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- W2077953406 abstract "Inhibition constants (Kis) were used as an estimate of the ability of various nucleoside analogues to be recognized as substrates by the deoxythymidine kinases (dTKs) of a 5-methoxymethyldeoxyuridine-resistant (MMdUr) mutant of herpes simplex virus type 1 (HSV-1) and its parent wild-type (wt). It was found that the Kis for the 5-position analogues MMdU, [E]-5-(2-bromovinyl)deoxyuridine, bromodeoxyuridine and iododeoxyuridine were increased approximately three-to fivefold, suggesting that they were poorer substrates for the MMdUr dTK than for the wt dTK. With the 2' analogues arabinosylthymine and 2' fluoro 5-methylarabinosyluracil, however, the Kis were increased to a much greater extent, 80- and 240-fold, respectively. These findings suggest that the resistance of the mutant MMdUr to these analogues may be due to a mutation(s) in the viral dTK that directly affects binding at the 2' recognition site and indirectly at the 5, while still allowing substantial activity with the natural substrate deoxythymidine." @default.
- W2077953406 created "2016-06-24" @default.
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- W2077953406 date "1983-12-01" @default.
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- W2077953406 title "Alterations in the Recognition of Nucleoside Analogues as Substrates by the Deoxythymidine Kinase of a 5-Methoxymethyldeoxyuridine-resistant Mutant of Herpes Simplex Virus Type 1" @default.
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- W2077953406 doi "https://doi.org/10.1099/0022-1317-64-12-2767" @default.
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