PTPN2

PTPN2
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1L8K
Identifiers
Aliases	PTPN2, PTN2, PTPT, TC-PTP, TCELLPTP, TCPTP, protein tyrosine phosphatase, non-receptor type 2, protein tyrosine phosphatase non-receptor type 2
External IDs	OMIM: 176887; MGI: 97806; HomoloGene: 7497; GeneCards: PTPN2; OMA:PTPN2 - orthologs
Gene location (Human) Chr. Chromosome 18 (human) Band 18p11.21 Start 12,785,478 bp End 12,929,643 bp
Gene location (Mouse) Chr. Chromosome 18 (mouse) Band 18|18 E1 Start 67,798,581 bp End 67,857,665 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in tendon of biceps brachii monocyte granulocyte tonsil cartilage tissue parotid gland oocyte lymph node body of pancreas gonad Top expressed in otic placode saccule condyle primary oocyte fossa Paneth cell hair follicle secondary oocyte submandibular gland primitive streak More reference expression data BioGPS n/a
Gene ontology Molecular function protein binding protein kinase binding phosphatase activity integrin binding phosphoprotein phosphatase activity syntaxin binding non-membrane spanning protein tyrosine phosphatase activity receptor tyrosine kinase binding hydrolase activity protein tyrosine phosphatase activity STAT family protein binding Cellular component cytoplasm membrane plasma membrane endoplasmic reticulum nucleus endoplasmic reticulum-Golgi intermediate compartment nucleoplasm cytosol Biological process negative regulation of type I interferon-mediated signaling pathway negative regulation of epidermal growth factor receptor signaling pathway positive regulation of PERK-mediated unfolded protein response dephosphorylation negative regulation of interleukin-4-mediated signaling pathway positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway negative regulation of interleukin-6-mediated signaling pathway negative regulation of cell population proliferation protein dephosphorylation negative regulation of interleukin-2-mediated signaling pathway regulation of interferon-gamma-mediated signaling pathway negative regulation of protein tyrosine kinase activity regulation of hepatocyte growth factor receptor signaling pathway negative regulation of platelet-derived growth factor receptor-beta signaling pathway insulin receptor signaling pathway negative regulation of interferon-gamma-mediated signaling pathway glucose homeostasis negative regulation of chemotaxis negative regulation of tumor necrosis factor-mediated signaling pathway negative regulation of macrophage differentiation negative regulation of T cell receptor signaling pathway negative regulation of positive thymic T cell selection negative regulation of insulin receptor signaling pathway T cell differentiation negative regulation of ERK1 and ERK2 cascade erythrocyte differentiation negative regulation of lipid storage B cell differentiation peptidyl-tyrosine dephosphorylation positive regulation of gluconeogenesis negative regulation of macrophage colony-stimulating factor signaling pathway negative regulation of inflammatory response negative regulation of transcription by RNA polymerase II negative regulation of tyrosine phosphorylation of STAT protein cellular response to cytokine stimulus Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 5771 19255 Ensembl ENSG00000175354 ENSMUSG00000024539 UniProt P17706 Q06180 RefSeq (mRNA) NM_001207013 NM_001308287 NM_002828 NM_080422 NM_080423 NM_001127177 NM_008977 RefSeq (protein) NP_001193942 NP_001295216 NP_002819 NP_536347 NP_536348 NP_001120649 NP_033003 Location (UCSC) Chr 18: 12.79 – 12.93 Mb Chr 18: 67.8 – 67.86 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Tyrosine-protein phosphatase non-receptor type 2 is an enzyme that in humans is encoded by the PTPN2 gene.

The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. Members of the PTP family share a highly conserved catalytic motif, which is essential for the catalytic activity. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation.

Epidermal growth factor receptor and the adaptor protein Shc were reported to be substrates of this PTP, which suggested the roles in growth factor mediated cell signaling. Three alternatively spliced variants of this gene, which encode isoforms differing at their extreme C-termini, have been described.

The different C-termini are thought to determine the substrate specificity, as well as the cellular localization of the isoforms. Two highly related but distinctly processed pseudogenes that localize to distinct chromosomes have been reported.

Further reading

• Baumgartner, CK, Ebrahimi-Nik, H, Iracheta-Vellve, A (2023). "The PTPN2/PTPN1 inhibitor ABBV-CLS-484 unleashes potent anti-tumour immunity". Nature. 622 (7984): 850–862. Bibcode:2023Natur.622..850B. doi:10.1038/s41586-023-06575-7. PMC 10599993. PMID 37794185.
• LaFleur MW, Nguyen TH, Coxe MA (2019). "PTPN2 regulates the generation of exhausted CD8+ T cell subpopulations and restrains tumor immunity". Nat. Immunol. 20 (10): 1335–1347. doi:10.1038/s41590-019-0480-4. PMC 6754306. PMID 31527834.
• Manguso RT, Pope HW, Zimmer MD (2017). "In vivo CRISPR screening identifies Ptpn2 as a cancer immunotherapy target". Nature. 547 (7664): 413–418. doi:10.1038/nature23270. PMC 5924693. PMID 28723893.
• Mosinger B, Tillmann U, Westphal H, Tremblay ML (1992). "Cloning and characterization of a mouse cDNA encoding a cytoplasmic protein-tyrosine-phosphatase". Proc. Natl. Acad. Sci. U.S.A. 89 (2): 499–503. Bibcode:1992PNAS...89..499M. doi:10.1073/pnas.89.2.499. PMC 48266. PMID 1731319.
• Swarup G, Kamatkar S, Radha V, Rema V (1991). "Molecular cloning and expression of a protein-tyrosine phosphatase showing homology with transcription factors Fos and Jun". FEBS Lett. 280 (1): 65–9. Bibcode:1991FEBSL.280...65S. doi:10.1016/0014-5793(91)80205-H. PMID 1849097. S2CID 10568838.
• Cool DE, Tonks NK, Charbonneau H, et al. (1989). "cDNA isolated from a human T-cell library encodes a member of the protein-tyrosine-phosphatase family". Proc. Natl. Acad. Sci. U.S.A. 86 (14): 5257–61. Bibcode:1989PNAS...86.5257C. doi:10.1073/pnas.86.14.5257. PMC 297600. PMID 2546150.
• Lorenzen JA, Dadabay CY, Fischer EH (1995). "COOH-terminal sequence motifs target the T cell protein tyrosine phosphatase to the ER and nucleus". J. Cell Biol. 131 (3): 631–43. doi:10.1083/jcb.131.3.631. PMC 2120615. PMID 7593185.
• Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
• Johnson CV, Cool DE, Glaccum MB, et al. (1993). "Isolation and mapping of human T-cell protein tyrosine phosphatase sequences: localization of genes and pseudogenes discriminated using fluorescence hybridization with genomic versus cDNA probes". Genomics. 16 (3): 619–29. doi:10.1006/geno.1993.1239. PMID 8325634.
• Tiganis T, Flint AJ, Adam SA, Tonks NK (1997). "Association of the T-cell protein tyrosine phosphatase with nuclear import factor p97". J. Biol. Chem. 272 (34): 21548–57. doi:10.1074/jbc.272.34.21548. PMID 9261175.
• Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
• Tiganis T, Bennett AM, Ravichandran KS, Tonks NK (1998). "Epidermal growth factor receptor and the adaptor protein p52Shc are specific substrates of T-cell protein tyrosine phosphatase". Mol. Cell. Biol. 18 (3): 1622–34. doi:10.1128/MCB.18.3.1622. PMC 108877. PMID 9488479.
• Tiganis T, Kemp BE, Tonks NK (1999). "The protein-tyrosine phosphatase TCPTP regulates epidermal growth factor receptor-mediated and phosphatidylinositol 3-kinase-dependent signaling". J. Biol. Chem. 274 (39): 27768–75. doi:10.1074/jbc.274.39.27768. PMID 10488121.
• Iversen LF, Moller KB, Pedersen AK, et al. (2002). "Structure determination of T cell protein-tyrosine phosphatase". J. Biol. Chem. 277 (22): 19982–90. doi:10.1074/jbc.M200567200. PMID 11907034.
• Simoncic PD, Lee-Loy A, Barber DL, et al. (2002). "The T cell protein tyrosine phosphatase is a negative regulator of janus family kinases 1 and 3". Curr. Biol. 12 (6): 446–53. Bibcode:2002CBio...12..446S. doi:10.1016/S0960-9822(02)00697-8. PMID 11909529. S2CID 16693906.
• ten Hoeve J, de Jesus Ibarra-Sanchez M, Fu Y, et al. (2002). "Identification of a nuclear Stat1 protein tyrosine phosphatase". Mol. Cell. Biol. 22 (16): 5662–8. doi:10.1128/MCB.22.16.5662-5668.2002. PMC 133976. PMID 12138178.
• Zhu W, Mustelin T, David M (2002). "Arginine methylation of STAT1 regulates its dephosphorylation by T cell protein tyrosine phosphatase". J. Biol. Chem. 277 (39): 35787–90. doi:10.1074/jbc.C200346200. PMID 12171910.
• Yamamoto T, Sekine Y, Kashima K, et al. (2002). "The nuclear isoform of protein-tyrosine phosphatase TC-PTP regulates interleukin-6-mediated signaling pathway through STAT3 dephosphorylation". Biochem. Biophys. Res. Commun. 297 (4): 811–7. doi:10.1016/S0006-291X(02)02291-X. hdl:2115/28124. PMID 12359225.
• Gupta S, Radha V, Sudhakar Ch, Swarup G (2003). "A nuclear protein tyrosine phosphatase activates p53 and induces caspase-1-dependent apoptosis". FEBS Lett. 532 (1–2): 61–6. doi:10.1016/S0014-5793(02)03628-1. PMID 12459463. S2CID 33468275.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Galic S, Klingler-Hoffmann M, Fodero-Tavoletti MT, et al. (2003). "Regulation of insulin receptor signaling by the protein tyrosine phosphatase TCPTP". Mol. Cell. Biol. 23 (6): 2096–108. doi:10.1128/MCB.23.6.2096-2108.2003. PMC 149470. PMID 12612081.