Source:http://linkedlifedata.com/resource/pubmed/id/18802636
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
18
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pubmed:dateCreated |
2008-9-19
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pubmed:abstractText |
The role of local geometric and stereo-electronic effects in tuning the preference for different cross-linked adducts between thymine and purinic bases has been analyzed by a computational approach rooted in density functional theory. Our study points out that G--T and T--G tandem lesions are produced according to the same mechanism as A--T and T--A intrastrand adducts, and in both cases purine--T adducts are preferred rather than the opposite sequences. Moreover, use of conceptual DFT tools allows the rationalization of the preferential occurrence of G--T and T--G tandem lesions in place of their A--T and T--A counterparts.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1477-0539
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
21
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3300-5
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pubmed:meshHeading |
pubmed-meshheading:18802636-Electrons,
pubmed-meshheading:18802636-Gases,
pubmed-meshheading:18802636-Guanine,
pubmed-meshheading:18802636-Hydroxyl Radical,
pubmed-meshheading:18802636-Kinetics,
pubmed-meshheading:18802636-Models, Molecular,
pubmed-meshheading:18802636-Molecular Structure,
pubmed-meshheading:18802636-Oxidation-Reduction,
pubmed-meshheading:18802636-Thermodynamics,
pubmed-meshheading:18802636-Thymine
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pubmed:year |
2008
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pubmed:articleTitle |
Formation of cross-linked adducts between guanine and thymine mediated by hydroxyl radical and one-electron oxidation: a theoretical study.
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pubmed:affiliation |
Laboratoire Lésions des Acides Nucléiques, INAC/SCIB, UMR-E 3 (CEA/UJF), CEA-Grenoble, 17 rue des Martyrs, 38054, Grenoble cedex 9, France.
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pubmed:publicationType |
Journal Article
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