Abstract
Background: The two-metal-ion mechanism of the nucleotidyl transfer reaction by RNA/DNA polymerases has not been adequately elucidated due to lack of temporal resolution. Results: Soak-trigger-freeze x-ray crystallography revealed structures of natural, time-resolved intermediates of transcript initiation. Conclusion: First structural evidence shows that catalytic metal binds after the nucleotide and nucleotide-binding metal and right before reaction chemistry. Significance: Time-dependent soak-trigger-freeze x-ray crystallography can yield functionally relevant high resolution information to study enzyme reactions. © 2013 by The American Society for Biochemistry and Molecular Biology, Inc.
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CITATION STYLE
Basu, R. S., & Murakami, K. S. (2013). Watching the bacteriophage N4 RNA polymerase transcription by time-dependent soak-trigger-freeze x-ray crystallography. Journal of Biological Chemistry, 288(5), 3305–3311. https://doi.org/10.1074/jbc.M112.387712
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