Branch migration during homologous recombination: assembly of a RuvAB-holliday junction complex in vitro
Author:
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology
Reference27 articles.
1. Nucleotide sequencing of the ruv region of E. coli K-12 reveals a LexA regulated operon encoding two genes;Benson;Nucl. Acids Res.,1988
2. Evidence of abortive recombination in ruv mutants of Escherichia coli K-12;Benson;Mol. Gen. Genet.,1991
3. Overproduction, purification, and ATPase activity of the Escherichia coli RuvB protein involved in DNA repair;Iwasaki;J. Bacteriol.,1989
4. Escherichia coli RuvA and RuvB proteins specifically interact with Holliday junctions and promote branch migration;Iwasaki;Genes Dev.,1992
5. Sliding clamps of DNA polymerases;Kuriyan;J. Mol. Biol.,1993
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1. Facilitating stable gene integration expression and copy number amplification in Bacillus subtilis through a reversible homologous recombination switch;Synthetic and Systems Biotechnology;2024-09
2. Mechanism of AAA+ ATPase-mediated RuvAB–Holliday junction branch migration;Nature;2022-08-24
3. DisA Restrains the Processing and Cleavage of Reversed Replication Forks by the RuvAB-RecU Resolvasome;International Journal of Molecular Sciences;2021-10-20
4. Biochemical and structural characterization of the Holliday junction resolvase RuvC from Pseudomonas aeruginosa;Biochemical and Biophysical Research Communications;2020-04
5. Homologous Recombination under the Single-Molecule Fluorescence Microscope;International Journal of Molecular Sciences;2019-12-03
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