GlyConnect

taxonomy (10) protein (27) source (16) structure (260) composition (115) disease (2) reference (36) site (34) peptide (0)

Taxonomy

Protein

Source

Reported structure

Composition

Disease

Reference

Site-specific glycan microheterogeneity of inter-alpha-trypsin inhibitor heavy chain H4 (2014 - Chandler KB, Brnakova Z, Sanda M, Wang S, Stalnaker SH, Bridger R, Zhao P, Wells L, Edwards NJ, Goldman R.) / Status : Reviewed
Site-specific characterization of cell membrane N-glycosylation with integrated hydrophilic interaction chromatography solid phase extraction and LC-MS/MS (2014 - Chen R, Seebun D, Ye M, Zou H, Figeys D) / Status : Reviewed
Structural characterization of recombinant soluble rat neuroligin 1: mapping of secondary structure and glycosylation by mass spectrometry. (2004 - Hoffman RC, Jennings LL, Tsigelny I, Comoletti D, Flynn RE, Sudhof TC, Taylor P) / Status : Reviewed
Characterization of the glycosylation profiles of Alzheimer's beta -secretase protein Asp-2 expressed in a variety of cell lines. (2001 - Charlwood J, Dingwall C, Matico R, Hussain I, Johanson K, Moore S, Powell DJ, Skehel JM, Ratcliffe S, Clarke B, Trill J, Sweitzer S, Camilleri P) / Status : Reviewed
Structural analysis of sulfated N-linked oligosaccharides in erythropoietin (2001 - Kawasaki, Haishima, Ohta, Itoh, Hyuga, Hayakawa) / Status : Reviewed
Hierarchy of post-translational modifications involved in the circulatory longevity of glycoproteins. Demonstration of concerted contributions of glycan sialylation and subunit assembly to the pharmacokinetic behavior of bovine acetylcholinesterase. (2000 - Kronman C, Chitlaru T, Elhanany E, Velan B, Shafferman A) / Status : Reviewed
N-linked oligosaccharide structures in the diamine oxidase from porcine kidney. (2000 - Huang Y, Mechref Y, Novotny M) / Status : Reviewed
Alternative O-glycosylation/O-phosphorylation of the murine estrogen receptor beta. (2000 - Cheng X, Cole R, Zaia J, Hart G) / Status : Reviewed
Metabolic shifts do not influence the glycosylation patterns of a recombinant fusion protein expressed in BHK cells. (2000 - Cruz H, Peixoto C, Nimtz M, Alves P, Dias E, Moreira J, Carrondo M) / Status : Reviewed
Carbohydrate structures of soluble human L-selectin recombinantly expressed in baby-hamster kidney cells. (2000 - Gohlke M, Mach U, Nuck R, Zimmermann-Kordmann M, Grunow D, Fieger C, Volz B, Tauber R, Petri T, Debus N, Reutter W) / Status : Reviewed
Structure of the asparagine-linked sugar chains of porcine kidney and human urine cerebroside sulfate activator protein. (2000 - Faull K, Johnson J, Kim M, To T, Whitelegge J, Stevens R, Fluharty C, Fluharty A) / Status : Reviewed
SV40 large T antigen is modified with O-linked N-acetylglucosamine but not with other forms of glycosylation. (1998 - Medina L, Grove K, Haltiwanger R) / Status : Reviewed
N-glycan structures of a recombinant mouse soluble Fcgamma receptor II. (1998 - Takahashi N, Yamada W, Masuda K, Araki H, Tsukamoto Y, Galinha A, Sauts C, Kato K, Shimada I) / Status : Reviewed
An evaluation of sialation of the nucleoporin p62. (1998 - Fang B, Hanover J, Miller M) / Status : Reviewed
Characterization of recombinant human plasma lecithin: cholesterol acyltransferase (LCAT): N-linked carbohydrate structures and catalytic properties. (1998 - Lacko A, Reason A, Nuckolls C, Kudchodkar B, Nair M, Sundarrajan G, Pritchard P, Morris H, Dell A) / Status : Reviewed
Recognition signal for C-mannosylation of Trp-7 in RNase 2 consists of sequence Trp-x-x-Trp. (1998 - Krieg J, Hartmann S, Vicentini A, Glsner W, Hess D, Hofsteenge J) / Status : Reviewed
C-Mannosylation of human RNase 2 is an intracellular process performed by a variety of cultured cells. (1997 - Krieg J, Glasner W, Vicentini A, Doucey M, Loffler A, Hess D, Hofsteenge J) / Status : Reviewed
Biological and physicochemical characterization of recombinant human erythropoietins fractionated by Mono Q column chromatography and their modification with sialyltransferase. (1996 - Morimoto K, Tsuda E, Said A, Uchida E, Hatakeyama S, Ueda M, Hayakawa T) / Status : Reviewed
Peptide, disulfide, and glycosylation mapping of recombinant human thrombopoietin from ser1 to Arg246. (1996 - Hoffman RC, Andersen H, Walker K, Krakover JD, Patel S, Stamm MR, Osborn SG) / Status : Reviewed
Identification and structural characterization of a mannose-6-phosphate containing oligomannosidic N-glycan from human erythropoietin secreted by recombinant BHK-21 cells. (1995 - Nimtz M, Wray V, Rdiger A, Conradt H) / Status : Reviewed
Structural determination of two N-linked glycans isolated from recombinant human lactoferrin expressed in BHK cells. (1995 - Legrand D, Salmon V, Coddeville B, Benaissa M, Plancke Y, Spik G) / Status : Reviewed
A strategy for the mapping of N-glycans by high-performance capillary electrophoresis. (1994 - Hermentin P, Doenges R, Witzel R, Hokke C, Vliegenthart J, Kamerling J, Conradt H, Nimtz M, Brazel D) / Status : Reviewed
Glycosylation of glycoprotein 55 encoded by the anaemia-inducing strain of Friend spleen focus-forming virus. (1994 - Volker J, Geyer H, Geyer R) / Status : Reviewed
Human serum amyloid P component is an invariant constituent of amyloid deposits and has a uniquely homogeneous glycostructure. (1994 - Pepys M, Rademacher T, Amatayakul-Chantler S, Williams P, Noble G, Hutchinson W, Hawkins P, Nelson S, Gallimore J, Herbert J) / Status : Reviewed
Structures of sialylated oligosaccharides of human erythropoietin expressed in recombinant BHK-21 cells. (1993 - Nimtz M, Martin W, Wray V, Klppel K, Augustin J, Conradt H) / Status : Reviewed
Human non-secretory ribonucleases. II. Structural characterization of the N-glycans of the kidney, liver and spleen enzymes by NMR spectroscopy and electrospray mass spectrometry. (1993 - Lawrence C, Little P, Little B, Glushka J, van Halbeek H, Alhadeff J) / Status : Reviewed
Novel Asn-linked oligosaccharides terminating in GalNAc beta (1-->4)[Fuc alpha (1-->3)]GlcNAc beta (1-->.) are present in recombinant human protein C expressed in human kidney 293 cells. (1993 - Yan S, Chao Y, van Halbeek H) / Status : Reviewed
Accumulation of pentamannose oligosaccharides in human mononuclear leukocytes by action of swainsonine, an inhibitor of glycoprotein processing. (1993 - Kang M, Bowlin T, Vijay I, Sunkara S) / Status : Reviewed
Carbohydrate structure of Marburg virus glycoprotein. (1992 - Geyer H, Will C, Feldmann H, Klenk H, Geyer R) / Status : Reviewed
The asparagine-linked oligosaccharides on tissue factor pathway inhibitor terminate with SO4-4GalNAc beta 1, 4GlcNAc beta 1,2 Mana alpha. (1992 - Smith P, Skelton T, Fiete D, Dharmesh S, Beranek M, MacPhail L, Broze G, Baenziger J) / Status : Reviewed
Human plasma and recombinant factor VII. Characterization of O-glycosylations at serine residues 52 and 60 and effects of site-directed mutagenesis of serine 52 to alanine. (1991 - Bjoern S, Foster D, Thim L, Wiberg F, Christensen M, Komiyama Y, Pedersen A, Kisiel W) / Status : Reviewed
Characterization of a posttranslational fucosylation in the growth factor domain of urinary plasminogen activator. (1991 - Buko A, Kentzer E, Petros A, Menon G, Zuiderweg E, Sarin V) / Status : Reviewed
Expression of human interleukin-2 in recombinant baby hamster kidney, Ltk-, and Chinese hamster ovary cells. Structure of O-linked carbohydrate chains and their location within the polypeptide. (1989 - Conradt H, Nimtz M, Dittmar K, Lindenmaier W, Hoppe J, Hauser H) / Status : Reviewed
Comparative structural study of N-linked oligosaccharides of urinary and recombinant erythropoietins. (1988 - Tsuda E, Goto M, Murakami A, Akai K, Ueda M, Kawanishi G, Takahashi N, Sasaki R, Chiba H, Ishihara H) / Status : Reviewed
Characterization and analysis of branched-chain N-acetylglucosaminyl oligosaccharides accumulating in Sandhoff disease tissue. Evidence that biantennary bisected oligosaccharide side chains of glycoproteins are abundant substrates for lysosomes. (1985 - Warner TG, deKremer RD, Sjoberg ER, Mock AK) / Status : Reviewed
Comparative study of the oligosaccharides released from baby hamster kidney cells and their polyoma transformant by hydrazinolysis. (1984 - Yamashita K, Ohkura T, Tachibana Y, Takasaki S, Kobata A) / Status : Reviewed

Reported glycosite

Adipocyte plasma membrane-associated protein / Homo sapiens
- Asn-160
Beta-secretase-fc fusion protein / Homo sapiens
- Undefined site
Coagulation factor VII / Homo sapiens
- Ser-112
- Ser-120
Erythropoietin / Homo sapiens
- Undefined site
- Asn-51
IgG-IL2 fusion protein / Homo sapiens
- Undefined site
Inter-alpha-trypsin inhibitor heavy chain h4 / Homo sapiens
- Asn-81
- Asn-207
- Asn-274
- Asn-517
- Asn-577
Interleukin-2 / Homo sapiens
- Thr-23
L-selectin / Homo sapiens
- Undefined site
Lactotransferrin / Homo sapiens
- Undefined site
Non-secretory ribonuclease / Homo sapiens
- Undefined site
- Trp-34
Phosphatidylcholine-sterol acyltransferase / Homo sapiens
- Undefined site
Recombinant urokinase-type plasminogen activator / Homo sapiens
- Undefined site
Serum amyloid p-component / Homo sapiens
- Asn-51
Thrombopoietin / Homo sapiens
- Undefined site
Tissue factor pathway inhibitor / Homo sapiens
- Undefined site
Vitamin k-dependent protein c / Homo sapiens
- Undefined site
Acetylcholinesterase / Bos taurus
- Undefined site
Rnase 2.4 / Fusion - homo sapiens/sus scrofa
- Trp-34
Estrogen receptor beta / Mus musculus
- Undefined site
Low affinity immunoglobulin gamma Fc region receptor II / Mus musculus
- Undefined site
Neuroligin 1 / Rattus norvegicus
- Undefined site
Nuclear pore glycoprotein p62 / Rattus norvegicus
- Undefined site
Amiloride-sensitive amine oxidase / Sus scrofa
- Undefined site
Saposin b / Sus scrofa
- Asn-21
Large t antigen / Simian virus 40
- Undefined site
Gp55 / Friend spleen focus-forming virus (anemia inducing strain)
- Undefined site
Structural glycoprotein / Marburg virus (strain musoke)
- Undefined site

Mass spectrometry observed peptide

- O-Linked / No-core (avg mass : 164.1583)
- O-Linked / Undefined core (avg mass : 180.1577)
- C-Linked / Undefined core (avg mass : 180.1577)
- O-Linked / Core 0 (avg mass : 221.2103)
- N-Linked/O-Linked / Truncated If N-Linked (avg mass : 221.2103)
- O-Linked / No-core (avg mass : 312.2738)
- O-Linked / Core 1 (avg mass : 383.3527)
- O-Linked / Undefined core (avg mass : 383.3527)
- O-Linked / No-core (avg mass : 444.3899)
- N-Linked / No-core (avg mass : 570.5483)
- O-Linked / Core 2 (avg mass : 586.5477)
- O-Linked / Undefined core (avg mass : 674.6106)
- O-Linked / Undefined core (avg mass : 674.6106)
- O-Linked / Core 1 (avg mass : 674.6106)
- N-Linked / No-core (avg mass : 732.6907)
- O-Linked / Core 2 (avg mass : 748.6901)
- O-Linked / Undefined core (avg mass : 820.7536)
- N-Linked / No-core (avg mass : 894.8331)
- N-Linked / No-core (avg mass : 894.8331)
- O-Linked / Core 1 (avg mass : 965.8685)
- O-Linked / Core 1 (avg mass : 965.8685)
- N-Linked / High-Mannose (avg mass : 1031.9223)
- N-Linked / Pauci-Mannose (avg mass : 1056.9755)
- N-Linked / High-Mannose (avg mass : 1072.9749)
- N-Linked / Pauci-Mannose (avg mass : 1072.9749)
- O-Linked / Core 2 (avg mass : 1114.0275)
- O-Linked / Core 2 (avg mass : 1114.0275)
- N-Linked / No-core (avg mass : 1114.0275)
- N-Linked / Hybrid (avg mass : 1219.1179)
- N-Linked / Hybrid (avg mass : 1235.1173)
- N-Linked / High-Mannose (avg mass : 1235.1173)
- N-Linked / Complex (avg mass : 1260.1705)
- N-Linked / Complex (avg mass : 1260.1705)
- N-Linked / Complex (avg mass : 1260.1705)
- N-Linked / Complex (avg mass : 1276.1699)
- N-Linked / Complex (avg mass : 1317.2225)
- N-Linked / No-core (avg mass : 1317.2225)
- N-Linked / Complex (avg mass : 1317.2225)
- N-Linked / No-core (avg mass : 1317.2225)
- N-Linked / Hybrid (avg mass : 1381.2603)
- N-Linked / High-Mannose (avg mass : 1397.2597)
- N-Linked / High-Mannose (avg mass : 1397.2597)
- N-Linked / High-Mannose (avg mass : 1397.2597)
- N-Linked / Complex (avg mass : 1422.3129)
- N-Linked / Complex (avg mass : 1422.3129)
- N-Linked / Complex (avg mass : 1463.3655)
- N-Linked / Complex (avg mass : 1463.3655)
- N-Linked / Complex (avg mass : 1463.3655)
- N-Linked / Complex (avg mass : 1479.3649)
- N-Linked / Complex (avg mass : 1479.3649)
- N-Linked / High-Mannose (avg mass : 1559.4021)
- N-Linked / High-Mannose (avg mass : 1559.4021)
- N-Linked / High-Mannose (avg mass : 1559.4021)
- N-Linked / High-Mannose (avg mass : 1559.4021)
- N-Linked / Hybrid (avg mass : 1600.4547)
- N-Linked / Complex (avg mass : 1625.5079)
- N-Linked / Complex (avg mass : 1625.5079)
- N-Linked / Complex (avg mass : 1625.5079)
- N-Linked / Complex (avg mass : 1625.5079)
- N-Linked / Complex (avg mass : 1625.5079)
- N-Linked / Complex (avg mass : 1641.5073)
- N-Linked / Complex (avg mass : 1641.5073)
- N-Linked / Complex (avg mass : 1666.5605)
- N-Linked / Complex (avg mass : 1666.5605)
- N-Linked / Complex (avg mass : 1666.5605)
- N-Linked / Hybrid (avg mass : 1680.4346)
- N-Linked / Complex (avg mass : 1682.5599)
- N-Linked / Complex (avg mass : 1713.5708)
- N-Linked / High-Mannose (avg mass : 1721.5445)
- N-Linked / High-Mannose (avg mass : 1721.5445)
- N-Linked / High-Mannose (avg mass : 1721.5445)
- N-Linked / High-Mannose (avg mass : 1721.5445)
- N-Linked / High-Mannose (avg mass : 1721.5445)
- N-Linked / Hybrid (avg mass : 1746.5977)
- N-Linked / Complex (avg mass : 1770.6228)
- N-Linked / Complex (avg mass : 1787.6503)
- N-Linked / Complex (avg mass : 1787.6503)
- N-Linked / Complex (avg mass : 1787.6503)
- N-Linked / Complex (avg mass : 1787.6503)
- N-Linked / Complex (avg mass : 1803.6767)
- N-Linked / Complex (avg mass : 1828.7029)
- N-Linked / Complex (avg mass : 1828.7029)
- N-Linked / Complex (avg mass : 1828.7029)
- N-Linked / Complex (avg mass : 1844.7023)
- N-Linked / Complex (avg mass : 1869.7555)
- N-Linked / Complex (avg mass : 1869.7555)
- N-Linked / High-Mannose (avg mass : 1883.6869)
- N-Linked / High-Mannose (avg mass : 1883.6869)
- N-Linked / High-Mannose (avg mass : 1883.6869)
- N-Linked / Complex (avg mass : 1883.7409)
- N-Linked / Complex (avg mass : 1916.7658)
- N-Linked / Complex (avg mass : 1916.7658)
- N-Linked / Complex (avg mass : 1916.7658)
- N-Linked / Complex (avg mass : 1932.7652)
- N-Linked / Complex (avg mass : 1932.7652)
- N-Linked / Complex (avg mass : 1932.7652)
- N-Linked / Complex (avg mass : 1933.7933)
- N-Linked / Complex (avg mass : 1933.7933)
- N-Linked / Complex (avg mass : 1949.7927)
- N-Linked / Complex (avg mass : 1949.8197)
- N-Linked / Complex (avg mass : 1949.8197)
- N-Linked / Complex (avg mass : 1974.8459)
- N-Linked / Complex (avg mass : 1990.8453)
- N-Linked / Complex (avg mass : 1990.8453)
- N-Linked / Complex (avg mass : 1990.8453)
- N-Linked / Complex (avg mass : 2006.8447)
- N-Linked / Complex (avg mass : 2006.8447)
- N-Linked / Complex (avg mass : 2006.8447)
- N-Linked / Complex (avg mass : 2006.8447)
- N-Linked / Complex (avg mass : 2015.8985)
- N-Linked / Complex (avg mass : 2015.8985)
- N-Linked / Complex (avg mass : 2015.8985)
- N-Linked / High-Mannose (avg mass : 2045.8293)
- N-Linked / Complex (avg mass : 2053.882)
- N-Linked / Complex (avg mass : 2053.882)
- N-Linked / Complex (avg mass : 2078.9082)
- N-Linked / Complex (avg mass : 2078.9082)
- N-Linked / Complex (avg mass : 2078.9082)
- N-Linked / Complex (avg mass : 2078.9082)
- N-Linked / Complex (avg mass : 2078.9082)
- N-Linked / Complex (avg mass : 2078.9082)
- N-Linked / Complex (avg mass : 2078.9082)
- N-Linked / Complex (avg mass : 2111.9351)
- N-Linked / Complex (avg mass : 2119.9608)
- N-Linked / Complex (avg mass : 2119.9608)
- N-Linked / Complex (avg mass : 2119.9608)
- N-Linked / Undefined core (avg mass : 2119.9608)
- N-Linked / Complex (avg mass : 2136.9883)
- N-Linked / Complex (avg mass : 2152.9877)
- N-Linked / Complex (avg mass : 2152.9877)
- N-Linked / Complex (avg mass : 2152.9877)
- N-Linked / Complex (avg mass : 2152.9877)
- N-Linked / Undefined core (avg mass : 2152.9877)
- N-Linked / Complex (avg mass : 2152.9877)
- N-Linked / Complex (avg mass : 2152.9877)
- N-Linked / Complex (avg mass : 2161.0134)
- N-Linked / Complex (avg mass : 2162.0415)
- N-Linked / Complex (avg mass : 2194.0403)
- N-Linked / Complex (avg mass : 2200.025)
- N-Linked / Complex (avg mass : 2224.0231)
- N-Linked / Complex (avg mass : 2224.0231)
- N-Linked / Complex (avg mass : 2224.0231)
- N-Linked / Complex (avg mass : 2224.0231)
- N-Linked / Complex (avg mass : 2225.0512)
- N-Linked / Complex (avg mass : 2225.0512)
- N-Linked / Complex (avg mass : 2225.0512)
- N-Linked / Complex (avg mass : 2266.1038)
- N-Linked / Complex (avg mass : 2266.1038)
- N-Linked / Complex (avg mass : 2266.1038)
- N-Linked / Complex (avg mass : 2282.1032)
- N-Linked / Complex (avg mass : 2282.1032)
- N-Linked / Complex (avg mass : 2299.1307)
- N-Linked / Complex (avg mass : 2307.1564)
- N-Linked / Complex (avg mass : 2356.1827)
- N-Linked / Complex (avg mass : 2370.1661)
- N-Linked / Complex (avg mass : 2370.1661)
- N-Linked / Complex (avg mass : 2370.1661)
- N-Linked / Complex (avg mass : 2370.1661)
- N-Linked / Complex (avg mass : 2370.1661)
- N-Linked / Complex (avg mass : 2370.1661)
- N-Linked / Complex (avg mass : 2370.1661)
- N-Linked / Complex (avg mass : 2372.1821)
- N-Linked / Complex (avg mass : 2372.1821)
- N-Linked / Complex (avg mass : 2372.1821)
- N-Linked / Complex (avg mass : 2411.2187)
- N-Linked / Complex (avg mass : 2411.2187)
- N-Linked / Complex (avg mass : 2411.2187)
- N-Linked / Complex (avg mass : 2444.2456)
- N-Linked / Complex (avg mass : 2444.2456)
- N-Linked / Complex (avg mass : 2444.2456)
- N-Linked / Complex (avg mass : 2444.2456)
- N-Linked / Complex (avg mass : 2485.2982)
- N-Linked / Undefined core (avg mass : 2485.2982)