enow.com Web Search

Search results

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

    en.wikipedia.org/wiki/Pyrimidine_dimer

    Cyclobutane pyrimidine dimer (CPD) is a dimer which features a four-membered ring formed by the fusion of two double-bonded carbons from adjacent pyrimidines. CPDs disrupt the formation of the base pair during DNA replication, potentially leading to mutations. [8] [9] [10]

  3. Nucleotide base - Wikipedia

    en.wikipedia.org/wiki/Nucleotide_base

    Similarly, the simple-ring structure of cytosine, uracil, and thymine is derived of pyrimidine, so those three bases are called the pyrimidine bases. [ 6 ] Each of the base pairs in a typical double- helix DNA comprises a purine and a pyrimidine: either an A paired with a T or a C paired with a G.

  4. Ribonucleotide - Wikipedia

    en.wikipedia.org/wiki/Ribonucleotide

    Both RNA and DNA contain two major purine bases, adenine (A) and guanine (G), and two major pyrimidines. In both DNA and RNA, one of the pyrimidines is cytosine (C). However, DNA and RNA differ in the second major pyrimidine. DNA contains thymine (T) while RNA contains uracil (U).

  5. Chargaff's rules - Wikipedia

    en.wikipedia.org/wiki/Chargaff's_rules

    The origin of the deviation from Chargaff's rule in the organelles has been suggested to be a consequence of the mechanism of replication. [13] During replication the DNA strands separate. In single stranded DNA, cytosine spontaneously slowly deaminates to adenosine (a C to A transversion). The longer the strands are separated the greater the ...

  6. DNA replication - Wikipedia

    en.wikipedia.org/wiki/DNA_replication

    In vitro single-molecule experiments (using optical tweezers and magnetic tweezers) have found synergetic interactions between the replisome enzymes (helicase, polymerase, and Single-strand DNA-binding protein) and with the DNA replication fork enhancing DNA-unwinding and DNA-replication. [14] These results lead to the development of kinetic ...

  7. 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.

  8. Nucleoside - Wikipedia

    en.wikipedia.org/wiki/Nucleoside

    Nucleosides are glycosylamines that can be thought of as nucleotides without a phosphate group.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.

  9. Nucleic acid metabolism - Wikipedia

    en.wikipedia.org/wiki/Nucleic_acid_metabolism

    This regulation helps to keep the purine/pyrimidine amounts similar, which is beneficial because equal amounts of purines and pyrimidines are required for DNA synthesis. [1] [6] Deficiencies of enzymes involved in pyrimidine synthesis can lead to the genetic disease Orotic aciduria which causes excessive excretion of orotic acid in the urine ...