PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
34855283-7	2021	More interestingly, almost all LacdiNAc-containing N-glycopeptides were enhanced in ICC tumor but not in HCC tumor, and this phenomenon was further confirmed by lectin histochemistry and the high expression of beta1-4 GalNAc transferases in ICC at both mRNA and protein expression levels.	n-glycopeptides	51-66	immunoglobulin kappa variable 6D-41 (non-functional)	Homo sapiens	210-217
17918875-2	2007	The use of alpha(2-3,6,8,9) neuraminidase is central to isolate sialylated N-glycopeptides out of a complex peptide mixture.	n-glycopeptides	75-90	neuraminidase 1	Homo sapiens	28-41
17154134-3	2006	It was demonstrated that the ZIC-HILIC separation column has a selectivity for sialylated N-glycopeptides and a high capability for separation based on the structural recognition of sialylated N-glycan isomers as well as for the previously reported neutral N-glycans and N-glycopeptides.	n-glycopeptides	90-105	Zic family member 1	Homo sapiens	29-32
17154134-3	2006	It was demonstrated that the ZIC-HILIC separation column has a selectivity for sialylated N-glycopeptides and a high capability for separation based on the structural recognition of sialylated N-glycan isomers as well as for the previously reported neutral N-glycans and N-glycopeptides.	n-glycopeptides	271-286	Zic family member 1	Homo sapiens	29-32
34296732-7	2021	The inherent properties endowed the nanocomposite with excellent enrichment performance for N-glycopeptides: excellent selectivity (1 : 2000, IgG/BSA, m/m), an ultralow detection limit (0.05 fmol muL-1), and a good size-exclusion effect (1 : 500, IgG digests/BSA, m/m).	n-glycopeptides	92-107	mitochondrial E3 ubiquitin protein ligase 1	Homo sapiens	196-201
34779613-6	2021	Finally, our results illustrated the aberrant sialylation of haptoglobin (Hp) in hepatocellular carcinoma (HCC), where the ratios of alpha2,3 to alpha2,6 sialylation of seven N-glycopeptides were found to be significantly altered (p < 0.01) in HCC individuals (n = 27) compared with healthy controls (n = 27).	n-glycopeptides	175-190	haptoglobin	Homo sapiens	61-72
34779613-6	2021	Finally, our results illustrated the aberrant sialylation of haptoglobin (Hp) in hepatocellular carcinoma (HCC), where the ratios of alpha2,3 to alpha2,6 sialylation of seven N-glycopeptides were found to be significantly altered (p < 0.01) in HCC individuals (n = 27) compared with healthy controls (n = 27).	n-glycopeptides	175-190	glycoprotein hormone subunit alpha 2	Homo sapiens	133-151
34436504-0	2021	PRM-MS Quantitative Analysis of Isomeric N-Glycopeptides Derived from Human Serum Haptoglobin of Patients with Cirrhosis and Hepatocellular Carcinoma.	n-glycopeptides	41-56	haptoglobin	Homo sapiens	82-93
34436504-6	2021	Strategic combinations of the significant N-glycopeptides, either with alpha-fetoprotein (AFP) or themselves, better estimate the areas under the curve (AUC) of their respective receiver operating characteristic (ROC) curves with respect to AFP.	n-glycopeptides	42-57	alpha fetoprotein	Homo sapiens	90-93
34436504-6	2021	Strategic combinations of the significant N-glycopeptides, either with alpha-fetoprotein (AFP) or themselves, better estimate the areas under the curve (AUC) of their respective receiver operating characteristic (ROC) curves with respect to AFP.	n-glycopeptides	42-57	alpha fetoprotein	Homo sapiens	241-244
34436504-7	2021	The combination of AFP with the isomeric sialylated fucosylated N-glycopeptides Asn207 + 5-6-1-2 and Asn207 + 5-6-1-3, resulted with an AUC value of 0.98, while the AUC value for AFP alone was 0.85.	n-glycopeptides	64-79	alpha fetoprotein	Homo sapiens	19-22
34436504-7	2021	The combination of AFP with the isomeric sialylated fucosylated N-glycopeptides Asn207 + 5-6-1-2 and Asn207 + 5-6-1-3, resulted with an AUC value of 0.98, while the AUC value for AFP alone was 0.85.	n-glycopeptides	64-79	alpha fetoprotein	Homo sapiens	179-182
34126284-7	2021	In contrast, the human alpha-l-fucosidase (FucA1) showed low activity on truncated Fucalpha1,6GlcNAc substrates but was able to remove core fucose from intact and full-length core-fucosylated N-glycopeptides and N-glycoproteins.	n-glycopeptides	192-207	alpha-L-fucosidase 1	Homo sapiens	43-48
34236361-2	2021	We describe here a facile chemoenzymatic synthesis of core-fucosylated N-glycopeptides derived from the SARS-CoV-2 Spike protein and their binding with glycan-dependent neutralizing antibody S309 and human lectin CLEC4G.	n-glycopeptides	71-86	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	115-120
34236361-2	2021	We describe here a facile chemoenzymatic synthesis of core-fucosylated N-glycopeptides derived from the SARS-CoV-2 Spike protein and their binding with glycan-dependent neutralizing antibody S309 and human lectin CLEC4G.	n-glycopeptides	71-86	C-type lectin domain family 4 member G	Homo sapiens	213-219
35573732-7	2022	Moreover, the alterations of LAMP2 site-specific intact N-glycopeptides were comprehensively assessed.	n-glycopeptides	56-71	lysosomal associated membrane protein 2	Homo sapiens	29-34
35510762-6	2022	The experimental results demonstrated that 217 N-glycosylation sites were identified in 283 N-glycopeptides, corresponding to 95 glycoproteins identified from 10 muL human serum by the nano-LC-MS/MS analysis, revealing the great potential of the novel ZIF-8/SAP hydrogel for glycopeptide enrichment and glycoproteomic research.	n-glycopeptides	92-107	SH2 domain containing 1A	Homo sapiens	258-261
34105527-3	2021	Under the synergistic effect of hydrogen bonding and electrostatic adsorption, Fe3O4@PANI can rapidly and easily enrich N-glycopeptides derived from standard protein (bovine fetuin and transferrin) tryptic digests and serum haptoglobin tryptic digests.	n-glycopeptides	120-135	serotransferrin	Bos taurus	185-196
34178943-7	2021	We have newly identified systemic site-specific N-glycosylation alterations underlying T2D patients in the complement activation pathways, including decreased levels of N-glycopeptides from C1s, MASP1, and CFP proteins, and increased levels of N-glycopeptides from C2, C4, C4BPA, C4BPB, and CFH.	n-glycopeptides	169-184	complement C1s	Homo sapiens	190-193
35559953-7	2022	We identified 79 N-glycopeptides from 15 different proteins and found that proteins including immunoglobulin A1, polymeric immunoglobulin receptor, and lactotransferrin displayed significant glycan heterogeneity.	n-glycopeptides	17-32	megakaryocyte and platelet inhibitory receptor G6b	Homo sapiens	123-146
35559953-7	2022	We identified 79 N-glycopeptides from 15 different proteins and found that proteins including immunoglobulin A1, polymeric immunoglobulin receptor, and lactotransferrin displayed significant glycan heterogeneity.	n-glycopeptides	17-32	lactotransferrin	Homo sapiens	152-168
35604151-0	2022	A Spin-Tip Enrichment Strategy for Simultaneous Analysis of N-Glycopeptides and Phosphopeptides from Human Pancreatic Tissues.	n-glycopeptides	60-75	spindlin 1	Homo sapiens	2-6
35602943-3	2022	Further study showed that indole-3-acetic acid (IAA) levels were undetectable in mns1 mns2 mns3 at normal condition and recovered at alkaline condition, which corroborate our N-glycopeptide profiling, from which N-glycopeptides related with IAA biosynthesis, amino acid conjugates hydrolysis, and response showed differential abundance between normal and alkaline conditions in mns1 mns2 mns3.	n-glycopeptides	212-227	alpha-mannosidase 1	Arabidopsis thaliana	81-90
33889548-6	2021	Then, the alteration of site-specific intact N-glycopeptides of PON1 was comprehensively assessed by using Immunoprecipitation (IP) and mass spectrometry based 16O/18O C-terminal labeling quantification method to distinguish AFP-negative HCC from LC patients in a validation set (n = 64).	n-glycopeptides	45-60	paraoxonase 1	Homo sapiens	64-68
33406838-7	2021	Our recently developed liquid chromatography-mass spectrometry methodology allowed us to identify LacdiNAc structural motifs on all occupied N-glycopeptides and polyLacNAc structures on six glycopeptides of the spike protein.	n-glycopeptides	141-156	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	211-216
30370771-0	2019	Differential Quantitative Determination of Site-Specific Intact N-Glycopeptides in Serum Haptoglobin between Hepatocellular Carcinoma and Cirrhosis Using LC-EThcD-MS/MS.	n-glycopeptides	64-79	haptoglobin	Homo sapiens	89-100
32892942-8	2020	Moreover, in the LC-MS/MS analysis of real biological sample, a total of 344 unique N-glycosites in 598 unique N-glycopeptides from 172 N-glycoproteins were identified from 2 muL human serum after deglycosylated by PNGase F, and 825 intact N-glycopeptides with different types of glycoform were detected when directly analyzed the N-glycopeptides enriched by PAM-OH HMS.	n-glycopeptides	111-126	N-glycanase 1	Homo sapiens	215-221
32892942-8	2020	Moreover, in the LC-MS/MS analysis of real biological sample, a total of 344 unique N-glycosites in 598 unique N-glycopeptides from 172 N-glycoproteins were identified from 2 muL human serum after deglycosylated by PNGase F, and 825 intact N-glycopeptides with different types of glycoform were detected when directly analyzed the N-glycopeptides enriched by PAM-OH HMS.	n-glycopeptides	111-126	peptidylglycine alpha-amidating monooxygenase	Homo sapiens	359-362
31517451-3	2019	The protocols include sample preparation of a 1:1 mixture of light (-CH3 )2 and heavy (-13 CD2 H)2 dimethylated intact N-glycopeptides from LO2 and HepG2 cells, RPLC-pentaHILIC 2DLC separation of the mixture, intact N-glycopeptide database search and identification using GPSeeker, and quantitation of differentially expressed intact N-glycopeptides using the quantitation module GPSeekerQuan.	n-glycopeptides	119-134	CD2 molecule	Homo sapiens	91-94
31393126-6	2019	A total of 50 N-glycopeptides and 30 N-glycans have been site-specific glycosylation profiled in major royal jelly protein 1 (MRJP1) and MRJP2 of RJ for the first time.	n-glycopeptides	14-29	major royal jelly protein 1	Apis mellifera	126-131
31393126-6	2019	A total of 50 N-glycopeptides and 30 N-glycans have been site-specific glycosylation profiled in major royal jelly protein 1 (MRJP1) and MRJP2 of RJ for the first time.	n-glycopeptides	14-29	major royal jelly protein 2	Apis mellifera	137-142
31079452-4	2019	Using the AXL receptor tyrosine kinase (AXL) as a model glycoprotein with multiple N-glycosylation sites, we show that those LCMS features that could be grouped into graph networks on the basis of glycan mass and retention time differences were actually N-glycopeptides with the same peptide backbone but different N-glycan compositions.	n-glycopeptides	254-269	AXL receptor tyrosine kinase	Homo sapiens	10-13
31079452-4	2019	Using the AXL receptor tyrosine kinase (AXL) as a model glycoprotein with multiple N-glycosylation sites, we show that those LCMS features that could be grouped into graph networks on the basis of glycan mass and retention time differences were actually N-glycopeptides with the same peptide backbone but different N-glycan compositions.	n-glycopeptides	254-269	AXL receptor tyrosine kinase	Homo sapiens	40-43
31079452-8	2019	GlycopeptideGraphMS detected more than 500 unique N-glycopeptides from AXL, triple the number found by a database search with Byonic software, and detected incorrect assignments due to a nonspecific protease cleavage.	n-glycopeptides	50-65	AXL receptor tyrosine kinase	Homo sapiens	71-74
32412768-3	2020	Herein, we have performed a comprehensive screening of site-specific N-glycopeptides in serum haptoglobin (Hp), a reporter molecule for aberrant glycosylation in HCC, to characterize glycopeptide markers for NASH-related HCCs.	n-glycopeptides	69-84	haptoglobin	Homo sapiens	94-105
32412768-6	2020	Receiver operating characteristic (ROC) curve analysis demonstrated that the N-glycopeptides at sites N184 and N241 bearing a monofucosylated tri-antennary glycan A3G3F1S3, had the best diagnostic performance in detection of early NASH HCC, area under the curve (AUC) = 0.733 and 0.775, respectively, whereas alpha-fetoprotein (AFP) had an AUC of 0.692.	n-glycopeptides	77-92	alpha fetoprotein	Homo sapiens	309-326
32412768-6	2020	Receiver operating characteristic (ROC) curve analysis demonstrated that the N-glycopeptides at sites N184 and N241 bearing a monofucosylated tri-antennary glycan A3G3F1S3, had the best diagnostic performance in detection of early NASH HCC, area under the curve (AUC) = 0.733 and 0.775, respectively, whereas alpha-fetoprotein (AFP) had an AUC of 0.692.	n-glycopeptides	77-92	alpha fetoprotein	Homo sapiens	328-331
32306330-4	2020	Recently, the recombinant Fbs1 derivative protein has been developed as a tool for comprehensive enrichment of N-glycopeptides.	n-glycopeptides	111-126	F-box protein 2	Homo sapiens	26-30
31377859-6	2019	When using MagG@PEI@HA, 376 N-glycopeptides derived from 102 glycoproteins were identified, both from a 2 muL serum sample.	n-glycopeptides	28-43	tripartite motif containing 37	Homo sapiens	106-109
30798070-4	2019	Using the high-temperature RPLC method, alpha2-6-linked sialylated N-glycopeptides were eluted first, followed by alpha2-3-linked isomers.	n-glycopeptides	67-82	immunoglobulin binding protein 1	Homo sapiens	40-48
30370771-2	2019	Herein, we developed a workflow that involved advanced methodologies, the EThcD-MS/MS fragmentation method and data interpretation software, for differential analysis of the microheterogeneity of site-specific intact N-glycopeptides of serum haptoglobin between early hepatocellular carcinoma (HCC) and liver cirrhosis.	n-glycopeptides	217-232	haptoglobin	Homo sapiens	242-253
28534482-0	2017	An engineered high affinity Fbs1 carbohydrate binding protein for selective capture of N-glycans and N-glycopeptides.	n-glycopeptides	101-116	fibrosin	Homo sapiens	28-32
29557479-7	2018	We found that boronic acid chemistry in this study preferred to capture glycopeptides with high mannose glycans, ZIC-HILIC enriched most N-glycopeptides and did not show significant preference during enrichment and PGC was not suitable for separating glycopeptides with a long amino acid sequence.	n-glycopeptides	137-152	zinc finger protein of the cerebellum 1	Mus musculus	113-116
29237727-6	2018	To demonstrate the precision of the approach, we also profiled N-glycopeptides from the mutant (xylt) of beta-1,2-xylosyltransferase, an enzyme in the N-glycan biosynthetic pathway.	n-glycopeptides	63-78	beta-1,2-xylosyltransferase	Arabidopsis thaliana	105-132
29806066-2	2018	In this work, we used separation involving hydrophilic interaction liquid chromatography using a superficially porous particle HALO  penta-HILIC column with tandem mass spectrometric detection for the analysis of N-glycopeptides of hemopexin.	n-glycopeptides	213-228	hemopexin	Homo sapiens	232-241
29644550-0	2018	Distinctive and Complementary MS2 Fragmentation Characteristics for Identification of Sulfated Sialylated N-Glycopeptides by nanoLC-MS/MS Workflow.	n-glycopeptides	106-121	MS2	Homo sapiens	30-33
29687791-0	2018	Site-specific characterization and quantitation of N-glycopeptides in PKM2 knockout breast cancer cells using DiLeu isobaric tags enabled by electron-transfer/higher-energy collision dissociation (EThcD).	n-glycopeptides	51-66	pyruvate kinase M1/2	Homo sapiens	70-74
29502397-8	2018	A total of 67 N-glycopeptides were identified from the PSA pooled from the patients.	n-glycopeptides	14-29	kallikrein related peptidase 3	Homo sapiens	55-58
27760464-6	2016	165 site-specific N-glycopeptides representative of all N-glycosylation sites were identified from AGP 1 and AGP 2 isoforms.	n-glycopeptides	18-33	orosomucoid 1	Homo sapiens	99-104
27760464-6	2016	165 site-specific N-glycopeptides representative of all N-glycosylation sites were identified from AGP 1 and AGP 2 isoforms.	n-glycopeptides	18-33	orosomucoid 2	Homo sapiens	109-114
25374123-3	2014	Here, we systematically analyzed the site-specific N-glycopeptides of vitronectin in human plasma by tandem mass spectrometry combined with immunoprecipitation and hydrophilic interaction liquid chromatography (HILIC) enrichment.	n-glycopeptides	51-66	vitronectin	Homo sapiens	70-81
27565792-5	2016	Additionally, 37 fucosylated N-glycopeptides were newly identified from nine liver-secreted proteins, including alpha-1-antichymotrypsin, alpha-1-antitrypsin, alpha-2-HS-glycoprotein, ceruloplasmin, alpha-1-acid glycoprotein 1/2, alpha-2-macroglobulin, serotransferrin, and beta-2-glycoprotein 1.	n-glycopeptides	29-44	serpin family A member 3	Homo sapiens	112-136
27565792-5	2016	Additionally, 37 fucosylated N-glycopeptides were newly identified from nine liver-secreted proteins, including alpha-1-antichymotrypsin, alpha-1-antitrypsin, alpha-2-HS-glycoprotein, ceruloplasmin, alpha-1-acid glycoprotein 1/2, alpha-2-macroglobulin, serotransferrin, and beta-2-glycoprotein 1.	n-glycopeptides	29-44	serpin family A member 1	Homo sapiens	138-157
27565792-5	2016	Additionally, 37 fucosylated N-glycopeptides were newly identified from nine liver-secreted proteins, including alpha-1-antichymotrypsin, alpha-1-antitrypsin, alpha-2-HS-glycoprotein, ceruloplasmin, alpha-1-acid glycoprotein 1/2, alpha-2-macroglobulin, serotransferrin, and beta-2-glycoprotein 1.	n-glycopeptides	29-44	ceruloplasmin	Homo sapiens	184-197
27565792-5	2016	Additionally, 37 fucosylated N-glycopeptides were newly identified from nine liver-secreted proteins, including alpha-1-antichymotrypsin, alpha-1-antitrypsin, alpha-2-HS-glycoprotein, ceruloplasmin, alpha-1-acid glycoprotein 1/2, alpha-2-macroglobulin, serotransferrin, and beta-2-glycoprotein 1.	n-glycopeptides	29-44	orosomucoid 1	Homo sapiens	199-228
27565792-5	2016	Additionally, 37 fucosylated N-glycopeptides were newly identified from nine liver-secreted proteins, including alpha-1-antichymotrypsin, alpha-1-antitrypsin, alpha-2-HS-glycoprotein, ceruloplasmin, alpha-1-acid glycoprotein 1/2, alpha-2-macroglobulin, serotransferrin, and beta-2-glycoprotein 1.	n-glycopeptides	29-44	alpha-2-macroglobulin	Homo sapiens	230-251
27565792-5	2016	Additionally, 37 fucosylated N-glycopeptides were newly identified from nine liver-secreted proteins, including alpha-1-antichymotrypsin, alpha-1-antitrypsin, alpha-2-HS-glycoprotein, ceruloplasmin, alpha-1-acid glycoprotein 1/2, alpha-2-macroglobulin, serotransferrin, and beta-2-glycoprotein 1.	n-glycopeptides	29-44	transferrin	Homo sapiens	253-268
27565792-5	2016	Additionally, 37 fucosylated N-glycopeptides were newly identified from nine liver-secreted proteins, including alpha-1-antichymotrypsin, alpha-1-antitrypsin, alpha-2-HS-glycoprotein, ceruloplasmin, alpha-1-acid glycoprotein 1/2, alpha-2-macroglobulin, serotransferrin, and beta-2-glycoprotein 1.	n-glycopeptides	29-44	apolipoprotein H	Homo sapiens	274-295
27591658-1	2016	In this work, we describe a multivariate data analysis approach for data exploration and classification of the complex and large data sets generated to study the alteration of human transferrin (Tf) N-glycopeptides in patients with congenital disorders of glycosylation (CDG).	n-glycopeptides	199-214	transferrin	Homo sapiens	182-193
27591658-1	2016	In this work, we describe a multivariate data analysis approach for data exploration and classification of the complex and large data sets generated to study the alteration of human transferrin (Tf) N-glycopeptides in patients with congenital disorders of glycosylation (CDG).	n-glycopeptides	199-214	transferrin	Homo sapiens	195-197
27519006-3	2016	Detailed site-specific reference glycoprofiles of purified basigin were manually established using ion-trap CID-MS/MS and high-resolution Q-Exactive Orbitrap HCD-MS/MS of tryptic N-glycopeptides and released N-glycans.	n-glycopeptides	179-194	basigin (Ok blood group)	Homo sapiens	59-66
27139140-0	2016	pGlyco: a pipeline for the identification of intact N-glycopeptides by using HCD- and CID-MS/MS and MS3.	n-glycopeptides	52-67	MS3	Homo sapiens	100-103
26700048-4	2016	As a result of their higher hydrophilicity N-glycopeptides comprising short peptide backbones are preferably accumulated by the ZIC-HILIC-based separation procedure.	n-glycopeptides	43-58	Zic family member 1	Homo sapiens	128-131
25374123-4	2014	Vitronectin was purified with immunoprecipitation by monoclonal antibody from plasma and digested to tryptic N-glycopeptides.Then, enrichment with HILIC materials was used and followed by analysis with nano-LC/MS/MS.	n-glycopeptides	109-124	vitronectin	Homo sapiens	0-11
25374123-8	2014	As a result, a total of 17 site-specific N-glycopeptides were completely identified in all of the three N-glycosylation sites of vitronectin in human plasma, including 12 N-glycopeptides first reported.	n-glycopeptides	41-56	vitronectin	Homo sapiens	129-140
25374123-8	2014	As a result, a total of 17 site-specific N-glycopeptides were completely identified in all of the three N-glycosylation sites of vitronectin in human plasma, including 12 N-glycopeptides first reported.	n-glycopeptides	171-186	vitronectin	Homo sapiens	129-140
24668066-1	2014	Conventional N-glycoproteome analysis usually applies C18 reversed-phase (RP) adsorbent for sample purification, which will lead to unavoidable sample loss due to the high hydrophilicity of N-glycopeptides.	n-glycopeptides	190-205	Bardet-Biedl syndrome 9	Homo sapiens	54-57
24668066-3	2014	It was observed that the small hydrophilic N-glycopeptides that cannot retain onto C18 adsorbent can be captured by the graphitized carbon, while the large hydrophobic N-glycopeptides that cannot retain onto the graphitized carbon can be feasibly captured by the C18 adsorbent.	n-glycopeptides	43-58	Bardet-Biedl syndrome 9	Homo sapiens	83-86
24668066-4	2014	Comparing with sample purification by using C18 adsorbent only, 28.5 % more N-glycopeptides were identified by combining both C18 and PGC adsorbents.	n-glycopeptides	76-91	Bardet-Biedl syndrome 9	Homo sapiens	44-47
24668066-4	2014	Comparing with sample purification by using C18 adsorbent only, 28.5 % more N-glycopeptides were identified by combining both C18 and PGC adsorbents.	n-glycopeptides	76-91	Bardet-Biedl syndrome 9	Homo sapiens	126-129
22223312-3	2012	The experimental data showed that the microcolumn could efficiently and reproducibly isolate N-glycopeptides from enzymatic mixtures of ovalbumin, fetuin, haptoglobin and human plasma.	n-glycopeptides	93-108	haptoglobin	Homo sapiens	155-166
23028207-2	2012	Herein, the detailed N-glycosylation pattern of human serum alpha-2-macroglobulin was studied using an integrative approach, including permethylation of N-glycans, collision induced dissociation (CID) and electron transfer dissociation (ETD) of chymotryptic N-glycopeptides, and partial deglycosylation of chymotryptic N-glycopeptides with endo-beta-N-acetylglucosaminidase F3 (Endo F3).	n-glycopeptides	258-273	alpha-2-macroglobulin	Homo sapiens	60-81
23028207-2	2012	Herein, the detailed N-glycosylation pattern of human serum alpha-2-macroglobulin was studied using an integrative approach, including permethylation of N-glycans, collision induced dissociation (CID) and electron transfer dissociation (ETD) of chymotryptic N-glycopeptides, and partial deglycosylation of chymotryptic N-glycopeptides with endo-beta-N-acetylglucosaminidase F3 (Endo F3).	n-glycopeptides	319-334	alpha-2-macroglobulin	Homo sapiens	60-81