PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9643019-5	1998	METHODS: (1) Lipid peroxides were formed by incubation of linoleic acid with lipoxygenase from soybean, separated by thin layer chromatography and incubated with tetramethylbenzidine.	Lipid Peroxides	13-28	linoleate 9S-lipoxygenase-4	Glycine max	77-89	
3122826-5	1987	Lipoxygenase catalyzes the oxidation of NDGA by LOOH at a rate that is consistent with the independently determined rate constant for the reduction of Eox by NDGA.	Lipid Peroxides	48-52	linoleate 9S-lipoxygenase-4	Glycine max	0-12	
3122826-7	1987	Because the catalytically inactive Ered is oxidized by fatty acid hydroperoxides (e.g., LOOH) to give the active Eox, reducing agents such as NDGA are most effective as lipoxygenase inhibitors at low hydroperoxide concentrations.	Lipid Peroxides	55-80	linoleate 9S-lipoxygenase-4	Glycine max	169-181	
3122826-7	1987	Because the catalytically inactive Ered is oxidized by fatty acid hydroperoxides (e.g., LOOH) to give the active Eox, reducing agents such as NDGA are most effective as lipoxygenase inhibitors at low hydroperoxide concentrations.	Lipid Peroxides	88-92	linoleate 9S-lipoxygenase-4	Glycine max	169-181	
3122826-8	1987	Our results suggest that in vivo, where lipid hydroperoxides are maintained at low steady-state levels, reduction of lipoxygenase from the ferric to ferrous state may be important in the regulation of lipoxygenase activity and hence leukotriene biosynthesis.	Lipid Peroxides	40-60	linoleate 9S-lipoxygenase-4	Glycine max	117-129	
9643019-11	1998	(2) In the isolated retinae of pigs lipid peroxides became visible as electron-dense structures in the rod outer segments (ROS) after treatment with lipoxygenase and were lacking in the other parts of the retina.	Lipid Peroxides	36-51	linoleate 9S-lipoxygenase-4	Glycine max	149-161	
9643019-12	1998	Without treatment with lipoxygenase lipid peroxides were only infrequently seen in ROS.	Lipid Peroxides	36-51	linoleate 9S-lipoxygenase-4	Glycine max	23-35	
3138991-5	1988	The data clearly indicate, for the first time, that H2O2 can efficiently replace fatty acid hydroperoxide in a xenobiotic oxidation reaction medicated by the hydroperoxidase activity of lipoxygenase.	Lipid Peroxides	81-105	linoleate 9S-lipoxygenase-4	Glycine max	186-198	
3101541-0	1986	Determination of stereochemistry in the fatty acid hydroperoxide products of lipoxygenase catalysis.	Lipid Peroxides	40-64	linoleate 9S-lipoxygenase-4	Glycine max	77-89	
9643019-6	1998	(2) Lipid peroxides were formed by incubation of porcine retinae with soybean lipoxygenase in an oxygensaturated atmosphere.	Lipid Peroxides	4-19	linoleate 9S-lipoxygenase-4	Glycine max	78-90	
7918597-11	1994	These results strongly suggest that lipoxygenase not only generates lipid hydroperoxides but can also generate superoxide via oxidation of pyridine nucleotides and may, therefore, significantly contribute to oxidative stress in cells.	Lipid Peroxides	68-88	linoleate 9S-lipoxygenase-4	Glycine max	36-48	
8679548-0	1996	Role of lipid hydroperoxides in the activation of 15-lipoxygenase.	Lipid Peroxides	8-28	linoleate 9S-lipoxygenase-4	Glycine max	53-65	
8769897-2	1996	Linoleic acid (LA) and its hydroperoxide 13-L-hydroperoxylinoleic acid (LOOH) prepared with soybean lipoxygenase inhibited the response of GABARs in the presence of GABA at high concentrations.	Lipid Peroxides	72-76	linoleate 9S-lipoxygenase-4	Glycine max	100-112	
1903070-7	1991	The results obtained in this paper for the cooxidation process of hemin and hemoglobin by lipoxygenase can be rationalized in terms of hemin binding at or near to the catalytic center, resulting in a lesser binding of linoleic acid and an enhanced release of radicals, and pigment bleaching by radicals and lipid hydroperoxides.	Lipid Peroxides	307-327	linoleate 9S-lipoxygenase-4	Glycine max	90-102	
1510955-0	1992	Effect of lipid hydroperoxide on lipoxygenase kinetics.	Lipid Peroxides	10-29	linoleate 9S-lipoxygenase-4	Glycine max	33-45