Difference between revisions of "Phosphatase Subfamily STS"

Revision as of 18:05, 29 May 2015

Phosphatase Classification: Fold HP: Superfamily HP (histidine phosphatase): HP, branch1 family: Subfamily STS

STS is protein tyrosine phosphatase involved in T-cell receptor signaling. In particular, STS dephosphorylates kinases Syk and ZAP-70 of Syk subfamily. STS is conserved in metazoan.

Evolution

STS subfamily is found in most metazoan. Human has two STSs: STS-1 (TULA-2 or UBASH3B) and STS-2 (TULA-1 or UBASH3A). STS-2 is present in lobe-finned fish, birds and mammals, but not other bony fishes. STS-1 emerged earlier than STS-2, which is found in most metazoan, from sponge to insects, fishes, birds, and mammals. C. elegans has five STS genes, but all of them lack UBA and SH3 domains.

Domain

Typical STS consists of four domains: UBA (ubiquitin-associated domain), 2H phosphoesterase [1], SH3 and HP2 phosphatase domain.

Functions

Human STS-1 and STS-2 are involved in T Cell Receptor (TCR) signaling pathways by regulating kinase Syk and ZAP-70, two members of Syk kinase subfamily. STS-2 is predominantly in naive and mature T cells , whereas STS-1 is expressed ubiquitously.

STS-1 decreases tyrosine phosphorylation of Syk in vivo and in vitro [2, 3]. Inactivated STS-1 increases tyrosine phosphorylation of Syk in cells co-transfected to overexpress these proteins, thus acting as a dominant-negative form that suppresses dephosphorylation of Syk caused by endogenous STS-1. However, the same assay on STS-2 shows the phosphatase activity of STS-2 is negligible compared to STS-1. The UBA domain of STS-2 and SH3-dependent Cbl-binding are required for this function [4]. In addition, both STS-1 and STS-2 regulates kinase ZAP-70 activation [3].

Human STS-1 can also dephosphorylate phospho-tyrosines on EGFR. The histidine phosphatase domain of STS-1, but not of STS-2, dephosphorylates the EGFR at multiple tyrosines, and thereby terminating its signalling and endocytosis [5].

References

1. Mazumder R, Iyer LM, Vasudevan S, and Aravind L. Detection of novel members, structure-function analysis and evolutionary classification of the 2H phosphoesterase superfamily. Nucleic Acids Res. 2002 Dec 1;30(23):5229-43. DOI:10.1093/nar/gkf645 | PubMed ID:12466548 | HubMed [mazumder02]
2. Chen X, Ren L, Kim S, Carpino N, Daniel JL, Kunapuli SP, Tsygankov AY, and Pei D. Determination of the substrate specificity of protein-tyrosine phosphatase TULA-2 and identification of Syk as a TULA-2 substrate. J Biol Chem. 2010 Oct 8;285(41):31268-76. DOI:10.1074/jbc.M110.114181 | PubMed ID:20670933 | HubMed [chen10]
3. Carpino N, Turner S, Mekala D, Takahashi Y, Zang H, Geiger TL, Doherty P, and Ihle JN. Regulation of ZAP-70 activation and TCR signaling by two related proteins, Sts-1 and Sts-2. Immunity. 2004 Jan;20(1):37-46. DOI:10.1016/s1074-7613(03)00351-0 | PubMed ID:14738763 | HubMed [carpino04]
4. Agrawal R, Carpino N, and Tsygankov A. TULA proteins regulate activity of the protein tyrosine kinase Syk. J Cell Biochem. 2008 Jun 1;104(3):953-64. DOI:10.1002/jcb.21678 | PubMed ID:18189269 | HubMed [STS_2]
5. Raguz J, Wagner S, Dikic I, and Hoeller D. Suppressor of T-cell receptor signalling 1 and 2 differentially regulate endocytosis and signalling of receptor tyrosine kinases. FEBS Lett. 2007 Oct 2;581(24):4767-72. DOI:10.1016/j.febslet.2007.08.077 | PubMed ID:17880946 | HubMed [STS_1]