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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
Názov 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 Aut.údaje Helmut Sigel ... [et al.] Autor Sigel Helmut (20%)
Spoluautori Song Bin (16%)
Blindauer Claudia A. (16%)
Kapinos Larisa E. (16%)
Gregáň Fridrich 1944- (16%) UMBFP08 - Katedra chémie
Prónayová Nadja (16%)
Zdroj.dok. Chemical Communications. No. 8 (1999), pp. 743-744. - Cambridge : The Royal Society of Chemistry, 1999 Kľúč.slová metal ion complexes aqueous solution derivatives hydrolysis Jazyk dok. angličtina Krajina Veľká Británia Systematika 54 Kategória publikačnej činnosti ADC Číslo archívnej kópie 26159 Kategória ohlasu 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.
Katal.org. BB301 - Univerzitná knižnica Univerzity Mateja Bela v Banskej Bystrici Báza dát xpca - PUBLIKAČNÁ ČINNOSŤ Odkazy PERIODIKÁ-Súborný záznam periodika nerozpoznaný
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