D M Hovorun

Summary

Affiliation: National Academy of Sciences of Ukraine
Country: Ukraine

Publications

  1. ncbi request reprint The prototropic tautomerism of nitrogen bases: a new insight into the old problem
    D M Hovorun
    Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine, Kyiv
    Ukr Biokhim Zh 71:5-10. 1999
  2. ncbi request reprint Recognition modes of hypoxanthine, xanthine and their derivatives by amino acid carboxylic group: UV spectroscopic and quantum chemical data
    S P Samijlenko
    Institute of Molecular Biology and Genetics, NAS of Ukraine, Kyiv
    Ukr Biokhim Zh 73:61-71. 2001
  3. ncbi request reprint [Specific interactions of isoguanine with the neutral and deprotonated carboxylic group of amino acids: results of model quantum chemical calculations]
    S P Samiĭlenko
    Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine, Kyiv
    Ukr Biokhim Zh 73:147-51. 2001
  4. ncbi request reprint Specific interactions of deprotonated carboxylic group with uracil and thymine provoke diketo-->keto-enol tautomeric transition in bases
    S P Samijlenko
    Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine, Kyiv
    Ukr Biokhim Zh 73:128-31. 2001

Collaborators

  • S P Samijlenko
  • A L Potyahaylo
  • S P Samiĭlenko
  • A V Stepanyugin
  • M E Dzerzhyns'kyĭ
  • A L Potiahaĭlo
  • I M Kolomiets
  • A V Stepaniuhin
  • T V Bohdan
  • I V Kondratyuk

Detail Information

Publications4

  1. ncbi request reprint The prototropic tautomerism of nitrogen bases: a new insight into the old problem
    D M Hovorun
    Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine, Kyiv
    Ukr Biokhim Zh 71:5-10. 1999
    ..A biological significance of the data obtained, which are generalized and may be extended from the authors point of view to more wide range of objects, amino acids included...
  2. ncbi request reprint Recognition modes of hypoxanthine, xanthine and their derivatives by amino acid carboxylic group: UV spectroscopic and quantum chemical data
    S P Samijlenko
    Institute of Molecular Biology and Genetics, NAS of Ukraine, Kyiv
    Ukr Biokhim Zh 73:61-71. 2001
    ..Substitution of the C8H group by N in 8-azaXan does not change the interaction specificity of the base with two forms of carboxylic group...
  3. ncbi request reprint [Specific interactions of isoguanine with the neutral and deprotonated carboxylic group of amino acids: results of model quantum chemical calculations]
    S P Samiĭlenko
    Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine, Kyiv
    Ukr Biokhim Zh 73:147-51. 2001
    ..By contrast, the neutral carboxylic group forms the most stable complex with the ground-state isoGua tautomer N3HN9H...
  4. ncbi request reprint Specific interactions of deprotonated carboxylic group with uracil and thymine provoke diketo-->keto-enol tautomeric transition in bases
    S P Samijlenko
    Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine, Kyiv
    Ukr Biokhim Zh 73:128-31. 2001
    ....