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  2. Deoxyribose - Wikipedia

    en.wikipedia.org/wiki/Deoxyribose

    Deoxyribose, or more precisely 2-deoxyribose, is a monosaccharide with idealized formula H−(C=O)−(CH 2)−(CHOH) 3 −H. Its name indicates that it is a deoxy sugar, meaning that it is derived from the sugar ribose by loss of a hydroxy group. Discovered in 1929 by Phoebus Levene, [4] deoxyribose is most notable for its presence in DNA.

  3. Ribose - Wikipedia

    en.wikipedia.org/wiki/Ribose

    L-Ribose Fischer Projection. Ribose is a simple sugar and carbohydrate with molecular formula C 5 H 10 O 5 and the linear-form composition H−(C=O)−(CHOH) 4 −H. The naturally occurring form, d-ribose, is a component of the ribonucleotides from which RNA is built, and so this compound is necessary for coding, decoding, regulation and expression of genes.

  4. Nucleic acid structure - Wikipedia

    en.wikipedia.org/wiki/Nucleic_acid_structure

    5-carbon sugar which is called deoxyribose (found in DNA) and ribose (found in RNA). One or more phosphate groups. [1] The nitrogen bases adenine and guanine are purine in structure and form a glycosidic bond between their 9 nitrogen and the 1' -OH group of the deoxyribose.

  5. Ribonucleotide - Wikipedia

    en.wikipedia.org/wiki/Ribonucleotide

    The general structure of a ribonucleotide consists of a phosphate group, a ribose sugar group, and a nucleobase, in which the nucleobase can either be adenine, guanine, cytosine, or uracil. Without the phosphate group, the composition of the nucleobase and sugar is known as a nucleoside.

  6. L-Deoxyribose - Wikipedia

    en.wikipedia.org/wiki/L-Deoxyribose

    l-Deoxyribose is an organic compound with formula C 5 H 10 O 4. It is a synthetic monosaccharide, a stereoisomer (mirror image) of the natural compound d-deoxyribose. l-Deoxyribose can be synthesized from d-galactose. [3] It has been used in chemical research, e.g. in the synthesis of mirror-image DNA. [4]

  7. Deoxyribonucleotide - Wikipedia

    en.wikipedia.org/wiki/Deoxyribonucleotide

    The nitrogenous bases are either purines or pyrimidines, heterocycles whose structures support the specific base-pairing interactions that allow nucleic acids to carry information. The base is always bonded to the 1'-carbon of the deoxyribose, an analog of ribose in which the hydroxyl group of the 2'-carbon is replaced with a hydrogen atom.

  8. Nucleic acid tertiary structure - Wikipedia

    en.wikipedia.org/.../Nucleic_acid_tertiary_structure

    Ribose Zippers: View of a canonical ribose zipper between two RNA backbones. [33] The ribose zipper is an RNA tertiary structural element in which two RNA chains are held together by hydrogen bonding interactions involving the 2’OH of ribose sugars on different strands. The 2'OH can behave as both hydrogen bond donor and acceptor, which ...

  9. Nucleotide base - Wikipedia

    en.wikipedia.org/wiki/Nucleotide_base

    At the sides of nucleic acid structure, phosphate molecules successively connect the two sugar-rings of two adjacent nucleotide monomers, thereby creating a long chain biomolecule. These chain-joins of phosphates with sugars ( ribose or deoxyribose ) create the "backbone" strands for a single- or double helix biomolecule.