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Drug-nucleic acid interactions: conformational flexibility at the intercalation site.

The conformational features of the intercalation site in polynucleotides were examined. We found that, for all the crystal structures of drug-dinucleoside complexes studied thus far, two torsion angles differ from those found in A RNA (phi and chi) and that alternate sugar puckering is not a prerequ...

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Publicat a:Proc Natl Acad Sci U S A
Autors principals: Berman, H M, Neidle, S, Stodola, R K
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 1978
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Accés en línia:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC411350/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/273246/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.75.2.828
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