PRSS53
Serine protease 53
Also known as: POL3S, PRS53_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q2L4Q9
- Gene
- PRSS53
- Ensembl
- ENSG00000151006
- Chromosome
- 16
- Canonical length
- 553 aa
- Protein class
- Enzymes, Predicted secreted proteins
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
Predicted to enable serine-type endopeptidase activity. Predicted to be involved in proteolysis. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
553 residues, UniProt reviewed canonical sequence.
>Q2L4Q9|PRSS53
1 MKWCWGPVLL IAGATVLMEG LQAAQRACGQ RGPGPPKPQE GNTVPGEWPW QASVRRQGAH
61 ICSGSLVADT WVLTAAHCFE KAAATELNSW SVVLGSLQRE GLSPGAEEVG VAALQLPRAY
121 NHYSQGSDLA LLQLAHPTTH TPLCLPQPAH RFPFGASCWA TGWDQDTSDA PGTLRNLRLR
181 LISRPTCNCI YNQLHQRHLS NPARPGMLCG GPQPGVQGPC QGDSGGPVLC LEPDGHWVQA
241 GIISFASSCA QEDAPVLLTN TAAHSSWLQA RVQGAAFLAQ SPETPEMSDE DSCVACGSLR
301 TAGPQAGAPS PWPWEARLMH QGQLACGGAL VSEEAVLTAA HCFIGRQAPE EWSVGLGTRP
361 EEWGLKQLIL HGAYTHPEGG YDMALLLLAQ PVTLGASLRP LCLPYPDHHL PDGERGWVLG
421 RARPGAGISS LQTVPVTLLG PRACSRLHAA PGGDGSPILP GMVCTSAVGE LPSCEGLSGA
481 PLVHEVRGTW FLAGLHSFGD ACQGPARPAV FTALPAYEDW VSSLDWQVYF AEEPEPEAEP
541 GSCLANISQP TSCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PRSS53 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.26
- Highest tissue expression
- 9.8 nTPM
Expression across tissuesHPA
Tissue
- liver: 9.8 nTPM
- skin: 2.4 nTPM
- cerebellum: 2.3 nTPM
- prostate: 0.9 nTPM
- blood vessel: 0.7 nTPM
- kidney: 0.7 nTPM
Single-cell type
- brain excitatory neurons: 5.5 nCPM
- brain inhibitory neurons: 5 nCPM
- other brain neurons: 4 nCPM
- astrocytes: 3.4 nCPM
- oligodendrocytes: 3.4 nCPM
- microglia: 2.8 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 1 nTPM
- cerebral cortex: 0.8 nTPM
- hippocampal formation: 0.8 nTPM
- hypothalamus: 0.8 nTPM
- medulla oblongata: 0.7 nTPM
- pons: 0.7 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)
- 1.36
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.49
- DepMap mean gene effect
- 0.1
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PRSS53 as an antibody target. Whether an autoantibody or antibody against PRSS53 could matter depends on whether native PRSS53 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PRSS53 is annotated as secreted, so native PRSS53 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label PRSS53 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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