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  2. Oligosaccharide - Wikipedia

    en.wikipedia.org/wiki/Oligosaccharide

    Oligosaccharides that participate in O-linked glycosylation are attached to threonine or serine on the hydroxyl group of the side chain. [7] O-linked glycosylation occurs in the Golgi apparatus, where monosaccharide units are added to a complete polypeptide chain. Cell surface proteins and extracellular proteins are O-glycosylated. [10]

  3. Chitin - Wikipedia

    en.wikipedia.org/wiki/Chitin

    Chitin is a modified polysaccharide that contains nitrogen; it is synthesized from units of N-acetyl-D-glucosamine (to be precise, 2-(acetylamino)-2-deoxy-D-glucose). These units form covalent β-(1→4)-linkages (like the linkages between glucose units forming cellulose).

  4. O-linked glycosylation - Wikipedia

    en.wikipedia.org/wiki/O-linked_glycosylation

    Galactose or glucose sugars can be attached to a hydroxyl group of ceramide lipids in a different form of O-glycosylation, as it does not occur on proteins. [6] This forms glycosphingolipids, which are important for the localisation of receptors in membranes. [8]

  5. Cellulose - Wikipedia

    en.wikipedia.org/wiki/Cellulose

    The chemical formula of cellulose is (C 6 H 10 O 5) n where n is the degree of polymerization and represents the number of glucose groups. [21] Plant-derived cellulose is usually found in a mixture with hemicellulose, lignin, pectin and other substances, while bacterial cellulose is quite pure, has a much higher water content and higher tensile ...

  6. Glycoprotein - Wikipedia

    en.wikipedia.org/wiki/Glycoprotein

    The process of glycosylation (binding a carbohydrate to a protein) is a post-translational modification, meaning it happens after the production of the protein. [3] Glycosylation is a process that roughly half of all human proteins undergo and heavily influences the properties and functions of the protein. [ 3 ]

  7. Glycosyl - Wikipedia

    en.wikipedia.org/wiki/Glycosyl

    The β-D-glucopyranosyl group which is obtained by the removal of the hemiacetal hydroxyl group (bottom right) from β-D-glucopyranoseIn organic chemistry, a glycosyl group is a univalent free radical or substituent structure obtained by removing the hydroxyl (−OH) group from the hemiacetal (−CH(OH)O−) group found in the cyclic form of a monosaccharide and, by extension, of a lower ...

  8. Polysaccharide - Wikipedia

    en.wikipedia.org/wiki/Polysaccharide

    Cellulose is a polymer made with repeated glucose units bonded together by beta-linkages. Humans and many animals lack an enzyme to break the beta-linkages, so they do not digest cellulose. Certain animals, such as termites can digest cellulose, because bacteria possessing the enzyme are present in their gut. Cellulose is insoluble in water.

  9. Glucose - Wikipedia

    en.wikipedia.org/wiki/Glucose

    The reason for glucose having the most stable cyclic form of all the aldohexoses is that its hydroxy groups (with the exception of the hydroxy group on the anomeric carbon of d-glucose) are in the equatorial position. Presumably, glucose is the most abundant natural monosaccharide because it is less glycated with proteins than other ...