An ab initio quantum chemistry study on N-glycosidic bond stabilities of hydroxyl radical modified guanosine analogs
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry
Reference23 articles.
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1. The activation of N-glycosidic bond cleavage performed by base-excision repair enzyme hOGG1; theoretical study of the role of Lys 249 residue in activation of G, OxoG and FapyG;RSC Adv.;2014
2. Theoretical study of the pre- and post-translational effects of adenine and thymine tautomers and methyl derivatives;Journal of Molecular Modeling;2013-05-31
3. Pyramidalization of the Glycosidic Nitrogen Provides the Way for Efficient Cleavage of the N-Glycosidic Bond of 8-OxoG with the hOGG1 DNA Repair Protein;The Journal of Physical Chemistry B;2012-10-09
4. Oligonucleotide Incorporation and Base Pair Stability of 9-Deaza-2′-deoxyguanosine, an Analogue of 8-Oxo-2′-deoxyguanosine;The Journal of Organic Chemistry;2010-07-29
5. The effect of oxidation on the stability of G:C base pair: a MP2 study;Structural Chemistry;2010-06-15
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