Summary information and primary citation
- PDB-id
-
5yv0;
DSSR-derived features in text and
JSON formats
- Class
- DNA binding protein-DNA
- Method
- X-ray (2.09 Å)
- Summary
- DNA polymerase iv - DNA ternary complex 12
- Reference
-
Kottur J, Nair DT (2018): "Pyrophosphate
hydrolysis is an intrinsic and critical step of the DNA
synthesis reaction." Nucleic Acids Res.,
46, 5875-5885. doi: 10.1093/nar/gky402.
- Abstract
- DNA synthesis by DNA polymerases (dPols) is central to
duplication and maintenance of the genome in all living
organisms. dPols catalyze the formation of a phosphodiester
bond between the incoming deoxynucleoside triphosphate and
the terminal primer nucleotide with the release of a
pyrophosphate (PPi) group. It is believed that formation of
the phosphodiester bond is an endergonic reaction and PPi
has to be hydrolyzed by accompanying pyrophosphatase
enzymes to ensure that the free energy change of the DNA
synthesis reaction is negative and it can proceed in the
forward direction. The fact that DNA synthesis proceeds in
vitro in the absence of pyrophosphatases represents a
long-standing conundrum regarding the thermodynamics of the
DNA synthesis reaction. Using time-resolved
crystallography, we show that hydrolysis of PPi is an
intrinsic and critical step of the DNA synthesis reaction
catalyzed by dPols. The hydrolysis of PPi occurs after the
formation of the phosphodiester bond and ensures that the
DNA synthesis reaction is energetically favorable without
the need for additional enzymes. Also, we observe that DNA
synthesis is a two Mg2+ ion assisted stepwise associative
SN2 reaction. Overall, this study provides deep temporal
insight regarding the primary enzymatic reaction
responsible for genome duplication.