PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
18984910-2	2009	In this study, we employed a LC-MS/MS assay to demonstrate that residues 38-51 of apoC-I are significantly protected from proteolysis in the presence of 1,2-dimyristoyl-3-sn-glycero-phosphocholine (DMPC).	Dimyristoylphosphatidylcholine	198-202	apolipoprotein C1	Homo sapiens	82-88	
18984910-5	2009	In contrast to wild-type apoC-I (WT), which binds DMPC vesicles with an apparent Kd [Kd(app)] of 0.89 microM, apoC-I(F42A) and apoC-I(F46A) possess 2-fold weaker affinities for DMPC with Kd(app) of 1.52 microM and 1.58 microM, respectively.	Dimyristoylphosphatidylcholine	50-54	apolipoprotein C1	Homo sapiens	25-31	
18984910-5	2009	In contrast to wild-type apoC-I (WT), which binds DMPC vesicles with an apparent Kd [Kd(app)] of 0.89 microM, apoC-I(F42A) and apoC-I(F46A) possess 2-fold weaker affinities for DMPC with Kd(app) of 1.52 microM and 1.58 microM, respectively.	Dimyristoylphosphatidylcholine	177-181	apolipoprotein C1	Homo sapiens	25-31	
18984910-6	2009	However, apoC-I(F46G), apoC-I(F42A/F46A), apoC-I(F42G), and apoC-I(F42G/F46G) bind significantly weaker to DMPC with Kd(app) of 2.24 microM, 3.07 microM, 4.24 microM, and 10.1 microM, respectively.	Dimyristoylphosphatidylcholine	107-111	apolipoprotein C1	Homo sapiens	9-15	
18984910-6	2009	However, apoC-I(F46G), apoC-I(F42A/F46A), apoC-I(F42G), and apoC-I(F42G/F46G) bind significantly weaker to DMPC with Kd(app) of 2.24 microM, 3.07 microM, 4.24 microM, and 10.1 microM, respectively.	Dimyristoylphosphatidylcholine	107-111	apolipoprotein C1	Homo sapiens	23-29	
18984910-6	2009	However, apoC-I(F46G), apoC-I(F42A/F46A), apoC-I(F42G), and apoC-I(F42G/F46G) bind significantly weaker to DMPC with Kd(app) of 2.24 microM, 3.07 microM, 4.24 microM, and 10.1 microM, respectively.	Dimyristoylphosphatidylcholine	107-111	apolipoprotein C1	Homo sapiens	23-29	
18984910-6	2009	However, apoC-I(F46G), apoC-I(F42A/F46A), apoC-I(F42G), and apoC-I(F42G/F46G) bind significantly weaker to DMPC with Kd(app) of 2.24 microM, 3.07 microM, 4.24 microM, and 10.1 microM, respectively.	Dimyristoylphosphatidylcholine	107-111	apolipoprotein C1	Homo sapiens	23-29	
18984910-7	2009	Sedimentation velocity studies subsequently show that the protein/DMPC complexes formed by these apoC-I mutants sediment at 6.5S, 6.7S, 6.5S, and 8.0S, respectively.	Dimyristoylphosphatidylcholine	66-70	apolipoprotein C1	Homo sapiens	97-103