Identification by UV resonance Raman spectroscopy of an imino tautomer of 5-hydroxy-2'-deoxycytidine, a powerful base analog transition mutagen with a much higher unfavored tautomer frequency than that of the natural residue 2'-deoxycytidine-Reference-Cited by-同舟云学术

Identification by UV resonance Raman spectroscopy of an imino tautomer of 5-hydroxy-2'-deoxycytidine, a powerful base analog transition mutagen with a much higher unfavored tautomer frequency than that of the natural residue 2'-deoxycytidine

Published:1999-04-13 Issue:8 Volume:96 Page:4500-4505
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Suen W.,Spiro T. G.,Sowers L. C.,Fresco J. R.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference25 articles.

1. Genetical Implications of the Structure of Deoxyribonucleic Acid

2. Complementary base pairing and the origin of substitution mutations

3. Tautomerism of purines. I. N(7)H .dha. N(9)H equilibrium in adenine

4. Quantum-Mechanical Prediction of Tautomeric Equilibria

5. Mutation spectrum of copper-induced DNA damage.

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