PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
20655881-6	2010	A homology model for wild-type Bo AChE was built using the recently published crystal structure of human AChE and used to generate models of 2-PAM and HI-6 bound to the active-sites of GF- and VR-inhibited Bo AChEs before nucleophilic attack.	pralidoxime	141-146	acetylcholinesterase	Bos taurus	34-38	
20655881-7	2010	Results revealed that the peripheral anionic site (PAS) of AChE as a whole plays a critical role in the reactivation of nerve agent-inhibited AChE by all 4 bis-pyridinium oximes examined, but not by the mono-pyridinium oxime 2-PAM.	pralidoxime	225-230	acetylcholinesterase	Bos taurus	59-63	
20655881-7	2010	Results revealed that the peripheral anionic site (PAS) of AChE as a whole plays a critical role in the reactivation of nerve agent-inhibited AChE by all 4 bis-pyridinium oximes examined, but not by the mono-pyridinium oxime 2-PAM.	pralidoxime	225-230	acetylcholinesterase	Bos taurus	142-146	
17869525-3	2007	Except in the case of DFP-inhibited HF AChE test of 2-PAM, the activities of 6a are much higher than the activities of 2-PAM and HI-6 which are AChE reactivators currently in use.	pralidoxime	119-124	acetylcholinesterase	Bos taurus	144-148	
8161944-10	1994	The present results also offer an explanation for another recent report, in which anomalous results were presented for decarbamylation of physostigmine-inhibited and carbaryl-inhibited erythrocyte acetylcholinesterase in the presence of 2-PAM or HI-6.	pralidoxime	237-242	acetylcholinesterase	Bos taurus	197-217