PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
31974202-6	2021	Neuraminidase treatment induces unfolding of the O-glycosylated mechanosensory domain in GPIbalpha as monitored by single-molecule force spectroscopy, increases the exposure of the ADAM17 shedding cleavage site in the mechanosensory domain on the platelet surface, and induces ligand-independent GPIb-IX signaling in human and murine platelets.	insulin, glycosylated	49-63	neuraminidase 1	Homo sapiens	0-13
31974202-6	2021	Neuraminidase treatment induces unfolding of the O-glycosylated mechanosensory domain in GPIbalpha as monitored by single-molecule force spectroscopy, increases the exposure of the ADAM17 shedding cleavage site in the mechanosensory domain on the platelet surface, and induces ligand-independent GPIb-IX signaling in human and murine platelets.	insulin, glycosylated	49-63	glycoprotein Ib platelet subunit alpha	Homo sapiens	89-98
31974202-6	2021	Neuraminidase treatment induces unfolding of the O-glycosylated mechanosensory domain in GPIbalpha as monitored by single-molecule force spectroscopy, increases the exposure of the ADAM17 shedding cleavage site in the mechanosensory domain on the platelet surface, and induces ligand-independent GPIb-IX signaling in human and murine platelets.	insulin, glycosylated	49-63	ADAM metallopeptidase domain 17	Homo sapiens	181-187
31616924-5	2020	APOE is O-glycosylated at several sites: Thr8, Thr18, Thr194, Ser197, Thr289, Ser290, and Ser296.	insulin, glycosylated	8-22	apolipoprotein E	Homo sapiens	0-4
32064614-8	2020	We reveal that an O-glycosylated AGP21 peptide, which is positively regulated by BZR1, a transcription factor activated by BR signaling, affects RH cell fate by altering GL2 expression in a BIN2-dependent manner.	insulin, glycosylated	18-32	arabinogalactan protein 21	Arabidopsis thaliana	33-38
32064614-8	2020	We reveal that an O-glycosylated AGP21 peptide, which is positively regulated by BZR1, a transcription factor activated by BR signaling, affects RH cell fate by altering GL2 expression in a BIN2-dependent manner.	insulin, glycosylated	18-32	Brassinosteroid signaling positive regulator (BZR1) family protein	Arabidopsis thaliana	81-85
32064614-8	2020	We reveal that an O-glycosylated AGP21 peptide, which is positively regulated by BZR1, a transcription factor activated by BR signaling, affects RH cell fate by altering GL2 expression in a BIN2-dependent manner.	insulin, glycosylated	18-32	HD-ZIP IV family of homeobox-leucine zipper protein with lipid-binding START domain-containing protein	Arabidopsis thaliana	170-173
32064614-8	2020	We reveal that an O-glycosylated AGP21 peptide, which is positively regulated by BZR1, a transcription factor activated by BR signaling, affects RH cell fate by altering GL2 expression in a BIN2-dependent manner.	insulin, glycosylated	18-32	Protein kinase superfamily protein	Arabidopsis thaliana	190-194
31894262-4	2020	GALNT6 O-glycosylated LGALS3BP in breast cancer cells, whereas knockdown of GALNT6 by siRNA led to the inhibition of both the O-glycosylation and secretion of LGALS3BP, resulting in the suppression of breast cancer cell growth.	insulin, glycosylated	7-21	polypeptide N-acetylgalactosaminyltransferase 6	Homo sapiens	0-6
31894262-4	2020	GALNT6 O-glycosylated LGALS3BP in breast cancer cells, whereas knockdown of GALNT6 by siRNA led to the inhibition of both the O-glycosylation and secretion of LGALS3BP, resulting in the suppression of breast cancer cell growth.	insulin, glycosylated	7-21	galectin 3 binding protein	Homo sapiens	22-30
31894262-5	2020	Notably, LGALS3BP is potentially O-glycosylated at three sites (T556, T571 and S582) by GALNT6, thereby promoting autocrine cell growth, whereas the expression of LGALS3BP with three Ala substitutions (T556A, T571A and S582A) in cells drastically reduced GALNT6-dependent LGALS3BP O-glycosylation and secretion, resulting in suppression of autocrine growth-promoting effect.	insulin, glycosylated	33-47	galectin 3 binding protein	Homo sapiens	9-17
31894262-5	2020	Notably, LGALS3BP is potentially O-glycosylated at three sites (T556, T571 and S582) by GALNT6, thereby promoting autocrine cell growth, whereas the expression of LGALS3BP with three Ala substitutions (T556A, T571A and S582A) in cells drastically reduced GALNT6-dependent LGALS3BP O-glycosylation and secretion, resulting in suppression of autocrine growth-promoting effect.	insulin, glycosylated	33-47	polypeptide N-acetylgalactosaminyltransferase 6	Homo sapiens	88-94
31894262-5	2020	Notably, LGALS3BP is potentially O-glycosylated at three sites (T556, T571 and S582) by GALNT6, thereby promoting autocrine cell growth, whereas the expression of LGALS3BP with three Ala substitutions (T556A, T571A and S582A) in cells drastically reduced GALNT6-dependent LGALS3BP O-glycosylation and secretion, resulting in suppression of autocrine growth-promoting effect.	insulin, glycosylated	33-47	polypeptide N-acetylgalactosaminyltransferase 6	Homo sapiens	255-261
31615765-8	2019	Biochemical analysis for various post-translational modifications demonstrated that secreted invadolysin is both N- and O-glycosylated, but not apparently GPI-linked.	insulin, glycosylated	120-134	leishmanolysin like peptidase	Homo sapiens	93-104
31696111-1	2019	Mucins and mucin-like molecules are highly O-glycosylated proteins present on the cell surface of mammals and other organisms.	insulin, glycosylated	43-57	LOC100508689	Homo sapiens	11-16
31930159-4	2019	In our investigation of the intracellular trafficking of N-glycosylated serine proteases, we used an inhibitor of alpha-glucosidases I and II to block the trimming of triglucosylated oligosaccharides, thereby inhibiting calnexin-assisted glycoprotein folding.	insulin, glycosylated	57-78	calnexin	Homo sapiens	220-228
31930159-5	2019	The study helped us to discover a key role of calnexin in the folding, ER exiting, and extracellular expression of N-glycosylated serine proteases such as corin, enteropeptidase, and prothrombin.	insulin, glycosylated	115-136	calnexin	Homo sapiens	46-54
31930159-5	2019	The study helped us to discover a key role of calnexin in the folding, ER exiting, and extracellular expression of N-glycosylated serine proteases such as corin, enteropeptidase, and prothrombin.	insulin, glycosylated	115-136	corin, serine peptidase	Homo sapiens	155-160
31930159-5	2019	The study helped us to discover a key role of calnexin in the folding, ER exiting, and extracellular expression of N-glycosylated serine proteases such as corin, enteropeptidase, and prothrombin.	insulin, glycosylated	115-136	transmembrane serine protease 15	Homo sapiens	162-177