scholarly journals Corrections for Amit et al., Direct observation of RuvAB-catalyzed branch migration of single Holliday junctions and Dawid et al., Single-molecule study of RuvAB-mediated Holliday-junction migration

2006 ◽  
Vol 103 (33) ◽  
pp. 12654-12654
2004 ◽  
Vol 44 (supplement) ◽  
pp. S134
Author(s):  
Y.-W. Han ◽  
T. Tani ◽  
M. Hayashi ◽  
T. Hishida ◽  
H. Iwasaki ◽  
...  

2008 ◽  
Vol 95 (9) ◽  
pp. 4372-4383 ◽  
Author(s):  
Mikhail A. Karymov ◽  
Mathivanan Chinnaraj ◽  
Aleksey Bogdanov ◽  
Annankoil R. Srinivasan ◽  
Guohui Zheng ◽  
...  

2018 ◽  
Vol 207 ◽  
pp. 251-265
Author(s):  
Subhas C. Bera ◽  
Tapas Paul ◽  
A. N. Sekar Iyengar ◽  
Padmaja P. Mishra

We have investigated the isomerization dynamics and plausible energy landscape of 4-way Holliday junctions (4WHJs) bound to integration host factor (IHF, a DNA binding protein), considering the effect of applied external force, by single-molecule FRET methods.


2005 ◽  
Vol 102 (23) ◽  
pp. 8186-8191 ◽  
Author(s):  
M. Karymov ◽  
D. Daniel ◽  
O. F. Sankey ◽  
Y. L. Lyubchenko

2019 ◽  
Author(s):  
Sujay Ray ◽  
Nibedita Pal ◽  
Nils G. Walter

AbstractHomologous recombination forms and resolves an entangled DNA Holliday Junction (HJ) critical for achieving genome repair. We use single-molecule observation and cluster analysis to probe how prototypic bacterial resolvase RuvC selects two of four possible HJ strands for cleavage. RuvC first exploits, then constrains intrinsic HJ isomer exchange and branch migration dynamics to direct cleavage toward only a desired, catalytically competent HJ conformation, thus controlling recombination products.


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