| Literature DB >> 27480935 |
Hanwool Yoon1, Arieh Warshel2.
Abstract
Understanding the origin of discrimination between rNTP and dNTP by DNA/RNA polymerases is important both for gaining fundamental knowledge on the corresponding systems and for advancing the design of specific drugs. This work explores the nature of this discrimination by systematic calculations of the transition state (TS) binding energy in RB69 DNA polymerase (gp43) and T7 RNA polymerase. The calculations reproduce the observed trend, in particular when they included the water contribution obtained by the water flooding approach. Our detailed study confirms the idea that the discrimination is due to the steric interaction between the 2'OH and Tyr416 in DNA polymerase, while the electrostatic interaction is the source of the discrimination in RNA polymerase. Proteins 2016; 84:1616-1624.Entities:
Keywords: DNA polymerase; RNA polymerase; enzyme catalysis; free energy perturbation; internal water in proteins; sugar selectivity
Mesh:
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Year: 2016 PMID: 27480935 PMCID: PMC5073073 DOI: 10.1002/prot.25104
Source DB: PubMed Journal: Proteins ISSN: 0887-3585