PTPN3
Tyrosine-protein phosphatase non-receptor type 3
Also known as: PTN3_HUMAN, PTPH1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P26045
- Gene
- PTPN3
- Ensembl
- ENSG00000070159
- Chromosome
- 9
- Canonical length
- 913 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This protein contains a C-terminal PTP domain and an N-terminal domain homologous to the band 4.1 superfamily of cytoskeletal-associated proteins. P97, a cell cycle regulator involved in a variety of membrane related functions, has been shown to be a substrate of this PTP. This PTP was also found to interact with, and be regulated by adaptor protein 14-3-3 beta. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]
Canonical amino-acid sequenceUniProt
913 residues, UniProt reviewed canonical sequence.
>P26045|PTPN3
1 MTSRLRALGG RINNIRTSEL PKEKTRSEVI CSIHFLDGVV QTFKVTKQDT GQVLLDMVHN
61 HLGVTEKEYF GLQHDDDSVD SPRWLEASKA IRKQLKGGFP CTLHFRVRFF IPDPNTLQQE
121 QTRHLYFLQL KMDICEGRLT CPLNSAVVLA SYAVQSHFGD YNSSIHHPGY LSDSHFIPDQ
181 NEDFLTKVES LHEQHSGLKQ SEAESCYINI ARTLDFYGVE LHSGRDLHNL DLMIGIASAG
241 VAVYRKYICT SFYPWVNILK ISFKRKKFFI HQRQKQAESR EHIVAFNMLN YRSCKNLWKS
301 CVEHHTFFQA KKLLPQEKNV LSQYWTMGSR NTKKSVNNQY CKKVIGGMVW NPAMRRSLSV
361 EHLETKSLPS RSPPITPNWR SPRLRHEIRK PRHSSADNLA NEMTYITETE DVFYTYKGSL
421 APQDSDSEVS QNRSPHQESL SENNPAQSYL TQKSSSSVSP SSNAPGSCSP DGVDQQLLDD
481 FHRVTKGGST EDASQYYCDK NDNGDSYLVL IRITPDEDGK FGFNLKGGVD QKMPLVVSRI
541 NPESPADTCI PKLNEGDQIV LINGRDISEH THDQVVMFIK ASRESHSREL ALVIRRRAVR
601 SFADFKSEDE LNQLFPEAIF PMCPEGGDTL EGSMAQLKKG LESGTVLIQF EQLYRKKPGL
661 AITFAKLPQN LDKNRYKDVL PYDTTRVLLQ GNEDYINASY VNMEIPAANL VNKYIATQGP
721 LPHTCAQFWQ VVWDQKLSLI VMLTTLTERG RTKCHQYWPD PPDVMNHGGF HIQCQSEDCT
781 IAYVSREMLV TNTQTGEEHT VTHLQYVAWP DHGVPDDSSD FLEFVNYVRS LRVDSEPVLV
841 HCSAGIGRTG VLVTMETAMC LTERNLPIYP LDIVRKMRDQ RAMMVQTSSQ YKFVCEAILR
901 VYEEGLVQML DPSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PTPN3 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 60 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 60 nTPM
- tongue: 44 nTPM
- skin: 28 nTPM
- liver: 27 nTPM
- kidney: 22 nTPM
- heart muscle: 20 nTPM
Single-cell type
- myonuclei: 344 nCPM
- distal convoluted tubule cells: 303 nCPM
- renal connecting tubule cells: 267 nCPM
- esophageal apical cells: 237 nCPM
- loop of henle epithelial cells: 227 nCPM
- ependymal cells: 200 nCPM
Immune cell
- neutrophil: 0.4 nTPM
- classical monocyte: 0.1 nTPM
- eosinophil: 0.1 nTPM
- non-classical monocyte: 0.1 nTPM
- basophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- thalamus: 64 nTPM
- midbrain: 37 nTPM
- choroid plexus: 27 nTPM
- amygdala: 22 nTPM
- cerebral cortex: 14 nTPM
- hypothalamus: 14 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)
- 0.57
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.71
- DepMap mean gene effect
- 0
- 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
- MAPK cascade
- negative regulation of epidermal growth factor receptor signaling pathway
- negative regulation of membrane protein ectodomain proteolysis
- negative regulation of mitotic cell cycle
- regulation of membrane depolarization during action potential
- regulation of sodium ion transmembrane transport
Molecular functions
- ATPase binding
- cytoskeletal protein binding
- phosphotyrosine residue binding
- protein tyrosine phosphatase activity
- sodium channel regulator activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Tyrosine-specific protein phosphatase, PTPase domain
- FERM domain
- Tyrosine-specific protein phosphatases domain
- PDZ domain
- Protein-tyrosine phosphatase, catalytic
- PH-like domain superfamily
- Protein-tyrosine phosphatase, non-receptor type-3, -4
- FERM/acyl-CoA-binding protein superfamily
- Protein-tyrosine phosphatase, active site
- FERM, N-terminal
- FERM, C-terminal PH-like domain
- FERM conserved site
- FERM central domain
- Band 4.1 domain
- Protein-tyrosine phosphatase-like
- Ubiquitin-like domain superfamily
- FERM superfamily, second domain
- PDZ superfamily
- PTPN3/4, FERM domain C-lobe
- Protein-tyrosine phosphatase
- FERM central domain
- PDZ domain
- FERM N-terminal domain
- FERM C-terminal PH-like domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PTPN3 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 PTPN3 as an antibody target. Whether an autoantibody or antibody against PTPN3 could matter depends on whether native PTPN3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PTPN3 is annotated at the cell surface, where native PTPN3 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label PTPN3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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