PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 7836415-1 1995 A novel protein kinase (named PKD) with an NH2-terminal region containing two cysteine-rich motifs has been expressed in COS-7 cells and identified as a receptor for phorbol esters. Phorbol Esters 166-180 protein kinase D1 Mus musculus 30-33 10197446-1 1999 The novel mouse serine-threonine kinase protein kinase D (PKD) is activated in intact Swiss 3T3 cells stimulated by phorbol esters, cell permeant diacylglycerols, bryostatin, neuropeptides and growth factors via a phosphorylation-dependent mechanism requiring protein kinase C (PKC) activity. Phorbol Esters 116-130 protein kinase D1 Mus musculus 40-56 10197446-1 1999 The novel mouse serine-threonine kinase protein kinase D (PKD) is activated in intact Swiss 3T3 cells stimulated by phorbol esters, cell permeant diacylglycerols, bryostatin, neuropeptides and growth factors via a phosphorylation-dependent mechanism requiring protein kinase C (PKC) activity. Phorbol Esters 116-130 protein kinase D1 Mus musculus 58-61 10197446-4 1999 Replacement of serines 744 and 748 with alanine prevented activation of the overexpressed PKD form upon phorbol ester treatment of cells, whereas replacement with glutamic acid results in full constitutive activation. Phorbol Esters 104-117 protein kinase D1 Mus musculus 90-93 10197446-6 1999 In vivo 32P-labeling and two-dimensional phosphopeptide mapping of PKD and catalytically inactive PKD mutants at serine 744, 748 or at both residues revealed that phorbol ester-sensitive phosphopeptides could be selectively eliminated from patterns observed as a result of these mutations. Phorbol Esters 163-176 protein kinase D1 Mus musculus 67-70 10197446-6 1999 In vivo 32P-labeling and two-dimensional phosphopeptide mapping of PKD and catalytically inactive PKD mutants at serine 744, 748 or at both residues revealed that phorbol ester-sensitive phosphopeptides could be selectively eliminated from patterns observed as a result of these mutations. Phorbol Esters 163-176 protein kinase D1 Mus musculus 98-101 11514571-0 2001 Protein kinase D potentiates DNA synthesis and cell proliferation induced by bombesin, vasopressin, or phorbol esters in Swiss 3T3 cells. Phorbol Esters 103-117 protein kinase D1 Mus musculus 0-16 9295346-1 1997 Protein kinase D (PKD) is a serine/threonine protein kinase that is activated by phorbol esters via protein kinase C in intact cells. Phorbol Esters 81-95 protein kinase D1 Mus musculus 0-16 9295346-1 1997 Protein kinase D (PKD) is a serine/threonine protein kinase that is activated by phorbol esters via protein kinase C in intact cells. Phorbol Esters 81-95 protein kinase D1 Mus musculus 18-21 8947045-1 1996 Protein kinase D (PKD) is a serine/threonine protein kinase that is directly stimulated in vitro by phorbol esters and diacylglycerol in the presence of phospholipids. Phorbol Esters 100-114 protein kinase D1 Mus musculus 0-16 8947045-1 1996 Protein kinase D (PKD) is a serine/threonine protein kinase that is directly stimulated in vitro by phorbol esters and diacylglycerol in the presence of phospholipids. Phorbol Esters 100-114 protein kinase D1 Mus musculus 18-21 8947045-3 1996 Our results demonstrate that tumour-promoting phorbol esters, membrane-permeant diacylglycerol and serum growth factors rapidly induced PKD activation in immortalized cell lines (e.g. Swiss 3T3 and Rat-1 cells), in secondary cultures of mouse embryo fibroblasts and in COS-7 cells transiently transfected with a PKD expression construct. Phorbol Esters 46-60 protein kinase D1 Mus musculus 136-139 8947045-3 1996 Our results demonstrate that tumour-promoting phorbol esters, membrane-permeant diacylglycerol and serum growth factors rapidly induced PKD activation in immortalized cell lines (e.g. Swiss 3T3 and Rat-1 cells), in secondary cultures of mouse embryo fibroblasts and in COS-7 cells transiently transfected with a PKD expression construct. Phorbol Esters 46-60 protein kinase D1 Mus musculus 312-315 19124542-6 2009 In contrast, the phorbol ester PMA (phorbol-12-myristate-13-acetate, a pharmacological mimic of the downstream mediator diacylglycerol in alpha-adrenergic signalling), caused continuous PKD-dependent HDAC5-GFP nuclear efflux and maintained PKD1-mPlum redistribution. Phorbol Esters 17-30 protein kinase D1 Mus musculus 186-189 22311617-9 2012 In addition, PKD2-deficient lymphocytes, as well as DT40 cells devoid of any PKD isoforms, could activate Rap1 in response to B-cell receptor ligation or phorbol ester treatment. Phorbol Esters 154-167 protein kinase D1 Mus musculus 13-16