XPNPEP1
Xaa-Pro aminopeptidase 1
Also known as: XPNPEP, XPNPEPL, XPNPEPL1, XPP1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NQW7
- Gene
- XPNPEP1
- Ensembl
- ENSG00000108039
- Chromosome
- 10
- Canonical length
- 623 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes the cytosolic form of a metalloaminopeptidase that catalyzes the cleavage of the N-terminal amino acid adjacent to a proline residue. The gene product may play a role in degradation and maturation of tachykinins, neuropeptides, and peptide hormones. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Nov 2009]
Canonical amino-acid sequenceUniProt
623 residues, UniProt reviewed canonical sequence.
>Q9NQW7|XPNPEP1
1 MPPKVTSELL RQLRQAMRNS EYVTEPIQAY IIPSGDAHQS EYIAPCDCRR AFVSGFDGSA
61 GTAIITEEHA AMWTDGRYFL QAAKQMDSNW TLMKMGLKDT PTQEDWLVSV LPEGSRVGVD
121 PLIIPTDYWK KMAKVLRSAG HHLIPVKENL VDKIWTDRPE RPCKPLLTLG LDYTGISWKD
181 KVADLRLKMA ERNVMWFVVT ALDEIAWLFN LRGSDVEHNP VFFSYAIIGL ETIMLFIDGD
241 RIDAPSVKEH LLLDLGLEAE YRIQVHPYKS ILSELKALCA DLSPREKVWV SDKASYAVSE
301 TIPKDHRCCM PYTPICIAKA VKNSAESEGM RRAHIKDAVA LCELFNWLEK EVPKGGVTEI
361 SAADKAEEFR RQQADFVDLS FPTISSTGPN GAIIHYAPVP ETNRTLSLDE VYLIDSGAQY
421 KDGTTDVTRT MHFGTPTAYE KECFTYVLKG HIAVSAAVFP TGTKGHLLDS FARSALWDSG
481 LDYLHGTGHG VGSFLNVHEG PCGISYKTFS DEPLEAGMIV TDEPGYYEDG AFGIRIENVV
541 LVVPVKTKYN FNNRGSLTFE PLTLVPIQTK MIDVDSLTDK ECDWLNNYHL TCRDVIGKEL
601 QKQGRQEALE WLIRETQPIS KQHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against XPNPEP1 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)
- 0.22
- Highest tissue expression
- 60 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 60 nTPM
- small intestine: 58 nTPM
- duodenum: 49 nTPM
- rectum: 38 nTPM
- colon: 30 nTPM
- salivary gland: 29 nTPM
Single-cell type
- platelets: 448 nCPM
- pancreatic acinar cells: 135 nCPM
- megakaryocytes: 111 nCPM
- enterocytes: 100 nCPM
- goblet cells: 81 nCPM
- foveolar cells: 62 nCPM
Immune cell
- myeloid DC: 46 nTPM
- intermediate monocyte: 42 nTPM
- non-classical monocyte: 37 nTPM
- plasmacytoid DC: 36 nTPM
- NK-cell: 31 nTPM
- total PBMC: 30 nTPM
Brain region
- choroid plexus: 22 nTPM
- hippocampal formation: 17 nTPM
- white matter: 14 nTPM
- cerebral cortex: 14 nTPM
- thalamus: 14 nTPM
- hypothalamus: 14 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)
- 0.4
- gnomAD pLI
- 0.33
- gnomAD missense Z
- 2.42
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- aminopeptidase activity
- manganese ion binding
- metalloaminopeptidase activity
- protein homodimerization activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Creatinase, N-terminal
- Peptidase M24
- Peptidase M24B, X-Pro dipeptidase/aminopeptidase P, conserved site
- Creatinase/Aminopeptidase P/Spt16, N-terminal
- Peptidase M24, C-terminal domain
- Aminopeptidase P
- Creatinase/aminopeptidase-like
- Xaa-Pro aminopeptidase P
- Metallopeptidase family M24
- Creatinase/Prolidase N-terminal domain
- C-terminal region of peptidase_M24
- Creatinase/Prolidase N-terminal domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads XPNPEP1 as an antibody target. Whether an autoantibody or antibody against XPNPEP1 could matter depends on whether native XPNPEP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
XPNPEP1 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 XPNPEP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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