Covalent Modification of N3 of Guanine by (+)-CC-1065 Results in Protonation of the Cross-Strand Cytosine
- 1 January 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (3) , 629-630
- https://doi.org/10.1021/ja9632264
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Solution Structure of the Covalent Duocarmycin A-DNA Duplex ComplexJournal of Molecular Biology, 1995
- A Novel Property of Duocarmycin and Its Analogs for Covalent Reaction with DNAJournal of the American Chemical Society, 1994
- DNA interstrand cross-links induced by the cyclopropylpyrroloindole antitumor agent bizelesin are reversible upon exposure to alkaliBiochemistry, 1993
- Sequence-selective guanine reactivity by duocarmycin AChemical Research in Toxicology, 1993
- 5'-CGA sequence is a strong motif for homo base-paired parallel-stranded DNA duplex as revealed by NMR analysis.Proceedings of the National Academy of Sciences, 1993
- NMR structural studies of intramolecular (Y+)n.cntdot.(R+)n(Y-)n DNA triplexes in solution: imino and amino proton and nitrogen markers of G.cntdot.AT base triple formationBiochemistry, 1991
- Determination of the major tautomeric form of the covalently modified adenine in the (+)-CC-1065-DNA adduct by proton and nitrogen-15 NMR studiesBiochemistry, 1990
- NMR studies of DNA (R+)n.cntdot.(Y-)n.cntdot.(Y+)n triple helixes in solution: imino and amino proton markers of T.cntdot.A.cntdot.T and C.cntdot.G.cntdot.C+ base-triple formationBiochemistry, 1989
- Complementary base pairing and the origin of substitution mutationsNature, 1976
- Genetical Implications of the Structure of Deoxyribonucleic AcidNature, 1953