PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
31491074-10	2019	The in silico molecular docking and dynamics simulation studies of lead compounds affirmed their consensual binding interactions with PAS-AChE and aspartate dyad of BACE-1.	Protactinium	134-137	acetylcholinesterase	Rattus norvegicus	138-142	
28797883-4	2017	Molecular modeling and kinetic studies revealed that compound 7f was a mixed-type inhibitor, which bond simultaneously to CAS and PAS of AChE, and it was also a competitive inhibitor, which occupied the active site of MAO-B.	Protactinium	130-133	acetylcholinesterase	Rattus norvegicus	137-141	
26058015-8	2015	Behavioral tests revealed that MCPs facilitated long-term learning and memory of the pups with PA through reducing oxidative damage and acetylcholinesterase (AChE) activity in the brain, and increasing hippocampus phosphorylated cAMP-response element binding protein (p-CREB) and brain derived neurotrophic factor (BDNF) expression.	Protactinium	95-97	acetylcholinesterase	Rattus norvegicus	136-156	
26058015-8	2015	Behavioral tests revealed that MCPs facilitated long-term learning and memory of the pups with PA through reducing oxidative damage and acetylcholinesterase (AChE) activity in the brain, and increasing hippocampus phosphorylated cAMP-response element binding protein (p-CREB) and brain derived neurotrophic factor (BDNF) expression.	Protactinium	95-97	acetylcholinesterase	Rattus norvegicus	158-162	
24941128-6	2014	The docking study of compound 4r with AChE enzyme showed that both CAS and PAS are occupied by the ligand.	Protactinium	75-78	acetylcholinesterase	Rattus norvegicus	38-42