PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
25003971-6	2014	PMA (10(-8) M), a PKC activator, increased Cu(I)-ATPase activity by 60%, whereas calphostin C and U73122 (PKC and PLC inhibitors, respectively) decreased the activity by 40%.	Tetradecanoylphorbol Acetate	0-3	dynein axonemal heavy chain 8	Homo sapiens	43-55	
8522995-6	1996	Activation of the ATPase was reversed by phorbol 12-myristate 13-acetate, an activator of protein kinase C, indicating that activation of Na+,K(+)-ATPase is due to decreased phosphorylation by protein kinase C. W-7 or cyclosporin, both inhibitors of calcineurin, prevented the activation of Na+,K(+)-ATPase by glutamate.	Tetradecanoylphorbol Acetate	41-72	dynein axonemal heavy chain 8	Homo sapiens	18-24	
12070036-6	2002	These granules are positive for the matrix enzyme gelatinase and the membrane subunit of the vacuolar H(+)/ATPase and can be recruited for exocytosis by treatment of neutrophils with phorbol myristate acetate.	Tetradecanoylphorbol Acetate	183-208	dynein axonemal heavy chain 8	Homo sapiens	36-113	
8873607-6	1996	TPA of skeletal SR at low and high Ca demonstrates that C12E8 induces aggregation of ATPase monomers and small oligomers.	Tetradecanoylphorbol Acetate	0-3	dynein axonemal heavy chain 8	Homo sapiens	85-91	
8873607-9	1996	Thus the TPA results provide a simple physical explanation for the functional effects: C12E8 inhibits the ATPase when it aggregates the enzyme (skeletal SR at high and low Ca; cardiac SR at high Ca), and the detergent activates when it dissociates ATPase oligomers (cardiac SR at low Ca).	Tetradecanoylphorbol Acetate	9-12	dynein axonemal heavy chain 8	Homo sapiens	106-112	
8873607-9	1996	Thus the TPA results provide a simple physical explanation for the functional effects: C12E8 inhibits the ATPase when it aggregates the enzyme (skeletal SR at high and low Ca; cardiac SR at high Ca), and the detergent activates when it dissociates ATPase oligomers (cardiac SR at low Ca).	Tetradecanoylphorbol Acetate	9-12	dynein axonemal heavy chain 8	Homo sapiens	248-254	
8522995-6	1996	Activation of the ATPase was reversed by phorbol 12-myristate 13-acetate, an activator of protein kinase C, indicating that activation of Na+,K(+)-ATPase is due to decreased phosphorylation by protein kinase C. W-7 or cyclosporin, both inhibitors of calcineurin, prevented the activation of Na+,K(+)-ATPase by glutamate.	Tetradecanoylphorbol Acetate	41-72	dynein axonemal heavy chain 8	Homo sapiens	147-153	
8522995-6	1996	Activation of the ATPase was reversed by phorbol 12-myristate 13-acetate, an activator of protein kinase C, indicating that activation of Na+,K(+)-ATPase is due to decreased phosphorylation by protein kinase C. W-7 or cyclosporin, both inhibitors of calcineurin, prevented the activation of Na+,K(+)-ATPase by glutamate.	Tetradecanoylphorbol Acetate	41-72	dynein axonemal heavy chain 8	Homo sapiens	147-153	
7912755-6	1994	On liquid culture with or without 5 x 10(-9) M 12-O-tetradecanoylphorbol-13-acetate (TPA) for 3 days, the blasts formed aggregates of proliferating and elongating cells on the wall of the flasks with a decline in CD34, numerous dendritic processes appeared on the cells and there was strong positivity for ATPase/ADPase, but no other changes in phenotype.	Tetradecanoylphorbol Acetate	47-83	dynein axonemal heavy chain 8	Homo sapiens	306-312	
7912755-6	1994	On liquid culture with or without 5 x 10(-9) M 12-O-tetradecanoylphorbol-13-acetate (TPA) for 3 days, the blasts formed aggregates of proliferating and elongating cells on the wall of the flasks with a decline in CD34, numerous dendritic processes appeared on the cells and there was strong positivity for ATPase/ADPase, but no other changes in phenotype.	Tetradecanoylphorbol Acetate	85-88	dynein axonemal heavy chain 8	Homo sapiens	306-312