PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
17849177-1	2008	PURPOSE: Eritoran (E5564) is a glycophospholipid that acts as a toll-like receptor 4 (TLR4) antagonist that is being tested as a treatment for severe sepsis and septic shock.	glycophospholipid	31-48	toll-like receptor 4	Oryctolagus cuniculus	64-84
17849177-1	2008	PURPOSE: Eritoran (E5564) is a glycophospholipid that acts as a toll-like receptor 4 (TLR4) antagonist that is being tested as a treatment for severe sepsis and septic shock.	glycophospholipid	31-48	toll-like receptor 4	Oryctolagus cuniculus	86-90
17090619-1	2007	Linker for activation of B cell (LAB)/non-T cell activation linker (NTAL) and phosphoprotein associated with glycophospholipid-enriched membrane microdomain (PAG)/Csk-binding protein (Cbp) are raft-associated transmembrane adaptor proteins with distinct functions in immediate/early phases of receptor signaling pathways.	glycophospholipid	109-126	linker for activation of T cells family member 2	Homo sapiens	68-72
16987101-7	2007	Notwithstanding, IPCs incorporated into glycosylphosphatidylinositol anchors of 4Delta.Lass5 show normal mobility on TLC and the ceramide- and raft-dependent traffic of Gas1p (glycophospholipid-anchored surface protein) from endoplasmic reticulum to Golgi remains almost normal.	glycophospholipid	176-193	ceramide synthase 5	Mus musculus	87-92
16987101-7	2007	Notwithstanding, IPCs incorporated into glycosylphosphatidylinositol anchors of 4Delta.Lass5 show normal mobility on TLC and the ceramide- and raft-dependent traffic of Gas1p (glycophospholipid-anchored surface protein) from endoplasmic reticulum to Golgi remains almost normal.	glycophospholipid	176-193	1,3-beta-glucanosyltransferase GAS1	Saccharomyces cerevisiae S288C	169-174
17090619-1	2007	Linker for activation of B cell (LAB)/non-T cell activation linker (NTAL) and phosphoprotein associated with glycophospholipid-enriched membrane microdomain (PAG)/Csk-binding protein (Cbp) are raft-associated transmembrane adaptor proteins with distinct functions in immediate/early phases of receptor signaling pathways.	glycophospholipid	109-126	phosphoprotein membrane anchor with glycosphingolipid microdomains 1	Homo sapiens	163-182
17090619-1	2007	Linker for activation of B cell (LAB)/non-T cell activation linker (NTAL) and phosphoprotein associated with glycophospholipid-enriched membrane microdomain (PAG)/Csk-binding protein (Cbp) are raft-associated transmembrane adaptor proteins with distinct functions in immediate/early phases of receptor signaling pathways.	glycophospholipid	109-126	phosphoprotein membrane anchor with glycosphingolipid microdomains 1	Homo sapiens	184-187
9242611-4	1997	The receptor designated decoy receptor 1 (DcR1) displayed properties of a glycophospholipid-anchored cell surface protein.	glycophospholipid	74-91	TNF receptor superfamily member 10c	Homo sapiens	24-40
11350953-5	2001	DcR1 is devoid of an intracellular domain and is anchored at the cell surface membrane by a glycophospholipid.	glycophospholipid	92-109	TNF receptor superfamily member 10c	Homo sapiens	0-4
9639537-0	1998	GPI anchor biosynthesis in yeast: phosphoethanolamine is attached to the alpha1,4-linked mannose of the complete precursor glycophospholipid.	glycophospholipid	123-140	glucose-6-phosphate isomerase	Homo sapiens	0-3
9242611-4	1997	The receptor designated decoy receptor 1 (DcR1) displayed properties of a glycophospholipid-anchored cell surface protein.	glycophospholipid	74-91	TNF receptor superfamily member 10c	Homo sapiens	42-46
8845756-1	1996	A soluble, monomeric form of acetylcholinesterase from mouse (mAChE), truncated at its carboxyl-terminal end, was generated from a cDNA encoding the glycophospholipid-linked form of the mouse enzyme by insertion of an early stop codon at position 549.	glycophospholipid	149-166	acetylcholinesterase	Mus musculus	29-49
9090058-5	1997	ORF O2145 shows 41.2% identity with the glycophospholipid-anchored surface glycoprotein Gas1p of S. cerevisiae and ORF O2197 has 53.2% identity to chromosome segregation protein Dis3p of Schizosaccharomyces pombe.	glycophospholipid	40-57	1,3-beta-glucanosyltransferase GAS1	Saccharomyces cerevisiae S288C	88-93
9090058-5	1997	ORF O2145 shows 41.2% identity with the glycophospholipid-anchored surface glycoprotein Gas1p of S. cerevisiae and ORF O2197 has 53.2% identity to chromosome segregation protein Dis3p of Schizosaccharomyces pombe.	glycophospholipid	40-57	exosome catalytic subunit DIS3	Saccharomyces cerevisiae S288C	178-183
8845756-1	1996	A soluble, monomeric form of acetylcholinesterase from mouse (mAChE), truncated at its carboxyl-terminal end, was generated from a cDNA encoding the glycophospholipid-linked form of the mouse enzyme by insertion of an early stop codon at position 549.	glycophospholipid	149-166	acetylcholinesterase	Mus musculus	62-67
7690370-4	1993	The phosphatidylinositol-specific enzyme, PIPLC, cleaved DAF from the surface of D54-MG cells, demonstrating that DAF is linked by a glycophospholipid anchor as has been shown for other cell types.	glycophospholipid	133-150	protein disulfide isomerase family A member 3	Homo sapiens	42-47
7690370-4	1993	The phosphatidylinositol-specific enzyme, PIPLC, cleaved DAF from the surface of D54-MG cells, demonstrating that DAF is linked by a glycophospholipid anchor as has been shown for other cell types.	glycophospholipid	133-150	CD55 molecule (Cromer blood group)	Homo sapiens	114-117
7688303-5	1993	No cross-reaction was detected with the following antigens: salt-soluble (SS) AChE from bovine brain, glycophospholipid-anchored AChE from human and bovine erythrocytes, DS-butyrylcholinesterase and SS-butyrylcholinesterase (BtChE) from the brains of human and bovine, DS-BtChE from chicken and BtChE from human serum.	glycophospholipid	102-119	acetylcholinesterase	Bos taurus	129-133
7686772-0	1993	Cholesterol regulates the cell surface expression of glycophospholipid-anchored CD14 antigen on human monocytes.	glycophospholipid	53-70	CD14 molecule	Homo sapiens	80-84
8449945-5	1993	However, splicing of exon 4 to exon 5, yielding a mRNA encoding the glycophospholipid-linked form of acetylcholinesterase, is seen primarily in erythroid and to a lesser extent in AtT-20 cells.	glycophospholipid	68-85	acetylcholinesterase (Cartwright blood group)	Homo sapiens	101-121
1346244-0	1992	A cDNA construct of tissue inhibitor of metalloproteinases (TIMP) linked to the last exon of Thy-1 confers glycophospholipid anchorage on this naturally secreted protein.	glycophospholipid	107-124	tissue inhibitor of metalloproteinase 1	Mus musculus	20-58
7687365-10	1993	Moreover, MOG appears to represent a novel member of this superfamily in that it possesses two potential transmembrane domains, in contrast to a single membrane-spanning domain or glycophospholipid anchor found in all other members of this superfamily.	glycophospholipid	180-197	myelin oligodendrocyte glycoprotein	Gallus gallus	10-13
1532143-0	1992	Endocytosis of glycophospholipid-anchored and transmembrane forms of CD4 by different endocytic pathways.	glycophospholipid	15-32	T-cell surface glycoprotein CD4	Cricetulus griseus	69-72
1346244-0	1992	A cDNA construct of tissue inhibitor of metalloproteinases (TIMP) linked to the last exon of Thy-1 confers glycophospholipid anchorage on this naturally secreted protein.	glycophospholipid	107-124	tissue inhibitor of metalloproteinase 1	Mus musculus	60-64
1346244-0	1992	A cDNA construct of tissue inhibitor of metalloproteinases (TIMP) linked to the last exon of Thy-1 confers glycophospholipid anchorage on this naturally secreted protein.	glycophospholipid	107-124	thymus cell antigen 1, theta	Mus musculus	93-98
1346244-6	1992	It is concluded that the last exon of Thy-1 has conferred the property of glycophospholipid anchorage on the normally secreted protein TIMP.	glycophospholipid	74-91	thymus cell antigen 1, theta	Mus musculus	38-43
1346244-6	1992	It is concluded that the last exon of Thy-1 has conferred the property of glycophospholipid anchorage on the normally secreted protein TIMP.	glycophospholipid	74-91	tissue inhibitor of metalloproteinase 1	Mus musculus	135-139
1824714-0	1991	Determinants for glycophospholipid anchoring of the Saccharomyces cerevisiae GAS1 protein to the plasma membrane.	glycophospholipid	17-34	1,3-beta-glucanosyltransferase GAS1	Saccharomyces cerevisiae S288C	77-81
1682315-0	1991	Characterization of glycophospholipid intermediate in the biosynthesis of glycophosphatidylinositol anchors accumulating in the Thy-1-negative lymphoma line SIA-b.	glycophospholipid	20-37	Thy-1 cell surface antigen	Homo sapiens	128-133
1674734-0	1991	Activation of T lymphocytes by cross-linking of glycophospholipid-anchored Thy-1 mobilizes separate pools of intracellular second messengers to those induced by the antigen-receptor/CD3 complex.	glycophospholipid	48-65	Thy-1 cell surface antigen	Homo sapiens	75-80
1961202-0	1991	Biosynthesis of glycophospholipid bound and secreted murine class I Qa-2 polypeptides.	glycophospholipid	16-33	Qa lymphocyte antigen 2 region	Mus musculus	68-72
1709701-0	1991	Human immunodeficiency virus infection and syncytium formation in HeLa cells expressing glycophospholipid-anchored CD4.	glycophospholipid	88-105	CD4 molecule	Homo sapiens	115-118
1709701-5	1991	This resulted in the anchoring of the extracellular domain of CD4 to the cell membrane via a glycophospholipid linkage.	glycophospholipid	93-110	CD4 molecule	Homo sapiens	62-65
1709701-6	1991	The glycophospholipid-anchored CD4 had a molecular size of approximately 56 to 62 kDa and was released following treatment of the cells with phosphatidylinositol-specific phospholipase C. HeLa cells expressing the CD4-DAF hybrid could be infected with HIV-1, as evidenced by reverse transcriptase activity, p24 core antigen content, and infectious virus production.	glycophospholipid	4-21	CD4 molecule	Homo sapiens	31-34
1709701-6	1991	The glycophospholipid-anchored CD4 had a molecular size of approximately 56 to 62 kDa and was released following treatment of the cells with phosphatidylinositol-specific phospholipase C. HeLa cells expressing the CD4-DAF hybrid could be infected with HIV-1, as evidenced by reverse transcriptase activity, p24 core antigen content, and infectious virus production.	glycophospholipid	4-21	CD4 molecule	Homo sapiens	214-217
1709701-6	1991	The glycophospholipid-anchored CD4 had a molecular size of approximately 56 to 62 kDa and was released following treatment of the cells with phosphatidylinositol-specific phospholipase C. HeLa cells expressing the CD4-DAF hybrid could be infected with HIV-1, as evidenced by reverse transcriptase activity, p24 core antigen content, and infectious virus production.	glycophospholipid	4-21	CD55 molecule (Cromer blood group)	Homo sapiens	218-221
1824714-7	1991	We conclude that glycophospholipid anchoring of Gas1p depends on the integrity of the C-terminal hydrophobic domain that is removed during anchor attachment.	glycophospholipid	17-34	1,3-beta-glucanosyltransferase GAS1	Saccharomyces cerevisiae S288C	48-53
1697596-0	1990	Complete and partial glycophospholipid anchors are found on a fusion protein consisting of luteinizing hormone beta subunit followed by a carboxyl-terminal domain of Thy-1.	glycophospholipid	21-38	lutropin subunit beta	Bos taurus	91-123
1983274-1	1990	Thy-1 is a major glycophospholipid (GPL)-anchored protein found on the surface of neurons, epithelial cells, fibroblasts and murine T-lymphomas.	glycophospholipid	17-34	thymus cell antigen 1, theta	Mus musculus	0-5
1697596-0	1990	Complete and partial glycophospholipid anchors are found on a fusion protein consisting of luteinizing hormone beta subunit followed by a carboxyl-terminal domain of Thy-1.	glycophospholipid	21-38	thymus cell antigen 1, theta	Mus musculus	166-171
1697596-1	1990	The Thy-1 antigen is anchored to the cell surface by a carboxyl-terminal glycophospholipid moiety.	glycophospholipid	73-90	thymus cell antigen 1, theta	Mus musculus	4-17
2129526-10	1990	Thus, it is concluded that the mature 5"-nucleotidase lacks the predicted COOH-terminal peptide extension (524-548), which has been replaced by the glycophospholipid functioning as the membrane anchor of 5"-nucleotidase.	glycophospholipid	148-165	5'-nucleotidase ecto	Homo sapiens	38-53
2129526-10	1990	Thus, it is concluded that the mature 5"-nucleotidase lacks the predicted COOH-terminal peptide extension (524-548), which has been replaced by the glycophospholipid functioning as the membrane anchor of 5"-nucleotidase.	glycophospholipid	148-165	5'-nucleotidase ecto	Homo sapiens	204-219
1688584-10	1990	The nature of the signal that directs posttranslational attachment of a glycophospholipid anchor to DAF is not known, but that signal is apparently spread over three exons and greater than 20 kb.	glycophospholipid	72-89	CD55 molecule (Cromer blood group)	Homo sapiens	100-103
33815382-4	2021	The TLR4/MD-2 complex can recognize the terminal motif of Gram-negative bacterial lipopolysaccharide (LPS)-a glycophospholipid lipid A.	glycophospholipid	109-126	toll like receptor 4	Homo sapiens	4-8
33815382-4	2021	The TLR4/MD-2 complex can recognize the terminal motif of Gram-negative bacterial lipopolysaccharide (LPS)-a glycophospholipid lipid A.	glycophospholipid	109-126	lymphocyte antigen 96	Homo sapiens	9-13
2904699-1	1988	Many plasma membrane proteins, including Thy-1, are anchored by a carboxyl terminal glycophospholipid.	glycophospholipid	84-101	Thy-1 cell surface antigen	Homo sapiens	41-46
2477368-1	1989	Decay accelerating factor (DAF) is a glycophospholipid-anchored membrane glycoprotein that protects mammalian host cells from inadvertant complement lysis.	glycophospholipid	37-54	CD55 molecule (Cromer blood group)	Homo sapiens	0-25
2477368-1	1989	Decay accelerating factor (DAF) is a glycophospholipid-anchored membrane glycoprotein that protects mammalian host cells from inadvertant complement lysis.	glycophospholipid	37-54	CD55 molecule (Cromer blood group)	Homo sapiens	27-30
2466338-1	1989	Decay accelerating factor (DAF) is anchored to the plasma membrane by a glycophospholipid (GPI) membrane anchor covalently attached to the COOH-terminus of the protein.	glycophospholipid	72-89	CD55 molecule (Cromer blood group)	Homo sapiens	0-25
2466338-1	1989	Decay accelerating factor (DAF) is anchored to the plasma membrane by a glycophospholipid (GPI) membrane anchor covalently attached to the COOH-terminus of the protein.	glycophospholipid	72-89	CD55 molecule (Cromer blood group)	Homo sapiens	27-30
2530453-0	1989	A glycophospholipid anchor is required for Qa-2-mediated T cell activation.	glycophospholipid	2-19	Qa lymphocyte antigen 2 region	Mus musculus	43-47
2831298-6	1988	We conclude that AChE from insect brain is attached to membranes via a glycophospholipid anchor.	glycophospholipid	71-88	Acetylcholine esterase	Drosophila melanogaster	17-21
2842340-8	1988	Taken together, these results suggest that CEA is anchored to the membrane by simultaneously occurring proteolysis of the carboxyl terminus and replacement by the glycophospholipid immediately after the synthesis.	glycophospholipid	163-180	CEA cell adhesion molecule 3	Homo sapiens	43-46
2451546-3	1988	DAF, AChE, and LAP are known to be anchored within cell membranes to glycophospholipid-containing phosphatidylinositol (PI).	glycophospholipid	69-86	CD55 molecule (Cromer blood group)	Homo sapiens	0-3
2451546-3	1988	DAF, AChE, and LAP are known to be anchored within cell membranes to glycophospholipid-containing phosphatidylinositol (PI).	glycophospholipid	69-86	acetylcholinesterase (Cartwright blood group)	Homo sapiens	5-9
3203325-3	1988	3H-Labeled precursors of glycophospholipid such as ethanolamine and stearic acid were incorporated into CEA produced by both normal and cancerous tissues, suggesting that CEA in normal mucosa is anchored to the cell membrane through a glycophospholipid as in cancerous tissues.	glycophospholipid	25-42	CEA cell adhesion molecule 3	Homo sapiens	104-107
3203325-3	1988	3H-Labeled precursors of glycophospholipid such as ethanolamine and stearic acid were incorporated into CEA produced by both normal and cancerous tissues, suggesting that CEA in normal mucosa is anchored to the cell membrane through a glycophospholipid as in cancerous tissues.	glycophospholipid	25-42	CEA cell adhesion molecule 3	Homo sapiens	171-174
3203325-3	1988	3H-Labeled precursors of glycophospholipid such as ethanolamine and stearic acid were incorporated into CEA produced by both normal and cancerous tissues, suggesting that CEA in normal mucosa is anchored to the cell membrane through a glycophospholipid as in cancerous tissues.	glycophospholipid	235-252	CEA cell adhesion molecule 3	Homo sapiens	104-107
3203325-3	1988	3H-Labeled precursors of glycophospholipid such as ethanolamine and stearic acid were incorporated into CEA produced by both normal and cancerous tissues, suggesting that CEA in normal mucosa is anchored to the cell membrane through a glycophospholipid as in cancerous tissues.	glycophospholipid	235-252	CEA cell adhesion molecule 3	Homo sapiens	171-174
2874887-1	1986	To investigate the mechanism of glycophospholipid anchoring of the surface antigen Thy-1, we have undertaken a comparative biosynthetic study using a wild-type Thy-1+ murine T lymphoma (BW5147) and a mutant T lymphoma (class E) that synthesizes Thy-1 but fails to express it on the plasma membrane.	glycophospholipid	32-49	thymus cell antigen 1, theta	Mus musculus	83-88
3277539-0	1988	The insulinomimetic effects of the polar head group of an insulin-sensitive glycophospholipid on pyruvate dehydrogenase in both subcellular and whole cell assays.	glycophospholipid	76-93	insulin	Homo sapiens	4-11
3277539-0	1988	The insulinomimetic effects of the polar head group of an insulin-sensitive glycophospholipid on pyruvate dehydrogenase in both subcellular and whole cell assays.	glycophospholipid	76-93	pyruvate dehydrogenase phosphatase catalytic subunit 1	Homo sapiens	97-119
3277539-1	1988	The polar head group that was released by treating an insulin-sensitive glycophospholipid with a phosphatidylinositol-specific phospholipase C (PI-PLC) stimulated pyruvate dehydrogenase (PDH) in both subcellular and whole cell assays.	glycophospholipid	72-89	insulin	Homo sapiens	54-61
3277539-1	1988	The polar head group that was released by treating an insulin-sensitive glycophospholipid with a phosphatidylinositol-specific phospholipase C (PI-PLC) stimulated pyruvate dehydrogenase (PDH) in both subcellular and whole cell assays.	glycophospholipid	72-89	pyruvate dehydrogenase phosphatase catalytic subunit 1	Homo sapiens	163-185
3277539-1	1988	The polar head group that was released by treating an insulin-sensitive glycophospholipid with a phosphatidylinositol-specific phospholipase C (PI-PLC) stimulated pyruvate dehydrogenase (PDH) in both subcellular and whole cell assays.	glycophospholipid	72-89	pyruvate dehydrogenase phosphatase catalytic subunit 1	Homo sapiens	187-190
3277539-10	1988	These data support the proposal that an early step in insulin action is the release of insulinomimetic polar head group from the insulin-sensitive glycophospholipid.	glycophospholipid	147-164	insulin	Homo sapiens	54-61
3277539-10	1988	These data support the proposal that an early step in insulin action is the release of insulinomimetic polar head group from the insulin-sensitive glycophospholipid.	glycophospholipid	147-164	insulin	Homo sapiens	87-94
2891709-1	1988	Defective glycophospholipid anchoring, rapid degradation, and secretion of Thy-1 glycoprotein.	glycophospholipid	10-27	Thy-1 cell surface antigen	Homo sapiens	75-80
2891709-2	1988	Thy-1 glycoprotein is a member of a class of proteins which are anchored to the plasma membrane via a covalently bound glycophospholipid.	glycophospholipid	119-136	Thy-1 cell surface antigen	Homo sapiens	0-5
2891709-19	1988	These observations are discussed with reference to the possibility that the lesions which characterize the mutants pertain to the biosynthesis of the glycophospholipid moiety of Thy-1.	glycophospholipid	150-167	Thy-1 cell surface antigen	Homo sapiens	178-183
2446389-1	1987	Decay accelerating factor (DAF) belongs to a novel group of membrane proteins anchored to the cell surface by a glycophospholipid membrane anchor that is covalently attached to the carboxyl terminus of the protein.	glycophospholipid	112-129	CD55 molecule (Cromer blood group)	Homo sapiens	0-25
2446389-1	1987	Decay accelerating factor (DAF) belongs to a novel group of membrane proteins anchored to the cell surface by a glycophospholipid membrane anchor that is covalently attached to the carboxyl terminus of the protein.	glycophospholipid	112-129	CD55 molecule (Cromer blood group)	Homo sapiens	27-30
2446389-2	1987	The last 37 amino acids of membrane DAF, when fused to the carboxyl terminus of a secreted protein, are sufficient to target the fusion protein to the plasma membrane by means of a glycophospholipid anchor.	glycophospholipid	181-198	CD55 molecule (Cromer blood group)	Homo sapiens	36-39
2881925-0	1987	The glycophospholipid anchor of Thy-1.	glycophospholipid	4-21	Thy-1 cell surface antigen	Homo sapiens	32-37
2881925-2	1987	The Thy-1 antigen of the surface of lymphocytes and neurons is anchored to the plasma membrane via a glycophospholipid moiety.	glycophospholipid	101-118	Thy-1 cell surface antigen	Homo sapiens	4-17
2888493-5	1987	In addition, the Thy-1 glycoprotein has the particularity of being anchored to the membrane via a glycophospholipid tail.	glycophospholipid	98-115	thymus cell antigen 1, theta	Mus musculus	17-22
2422055-4	1986	From these results we conclude that the glycophospholipid anchors of protozoan VSG and of AChE of the two vertebrates share common structural features, suggesting that this novel type of membrane anchor has been conserved during evolution.	glycophospholipid	40-57	acetylcholinesterase (Cartwright blood group)	Homo sapiens	90-94
2869796-0	1985	A glycophospholipid covalently attached to the C-terminus of the Thy-1 glycoprotein.	glycophospholipid	2-19	Thy-1 cell surface antigen	Rattus norvegicus	65-83
2865810-0	1985	A glycophospholipid tail at the carboxyl terminus of the Thy-1 glycoprotein of neurons and thymocytes.	glycophospholipid	2-19	Thy-1 cell surface antigen	Homo sapiens	57-62
26329338-6	2015	RESULTS: The metabolic pathways for carnitine, tryptophan, phenylalanine, arachidonic acid, and glycophospholipid were significantly upregulated in OA SF.	glycophospholipid	96-113	OAP	Homo sapiens	148-153
21512604-3	2011	Synthetic PIM/LM/LAM substructures are useful biochemical tools to delineate and dissect the fine details of mannose glycophospholipid biosynthesis and their interactions with host cells.	glycophospholipid	117-134	Pim-1 proto-oncogene, serine/threonine kinase	Homo sapiens	10-13
23952219-2	2013	A pro-inflammatory signaling cascade is initiated upon binding of membrane-associated portion of LPS, a glycophospholipid Lipid A, by a coreceptor protein MD-2, which results in a protective host innate immune response.	glycophospholipid	104-121	toll-like receptor 4	Mus musculus	97-100
23952219-2	2013	A pro-inflammatory signaling cascade is initiated upon binding of membrane-associated portion of LPS, a glycophospholipid Lipid A, by a coreceptor protein MD-2, which results in a protective host innate immune response.	glycophospholipid	104-121	lymphocyte antigen 96	Mus musculus	155-159