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Encyclopedia > Nucleobase

Chemical structure of adenine
Adenine
Download high resolution version (1163x1429, 7 KB) Wikipedia does not have an article with this exact name. ... Adenine is one of the two purine nucleobases used in forming nucleotides of the nucleic acids DNA and RNA. In DNA, adenine (A) binds to thymine (T) via two hydrogen bonds to assist in stabilizing the nucleic acid structures. ...


Chemical structure of guanine
Guanine
Download high resolution version (1724x1429, 9 KB) Wikipedia does not have an article with this exact name. ... Guanine is one of the five main nucleobases found in nucleic acids (, DNA and RNA). ...

 
Chemical structure of thymine
Thymine
Chemical structure of cytosine
Cytosine
Download high resolution version (1269x1363, 6 KB) Wikipedia does not have an article with this exact name. ... Thymine, also known as 5-methyluracil, is a pyrimidine nucleobase. ... Download high resolution version (1014x1357, 5 KB) Wikipedia does not have an article with this exact name. ... Cytosine is one of the 5 main nucleobases used in storing and transporting genetic information within a cell in the nucleic acids DNA and RNA. It is a pyrimidine derivative, with a heterocyclic aromatic ring and two substituents attached (an amine group at position 4 and a keto group at...

  Results from FactBites:
 
Purine Nucleobase Transport in Amastigotes of Leishmania mexicana: Involvement in Allopurinol Uptake -- Al-Salabi and ... (3977 words)
Purine Nucleobase Transport in Amastigotes of Leishmania mexicana: Involvement in Allopurinol Uptake
nucleobase transporter that is responsible for the uptake of
A Leishmania major nucleobase transporter responsible for allopurinol uptake is a functional homolog of the Trypanosoma brucei H2 transporter.
TSRI - News and Publications (663 words)
Alternatively, interaction with a cationic nucleobase might activate the 2´ oxyanion nucleophile, or the nucleobase could act as a general acid to protonate the leaving group during the breaking of 5´ oxygen-phosphorus bonds (Fig.
A cationic nucleobase should contribute electrostatic stabilization to the transition state for both cleavage and ligation reactions, because the transition state is identical in forward and reverse reactions.
In contrast, a nucleobase that contributes general acid catalysis to the cleavage reaction should contribute general base catalysis to ligation as the 5´ oxygen becomes the nucleophile and the 2´ oxygen becomes the leaving group.
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