Dynamics: the missing link between structure and function of the viral RNA-dependent RNA polymerase?

被引:38
|
作者
Cameron, Craig E. [1 ]
Moustafa, Ibrahim M. [1 ]
Arnold, Jamie J. [1 ]
机构
[1] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
关键词
STATE KINETIC-ANALYSIS; RIBONUCLEOTIDE INCORPORATION; NUCLEOTIDYL TRANSFER; FINGERS SUBDOMAIN; TRIGGER LOOP; O-HELIX; FIDELITY; MUTANT; REPLICATION; RNA-POLYMERASE-(3D(POL));
D O I
10.1016/j.sbi.2009.10.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The structural basis for nucleotide incorporation fidelity remains an open question for all nucleic acid polymerases. Addressing this question for the viral RNA-dependent RNA polymerase (RdRp) is of particular, practical significance because it is a determinant of sensitivity to antiviral nucleosides and may be a determinant of viral virulence. All polymerases are thought to employ the same catalytic mechanism, but the rate of nucleotide incorporation can vary substantially. Here we review some of the recent work with the RdRp that leads us to suggest that structure provides only a partial understanding of RdRp function and dynamics may be the missing link.
引用
收藏
页码:768 / 774
页数:7
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