PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
17921317-0	2007	Two calcium-dependent protein kinases, CPK4 and CPK11, regulate abscisic acid signal transduction in Arabidopsis.	Abscisic Acid	64-77	calcium-dependent protein kinase 2	Arabidopsis thaliana	48-53
20978156-4	2011	It has been reported that four Arabidopsis (Arabidopsis thaliana) CDPKs, CPK3, CPK6, CPK4, and CPK11, are involved in abscisic acid signaling in guard cells.	Abscisic Acid	118-131	calcium-dependent protein kinase 2	Arabidopsis thaliana	95-100
17921317-2	2007	Here, we report that ABA stimulated two homologous CDPKs in Arabidopsis thaliana, CPK4 and CPK11.	Abscisic Acid	21-24	calcium-dependent protein kinase 2	Arabidopsis thaliana	91-96
17921317-3	2007	Loss-of-function mutations of CPK4 and CPK11 resulted in pleiotropic ABA-insensitive phenotypes in seed germination, seedling growth, and stomatal movement and led to salt insensitivity in seed germination and decreased tolerance of seedlings to salt stress.	Abscisic Acid	69-72	calcium-dependent protein kinase 2	Arabidopsis thaliana	39-44
17921317-3	2007	Loss-of-function mutations of CPK4 and CPK11 resulted in pleiotropic ABA-insensitive phenotypes in seed germination, seedling growth, and stomatal movement and led to salt insensitivity in seed germination and decreased tolerance of seedlings to salt stress.	Salts	167-171	calcium-dependent protein kinase 2	Arabidopsis thaliana	39-44
17921317-3	2007	Loss-of-function mutations of CPK4 and CPK11 resulted in pleiotropic ABA-insensitive phenotypes in seed germination, seedling growth, and stomatal movement and led to salt insensitivity in seed germination and decreased tolerance of seedlings to salt stress.	Salts	246-250	calcium-dependent protein kinase 2	Arabidopsis thaliana	39-44
17921317-5	2007	CPK4- or CPK11-overexpressing plants generally showed inverse ABA-related phenotypes relative to those of the loss-of-function mutants.	Abscisic Acid	62-65	calcium-dependent protein kinase 2	Arabidopsis thaliana	9-14
17921317-7	2007	The CPK4 and CPK11 kinases both phosphorylated two ABA-responsive transcription factors, ABF1 and ABF4, in vitro, suggesting that the two kinases may regulate ABA signaling through these transcription factors.	Abscisic Acid	51-54	calcium-dependent protein kinase 2	Arabidopsis thaliana	13-18
17921317-7	2007	The CPK4 and CPK11 kinases both phosphorylated two ABA-responsive transcription factors, ABF1 and ABF4, in vitro, suggesting that the two kinases may regulate ABA signaling through these transcription factors.	Abscisic Acid	159-162	calcium-dependent protein kinase 2	Arabidopsis thaliana	13-18
17921317-8	2007	These data provide in planta genetic evidence for the involvement of CDPK/calcium in ABA signaling at the whole-plant level and show that CPK4 and CPK11 are two important positive regulators in CDPK/calcium-mediated ABA signaling pathways.	Calcium	74-81	calcium-dependent protein kinase 2	Arabidopsis thaliana	147-152
17921317-8	2007	These data provide in planta genetic evidence for the involvement of CDPK/calcium in ABA signaling at the whole-plant level and show that CPK4 and CPK11 are two important positive regulators in CDPK/calcium-mediated ABA signaling pathways.	Abscisic Acid	85-88	calcium-dependent protein kinase 2	Arabidopsis thaliana	147-152
17921317-8	2007	These data provide in planta genetic evidence for the involvement of CDPK/calcium in ABA signaling at the whole-plant level and show that CPK4 and CPK11 are two important positive regulators in CDPK/calcium-mediated ABA signaling pathways.	Calcium	199-206	calcium-dependent protein kinase 2	Arabidopsis thaliana	147-152
17921317-8	2007	These data provide in planta genetic evidence for the involvement of CDPK/calcium in ABA signaling at the whole-plant level and show that CPK4 and CPK11 are two important positive regulators in CDPK/calcium-mediated ABA signaling pathways.	Abscisic Acid	216-219	calcium-dependent protein kinase 2	Arabidopsis thaliana	147-152
26829353-7	2016	Overexpression of GhDi19-1/-2 and their constitutively activated forms in Atcpk11 background could recover the salt- and ABA-insensitive phenotype of the mutant.	Salts	111-115	calcium-dependent protein kinase 2	Arabidopsis thaliana	74-81
8078458-2	1994	Northern blot analysis indicated that the mRNAs corresponding to the ATCDPK1 and ATCDPK2 genes are rapidly induced by drought and high-salt stress but not by low-temperature stress or heat stress.	Salts	135-139	calcium-dependent protein kinase 2	Arabidopsis thaliana	81-88
26829353-7	2016	Overexpression of GhDi19-1/-2 and their constitutively activated forms in Atcpk11 background could recover the salt- and ABA-insensitive phenotype of the mutant.	Abscisic Acid	121-124	calcium-dependent protein kinase 2	Arabidopsis thaliana	74-81
24019427-7	2013	Nitric oxide and reduced nicotinamide adenine dinucleotide phosphate oxidase-dependent reactive oxygen species generation (due to the function of Respiratory Burst Oxidase Homolog proteins D and F) are also involved downstream from the Ca(2+) signal in the Pep immune defense signal transduction cascade, as is the case with BRASSINOSTEROID-INSENSITIVE1 Associated Kinase1 and CPK5, CPK6, and CPK11.	Nitric Oxide	0-12	calcium-dependent protein kinase 2	Arabidopsis thaliana	393-398
26485342-5	2015	Here we show that simultaneous loss of calcium-dependent protein kinases CPK5, CPK6 and CPK11 affects Arabidopsis thaliana basal as well as elicitor- induced resistance to the necrotroph Botrytis cinerea, by affecting pathogen-induced ethylene production and accumulation of the ethylene biosynthetic enzymes 1-aminocyclopropane-1-carboxylic acid (ACC) synthase 2 (ACS2) and 6 (ACS6).	ethylene	235-243	calcium-dependent protein kinase 2	Arabidopsis thaliana	88-93
24738778-6	2014	Two ABA-activated calcium-dependent protein kinases, CPK4 and CPK11, phosphorylate the C-terminus of ACS6 and increase the stability of ACS6 in ethylene biosynthesis.	ethylene	144-152	calcium-dependent protein kinase 2	Arabidopsis thaliana	62-67
24019427-7	2013	Nitric oxide and reduced nicotinamide adenine dinucleotide phosphate oxidase-dependent reactive oxygen species generation (due to the function of Respiratory Burst Oxidase Homolog proteins D and F) are also involved downstream from the Ca(2+) signal in the Pep immune defense signal transduction cascade, as is the case with BRASSINOSTEROID-INSENSITIVE1 Associated Kinase1 and CPK5, CPK6, and CPK11.	nicotinamide adenine	25-45	calcium-dependent protein kinase 2	Arabidopsis thaliana	393-398
24019427-7	2013	Nitric oxide and reduced nicotinamide adenine dinucleotide phosphate oxidase-dependent reactive oxygen species generation (due to the function of Respiratory Burst Oxidase Homolog proteins D and F) are also involved downstream from the Ca(2+) signal in the Pep immune defense signal transduction cascade, as is the case with BRASSINOSTEROID-INSENSITIVE1 Associated Kinase1 and CPK5, CPK6, and CPK11.	Reactive Oxygen Species	87-110	calcium-dependent protein kinase 2	Arabidopsis thaliana	393-398
24019427-7	2013	Nitric oxide and reduced nicotinamide adenine dinucleotide phosphate oxidase-dependent reactive oxygen species generation (due to the function of Respiratory Burst Oxidase Homolog proteins D and F) are also involved downstream from the Ca(2+) signal in the Pep immune defense signal transduction cascade, as is the case with BRASSINOSTEROID-INSENSITIVE1 Associated Kinase1 and CPK5, CPK6, and CPK11.	Brassinosteroids	325-340	calcium-dependent protein kinase 2	Arabidopsis thaliana	393-398
22821939-7	2012	AtCDPK2 overexpression in atsc rescued the salt-sensitive phenotype of atsc.	Salts	43-47	calcium-dependent protein kinase 2	Arabidopsis thaliana	0-7