TYSND1
Peroxisomal leader peptide-processing protease
Also known as: MGC34695, NET41, TYSD1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q2T9J0
- Gene
- TYSND1
- Ensembl
- ENSG00000156521
- Chromosome
- 10
- Canonical length
- 566 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Centrosome,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a protease that removes the N-terminal peroxisomal targeting signal (PTS2) from proteins produced in the cytosol, thereby facilitating their import into the peroxisome. The encoded protein is also capable of removing the C-terminal peroxisomal targeting signal (PTS1) from proteins in the peroxisomal matrix. The full-length protein undergoes self-cleavage to produce shorter, potentially inactive, peptides. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Jan 2013]
Canonical amino-acid sequenceUniProt
566 residues, UniProt reviewed canonical sequence.
>Q2T9J0|TYSND1
1 MRRQWGSAMR AAEQAGCMVS ASRAGQPEAG PWSCSGVILS RSPGLVLCHG GIFVPFLRAG
61 SEVLTAAGAV FLPGDSCRDD LRLHVQWAPT AAGPGGGAER GRPGLCTPQC ASLEPGPPAP
121 SRGRPLQPRL PAELLLLLSC PAFWAHFARL FGDEAAEQWR FSSAARDDEV SEDEEADQLR
181 ALGWFALLGV RLGQEEVEEE RGPAMAVSPL GAVPKGAPLL VCGSPFGAFC PDIFLNTLSC
241 GVLSNVAGPL LLTDARCLPG TEGGGVFTAR PAGALVALVV APLCWKAGEW VGFTLLCAAA
301 PLFRAARDAL HRLPHSTAAL AALLPPEVGV PWGLPLRDSG PLWAAAAVLV ECGTVWGSGV
361 AVAPRLVVTC RHVSPREAAR VLVRSTTPKS VAIWGRVVFA TQETCPYDIA VVSLEEDLDD
421 VPIPVPAEHF HEGEAVSVVG FGVFGQSCGP SVTSGILSAV VQVNGTPVML QTTCAVHSGS
481 SGGPLFSNHS GNLLGIITSN TRDNNTGATY PHLNFSIPIT VLQPALQQYS QTQDLGGLRE
541 LDRAAEPVRV VWRLQRPLAE APRSKLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TYSND1 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)
- 0.26
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- testis: 13 nTPM
- esophagus: 11 nTPM
- skin: 10 nTPM
- vagina: 6 nTPM
- liver: 5.8 nTPM
- pancreas: 5.7 nTPM
Single-cell type
- late primary spermatocytes: 325 nCPM
- late spermatids: 305 nCPM
- early spermatids: 101 nCPM
- esophageal basal cells: 52 nCPM
- cytotrophoblasts: 46 nCPM
- esophageal suprabasal cells: 46 nCPM
Immune cell
- gdT-cell: 3.8 nTPM
- naive B-cell: 3.3 nTPM
- memory B-cell: 3 nTPM
- naive CD4 T-cell: 3 nTPM
- memory CD8 T-cell: 2.8 nTPM
- T-reg: 2.7 nTPM
Brain region
- medulla oblongata: 11 nTPM
- cerebellum: 9.9 nTPM
- cerebral cortex: 9.8 nTPM
- amygdala: 9.3 nTPM
- basal ganglia: 9.2 nTPM
- white matter: 9.1 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
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.98
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- selective
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
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Peptidase S1, PA clan
- Trypsin-like peptidase domain
- Peptidase S1A, Tysnd1
- Peroxisomal/glyoxysomal leader peptide-processing protease
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TYSND1 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 TYSND1 as an antibody target. Whether an autoantibody or antibody against TYSND1 could matter depends on whether native TYSND1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TYSND1 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 TYSND1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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