enow.com Web Search

  1. Ad

    related to: purine vs pyrimidine bases in food groups

Search results

  1. Results from the WOW.Com Content Network
  2. Purine - Wikipedia

    en.wikipedia.org/wiki/Purine

    Purines and pyrimidines make up the two groups of nitrogenous bases, including the two groups of nucleotide bases. The purine bases are guanine (G) and adenine (A) which form corresponding nucleosides-deoxyribonucleosides (deoxyguanosine and deoxyadenosine) with deoxyribose moiety and ribonucleosides (guanosine, adenosine) with

  3. Nucleotide base - Wikipedia

    en.wikipedia.org/wiki/Nucleotide_base

    The purine nitrogenous bases are characterized by their single amino group (−NH 2), at the C6 carbon in adenine and C2 in guanine. [5] Similarly, the simple-ring structure of cytosine, uracil, and thymine is derived of pyrimidine, so those three bases are called the pyrimidine bases. [6]

  4. Purine metabolism - Wikipedia

    en.wikipedia.org/wiki/Purine_metabolism

    Formyl groups build carbon-2 and carbon-8 in the purine ring system, which are the ones acting as bridges between two nitrogen atoms. A key regulatory step is the production of 5-phospho-α- D -ribosyl 1-pyrophosphate ( PRPP ) by ribose-phosphate diphosphokinase , which is activated by inorganic phosphate and inactivated by purine ribonucleotides.

  5. Nucleic acid structure - Wikipedia

    en.wikipedia.org/wiki/Nucleic_acid_structure

    Cytosine, thymine, and uracil are pyrimidines, hence the glycosidic bonds form between their 1 nitrogen and the 1' -OH of the deoxyribose. For both the purine and pyrimidine bases, the phosphate group forms a bond with the deoxyribose sugar through an ester bond between one of its negatively charged oxygen groups and the 5' -OH of the sugar. [2]

  6. Nucleic acid metabolism - Wikipedia

    en.wikipedia.org/wiki/Nucleic_acid_metabolism

    Thymidine synthesis first requires reduction of the uridine to deoxyuridine (see next section), before the base can be methylated to produce thymidine. [1] [5] ATP, a purine nucleotide, is an activator of pyrimidine synthesis, while CTP, a pyrimidine nucleotide, is an inhibitor of pyrimidine synthesis. This regulation helps to keep the purine ...

  7. Nucleoside - Wikipedia

    en.wikipedia.org/wiki/Nucleoside

    A nucleoside consists simply of a nucleobase (also termed a nitrogenous base) and a five-carbon sugar (ribose or 2'-deoxyribose) whereas a nucleotide is composed of a nucleobase, a five-carbon sugar, and one or more phosphate groups. In a nucleoside, the anomeric carbon is linked through a glycosidic bond to the N9 of a purine or the N1 of a ...

  8. Ribonucleotide - Wikipedia

    en.wikipedia.org/wiki/Ribonucleotide

    In living organisms, the most common bases for ribonucleotides are adenine (A), guanine (G), cytosine (C), or uracil (U). The nitrogenous bases are classified into two parent compounds, purine and pyrimidine. General Ribonucleotide Structure: phosphate group, Ribose, Nucleobase.

  9. Pyrimidine - Wikipedia

    en.wikipedia.org/wiki/Pyrimidine

    Pyrimidine (C 4 H 4 N 2; / p ɪ ˈ r ɪ. m ɪ ˌ d iː n, p aɪ ˈ r ɪ. m ɪ ˌ d iː n /) is an aromatic, heterocyclic, organic compound similar to pyridine (C 5 H 5 N). [3] One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has nitrogen atoms at positions 1 and 3 in the ring.

  1. Ad

    related to: purine vs pyrimidine bases in food groups