CTSE
Cathepsin E
Also known as: CATE_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P14091
- Gene
- CTSE
- Ensembl
- ENSG00000196188
- Chromosome
- 1
- Canonical length
- 396 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Vesicles
- Secretome location
- Intracellular and membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a member of the A1 family of peptidases. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This enzyme, an aspartic endopeptidase, may be involved in antigen processing and the maturation of secretory proteins. Elevated expression of this gene has been observed in neurodegeneration. [provided by RefSeq, Nov 2015]
Canonical amino-acid sequenceUniProt
396 residues, UniProt reviewed canonical sequence.
>P14091|CTSE
1 MKTLLLLLLV LLELGEAQGS LHRVPLRRHP SLKKKLRARS QLSEFWKSHN LDMIQFTESC
61 SMDQSAKEPL INYLDMEYFG TISIGSPPQN FTVIFDTGSS NLWVPSVYCT SPACKTHSRF
121 QPSQSSTYSQ PGQSFSIQYG TGSLSGIIGA DQVSVEGLTV VGQQFGESVT EPGQTFVDAE
181 FDGILGLGYP SLAVGGVTPV FDNMMAQNLV DLPMFSVYMS SNPEGGAGSE LIFGGYDHSH
241 FSGSLNWVPV TKQAYWQIAL DNIQVGGTVM FCSEGCQAIV DTGTSLITGP SDKIKQLQNA
301 IGAAPVDGEY AVECANLNVM PDVTFTINGV PYTLSPTAYT LLDFVDGMQF CSSGFQGLDI
361 HPPAGPLWIL GDVFIRQFYS VFDRGNNRVG LAPAVPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CTSE 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)
- 0.24
- Highest tissue expression
- 1,103 nTPM
Expression across tissuesHPA
Tissue
- stomach: 1,103 nTPM
- duodenum: 216 nTPM
- small intestine: 52 nTPM
- lung: 47 nTPM
- bone marrow: 28 nTPM
- rectum: 24 nTPM
Single-cell type
- foveolar cells: 1,602 nCPM
- alveolar cells type 1: 650 nCPM
- mucous neck cells: 401 nCPM
- transitional alveolar cells: 389 nCPM
- parietal cells: 309 nCPM
- gastric progenitor cells: 253 nCPM
Immune cell
- basophil: 0.5 nTPM
- neutrophil: 0.4 nTPM
- naive B-cell: 0.2 nTPM
- plasmacytoid DC: 0.2 nTPM
- classical monocyte: 0.1 nTPM
- gdT-cell: 0.1 nTPM
Brain region
- cerebellum: 2.5 nTPM
- white matter: 2.5 nTPM
- pons: 2.2 nTPM
- cerebral cortex: 2.1 nTPM
- thalamus: 2.1 nTPM
- medulla oblongata: 2 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)
- 1.62
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.3
- DepMap mean gene effect
- 0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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 CTSE as an antibody target. Whether an autoantibody or antibody against CTSE could matter depends on whether native CTSE is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CTSE 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 CTSE as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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