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RecG and UvsW catalyse robust DNA rewinding critical for stalled DNA replication fork rescue.

Manosas M, Perumal SK, Bianco PR, Ritort F, Benkovic SJ, Croquette V.

Nat Commun. 2013;4:2368. doi: 10.1038/ncomms3368. Erratum in: Nat Commun. 2014;5:4210. Bianco, Piero [corrected to Bianco, Piero R].


Characterization of the ATPase activity of RecG and RuvAB proteins on model fork structures reveals insight into stalled DNA replication fork repair.

Abd Wahab S, Choi M, Bianco PR.

J Biol Chem. 2013 Sep 13;288(37):26397-409. doi: 10.1074/jbc.M113.500223. Epub 2013 Jul 27.


Direct observation of stalled fork restart via fork regression in the T4 replication system.

Manosas M, Perumal SK, Croquette V, Benkovic SJ.

Science. 2012 Nov 30;338(6111):1217-20. doi: 10.1126/science.1225437.


Regression of replication forks stalled by leading-strand template damage: I. Both RecG and RuvAB catalyze regression, but RuvC cleaves the holliday junctions formed by RecG preferentially.

Gupta S, Yeeles JT, Marians KJ.

J Biol Chem. 2014 Oct 10;289(41):28376-87. doi: 10.1074/jbc.M114.587881. Epub 2014 Aug 19.


Crystallographic and NMR analyses of UvsW and UvsW.1 from bacteriophage T4.

Kerr ID, Sivakolundu S, Li Z, Buchsbaum JC, Knox LA, Kriwacki R, White SW.

J Biol Chem. 2007 Nov 23;282(47):34392-400. Epub 2007 Sep 17.


The phage T4 protein UvsW drives Holliday junction branch migration.

Webb MR, Plank JL, Long DT, Hsieh TS, Kreuzer KN.

J Biol Chem. 2007 Nov 23;282(47):34401-11. Epub 2007 Sep 5.


Interaction of T4 UvsW helicase and single-stranded DNA binding protein gp32 through its carboxy-terminal acidic tail.

Perumal SK, Nelson SW, Benkovic SJ.

J Mol Biol. 2013 Aug 23;425(16):2823-39. doi: 10.1016/j.jmb.2013.05.012. Epub 2013 Jun 1.


Interplay between DNA replication, recombination and repair based on the structure of RecG helicase.

Briggs GS, Mahdi AA, Weller GR, Wen Q, Lloyd RG.

Philos Trans R Soc Lond B Biol Sci. 2004 Jan 29;359(1441):49-59. Review.


UvsX recombinase and Dda helicase rescue stalled bacteriophage T4 DNA replication forks in vitro.

Kadyrov FA, Drake JW.

J Biol Chem. 2004 Aug 20;279(34):35735-40. Epub 2004 Jun 11.


Resolving Holliday junctions with Escherichia coli UvrD helicase.

Carter AS, Tahmaseb K, Compton SA, Matson SW.

J Biol Chem. 2012 Mar 9;287(11):8126-34. doi: 10.1074/jbc.M111.314047. Epub 2012 Jan 20.


Fork regression is an active helicase-driven pathway in bacteriophage T4.

Long DT, Kreuzer KN.

EMBO Rep. 2009 Apr;10(4):394-9. doi: 10.1038/embor.2009.13. Epub 2009 Mar 6.


Genome stability and the processing of damaged replication forks by RecG.

McGlynn P, Lloyd RG.

Trends Genet. 2002 Aug;18(8):413-9. Review.


A step backward in advancing DNA replication: rescue of stalled replication forks by RecG.

Dillingham MS, Kowalczykowski SC.

Mol Cell. 2001 Oct;8(4):734-6.


RecG interacts directly with SSB: implications for stalled replication fork regression.

Buss JA, Kimura Y, Bianco PR.

Nucleic Acids Res. 2008 Dec;36(22):7029-42. doi: 10.1093/nar/gkn795. Epub 2008 Nov 5.


Characterisation of the catalytically active form of RecG helicase.

McGlynn P, Mahdi AA, Lloyd RG.

Nucleic Acids Res. 2000 Jun 15;28(12):2324-32.


Substrate-selective repair and restart of replication forks by DNA translocases.

B├ętous R, Couch FB, Mason AC, Eichman BF, Manosas M, Cortez D.

Cell Rep. 2013 Jun 27;3(6):1958-69. doi: 10.1016/j.celrep.2013.05.002. Epub 2013 Jun 6.


Control of helicase loading in the coupled DNA replication and recombination systems of bacteriophage T4.

Branagan AM, Klein JA, Jordan CS, Morrical SW.

J Biol Chem. 2014 Jan 31;289(5):3040-54. doi: 10.1074/jbc.M113.505842. Epub 2013 Dec 14.

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