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Bioorg Med Chem Lett ; 16(4): 923-7, 2006 Feb 15.
Article in English | MEDLINE | ID: mdl-16300943

ABSTRACT

Helicases form an attractive protein family for drug discovery because they are involved in various human diseases. In this report, we show that it is possible to inhibit both the ATPase and the helicase activities of a DNA helicase with dibenzothiepins that bind at its nucleic acid binding site. These results suggest a drug discovery strategy to inhibit DNA helicases.


Subject(s)
DNA Helicases/antagonists & inhibitors , DNA/drug effects , Dibenzothiepins/pharmacology , Enzyme Inhibitors/pharmacology , Escherichia coli Proteins/antagonists & inhibitors , Adenosine Triphosphatases/antagonists & inhibitors , Binding Sites , Binding, Competitive/drug effects , Crystallography, X-Ray , DNA/chemistry , Dibenzothiepins/chemistry , Enzyme Inhibitors/chemistry , Escherichia coli/enzymology , Models, Molecular , Molecular Structure , Protein Conformation , Protein Structure, Tertiary , Structure-Activity Relationship
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