PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
9529088-7	1998	Hapten inhibition assays with monosaccharides and defined oligosaccharides showed that the inhibitory effects of MBP were abrogated by mannose or high-mannose type oligomannose-oligosaccharide.	high-mannose	146-158	myelin basic protein	Homo sapiens	113-116
18793148-9	2008	Genome analyses in Arabidopsis and rice revealed the presence of F-box proteins with a C-terminal lectin-related domain homologous with Nictaba, a jasmonate-inducible lectin from tobacco that was shown to interact with the core structure of high-mannose and complex N-glycans.	high-mannose	241-253	F-box protein PP2-B11-like	Nicotiana tabacum	98-104
18793148-9	2008	Genome analyses in Arabidopsis and rice revealed the presence of F-box proteins with a C-terminal lectin-related domain homologous with Nictaba, a jasmonate-inducible lectin from tobacco that was shown to interact with the core structure of high-mannose and complex N-glycans.	high-mannose	241-253	F-box protein PP2-B11-like	Nicotiana tabacum	167-173
15723043-5	2005	Both Fbs1 and Fbs2 proteins interacted with denatured glycoproteins, which were modified with not only high-mannose but also complex-type oligosaccharides, more efficiently than native proteins.	high-mannose	103-115	fibrosin	Homo sapiens	5-9
15723043-5	2005	Both Fbs1 and Fbs2 proteins interacted with denatured glycoproteins, which were modified with not only high-mannose but also complex-type oligosaccharides, more efficiently than native proteins.	high-mannose	103-115	F-box protein 6	Homo sapiens	14-18
12609975-2	2003	We found that the HCV envelope glycoprotein E2 binds the dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin (DC-SIGN) and the related liver endothelial cell lectin L-SIGN through high-mannose N-glycans.	high-mannose	207-219	CD209 molecule	Homo sapiens	137-144
12609975-2	2003	We found that the HCV envelope glycoprotein E2 binds the dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin (DC-SIGN) and the related liver endothelial cell lectin L-SIGN through high-mannose N-glycans.	high-mannose	207-219	C-type lectin domain family 4 member M	Homo sapiens	192-198
11076950-2	2001	To determine whether the carbohydrate recognition activity of IL-2 contributes to its physiological activity, the inhibitory effects of high-mannose type glycans on IL-2-dependent CTLL-2 cell proliferation were investigated.	high-mannose	136-148	interleukin 2	Mus musculus	165-169
11076950-5	2001	Among the components of this complex, only the IL-2 receptor alpha subunit was stained with Galanthus nivalis agglutinin which specifically recognizes high-mannose type glycans.	high-mannose	151-163	interleukin 2 receptor subunit alpha	Homo sapiens	47-66
20842142-2	2010	This effect is brought about by its specific binding to Man-alpha(1-2)-Man unit(s) of high-mannose type glycan (HMTG) bound to HIV gp120.	high-mannose	86-98	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	131-136
20559567-2	2010	The actinomycete-derived lectin actinohivin (AH) is highly specific to a cluster of high-mannose-type glycans uniquely found on the viral envelope (Env).	high-mannose	84-96	endogenous retrovirus group K member 20	Homo sapiens	148-151
20816211-4	2010	Frontal affinity chromatography (FAC) and cell-surface expressed lectin assay revealed that both OS-9 and XTP3-B recognize high-mannose type N-glycans that lack the terminal mannose on the C branch.	high-mannose	123-135	OS9 endoplasmic reticulum lectin	Homo sapiens	97-101
20816211-4	2010	Frontal affinity chromatography (FAC) and cell-surface expressed lectin assay revealed that both OS-9 and XTP3-B recognize high-mannose type N-glycans that lack the terminal mannose on the C branch.	high-mannose	123-135	endoplasmic reticulum lectin 1	Homo sapiens	106-112
19214580-4	2009	The lectins ConA, LCA, and DSA, which recognize high-mannose or complex types of N-linked glycans stain both apical and basolateral membranes of photoreceptor cells, whereas SBA, DBA, and ABA lectins, which bind to mucin-type O-glycans, label the inter-rhabdomeral space.	high-mannose	48-60	corona	Drosophila melanogaster	12-16
17084390-0	2006	Localization and in vitro binding studies suggest that the cytoplasmic/nuclear tobacco lectin can interact in situ with high-mannose and complex N-glycans.	high-mannose	120-132	F-box protein PP2-B11-like	Nicotiana tabacum	87-93
16713984-7	2006	Finally, by using biotinylated high-mannose N-glycans, we could visualize DC-SIGN-expressing cells in lymph node tissue.	high-mannose	31-43	CD209 molecule	Homo sapiens	74-81
7849022-6	1995	Here, we have identified protein--carbohydrate and carbohydrate--carbohydrate interactions and, in combination with previous knowledge from electrospray ionization mass spectrometry, have determined the composition of the heterogeneous high-mannose glycan in hu-sCD2(105).	high-mannose	236-248	stearoyl-CoA desaturase 5	Homo sapiens	262-266
1824724-1	1991	UDP-GlcNAc:alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I (GnT I; EC 2.4.1.101) catalyzes an essential first step in the conversion of high-mannose N-glycans to hybrid and complex N-glycans.	high-mannose	151-163	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Oryctolagus cuniculus	0-73
1824724-1	1991	UDP-GlcNAc:alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I (GnT I; EC 2.4.1.101) catalyzes an essential first step in the conversion of high-mannose N-glycans to hybrid and complex N-glycans.	high-mannose	151-163	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Oryctolagus cuniculus	75-80
2809279-1	1989	Plasma from normal outbred Swiss mice not previously given interferon (IFN) neutralized a glycosylated (high-mannose) recombinant murine IFN-beta made in yeast (rMuIFN-beta y).	high-mannose	104-116	interferon beta 1, fibroblast	Mus musculus	137-145
4043085-0	1985	High-mannose structure of apolipoprotein-B from low-density lipoproteins of human plasma.	high-mannose	0-12	apolipoprotein B	Homo sapiens	26-42
6774767-3	1980	The oligosaccharides on fibronectin were analyzed by gel electrophoresis for alterations in sensitivity to the enzyme endo-beta-N-acetylgluosaminidase H, which specifically cleaves the "high-mannose" class of asparagine-linked oligosaccharide.	high-mannose	186-198	fibronectin 1	Homo sapiens	24-35
31494931-2	2020	N-acetylglucosaminyltransferase I (MGAT1) plays an essential role in the conversion of processed high-mannose cores into complex or hybrid N-linked oligosaccharide structures.	high-mannose	97-109	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Homo sapiens	35-40
3875789-3	1985	When the status of the oligosaccharides present on these glycoproteins was examined, conversion of high-mannose [endo-beta-N-acetylglucosaminidase-(Endo H) sensitive] to complex-type (Endo H resistant) oligosaccharides diminished with decreasing temp.	high-mannose	99-111	O-GlcNAcase	Homo sapiens	118-146
6459926-1	1981	Distribution of high-mannose and complex oligosaccharides in cathepsin D and beta-hexosaminidase.	high-mannose	16-28	cathepsin D	Homo sapiens	61-72
6459926-1	1981	Distribution of high-mannose and complex oligosaccharides in cathepsin D and beta-hexosaminidase.	high-mannose	16-28	O-GlcNAcase	Homo sapiens	77-96
29401627-6	2018	We characterized the N-glycosylation profile of mouse colonic mucin (Muc)-2 by MS and showed that the interaction with mDectin-2 was mediated by high-mannose N-glycans.	high-mannose	145-157	LOC100508689	Homo sapiens	62-67
29401627-6	2018	We characterized the N-glycosylation profile of mouse colonic mucin (Muc)-2 by MS and showed that the interaction with mDectin-2 was mediated by high-mannose N-glycans.	high-mannose	145-157	C-type lectin domain family 4, member n	Mus musculus	119-128