Enzymatic bypass and the structural basis of miscoding opposite the DNA adduct 1,N2-ethenodeoxyguanosine by human DNA translesion polymerase η
Author:
Funder
National Cancer Institute
National Institute of Environmental Health Sciences
Vanderbilt-Ingram Cancer Center
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
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5. Formation of 1,N2- and N2,3-ethenoguanine derivatives from 2-halooxiranes: Isotopic labeling studies and formation of a hemiaminal derivative of N2-(2-oxoethyl)guanine;Guengerich;Chem. Res. Toxicol.,1993
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