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  2. Thymine - Wikipedia

    en.wikipedia.org/wiki/Thymine

    Thymine could also be a target for actions of 5-fluorouracil (5-FU) in cancer treatment. 5-FU can be a metabolic analog of thymine (in DNA synthesis) or uracil (in RNA synthesis). Substitution of this analog inhibits DNA synthesis in actively dividing cells. Thymine bases are frequently oxidized to hydantoins over time after the death of an ...

  3. Thymidine - Wikipedia

    en.wikipedia.org/wiki/Thymidine

    Thymidine (symbol dT or dThd), also known as deoxythymidine, deoxyribosylthymine, or thymine deoxyriboside, is a pyrimidine deoxynucleoside. Deoxythymidine is the DNA nucleoside T, which pairs with deoxyadenosine (A) in double-stranded DNA.

  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. Methylenetetrahydrofolate—tRNA-(uracil-5-)-methyltransferase

    en.wikipedia.org/wiki/Methylenetetrahydrofolate...

    In enzymology, a methylenetetrahydrofolate-tRNA-(uracil-5-)-methyltransferase (EC 2.1.1.74) is an enzyme that catalyzes the chemical reaction 5,10-methylenetetrahydrofolate + tRNA containing uridine at position 54 + FADH 2 ⇌ {\displaystyle \rightleftharpoons } tetrahydrofolate + tRNA containing ribothymidine at position 54 + FAD

  6. Uracil - Wikipedia

    en.wikipedia.org/wiki/Uracil

    Uracil (/ ˈ j ʊər ə s ɪ l /) (symbol U or Ura) is one of the four nucleotide bases in the nucleic acid RNA. The others are adenine (A), cytosine (C), and guanine (G). In RNA, uracil binds to adenine via two hydrogen bonds. In DNA, the uracil nucleobase is replaced by thymine (T). Uracil is a demethylated form of thymine.

  7. Ribonucleotide - Wikipedia

    en.wikipedia.org/wiki/Ribonucleotide

    The RNA chain is synthesized from the 5' end to the 3' end as the 3'-hydroxyl group of the last ribonucleotide in the chain acts as a nucleophile and launches a hydrophilic attack on the 5'-triphosphate of the incoming ribonucleotide, releasing pyrophosphate as a by-[6] product. Due to the physical properties of the nucleotides, the backbone of ...

  8. 5-Methyluridine - Wikipedia

    en.wikipedia.org/wiki/5-Methyluridine

    The chemical compound 5-methyluridine (symbol m 5 U or m5U), also called ribothymidine (rT) [footnote 1], is a pyrimidine nucleoside. It is the ribonucleoside counterpart to the deoxyribonucleoside thymidine, which lacks a hydroxyl group at the 2' position. 5-Methyluridine contains a thymine base joined to a ribose pentose sugar. [4] It is a ...

  9. Thymine dioxygenase - Wikipedia

    en.wikipedia.org/wiki/Thymine_dioxygenase

    In enzymology, a thymine dioxygenase (EC 1.14.11.6) is an enzyme that catalyzes the chemical reaction. thymine + 2-oxoglutarate + O 2 5-hydroxymethyluracil + succinate + CO 2. The 3 substrates of this enzyme are thymine, 2-oxoglutarate, and O 2, whereas its 3 products are 5-hydroxymethyluracil, succinate, and CO 2.