I came to a fork in the DNA and there was RecG
Author:
Funder
NIH
Publisher
Elsevier BV
Subject
Molecular Biology,Biophysics
Reference64 articles.
1. Characterization of the ATPase activity of RecG and RuvAB proteins on model fork structures reveals insight into stalled DNA replication fork repair;Abd Wahab;J. Biol. Chem.,2013
2. Escherichia coli CreBC is a global regulator of gene expression that responds to growth in minimal media;Avison;J. Biol. Chem.,2001
3. RuvAB is essential for replication forks reversal in certain replication mutants;Baharoglu;EMBO J.,2006
4. Resolution of Holliday junctions by RuvC resolvase: cleavage specificity and DNA distortion;Bennett;Cell,1993
5. DNA binding by the substrate specificity (wedge) domain of RecG helicase suggests a role in processivity;Briggs;J. Biol. Chem.,2005
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1. Revealing the DNA Unwinding Activity and Mechanism of Fork Reversal by RecG While Exposed to Variants of Stalled Replication-fork at Single-Molecular Resolution;Journal of Molecular Biology;2022-11
2. The Biochemical Mechanism of Fork Regression in Prokaryotes and Eukaryotes—A Single Molecule Comparison;International Journal of Molecular Sciences;2022-08-03
3. Revealing the DNA Unwinding Activity and Mechanism of Fork Reversal by Recg While Exposed to Variants of Stalled Replication-Fork at Single-Molecular Resolution;SSRN Electronic Journal;2022
4. Single Molecule Analysis of differential functional mechanisms of MtRecG while being exposed to variants of stalled replication-fork;2021-12-11
5. Insight into the biochemical mechanism of DNA helicases provided by bulk-phase and single-molecule assays;Methods;2021-12
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