PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
11356825-3	2001	The wild type showed spontaneous formation of higher molecular mass species in the absence of reducing agent, and its ATPase was activated by dithiothreitol.	Dithiothreitol	142-156	dynein axonemal heavy chain 8	Homo sapiens	118-124	
9741592-11	1998	However, when Cu2+ was used instead of Fe2+ in the Fenton reaction, ATPase inhibition could be prevented by DTT.	Dithiothreitol	108-111	dynein axonemal heavy chain 8	Homo sapiens	68-74	
8080446-14	1994	However, superoxide dismutase (500 U/mL) and dithiothreitol blocked artemisinin-hemin or hemin-mediated ATPase inhibition significantly (P < 0.001).	Dithiothreitol	45-59	dynein axonemal heavy chain 8	Homo sapiens	104-110	
2140277-1	1990	ATPase activity of the coupling factor 1, CF1, isolated from spinach chloroplasts, was enhanced by reduction with dithiothreitol.	Dithiothreitol	114-128	dynein axonemal heavy chain 8	Homo sapiens	0-6	
2140277-2	1990	Reduced thioredoxins from spinach chloroplasts, Escherichia coli and human lymphocytes replaced dithiothreitol as reductant and activator of the ATPase.	Dithiothreitol	96-110	dynein axonemal heavy chain 8	Homo sapiens	145-151	
2867898-4	1986	ATPase activity measured under dark, partially uncoupling conditions, following light activation with dithiothreitol and pyocyanine, was markedly enhanced by the presence of Mg2+ in the activation stage.	Dithiothreitol	102-116	dynein axonemal heavy chain 8	Homo sapiens	0-6	
6248505-1	1980	A high concentration (0.5 M) of a reducing agent such as dithiothreitol or 2-mercaptoethanol inactivated both crude (microsomal) and purified preparations of Na+,K+-ATPase only in the presence of detergent.	Dithiothreitol	57-71	dynein axonemal heavy chain 8	Homo sapiens	165-171	
17121824-7	2007	Treatment of H(2)O(2)-inactivated phosphorylated HMM or S1 with dithiothreitol partially reactivated the ATPase but had no effect on total ATP binding.	Dithiothreitol	64-78	dynein axonemal heavy chain 8	Homo sapiens	105-111	
10806188-10	2000	More than 60% of the drug-stimulated ATPase activity, however, was recovered after treatment with dithiothreitol.	Dithiothreitol	98-112	dynein axonemal heavy chain 8	Homo sapiens	37-43	
8241252-10	1993	Dithiothreitol was completely effective in preventing the tBHP-induced formation of TBARS as well as inhibition of the Ca-pump ATPase.	Dithiothreitol	0-14	dynein axonemal heavy chain 8	Homo sapiens	127-133	
8241252-13	1993	In the presence of mercaptosuccinate, a potent inhibitor of glutathione peroxidase, the ability of dithiothreitol to protect the Ca-pump ATPase from tBHP-induced inhibition was abolished.	Dithiothreitol	99-113	dynein axonemal heavy chain 8	Homo sapiens	137-143	
8241252-15	1993	These results may be interpreted to suggest that inhibition of the Ca-pump ATPase in intact RBCs occurs as a result of tBHP-induced oxidant stress and subsequent lipid peroxidation which can be prevented by certain antioxidants including butylated hydroxytoluene, stobadine, and thiol-containing compounds such as dithiothreitol.	Dithiothreitol	314-328	dynein axonemal heavy chain 8	Homo sapiens	75-81	
2159344-2	1990	Dithiothreitol reversed the inhibition of Cl(-)-stimulated ATPase induced by p-chloromercuribenzenesulfonate.	Dithiothreitol	0-14	dynein axonemal heavy chain 8	Homo sapiens	59-65	
6461650-6	1982	Trypsin treatment of dithiothreitol-activated CF1 resulted in a very rapid increase in Ca2+-ATPase activity and a corresponding rapid cleavage of the gamma subunit to a 25,000-dalton species.	Dithiothreitol	21-35	dynein axonemal heavy chain 8	Homo sapiens	92-98