PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 26234813-0 2015 Csk-Induced Phosphorylation of Src at Tyrosine 530 is Essential for H2O2-Mediated Suppression of ERK1/2 in Human Umbilical Vein Endothelial Cells. Hydrogen Peroxide 68-72 C-terminal Src kinase Homo sapiens 0-3 31125786-5 2019 Treatment with hydrogen peroxide inhibited this modification to a certain extent, but PIAS3, identified as the main specific SUMO E3 ligase for Csk, could significantly enhance SUMO1-Csk level. Hydrogen Peroxide 15-32 C-terminal Src kinase Homo sapiens 144-147 31125786-5 2019 Treatment with hydrogen peroxide inhibited this modification to a certain extent, but PIAS3, identified as the main specific SUMO E3 ligase for Csk, could significantly enhance SUMO1-Csk level. Hydrogen Peroxide 15-32 C-terminal Src kinase Homo sapiens 183-186 26234813-5 2015 Using siRNA, it was found that H2O2-induced suppression of ERK1/2 was dependent on Csk. Hydrogen Peroxide 31-35 C-terminal Src kinase Homo sapiens 83-86 26234813-7 2015 In conclusion, H2O2-induced Csk translocation to the plasma membrane leads to phosphorylation of Src at the tyrosine 530 residue resulting in a reduction of ERK1/2 phosphorylation. Hydrogen Peroxide 15-19 C-terminal Src kinase Homo sapiens 28-31 24632723-0 2014 SHP-2 binds to caveolin-1 and regulates Src activity via competitive inhibition of CSK in response to H2O2 in astrocytes. Hydrogen Peroxide 102-106 C-terminal Src kinase Homo sapiens 83-86 24632723-5 2014 In the presence of CSK siRNA, binding between caveolin-1 and SHP-2 was enhanced by H2O2 treatment, which led to reduced Src phosphorylation at tyrosine (Tyr) 530 and enhanced Src phosphorylation at Tyr 419. Hydrogen Peroxide 83-87 C-terminal Src kinase Homo sapiens 19-22 24632723-7 2014 Our results collectively indicate that SHP-2 alters Src kinase activity by interfering with the complex formation between CSK and phosphotyrosine caveolin-1 in the presence of H2O2, thus functions as a positive regulator in Src signaling under oxidative stress in brain astrocytes. Hydrogen Peroxide 176-180 C-terminal Src kinase Homo sapiens 122-125 24632723-6 2014 In contrast, siRNA targeting of SHP-2 facilitated H2O2-mediated interaction between caveolin-1 and CSK and enhanced Src phosphorylation at Tyr 530, leading to subsequent decrease in Src downstream signaling, such as focal adhesion kinase (FAK) and extracellular signal-related kinase (ERK). Hydrogen Peroxide 50-54 C-terminal Src kinase Homo sapiens 99-102 16814101-3 2006 This H2O2-induced kinase activation was significantly attenuated by a Src kinase inhibitor PP2, or by transient transfection of carboxyl-terminal Src kinase (CSK) that maintained Src in the dormant form. Hydrogen Peroxide 5-9 C-terminal Src kinase Homo sapiens 158-161 17349748-2 2007 The results demonstrate also that both platelet-derived growth factor (PDGF) and S1P-mediated NADPH oxidase activation and H2O2 production by Gi-protein coupled receptors (GPCRs) and c-Src kinase. Hydrogen Peroxide 123-127 C-terminal Src kinase Homo sapiens 183-195 17349748-5 2007 However, a different time course of H2O2 production in S1P-stimulated cells compared to that obtained in PDGF-stimulated cells has been observed, and this seems to be related to the different activation behavior of c-Src kinase induced after S1P or PDGF stimulation. Hydrogen Peroxide 36-40 C-terminal Src kinase Homo sapiens 215-227 17349748-6 2007 Finally, these data demonstrate that S1P-induced H2O2 production is necessary to maximize c-Src kinase activation, confirming that this is a redox regulated kinase. Hydrogen Peroxide 49-53 C-terminal Src kinase Homo sapiens 90-102 15958730-6 2005 Acute treatment with H(2)O(2) activated multiple signaling pathways, including the mitogen-activated protein kinases (MAPK) members (MAPK3/1-ERK2/1, MAPK8/9-JNK1/2, and MAPK11-p38(mapk)) and the c-src tyrosine kinase (CSK). Hydrogen Peroxide 21-29 C-terminal Src kinase Homo sapiens 195-216 15958730-6 2005 Acute treatment with H(2)O(2) activated multiple signaling pathways, including the mitogen-activated protein kinases (MAPK) members (MAPK3/1-ERK2/1, MAPK8/9-JNK1/2, and MAPK11-p38(mapk)) and the c-src tyrosine kinase (CSK). Hydrogen Peroxide 21-29 C-terminal Src kinase Homo sapiens 218-221 15958730-7 2005 Pharmacological studies demonstrated that, among these pathways, only the blockade of CSK activation abolished H(2)O(2)-induced CAV1 phosphorylation. Hydrogen Peroxide 111-119 C-terminal Src kinase Homo sapiens 86-89