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Items: 1 to 20 of 119

1.

Structural basis for translocation by AddAB helicase-nuclease and its arrest at χ sites.

Krajewski WW, Fu X, Wilkinson M, Cronin NB, Dillingham MS, Wigley DB.

Nature. 2014 Apr 17;508(7496):416-9. doi: 10.1038/nature13037. Epub 2014 Mar 16.

2.

Insights into Chi recognition from the structure of an AddAB-type helicase-nuclease complex.

Saikrishnan K, Yeeles JT, Gilhooly NS, Krajewski WW, Dillingham MS, Wigley DB.

EMBO J. 2012 Mar 21;31(6):1568-78. doi: 10.1038/emboj.2012.9. Epub 2012 Feb 3.

3.

The Bacillus subtilis AddAB helicase/nuclease is regulated by its cognate Chi sequence in vitro.

Chédin F, Ehrlich SD, Kowalczykowski SC.

J Mol Biol. 2000 Apr 21;298(1):7-20.

PMID:
10756102
4.

The AddAB helicase/nuclease forms a stable complex with its cognate chi sequence during translocation.

Chédin F, Handa N, Dillingham MS, Kowalczykowski SC.

J Biol Chem. 2006 Jul 7;281(27):18610-7. Epub 2006 Apr 21.

5.

Recombination hotspots and single-stranded DNA binding proteins couple DNA translocation to DNA unwinding by the AddAB helicase-nuclease.

Yeeles JT, van Aelst K, Dillingham MS, Moreno-Herrero F.

Mol Cell. 2011 Jun 24;42(6):806-16. doi: 10.1016/j.molcel.2011.04.012.

6.

Recombination hotspots attenuate the coupled ATPase and translocase activities of an AddAB-type helicase-nuclease.

Gilhooly NS, Dillingham MS.

Nucleic Acids Res. 2014 May;42(9):5633-43. doi: 10.1093/nar/gku188. Epub 2014 Mar 15.

7.

Structural features of Chi recognition in AddAB with implications for RecBCD.

Wilkinson M, Wigley DB.

Cell Cycle. 2014;13(18):2812-20. doi: 10.4161/15384101.2014.950892.

8.
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10.

The AddAB helicase-nuclease catalyses rapid and processive DNA unwinding using a single Superfamily 1A motor domain.

Yeeles JT, Gwynn EJ, Webb MR, Dillingham MS.

Nucleic Acids Res. 2011 Mar;39(6):2271-85. doi: 10.1093/nar/gkq1124. Epub 2010 Nov 10.

11.

Role of enzymes of homologous recombination in illegitimate plasmid recombination in Bacillus subtilis.

Meima R, Haijema BJ, Dijkstra H, Haan GJ, Venema G, Bron S.

J Bacteriol. 1997 Feb;179(4):1219-29.

12.

Single-molecule imaging of Bacteroides fragilis AddAB reveals the highly processive translocation of a single motor helicase.

Reuter M, Parry F, Dryden DT, Blakely GW.

Nucleic Acids Res. 2010 Jun;38(11):3721-31. doi: 10.1093/nar/gkq100. Epub 2010 Feb 25.

13.

An iron-sulfur cluster is essential for the binding of broken DNA by AddAB-type helicase-nucleases.

Yeeles JT, Cammack R, Dillingham MS.

J Biol Chem. 2009 Mar 20;284(12):7746-55. doi: 10.1074/jbc.M808526200. Epub 2009 Jan 7.

14.

A dual-nuclease mechanism for DNA break processing by AddAB-type helicase-nucleases.

Yeeles JT, Dillingham MS.

J Mol Biol. 2007 Aug 3;371(1):66-78. Epub 2007 May 25.

PMID:
17570399
15.

Dual nuclease and helicase activities of Helicobacter pylori AddAB are required for DNA repair, recombination, and mouse infectivity.

Amundsen SK, Fero J, Salama NR, Smith GR.

J Biol Chem. 2009 Jun 19;284(25):16759-66. doi: 10.1074/jbc.M109.005587. Epub 2009 Apr 24.

16.

Crystal structure of RecBCD enzyme reveals a machine for processing DNA breaks.

Singleton MR, Dillingham MS, Gaudier M, Kowalczykowski SC, Wigley DB.

Nature. 2004 Nov 11;432(7014):187-93.

PMID:
15538360
18.

Translocation by the RecB motor is an absolute requirement for {chi}-recognition and RecA protein loading by RecBCD enzyme.

Spies M, Dillingham MS, Kowalczykowski SC.

J Biol Chem. 2005 Nov 4;280(44):37078-87. Epub 2005 Jul 22.

19.

Uncoupling DNA translocation and helicase activity in PcrA: direct evidence for an active mechanism.

Soultanas P, Dillingham MS, Wiley P, Webb MR, Wigley DB.

EMBO J. 2000 Jul 17;19(14):3799-810.

20.

A single mutation, RecB(D1080A,) eliminates RecA protein loading but not Chi recognition by RecBCD enzyme.

Anderson DG, Churchill JJ, Kowalczykowski SC.

J Biol Chem. 1999 Sep 17;274(38):27139-44.

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