PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26512898-0	2015	Inhibition on Proteasome beta1 Subunit Might Contribute to the Anti-Cancer Effects of Fangchinoline in Human Prostate Cancer Cells.	fangchinoline	86-99	proteasome 20S subunit beta 1	Homo sapiens	14-38	
26512898-2	2015	Fangchinoline and its structure analogue, tetrandrine, exhibited direct binding affinity with recombinant human proteasome beta1 subunit and also inhibited its activity in vitro.	fangchinoline	0-13	proteasome 20S subunit beta 1	Homo sapiens	112-136	
26512898-3	2015	In cultured prostate PC-3 cells and LnCap cells, fangchinoline could dose-dependently inhibit cell proliferation and caspase-like activity of cellular proteasome which was mediated by proteasome beta1 subunit.	fangchinoline	49-62	proteasome 20S subunit beta 1	Homo sapiens	184-208	
26512898-8	2015	Over-expression of proteasome beta1 subunit by plasmid transfection increased sensitivity of cells to the cytotoxicity of fangchinoline while knockdown of proteasome beta1 subunit ameliorated cytotoxicity of fangchinoline in PC-3 cells.	fangchinoline	122-135	proteasome 20S subunit beta 1	Homo sapiens	19-43	
26512898-8	2015	Over-expression of proteasome beta1 subunit by plasmid transfection increased sensitivity of cells to the cytotoxicity of fangchinoline while knockdown of proteasome beta1 subunit ameliorated cytotoxicity of fangchinoline in PC-3 cells.	fangchinoline	208-221	proteasome 20S subunit beta 1	Homo sapiens	19-43	
26512898-8	2015	Over-expression of proteasome beta1 subunit by plasmid transfection increased sensitivity of cells to the cytotoxicity of fangchinoline while knockdown of proteasome beta1 subunit ameliorated cytotoxicity of fangchinoline in PC-3 cells.	fangchinoline	208-221	proteasome 20S subunit beta 1	Homo sapiens	155-179