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Why is the antiviral nucleotide analogue 9-[2-(phosphonomethoxy)ethyl]adenine in its diphosphorylated form (PMEApp(4-)) initially a better substrate for polymerases than (2 '-deoxy)adenosine 5 '-triphosphate (dATP(4-)/ATP(4-))? Considerations on the mechanism of nucleic acid polymerases
Title Why is the antiviral nucleotide analogue 9-[2-(phosphonomethoxy)ethyl]adenine in its diphosphorylated form (PMEApp(4-)) initially a better substrate for polymerases than (2 '-deoxy)adenosine 5 '-triphosphate (dATP(4-)/ATP(4-))? Considerations on the mechanism of nucleic acid polymerases Author info Helmut Sigel ... [et al.] Author Sigel Helmut (20%)
Co-authors Song Bin (16%)
Blindauer Claudia A. (16%)
Kapinos Larisa E. (16%)
Gregáň Fridrich 1944- (16%) UMBFP08 - Katedra chémie
Prónayová Nadja (16%)
Source document Chemical Communications. No. 8 (1999), pp. 743-744. - Cambridge : The Royal Society of Chemistry, 1999 Keywords metal ion complexes aqueous solution derivatives hydrolysis Language English Country Great Britian systematics 54 Public work category ADC No. of Archival Copy 26159 Repercussion category EVANS, Bradley S. - ZHAO, Changming - GAO, Jiangtao et al. Discovery of the antibiotic phosacetamycin via a new mass spectrometry-based method for phosphonic acid detection. In ACS chemical biology. ISSN 1554-8929, 2013, vol. 8, no. 5, pp. 908-913.
GUO, Y.H. - GE, Q.C. - LIN, H.K. et al. The role of copper(II) ion in regulating H-bonding and coulombic interactions in copper(II)/tripod/polyphosphate systems. In Transition metal chemistry. ISSN 0340-4285, 2003, vol. 28, no. 6, pp. 609-615.
Catal.org. BB301 - Univerzitná knižnica Univerzity Mateja Bela v Banskej Bystrici Database xpca - PUBLIKAČNÁ ČINNOSŤ References PERIODIKÁ-Súborný záznam periodika 
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Number of the records: 1