PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
11128586-3	2000	The results revealed that the binding region in HSA is longer than five subsites usually considered in the literature and suggested the presence of at least six subsites; four glycone binding sites (-4, -3, -2, -1) and two aglycone binding sites (+1, +2).	glycone	176-183	albumin	Homo sapiens	48-51
12782315-4	2003	The binding region of HSA is composed of four glycone and three aglycone-binding sites, while that of Tyr151Met is composed of four glycone and two aglycone-binding sites.	glycone	46-53	albumin	Homo sapiens	22-25
12782315-4	2003	The binding region of HSA is composed of four glycone and three aglycone-binding sites, while that of Tyr151Met is composed of four glycone and two aglycone-binding sites.	glycone	65-72	albumin	Homo sapiens	22-25
24900249-0	2011	Study of kaempferol glycoside as an insulin mimic reveals glycon to be the key active structure.	glycone	58-64	insulin	Homo sapiens	36-43
20114052-6	2010	The alpha-syn mutant E46K has a stronger affinity for GM3 than the wild-type protein, and the interaction is inhibited by 3"-sialyllactose (the glycone part of GM3).	glycone	144-151	synuclein alpha	Homo sapiens	4-13
9513044-6	1998	Overall, the consistent association of glycosylated and unglycosylated calreticulin with P-SG50 and unglycosylated HSPs suggests that P-SG/calreticulin is an active member of the cast of glycone/aglycone chaperones that cooperate to achieve cellular recovery from acute heat stress.	glycone	187-194	calreticulin	Cricetulus griseus	71-83
9513044-6	1998	Overall, the consistent association of glycosylated and unglycosylated calreticulin with P-SG50 and unglycosylated HSPs suggests that P-SG/calreticulin is an active member of the cast of glycone/aglycone chaperones that cooperate to achieve cellular recovery from acute heat stress.	glycone	187-194	calreticulin	Cricetulus griseus	134-151
34946583-1	2021	sp2-Iminosugar glycolipids (sp2-IGLs) represent a consolidated family of glycoconjugate mimetics encompassing a monosaccharide-like glycone moiety with a pseudoamide-type nitrogen replacing the endocyclic oxygen atom of carbohydrates and an axially-oriented lipid chain anchored at the pseudoanomeric position.	glycone	132-139	Sp2 transcription factor	Homo sapiens	0-3
7510794-0	1993	Inhibition of beta-N-acetylglucosaminidase by glycon-related analogues of the substrate.	glycone	46-52	O-GlcNAcase	Homo sapiens	14-42
34946583-1	2021	sp2-Iminosugar glycolipids (sp2-IGLs) represent a consolidated family of glycoconjugate mimetics encompassing a monosaccharide-like glycone moiety with a pseudoamide-type nitrogen replacing the endocyclic oxygen atom of carbohydrates and an axially-oriented lipid chain anchored at the pseudoanomeric position.	glycone	132-139	Sp2 transcription factor	Homo sapiens	28-31
31017416-3	2019	We found that PCs combining a LAMAN glycone-binding motif based on the 5 N,6 O-oxomethylidenemannojirimycin (OMJ) glycomimetic core and different aglycones, in either mono- or multivalent displays, elicit binding modes involving glycone and nonglycone enzyme regions that reinforce the protein folding and stabilization potential.	glycone	36-43	mannosidase alpha class 2B member 1	Homo sapiens	30-35
3234317-0	1988	Human acid beta-glucosidase: inhibition studies using glucose analogues and pH variation to characterize the normal and Gaucher disease glycon binding sites.	glycone	136-142	glucosylceramidase beta	Homo sapiens	6-27
3234317-1	1988	Comparative kinetic studies with glycon inhibitors were used to investigate the properties of the active site of human acid beta-glucosidase (EC 3.2.1.45) from normal placenta and spleens of type 1 Ashkenazi Jewish Gaucher disease (AJGD) patients.	glycone	33-39	glucosylceramidase beta	Homo sapiens	119-140
3234317-10	1988	The findings were consistent with a specific alteration in or near the glycon binding site which results in the functional abnormalities of the mutant AJGD acid beta-glucosidase.	glycone	71-77	glucosylceramidase beta	Homo sapiens	156-177
31398901-5	2019	Both the glycone moiety and the aglycone tail can be modified by using sp2-iminosugar precursors with different configurational profiles (d-gluco or d-galacto in this work) and varied thiols, as well as by oxidation of the sulfide adducts (to the corresponding sulfones in this work).	glycone	9-16	Sp2 transcription factor	Homo sapiens	71-74