Why is the antiviral nucleotide analogue 9-[2-(phosphonomethoxy)ethyl]adenine in its diphosphorylated form (PMEApp4−) initially a better substrate for polymerases than (2′-deoxy)adenosine 5′-triphosphate (dATP4−/ATP4−)? Considerations on the mechanism ...

  • Helmut Sigel, Bin Song, Claudia A. Blindauer, Larisa E. Kapinos, Fridrich Gregáň, Nadja Prónayová
  • Chemical Communications, January 1999, Royal Society of Chemistry
  • DOI: 10.1039/a901233h

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http://dx.doi.org/10.1039/a901233h

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