When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Nucleoside triphosphate - Wikipedia

    en.wikipedia.org/wiki/Nucleoside_triphosphate

    A nitrogenous base called hypoxanthine is assembled directly onto PRPP. [22] This results in a nucleotide called inosine monophosphate (IMP). IMP is then converted to either a precursor to AMP or GMP. Once AMP or GMP are formed, they can be phosphorylated by ATP to their diphosphate and triphosphate forms. [23]

  3. Dideoxynucleotide - Wikipedia

    en.wikipedia.org/wiki/Dideoxynucleotide

    That is, each nucleotide base of that particular type has a probability of being bonded to not a deoxynucleotide but rather a dideoxynucleotide, which ends chain elongation. Therefore, if the sample then undergoes electrophoresis, there will be a band present for each length at which the complement of the dideoxynucleotide is present.

  4. 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.

  5. 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.

  6. rNTP - Wikipedia

    en.wikipedia.org/wiki/RNTP

    The use of a steric gate residue present on the DNA polymerase prevents incorporation of rNTP by creating a steric clash between an active site amino acid residue on the DNA polymerase and the 2'-OH on the sugar base of the rNTP. This steric clash is absent when incorporating dNTP since the sugar base on dNTPs have a 2'-H instead of a 2'-OH.

  7. Nucleotide - Wikipedia

    en.wikipedia.org/wiki/Nucleotide

    This nucleotide contains the five-carbon sugar deoxyribose (at center), a nucleobase called adenine (upper right), and one phosphate group (left). The deoxyribose sugar joined only to the nitrogenous base forms a Deoxyribonucleoside called deoxyadenosine, whereas the whole structure along with the phosphate group is a nucleotide, a constituent of DNA with the name deoxyadenosine monophosphate.

  8. DNA synthesis - Wikipedia

    en.wikipedia.org/wiki/DNA_synthesis

    Each unit is joined when a covalent bond forms between its phosphate group and the pentose sugar of the next nucleotide, forming a sugar-phosphate backbone. DNA is a complementary, double stranded structure as specific base pairing (adenine and thymine, guanine and cytosine) occurs naturally when hydrogen bonds form between the nucleotide bases.

  9. Deoxyribonucleotide - Wikipedia

    en.wikipedia.org/wiki/Deoxyribonucleotide

    A deoxyribonucleotide is a nucleotide that contains deoxyribose. They are the monomeric units of the informational biopolymer , deoxyribonucleic acid ( DNA ). Each deoxyribonucleotide comprises three parts: a deoxyribose sugar ( monosaccharide ), a nitrogenous base , and one phosphoryl group . [ 1 ]