BIOMAT Database Logo BIOMAT Database Logo

[Structures of 9 oligosaccharides and glycopeptides containing large amounts of fucose excreted in the urine of 2 patients with fucosidosis]. 1977

G Strecker, and B Fournet, and G Spik, and J Montreuil, and P Durand, and M Tondeur

UI MeSH Term Description Entries
D007983 Lewis Blood Group Antigens Carbohydrate antigens structurally related to the ABH BLOOD-GROUP SYSTEM. They may occur as a modification of saccharide chains on glycolipids or glycoproteins on cell surfaces or in plasma, or as free oligosaccharides in secretions. Lewis antigens are not synthesized in blood cells. Instead Lewis glycolipids present in plasma are absorbed onto the surface of ERYTHROCYTES; LYMPHOCYTES; and PLATELETS. The phenotypes Le(a) and Le(b) are the result of the actions of two genes the Le gene (fucosyltransferase FUT3) and the Se gene (fucosyltransferase FUT2) on the precursor carbohydrate, glycolipid or glycoprotein. Other FUCOSYLTRANSFERASES can also synthesize the Lewis antigens. Blood Group Lewis Related Antigens,Lewis Antigen Related Tumor-Associated Antigens,Lewis Antigens,Lewis Blood Group Related Antigens,Lewis Blood Group Related Tumor-Associated Antigens,Lewis Blood-Group System,Lewis Related Antigens,Lewis System,Sialyl Lewis Antigens,Le Antigens,Le(a) Blood Group System,Antigens, Lewis,Antigens, Lewis Related,Antigens, Sialyl Lewis,Blood-Group System, Lewis,Lewis Antigen Related Tumor Associated Antigens,Lewis Blood Group Related Tumor Associated Antigens,Lewis Blood Group System
D009844 Oligosaccharides Carbohydrates consisting of between two (DISACCHARIDES) and ten MONOSACCHARIDES connected by either an alpha- or beta-glycosidic link. They are found throughout nature in both the free and bound form. Oligosaccharide
D002239 Carbohydrate Metabolism, Inborn Errors Dysfunctions of CARBOHYDRATE METABOLISM resulting from inborn genetic mutations that are inherited or acquired in utero. Carbohydrate Metabolism, Inborn Error
D002621 Chemistry A basic science concerned with the composition, structure, and properties of matter; and the reactions that occur between substances and the associated energy exchange.
D004186 Disaccharidases Enzymes belonging to the class of GLYCOSIDE HYDROLASES which break down DISACCHARIDES into simpler sugars, MONOSACCHARIDES. Disaccharidase
D005643 Fucose A six-member ring deoxysugar with the chemical formula C6H12O5. It lacks a hydroxyl group on the carbon at position 6 of the molecule. Deoxygalactose,alpha-Fucose,alpha Fucose
D005644 alpha-L-Fucosidase An enzyme that catalyzes the hydrolysis of an alpha L-fucoside to yield an alcohol and L-fucose. Deficiency of this enzyme can cause FUCOSIDOSIS. EC 3.2.1.51. Fucosidase,alpha-Fucosidase,alpha Fucosidase,alpha L Fucosidase
D005838 Genotype The genetic constitution of the individual, comprising the ALLELES present at each GENETIC LOCUS. Genogroup,Genogroups,Genotypes
D006020 Glycopeptides Proteins which contain carbohydrate groups attached covalently to the polypeptide chain. The protein moiety is the predominant group with the carbohydrate making up only a small percentage of the total weight. Glycopeptide
D006023 Glycoproteins Conjugated protein-carbohydrate compounds including MUCINS; mucoid, and AMYLOID glycoproteins. C-Glycosylated Proteins,Glycosylated Protein,Glycosylated Proteins,N-Glycosylated Proteins,O-Glycosylated Proteins,Glycoprotein,Neoglycoproteins,Protein, Glycosylated,Proteins, C-Glycosylated,Proteins, Glycosylated,Proteins, N-Glycosylated,Proteins, O-Glycosylated

Related Publications

G Strecker, and B Fournet, and G Spik, and J Montreuil, and P Durand, and M Tondeur
Characterization of oligosaccharides and glycopeptides excreted in the urine of GMl-gangliosidosis patients.
September 1975, Biochemical and biophysical research communications,
G Strecker, and B Fournet, and G Spik, and J Montreuil, and P Durand, and M Tondeur
The affinity of the fucose-binding lectin from Lotus tetragonolobus for glycopeptides and oligosaccharides accumulating in fucosidosis.
March 1979, Journal of neurochemistry,
G Strecker, and B Fournet, and G Spik, and J Montreuil, and P Durand, and M Tondeur
Urinary oligosaccharides of GM1-gangliosidosis. Structures of oligosaccharides excreted in the urine of type 1 but not in the urine of type 2 patients.
August 1981, The Journal of biological chemistry,
G Strecker, and B Fournet, and G Spik, and J Montreuil, and P Durand, and M Tondeur
ISOLATION OF FUCOSE-RICH GLYCOPEPTIDES FROM NORMAL URINE.
March 1965, Biochimica et biophysica acta,
G Strecker, and B Fournet, and G Spik, and J Montreuil, and P Durand, and M Tondeur
The structures of oligosaccharides excreted by sheep with swainsonine toxicosis.
October 1988, The Journal of biological chemistry,
G Strecker, and B Fournet, and G Spik, and J Montreuil, and P Durand, and M Tondeur
[2 hydroxyproline-containing glycopeptides from normal human urine].
April 1966, Biochimica et biophysica acta,
G Strecker, and B Fournet, and G Spik, and J Montreuil, and P Durand, and M Tondeur
Monocyte chemoattractant protein-1 is excreted in excessive amounts in the urine of patients with lupus nephritis.
December 1995, Laboratory investigation; a journal of technical methods and pathology,
G Strecker, and B Fournet, and G Spik, and J Montreuil, and P Durand, and M Tondeur
Enzymatic synthesis of fucose-containing galacto-oligosaccharides using β-galactosidase and identification of novel disaccharide structures.
February 2018, Glycoconjugate journal,
G Strecker, and B Fournet, and G Spik, and J Montreuil, and P Durand, and M Tondeur
Comparison of the urinary glycoconjugates excreted by patients with type I and type II fucosidosis.
January 1987, Clinical chemistry,
G Strecker, and B Fournet, and G Spik, and J Montreuil, and P Durand, and M Tondeur
[Quantitative analysis of oligosaccharides and glycopeptides in urine by gas chromatography--mass spectrometry].
February 1976, Lakartidningen,
Copied contents to your clipboard!