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Title
Redesigning the leaving group in nucleic acid polymerization
Authors
Keywords
-
Journal
FEBS LETTERS
Volume 586, Issue 15, Pages 2049-2056
Publisher
Wiley
Online
2012-03-04
DOI
10.1016/j.febslet.2012.02.033
References
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Related references
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- (2010) Anne Giraut et al. CHEMBIOCHEM
- Iminodiacetic-phosphoramidates as metabolic prototypes for diversifying nucleic acid polymerization in vivo
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- 3-Phosphono-l-alanine as pyrophosphate mimic for DNA synthesis using HIV-1 reverse transcriptase
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- δ-Di-carboxybutyl phosphoramidate of 2′-deoxycytidine-5′-monophosphate as substrate for DNA polymerization by HIV-1 reverse transcriptase
- (2009) Ivan Zlatev et al. BIOORGANIC & MEDICINAL CHEMISTRY
- Phosphodiester Substrates for Incorporation of Nucleotides in DNA Using HIV-1 Reverse Transcriptase
- (2009) Anne Giraut et al. CHEMBIOCHEM
- Nucleic acid polymerases use a general acid for nucleotidyl transfer
- (2009) Christian Castro et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Enzymatically Catalyzed DNA Synthesis UsingL-Asp-dGMP,L-Asp-dCMP, andL-Asp-dTMP
- (2008) Montserrat Terrazas et al. CHEMISTRY & BIODIVERSITY
- Utilization of a Deoxynucleoside Diphosphate Substrate by HIV Reverse Transcriptase
- (2008) Scott J. Garforth et al. PLoS One
- A consensus view of DNA binding by the C family of replicative DNA polymerases
- (2008) M. H. Lamers et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- DNA Polymerase β Fidelity: Halomethylene-Modified Leaving Groups in Pre-Steady-State Kinetic Analysis Reveal Differences at the Chemical Transition State†
- (2007) Christopher A. Sucato et al. BIOCHEMISTRY
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