scholarly article | Q13442814 |
P2093 | author name string | Michael P Myers | |
Nicholas K Tonks | |||
Lizabeth A Allison | |||
Shantá D Hinton | |||
Vincent R Roggero | |||
P2860 | cites work | Mathematical models of protein kinase signal transduction. | Q52039321 |
Principles behind the multifarious control of signal transduction | Q57393856 | ||
Gathering STYX: phosphatase-like form predicts functions for unique protein-interaction domains | Q22003889 | ||
Crystal structure of the tandem phosphatase domains of RPTP LAR | Q22009892 | ||
The IA-2 interactome | Q24293778 | ||
The phosphoinositide-3-phosphatase MTMR2 associates with MTMR13, a membrane-associated pseudophosphatase also mutated in type 4B Charcot-Marie-Tooth disease | Q24306773 | ||
Regulation of MBK-2/DYRK by CDK-1 and the pseudophosphatases EGG-4 and EGG-5 during the oocyte-to-embryo transition | Q24313264 | ||
A Ras-GTPase-activating protein SH3-domain-binding protein | Q24316153 | ||
P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphatase | Q24322705 | ||
Development of "substrate-trapping" mutants to identify physiological substrates of protein tyrosine phosphatases | Q24323070 | ||
A novel phosphorylation-dependent RNase activity of GAP-SH3 binding protein: a potential link between signal transduction and RNA stability | Q24522539 | ||
The archetype STYX/dead-phosphatase complexes with a spermatid mRNA-binding protein and is essential for normal sperm production | Q24529833 | ||
Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma | Q24532011 | ||
RasGAP-associated endoribonuclease G3Bp: selective RNA degradation and phosphorylation-dependent localization | Q24548269 | ||
The RasGAP-associated endoribonuclease G3BP assembles stress granules | Q24671936 | ||
Stress granules and processing bodies are dynamically linked sites of mRNP remodeling | Q24678779 | ||
Heregulin induces expression, ATPase activity, and nuclear localization of G3BP, a Ras signaling component, in human breast tumors | Q28206195 | ||
Rasputin, more promiscuous than ever: a review of G3BP | Q28298633 | ||
Protein tyrosine phosphatases: from genes, to function, to disease | Q29614826 | ||
RNA-binding proteins TIA-1 and TIAR link the phosphorylation of eIF-2 alpha to the assembly of mammalian stress granules | Q29615265 | ||
Modulation of p53 and MDM2 activity by novel interaction with Ras-GAP binding proteins (G3BP). | Q30158060 | ||
Rasputin, the Drosophila homologue of the RasGAP SH3 binding protein, functions in ras- and Rho-mediated signaling | Q30175218 | ||
Substrate-trapping techniques in the identification of cellular PTP targets | Q34374862 | ||
EWS-FLI1 target genes recovered from Ewing's sarcoma chromatin | Q34398493 | ||
LKB1-dependent signaling pathways | Q34535140 | ||
Formation of stress granules inhibits apoptosis by suppressing stress-responsive MAPK pathways | Q34845865 | ||
mRNA degradation machines in eukaryotic cells | Q35011995 | ||
The structure and regulation of myotubularin phosphatases | Q36313678 | ||
Myotubularin phosphatases: policing 3-phosphoinositides | Q36530570 | ||
Preferential oxidation of the second phosphatase domain of receptor-like PTP-alpha revealed by an antibody against oxidized protein tyrosine phosphatases | Q36603867 | ||
Differential regulation of MAP kinase signalling by dual-specificity protein phosphatases. | Q36819391 | ||
The JAK kinases: not just another kinase drug discovery target | Q37250023 | ||
Expression and function of IA-2 family proteins, unique neuroendocrine-specific protein-tyrosine phosphatases | Q37528867 | ||
A single mutation converts a novel phosphotyrosine binding domain into a dual-specificity phosphatase. | Q38289397 | ||
Crystal structure of the major diabetes autoantigen insulinoma-associated protein 2 reveals distinctive immune epitopes | Q40256865 | ||
A novel strategy for the development of selective active-site inhibitors of the protein tyrosine phosphatase-like proteins islet-cell antigen 512 (IA-2) and phogrin (IA-2beta). | Q40593923 | ||
G3BP is overexpressed in human tumors and promotes S phase entry | Q42832825 | ||
Pseudophosphatases: grab and hold on. | Q43251271 | ||
Modulation of specific protein expression levels by PTEN: identification of AKAP121, DHFR, G3BP, Rap1, and RCC1 as potential targets of PTEN. | Q46396119 | ||
IA-2 (islet cell antigen 512) is the primary target of humoral autoimmunity against type 1 diabetes-associated tyrosine phosphatase autoantigens. | Q50158841 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial 2.5 Generic | Q19113746 |
P6216 | copyright status | copyrighted | Q50423863 |
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | regulation of stress granule assembly | Q54810457 |
positive regulation of stress granule assembly | Q54810458 | ||
negative regulation of stress granule assembly | Q54810459 | ||
G3BP stress granule assembly factor 1 | Q21112719 | ||
Serine/threonine/tyrosine interacting like 1 | Q21135934 | ||
P304 | page(s) | 349-357 | |
P577 | publication date | 2010-04-14 | |
P1433 | published in | Biochemical Journal | Q864221 |
P1476 | title | The pseudophosphatase MK-STYX interacts with G3BP and decreases stress granule formation | |
P478 | volume | 427 |
Q51577082 | Analyzing Pseudophosphatase Function. |
Q39241478 | Antagonistic roles for STYX pseudophosphatases in neurite outgrowth |
Q27974726 | Atypical mitogen-activated protein kinase phosphatase implicated in regulating transition from pre-S-Phase asexual intraerythrocytic development of Plasmodium falciparum |
Q27309029 | G3BP-Caprin1-USP10 complexes mediate stress granule condensation and associate with 40S subunits |
Q21199585 | Genome-wide matching of genes to cellular roles using guilt-by-association models derived from single sample analysis |
Q27974727 | In silico characterization of an atypical MAPK phosphatase of Plasmodium falciparum as a suitable target for drug discovery |
Q24308033 | Insights into the suppressor of T-cell receptor (TCR) signaling-1 (Sts-1)-mediated regulation of TCR signaling through the use of novel substrate-trapping Sts-1 phosphatase variants |
Q36506947 | Japanese encephalitis virus core protein inhibits stress granule formation through an interaction with Caprin-1 and facilitates viral propagation |
Q47132858 | MK-STYX Alters the Morphology of Primary Neurons, and Outgrowths in MK-STYX Overexpressing PC-12 Cells Develop a Neuronal Phenotype |
Q36427519 | Phosphotyrosine recognition domains: the typical, the atypical and the versatile |
Q43638244 | Phylogenetic and genetic linkage between novel atypical dual-specificity phosphatases from non-metazoan organisms. |
Q24622527 | Protein tyrosine phosphatases--from housekeeping enzymes to master regulators of signal transduction |
Q64062337 | Pseudophosphatase MK-STYX Alters Histone Deacetylase 6 Cytoplasmic Localization, Decreases Its Phosphorylation, and Increases Detyrosination of Tubulin |
Q38142438 | Pseudophosphatases: methods of analysis and physiological functions |
Q37992291 | Regulation of stress granules in virus systems |
Q38634867 | The extended human PTPome: a growing tyrosine phosphatase family |
Q35494912 | The pseudophosphatase MK-STYX induces neurite-like outgrowths in PC12 cells. |
Q30009978 | The pseudophosphatase MK-STYX inhibits stress granule assembly independently of Ser149 phosphorylation of G3BP-1 |
Q31157967 | The pseudophosphatase MK-STYX physically and genetically interacts with the mitochondrial phosphatase PTPMT1 |
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