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  2. Pyranose - Wikipedia

    en.wikipedia.org/wiki/Pyranose

    If reaction is between the C-4 hydroxyl and the aldehyde, a furanose is formed instead. [1] The pyranose form is thermodynamically more stable than the furanose form, which can be seen by the distribution of these two cyclic forms in solution. [2] Formation of pyranose hemiacetal and representations of β-D-glucopyranose

  3. D-Ribose pyranase - Wikipedia

    en.wikipedia.org/wiki/D-Ribose_Pyranase

    The furanose form is more useful for cells, as it can be used in other reactions. For most cells, ribose is transported into the cell in the pyranose form. With this said, D-Ribose Pyranase needs to be present to convert the pyranose form into the furanose form. Beta-D-ribofuranose can then be converted to ribose-5-phosphate.

  4. Lyxose - Wikipedia

    en.wikipedia.org/wiki/Lyxose

    It has chemical formula C 5 H 10 O 5. It is a C'-2 carbon epimer of the sugar xylose. The name "lyxose" comes from reversing the prefix "xyl" in "xylose". Lyxose occurs only rarely in nature, for example, as a component of bacterial glycolipids. [1] D-Lyxose in both its furanose and pyranose forms

  5. Monosaccharide - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide

    Conversion between the furanose, acyclic, and pyranose forms of D-glucose Pyranose forms of some pentose sugars Pyranose forms of some hexose sugars For many monosaccharides (including glucose), the cyclic forms predominate, in the solid state and in solutions, and therefore the same name commonly is used for the open- and closed-chain isomers.

  6. Furanose - Wikipedia

    en.wikipedia.org/wiki/Furanose

    A furanose is a collective term for carbohydrates that have a chemical structure that includes a five-membered ring system consisting of four carbon atoms and one oxygen atom. The name derives from its similarity to the oxygen heterocycle furan , but the furanose ring does not have double bonds .

  7. File:D-Sorbose-Keto-Pyranose-Furanose.svg - Wikipedia

    en.wikipedia.org/wiki/File:D-Sorbose-Keto...

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  8. N-Acetylglucosamine - Wikipedia

    en.wikipedia.org/wiki/N-Acetylglucosamine

    O-GlcNAcylation is the process of adding a single N-acetylglucosamine sugar to the serine or threonine of a protein. [4] Comparable to phosphorylation, addition or removal of N-acetylglucosamine is a means of activating or deactivating enzymes or transcription factors. [4]

  9. Haworth projection - Wikipedia

    en.wikipedia.org/wiki/Haworth_projection

    A Haworth projection has the following characteristics: [3] Carbon is the implicit type of atom. In the example on the right, the atoms numbered from 1 to 6 are all carbon atoms. Carbon 1 is known as the anomeric carbon. Hydrogen atoms on carbon are implicit. In the example, atoms 1 to 6 have extra hydrogen atoms not depicted.

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