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