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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
1990-12-13
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pubmed:abstractText |
The interaction of a new group of 'quinomycin-like' antibiotics with the DNA duplexes d(ACGT)2 and d(GACGTC)2 has been investigated in solution by 1H NMR spectroscopy. By monitoring the intensity of intranucleotide base H6/H8 to deoxyribose H1'NOE cross-peaks we conclude that the terminal A-T basepairs flanking the CG bisintercalation site in the d(ACGT)2 complex adopt the Hoogsteen bonding scheme, with the purine base in a syn conformation. By comparison in the d(GACGTC)2 complex all glycosidic bond angles are anti, consistent with a preferred Watson-Crick basepairing scheme. Both DNA duplexes appear to be significantly unwound compared with the ligand-free DNAs. The data illustrate the influence of helical constraints on the stability of the Hoogsteen bonding scheme adjacent to the drug binding sites.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0014-5793
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
272
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
171-4
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:2226828-Anti-Bacterial Agents,
pubmed-meshheading:2226828-Base Composition,
pubmed-meshheading:2226828-Base Sequence,
pubmed-meshheading:2226828-Binding Sites,
pubmed-meshheading:2226828-Chemistry, Physical,
pubmed-meshheading:2226828-DNA,
pubmed-meshheading:2226828-Echinomycin,
pubmed-meshheading:2226828-Magnetic Resonance Spectroscopy,
pubmed-meshheading:2226828-Molecular Sequence Data,
pubmed-meshheading:2226828-Molecular Structure,
pubmed-meshheading:2226828-Nucleic Acid Conformation,
pubmed-meshheading:2226828-Physicochemical Phenomena
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pubmed:year |
1990
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pubmed:articleTitle |
Hoogsteen versus Watson-Crick A-T basepairing in DNA complexes of a new group of 'quinomycin-like' antibiotics.
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pubmed:affiliation |
Peter MacCallum Cancer Institute NMR Facility, Victorian College of Pharmacy, Parkville, Australia.
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pubmed:publicationType |
Journal Article,
Comparative Study
|