Correlation between sequence-dependent glycosylase repair and the thermal stability of oligonucleotide duplexes containing 1, N6-ethenoadenine (Q46639357)

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scientific article published in December 1998

Language	Label	Description	Also known as
English	Correlation between sequence-dependent glycosylase repair and the thermal stability of oligonucleotide duplexes containing 1, N6-ethenoadenine	scientific article published in December 1998

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scholarly article

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

Correlation between sequence-dependent glycosylase repair and the thermal stability of oligonucleotide duplexes containing 1, N6-ethenoadenine (English)

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

author name string

Hang B

1

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

Sági J

2

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

Singer B

3

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

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publication date

1 December 1998

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

Journal of Biological Chemistry

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

273

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

50

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Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

33406-33413

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

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Sequence specificity of guanine alkylation and repair.

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Splicing mutations in the CHO DHFR gene preferentially induced by (+/-)-3 alpha,4 beta-dihydroxy-1 alpha,2 alpha-epoxy-1,2,3,4- tetrahydrobenzo[c]phenanthrene

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Effect of 3' flanking neighbors on kinetics of pairing of dCTP or dTTP opposite O6-methylguanine in a defined primed oligonucleotide when Escherichia coli DNA polymerase I is used

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Sequence context is an important determinant in the mutagenic potential of 1,N6-ethenodeoxyadenosine (epsilonA): formation of epsilonA basepairs and elongation in defined templates

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Base analog and neighboring base effects on substrate specificity of recombinant human G:T mismatch-specific thymine DNA-glycosylase.

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Sequence-dependent modulation of nucleotide excision repair: the efficiency of the incision reaction is inversely correlated with the stability of the pre-incision UvrB-DNA complex

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Differential cleavage of oligonucleotides containing the benzene-derived adduct, 1,N6-benzetheno-dA, by the major human AP endonuclease HAP1 and Escherichia coli exonuclease III and endonuclease IV.

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Predicting DNA duplex stability from the base sequence

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21 January 2018

Comparison between DNA melting thermodynamics and DNA polymerase fidelity

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21 January 2018

DNA Repair Enzymes

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21 January 2018

Both purified human 1,N6-ethenoadenine-binding protein and purified human 3-methyladenine-DNA glycosylase act on 1,N6-ethenoadenine and 3-methyladenine

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Escherichia coli, Saccharomyces cerevisiae, rat and human 3-methyladenine DNA glycosylases repair 1,N6-ethenoadenine when present in DNA

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Targeted deletion of alkylpurine-DNA-N-glycosylase in mice eliminates repair of 1,N6-ethenoadenine and hypoxanthine but not of 3,N4-ethenocytosine or 8-oxoguanine

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Assessment of mutagenic efficiency of two carcinogen-modified nucleosides, 1,N6-ethenodeoxyadenosine and O4-methyldeoxythymidine, using polymerases of varying fidelity

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Mutagenic and genotoxic effects of three vinyl chloride-induced DNA lesions: 1,N6-ethenoadenine, 3,N4-ethenocytosine, and 4-amino-5-(imidazol-2-yl)imidazole.

1 reference

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1,N6-ethenodeoxyadenosine, a DNA adduct highly mutagenic in mammalian cells

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Endogenous DNA adducts: potential and paradox

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Purification and characterization of human 3-methyladenine-DNA glycosylase

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Purification and biochemical characterization of recombinant N-methylpurine-DNA glycosylase of the mouse.

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Structure, dynamics, and thermodynamics of mismatched DNA oligonucleotide duplexes d(CCCAGGG)2 and d(CCCTGGG)2.

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Human cells contain protein specifically binding to a single 1,N6-ethenoadenine in a DNA fragment

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Evidence for a common active site for cleavage of an AP site and the benzene-derived exocyclic adduct, 3,N4-benzetheno-dC, in the major human AP endonuclease

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NMR studies of the exocyclic 1,N6-ethenodeoxyadenosine adduct (epsilon dA) opposite thymidine in a DNA duplex. Nonplanar alignment of epsilon dA(anti) and dT(anti) at the lesion site

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Nearest neighbor thermodynamic parameters for internal G.A mismatches in DNA

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Effect of mismatched complementary strands and 5'-change in sequence context on the thermodynamics and structure of benzo[a]pyrene-modified oligonucleotides

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Kinetics of repair of O6-methylguanine in dna by O6-methylguanine-DNA methyltransferase in vitro and in vivo

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Conformational properties of the G.G mismatch in d(CGCGAATTGGCG)2 determined by NMR

1 reference

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Solution conformation of a deoxynucleotide containing tandem G.A mismatched base pairs and 3'-overhanging ends in d(GTGAACTT)2

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Thermodynamics of nonsymmetric tandem mismatches adjacent to G.C base pairs in RNA

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Identifiers

10.1074/JBC.273.50.33406

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/9837917

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