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Adenine-thymine interactions

Another pyrimidine base, uracil, is found in RNA instead of thymine. Base pairing between adenine and uracil involves two hydrogen bonds and resembles the adenine-thymine interaction. This type of base pairing is of importance in transcription, the synthesis of messenger RNA (see Section 14.2.5). [Pg.51]

Fig. 74 Selective binding and detachment of a PS-polymer via adenine/thymine interaction to/from a SAM surface. Reprinted with permission from [247]... Fig. 74 Selective binding and detachment of a PS-polymer via adenine/thymine interaction to/from a SAM surface. Reprinted with permission from [247]...
As found for other stacked base pairs, in the stacked thymine-thymine pair changes in the interaction energy upon rotation of one thymine unit are almost completely compensated for by solvation effects [99JPC(B)884]. The adenine-thymine (A-T) base pair, which possesses a significant degree of conformational... [Pg.52]

Adsorption of adenine and coadsorption of adenine-thymine and uracil-thymine on Au(lll) has been reported [300]. Adenine was chemisorbed in two different states. Mutual interaction between adenine and thymine was detectable only at... [Pg.873]

M. Isaacson, Interaction of 25keV electrons with the nucleic acid bases, Adenine, Thymine, Uracil. II. Inner shell excitation and inelastic scattering cross sections, J. Chem. Phys. 56 (1972) 1813. [Pg.378]

The BFPT process may take place whenever an excess electron is attached to a nucleobase interacting with a proton donor. In particular, the role of a proton donor could be filled by another nucleobase. Especially interesting are complementary base pairs, AT and GC, since these systems appear in DNA. In the case of the adenine-thymine base pair (AT), a combination of three proton donor and acceptor pairs of adenine with three proton donor and acceptor pairs of thymine leads to nine possible, planar, cyclic H-bonded complexes (see Figure 21-22 [49]). [Pg.646]

Considerable attention has also been devoted by several investigators to the theoretical study of the potential curves for hydrogen bonds of the guanine-cytosine and adenine-thymine base pairs. An accurate representation of this potential is important because the genetic code is contained in this interaction. Lowdin has suggested that mutations may be a result of a shift in position of the hydrogen bond protons in the base units of DNA via proton tunneling. " The idea of proton... [Pg.271]

Yet another effect of the action of Ag" has been described, namely, its interaction with nucleic acids [112]. The Ag" ion interacts preferentially with the bases found in DNA rather than with the phosphate group [113-118]. The reaction between Ag and a GC (guanine-cytosine) base pair proceeds via two steps, whereas that between Ag" and an AT (adenine-thymine) base pair requires only one step [116], Ag appears to be attached to the N atom... [Pg.362]

A wide assortment of different possible geometries for the uracil dimer were examined [127] in 1998. The most stable of all these contained a pair of NH- -O bonds, but another was identified, only slightly less stable than the others, in which one of these conventional H-bonds was replaced by CH- -O = C. There was no way of estimating the energetic contribution of this particular interaction, as it was secondary to the stronger NH- -O bond. A study of the adenine thymine pair [128] noted a blue shift of the C-H stretching frequency, an indication of a H-bond, but the authors did not attempt to extract an interaction energy. [Pg.272]


See other pages where Adenine-thymine interactions is mentioned: [Pg.19]    [Pg.74]    [Pg.19]    [Pg.74]    [Pg.64]    [Pg.579]    [Pg.64]    [Pg.212]    [Pg.659]    [Pg.68]    [Pg.1202]    [Pg.48]    [Pg.271]    [Pg.979]    [Pg.73]    [Pg.22]    [Pg.399]    [Pg.391]    [Pg.391]    [Pg.410]    [Pg.5]    [Pg.7]    [Pg.541]    [Pg.179]    [Pg.239]    [Pg.203]    [Pg.139]    [Pg.211]    [Pg.212]    [Pg.596]    [Pg.53]    [Pg.1625]    [Pg.189]    [Pg.303]    [Pg.189]    [Pg.541]    [Pg.5]    [Pg.287]    [Pg.17]    [Pg.25]    [Pg.136]   
See also in sourсe #XX -- [ Pg.91 ]

See also in sourсe #XX -- [ Pg.91 ]




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