PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
33794068-4	2021	We showed that SMAC/Diablo directly interacts with mitochondrial phosphatidylserine decarboxylase (PSD) and inhibits its catalytic activity during synthesis of phosphatidylethanolamine (PE) from phosphatidylserine (PS).	phosphatidylethanolamine	160-184	F-box and leucine rich repeat protein 15	Homo sapiens	99-102	
33794068-4	2021	We showed that SMAC/Diablo directly interacts with mitochondrial phosphatidylserine decarboxylase (PSD) and inhibits its catalytic activity during synthesis of phosphatidylethanolamine (PE) from phosphatidylserine (PS).	phosphatidylethanolamine	186-188	F-box and leucine rich repeat protein 15	Homo sapiens	99-102	
33794068-7	2021	Moreover, in the absence of SMAC/Diablo, PSD inhibited cancer cell proliferation by catalysing the overproduction of mitochondrial PE and depleting the cellular levels of PC, PE and PS.	phosphatidylethanolamine	131-133	F-box and leucine rich repeat protein 15	Homo sapiens	41-44	
33794068-7	2021	Moreover, in the absence of SMAC/Diablo, PSD inhibited cancer cell proliferation by catalysing the overproduction of mitochondrial PE and depleting the cellular levels of PC, PE and PS.	phosphatidylethanolamine	175-177	F-box and leucine rich repeat protein 15	Homo sapiens	41-44	
33794068-13	2021	Altogether, we demonstrated that phospholipid metabolism and PE synthesis regulated by the SMAC-PSD interaction are essential for cancer cell proliferation and may be potentially targeted for treating cancer.	phosphatidylethanolamine	61-63	F-box and leucine rich repeat protein 15	Homo sapiens	96-99