PTER
N-acetyltaurine hydrolase
Also known as: PTER_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96BW5
- Gene
- PTER
- Ensembl
- ENSG00000165983
- Chromosome
- 10
- Canonical length
- 349 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Enables N-acetyltaurine hydrolase activity. Involved in epithelial cell differentiation and taurine metabolic process. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
349 residues, UniProt reviewed canonical sequence.
>Q96BW5|PTER
1 MSSLSGKVQT VLGLVEPSKL GRTLTHEHLA MTFDCCYCPP PPCQEAISKE PIVMKNLYWI
61 QKNAYSHKEN LQLNQETEAI KEELLYFKAN GGGALVENTT TGISRDTQTL KRLAEETGVH
121 IISGAGFYVD ATHSSETRAM SVEQLTDVLM NEILHGADGT SIKCGIIGEI GCSWPLTESE
181 RKVLQATAHA QAQLGCPVII HPGRSSRAPF QIIRILQEAG ADISKTVMSH LDRTILDKKE
241 LLEFAQLGCY LEYDLFGTEL LHYQLGPDID MPDDNKRIRR VRLLVEEGCE DRILVAHDIH
301 TKTRLMKYGG HGYSHILTNV VPKMLLRGIT ENVLDKILIE NPKQWLTFKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PTER 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)
- 0.2
- Highest tissue expression
- 41 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 41 nTPM
- kidney: 29 nTPM
- hippocampal formation: 26 nTPM
- amygdala: 23 nTPM
- stomach: 13 nTPM
- liver: 13 nTPM
Single-cell type
- proximal tubule cells: 145 nCPM
- urothelial cells: 136 nCPM
- pancreatic acinar cells: 126 nCPM
- foveolar cells: 104 nCPM
- renal collecting duct intercalated cells: 88 nCPM
- alveolar cells type 2: 75 nCPM
Immune cell
- T-reg: 14 nTPM
- intermediate monocyte: 12 nTPM
- non-classical monocyte: 10 nTPM
- memory B-cell: 9.2 nTPM
- memory CD4 T-cell: 8.8 nTPM
- MAIT T-cell: 8.1 nTPM
Brain region
- basal ganglia: 51 nTPM
- hippocampal formation: 50 nTPM
- cerebral cortex: 41 nTPM
- amygdala: 32 nTPM
- white matter: 20 nTPM
- thalamus: 19 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)
- 1.82
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.64
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- selective
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
- zinc ion binding
- N-acetyltaurine hydrolase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Metal-dependent hydrolase
- Phosphotriesterase
- Aryldialkylphosphatase, zinc-binding site
- Phosphotriesterase family
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PTER as an antibody target. Whether an autoantibody or antibody against PTER could matter depends on whether native PTER is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PTER 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 PTER as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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