CPVL
Probable serine carboxypeptidase CPVL
Also known as: CPVL_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H3G5
- Gene
- CPVL
- Ensembl
- ENSG00000106066
- Chromosome
- 7
- Canonical length
- 476 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Endoplasmic reticulum
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
The protein encoded by this gene is a carboxypeptidase and bears strong sequence similarity to serine carboxypeptidases. Carboxypeptidases are a large class of proteases that act to cleave a single amino acid from the carboxy termini of proteins or peptides. The exact function of this protein, however, has not been determined. [provided by RefSeq, Jan 2017]
Canonical amino-acid sequenceUniProt
476 residues, UniProt reviewed canonical sequence.
>Q9H3G5|CPVL
1 MVGAMWKVIV SLVLLMPGPC DGLFRSLYRS VSMPPKGDSG QPLFLTPYIE AGKIQKGREL
61 SLVGPFPGLN MKSYAGFLTV NKTYNSNLFF WFFPAQIQPE DAPVVLWLQG GPGGSSMFGL
121 FVEHGPYVVT SNMTLRDRDF PWTTTLSMLY IDNPVGTGFS FTDDTHGYAV NEDDVARDLY
181 SALIQFFQIF PEYKNNDFYV TGESYAGKYV PAIAHLIHSL NPVREVKINL NGIAIGDGYS
241 DPESIIGGYA EFLYQIGLLD EKQKKYFQKQ CHECIEHIRK QNWFEAFEIL DKLLDGDLTS
301 DPSYFQNVTG CSNYYNFLRC TEPEDQLYYV KFLSLPEVRQ AIHVGNQTFN DGTIVEKYLR
361 EDTVQSVKPW LTEIMNNYKV LIYNGQLDII VAAALTERSL MGMDWKGSQE YKKAEKKVWK
421 IFKSDSEVAG YIRQAGDFHQ VIIRGGGHIL PYDQPLRAFD MINRFIYGKG WDPYVGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CPVL 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.22
- Highest tissue expression
- 206 nTPM
Expression across tissuesHPA
Tissue
- spleen: 206 nTPM
- choroid plexus: 192 nTPM
- thyroid gland: 122 nTPM
- kidney: 88 nTPM
- lymph node: 87 nTPM
- placenta: 80 nTPM
Single-cell type
- cardiomyocytes: 1,565 nCPM
- cdc: 1,103 nCPM
- kupffer cells: 547 nCPM
- hofbauer cells: 521 nCPM
- macrophages: 423 nCPM
- monocytes: 391 nCPM
Immune cell
- myeloid DC: 1,322 nTPM
- total PBMC: 1,143 nTPM
- classical monocyte: 1,140 nTPM
- intermediate monocyte: 955 nTPM
- non-classical monocyte: 330 nTPM
- plasmacytoid DC: 35 nTPM
Brain region
- cerebellum: 101 nTPM
- choroid plexus: 81 nTPM
- white matter: 47 nTPM
- medulla oblongata: 31 nTPM
- pons: 29 nTPM
- spinal cord: 24 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)
- 1.07
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.61
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CPVL 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 CPVL as an antibody target. Whether an autoantibody or antibody against CPVL could matter depends on whether native CPVL is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CPVL 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 CPVL as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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