NPEPL1
Probable aminopeptidase NPEPL1
Also known as: bA261P9.2, FLJ11583, PEPL1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NDH3
- Gene
- NPEPL1
- Ensembl
- ENSG00000215440
- Chromosome
- 20
- Canonical length
- 523 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Predicted to enable peptidase activity. Predicted to be involved in proteolysis. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
523 residues, UniProt reviewed canonical sequence.
>Q8NDH3|NPEPL1
1 MANVGLQFQA SAGDSDPQSR PLLLLGQLHH LHRVPWSHVR GKLQPRVTEE LWQAALSTLN
61 PNPTDSCPLY LNYATVAALP CRVSRHNSPS AAHFITRLVR TCLPPGAHRC IVMVCEQPEV
121 FASACALARA FPLFTHRSGA SRRLEKKTVT VEFFLVGQDN GPVEVSTLQC LANATDGVRL
181 AARIVDTPCN EMNTDTFLEE INKVGKELGI IPTIIRDEEL KTRGFGGIYG VGKAALHPPA
241 LAVLSHTPDG ATQTIAWVGK GIVYDTGGLS IKGKTTMPGM KRDCGGAAAV LGAFRAAIKQ
301 GFKDNLHAVF CLAENSVGPN ATRPDDIHLL YSGKTVEINN TDAEGRLVLA DGVSYACKDL
361 GADIILDMAT LTGAQGIATG KYHAAVLTNS AEWEAACVKA GRKCGDLVHP LVYCPELHFS
421 EFTSAVADMK NSVADRDNSP SSCAGLFIAS HIGFDWPGVW VHLDIAAPVH AGERATGFGV
481 ALLLALFGRA SEDPLLNLVS PLGCEVDVEE GDLGRDSKRR RLVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NPEPL1 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)
- 0.23
- Highest tissue expression
- 62 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 62 nTPM
- cerebellum: 58 nTPM
- kidney: 43 nTPM
- colon: 42 nTPM
- spleen: 42 nTPM
- thyroid gland: 42 nTPM
Single-cell type
- bergmann glia: 61 nCPM
- astrocytes: 52 nCPM
- breast lactating cells: 47 nCPM
- brain excitatory neurons: 29 nCPM
- oligodendrocyte progenitor cells: 28 nCPM
- ependymal cells: 28 nCPM
Immune cell
- basophil: 24 nTPM
- non-classical monocyte: 19 nTPM
- classical monocyte: 19 nTPM
- neutrophil: 14 nTPM
- intermediate monocyte: 13 nTPM
- myeloid DC: 11 nTPM
Brain region
- medulla oblongata: 25 nTPM
- choroid plexus: 25 nTPM
- thalamus: 24 nTPM
- basal ganglia: 22 nTPM
- cerebral cortex: 22 nTPM
- white matter: 21 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
- 0.51
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% 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
- Peptidase M17, leucyl aminopeptidase, C-terminal
- Peptidase M17, leucine aminopeptidase/peptidase B
- Cytosol aminopeptidase family, catalytic domain
- Probable aminopeptidase NPEPL1, N-terminal
- M17 aminopeptidase N-terminal domain 2
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads NPEPL1 as an antibody target. Whether an autoantibody or antibody against NPEPL1 could matter depends on whether native NPEPL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NPEPL1 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 NPEPL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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