Formation of S-[2-(N6-Deoxyadenosinyl)ethyl]glutathione in DNA and Replication Past the Adduct by Translesion DNA Polymerases
Author:
Affiliation:
1. Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0146, United States
Funder
National Institute of Environmental Health Sciences
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Toxicology,General Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.chemrestox.7b00022
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1. Enzymatic bypass of an N6-deoxyadenosine DNA–ethylene dibromide–peptide cross-link by translesion DNA polymerases;Journal of Biological Chemistry;2021-01
2. Protective Role of Glutathione against Peroxynitrite-Mediated DNA Damage During Acute Inflammation;Chemical Research in Toxicology;2020-09-07
3. The abundant DNA adduct N7-methyl deoxyguanosine contributes to miscoding during replication by human DNA polymerase η;Journal of Biological Chemistry;2019-06
4. Human Y-Family DNA Polymerase κ Is More Tolerant to Changes in Its Active Site Loop than Its Ortholog Escherichia coli DinB;Chemical Research in Toxicology;2017-08-19
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