNEGTVF
301 TFKTNRQSPN YRVINIDFRD PEESKWKVLV PEHEKDVLEW IACVRSNFLV LCYLHDVKNI
361 LQLHDLTTGA LLKTFPLDVG SIVGYSGQKK DTEIFYQFTS FLSPGIIYHC DLTKEELEPR
421 VFREVTVKGI DASDYQTVQI FYPSKDGTKI PMFIVHKKGI KLDGSHPAFL YGYGGFNISI
481 TPNYSVSRLI FVRHMGGILA VANIRGGGEY GETWHKGGIL ANKQNCFDDF QCAAEYLIKE
541 GYTSPKRLTI NGGSNGGLLV AACANQRPDL FGCVIAQVGV MDMLKFHKYT IGHAWTTDYG
601 CSDSKQHFEW LVKYSPLHNV KLPEADDIQY PSMLLLTADH DDRVVPLHSL KFIATLQYIV
661 GRSRKQSNPL LIHVDTKAGH GAGKPTAKVI EEVSDMFAFI ARCLNVDWIPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PREP 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)
- 0.2
- Highest tissue expression
- 61 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 61 nTPM
- tongue: 44 nTPM
- rectum: 35 nTPM
- colon: 30 nTPM
- skin: 25 nTPM
- duodenum: 22 nTPM
Single-cell type
- sertoli cells: 193 nCPM
- myonuclei: 184 nCPM
- cone photoreceptor cells: 184 nCPM
- enteric stem cells: 162 nCPM
- enteric transient amplifying cells: 136 nCPM
- syncytiotrophoblasts: 130 nCPM
Immune cell
- non-classical monocyte: 23 nTPM
- NK-cell: 20 nTPM
- memory CD8 T-cell: 17 nTPM
- intermediate monocyte: 17 nTPM
- MAIT T-cell: 17 nTPM
- myeloid DC: 17 nTPM
Brain region
- cerebral cortex: 25 nTPM
- thalamus: 18 nTPM
- white matter: 17 nTPM
- choroid plexus: 16 nTPM
- midbrain: 16 nTPM
- hypothalamus: 15 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)
- 0.43
- gnomAD pLI
- 0.08
- gnomAD missense Z
- 2.27
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- metallocarboxypeptidase activity
- oligopeptidase activity
- serine-type endopeptidase activity
- serine-type peptidase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PREP as an antibody target. Whether an autoantibody or antibody against PREP could matter depends on whether native PREP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PREP 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 PREP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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