Combinatorial control of the specificity of protein tyrosine phosphatases - PubMed (original) (raw)
Review
Combinatorial control of the specificity of protein tyrosine phosphatases
N K Tonks et al. Curr Opin Cell Biol. 2001 Apr.
Abstract
Protein tyrosine phosphatases (PTPs), the enzymes that dephosphorylate tyrosyl phosphoproteins, were initially believed to be few in number and serve a 'housekeeping' role in signal transduction. Recent work indicates that this is totally incorrect. Instead, PTPs comprise a large superfamily whose members play critical roles in a wide variety of cellular processes. Moreover, PTPs exhibit exquisite substrate specificity in vivo. Recent evidence has led us to propose that members of the PTP family achieve selectivity through different combinations of specific targeting strategies and intrinsic catalytic domain specificity.
Similar articles
- Mechanistic studies on protein tyrosine phosphatases.
Zhang ZY. Zhang ZY. Prog Nucleic Acid Res Mol Biol. 2003;73:171-220. doi: 10.1016/s0079-6603(03)01006-7. Prog Nucleic Acid Res Mol Biol. 2003. PMID: 12882518 Review. - The Extended Family of Protein Tyrosine Phosphatases.
Alonso A, Nunes-Xavier CE, Bayón Y, Pulido R. Alonso A, et al. Methods Mol Biol. 2016;1447:1-23. doi: 10.1007/978-1-4939-3746-2_1. Methods Mol Biol. 2016. PMID: 27514797 Review. - Bi-domain protein tyrosine phosphatases reveal an evolutionary adaptation to optimize signal transduction.
Ahuja LG, Gopal B. Ahuja LG, et al. Antioxid Redox Signal. 2014 May 10;20(14):2141-59. doi: 10.1089/ars.2013.5721. Epub 2013 Dec 21. Antioxid Redox Signal. 2014. PMID: 24206235 Review. - Functional studies of protein tyrosine phosphatases with chemical approaches.
Zhang ZY. Zhang ZY. Biochim Biophys Acta. 2005 Dec 30;1754(1-2):100-7. doi: 10.1016/j.bbapap.2005.09.005. Epub 2005 Sep 29. Biochim Biophys Acta. 2005. PMID: 16226063 Review. - Use of Dominant-Negative/Substrate Trapping PTP Mutations to Search for PTP Interactors/Substrates.
Radha V. Radha V. Methods Mol Biol. 2016;1447:243-65. doi: 10.1007/978-1-4939-3746-2_14. Methods Mol Biol. 2016. PMID: 27514810
Cited by
- Protein tyrosine phosphatase 1B modulates GSK3β/Nrf2 and IGFIR signaling pathways in acetaminophen-induced hepatotoxicity.
Mobasher MA, González-Rodriguez A, Santamaría B, Ramos S, Martín MÁ, Goya L, Rada P, Letzig L, James LP, Cuadrado A, Martín-Pérez J, Simpson KJ, Muntané J, Valverde AM. Mobasher MA, et al. Cell Death Dis. 2013 May 9;4(5):e626. doi: 10.1038/cddis.2013.150. Cell Death Dis. 2013. PMID: 23661004 Free PMC article. - Virtual screening, optimization, and identification of a novel specific PTP-MEG2 Inhibitor with potential therapy for T2DM.
Wang M, Li X, Dong L, Chen X, Xu W, Wang R. Wang M, et al. Oncotarget. 2016 Aug 9;7(32):50828-50834. doi: 10.18632/oncotarget.10341. Oncotarget. 2016. PMID: 27384997 Free PMC article. - Upregulation of PTP1B After Rat Spinal Cord Injury.
Zhu X, Zhou Y, Tao R, Zhao J, Chen J, Liu C, Xu Z, Bao G, Zhang J, Chen M, Shen J, Cheng C, Zhang D. Zhu X, et al. Inflammation. 2015 Oct;38(5):1891-902. doi: 10.1007/s10753-015-0169-2. Inflammation. 2015. PMID: 25894283 - Identification of a nuclear Stat1 protein tyrosine phosphatase.
ten Hoeve J, de Jesus Ibarra-Sanchez M, Fu Y, Zhu W, Tremblay M, David M, Shuai K. ten Hoeve J, et al. Mol Cell Biol. 2002 Aug;22(16):5662-8. doi: 10.1128/MCB.22.16.5662-5668.2002. Mol Cell Biol. 2002. PMID: 12138178 Free PMC article. - Contact inhibition of VEGF-induced proliferation requires vascular endothelial cadherin, beta-catenin, and the phosphatase DEP-1/CD148.
Grazia Lampugnani M, Zanetti A, Corada M, Takahashi T, Balconi G, Breviario F, Orsenigo F, Cattelino A, Kemler R, Daniel TO, Dejana E. Grazia Lampugnani M, et al. J Cell Biol. 2003 May 26;161(4):793-804. doi: 10.1083/jcb.200209019. J Cell Biol. 2003. PMID: 12771128 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
- P01 DK50654/DK/NIDDK NIH HHS/United States
- P30 C45508/PHS HHS/United States
- P50 HL56993/HL/NHLBI NIH HHS/United States
- R01 CA49152/CA/NCI NIH HHS/United States
- R01 CA53840/CA/NCI NIH HHS/United States
- R01 DK50693/DK/NIDDK NIH HHS/United States
- R01 GM55989/GM/NIGMS NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources