O6-Methylguanine in place of guanine causes asymmetric single-strand cleavage of DNA by some restriction enzymes
Author:
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi00458a039
Reference27 articles.
1. Use of short synthetic DNA duplexes as substrates for the restriction endonucleases Hpa II and Mno I.
2. The effects of substituted pyrimidines in DNAs on cleavage by sequence-specific endonucleases
3. Effect of nucleotide analogs on the cleavage of DNA by the restriction enzymes AluI, DdeI, HinfI, RsaI, and TaqI.
4. A study of side reactions occurring during synthesis of oligodeoxynucleotides containing O6-alkyldeoxyguanosine residues at preselected sites
5. The effects of base analogue substitutions on the cleavage by the EcoRI restriction endonuclease of octadeoxyribonucleotides containing modified EcoRI recognition sequences.
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1. Repair of O6-methylguanine adducts in human telomeric G-quadruplex DNA by O6-alkylguanine-DNA alkyltransferase;Nucleic Acids Research;2014-07-30
2. Lesion-specific DNA-binding and repair activities of human O6-alkylguanine DNA alkyltransferase;Nucleic Acids Research;2012-07-18
3. Cooperative cluster formation, DNA bending and base-flipping by O 6 -alkylguanine-DNA alkyltransferase;Nucleic Acids Research;2012-06-21
4. 6-Carboxyfluorescein and structurally similar molecules inhibit DNA binding and repair by O6-alkylguanine DNA alkyltransferase;DNA Repair;2011-12
5. Interactions of the Human T-cell Leukemia Virus Type-II Integrase with the Conserved CA in the Retroviral Long Terminal Repeat End;Journal of Biological Chemistry;2001-01
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