Dual Specificity of the Pyrimidine Analogue, 4-Methylpyridin-2-one, in DNA Replication
- 1 June 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (25), 6118-6119
- https://doi.org/10.1021/ja993291o
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- A specific partner for abasic damage in DNANature, 1999
- Minor Groove Interactions between Polymerase and DNA: More Essential to Replication than Watson−Crick Hydrogen Bonds?Journal of the American Chemical Society, 1999
- Efficient replication between non-hydrogen-bonded nucleoside shape analogsNature Structural & Molecular Biology, 1998
- A thymidine triphosphate shape analog lacking Watson–Crick pairing ability is replicated with high sequence selectivityProceedings of the National Academy of Sciences, 1997
- Difluorotoluene, a Nonpolar Isostere for Thymine, Codes Specifically and Efficiently for Adenine in DNA ReplicationJournal of the American Chemical Society, 1997
- Recognition by viral and cellular DNA polymerases of nucleosides bearing bases with nonstandard hydrogen bonding patterns.Proceedings of the National Academy of Sciences, 1995
- Enzymic recognition of the base pair between isocytidine and isoguanosineBiochemistry, 1993
- Enzymatic incorporation of a new base pair into DNA and RNA extends the genetic alphabetNature, 1990
- Enzymatic incorporation of a new base pair into DNA and RNAJournal of the American Chemical Society, 1989
- An unusual base pairing between pyrimidine and pyridine nucleotidesNucleic Acids Research, 1986