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== Function == | == Function == | ||
[[http://www.uniprot.org/uniprot/XERH_HELPY XERH_HELPY]] Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. Involved in chromosome segregation. May contribute to chromosome decatenation.<ref>PMID:22511919</ref> | [[http://www.uniprot.org/uniprot/XERH_HELPY XERH_HELPY]] Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. Involved in chromosome segregation. May contribute to chromosome decatenation.<ref>PMID:22511919</ref> | ||
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== Publication Abstract from PubMed == | |||
Bacterial Xer site-specific recombinases play an essential genome maintenance role by unlinking chromosome multimers, but their mechanism of action has remained structurally uncharacterized. Here, we present two high-resolution structures of Helicobacter pylori XerH with its recombination site DNA difH, representing pre-cleavage and post-cleavage synaptic intermediates in the recombination pathway. The structures reveal that activation of DNA strand cleavage and rejoining involves large conformational changes and DNA bending, suggesting how interaction with the cell division protein FtsK may license recombination at the septum. Together with biochemical and in vivo analysis, our structures also reveal how a small sequence asymmetry in difH defines protein conformation in the synaptic complex and orchestrates the order of DNA strand exchanges. Our results provide insights into the catalytic mechanism of Xer recombination and a model for regulation of recombination activity during cell division. | |||
Structural snapshots of Xer recombination reveal activation by synaptic complex remodeling and DNA bending.,Bebel A, Karaca E, Kumar B, Stark WM, Barabas O Elife. 2016 Dec 23;5. pii: e19706. doi: 10.7554/eLife.19706. PMID:28009253<ref>PMID:28009253</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
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== References == | == References == | ||
<references/> | <references/> | ||
Revision as of 10:16, 18 January 2017
Crystal structure of XerH site-specific recombinase bound to palindromic difH substrate: post-cleavage complexCrystal structure of XerH site-specific recombinase bound to palindromic difH substrate: post-cleavage complex
Structural highlights
Function[XERH_HELPY] Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. Involved in chromosome segregation. May contribute to chromosome decatenation.[1] Publication Abstract from PubMedBacterial Xer site-specific recombinases play an essential genome maintenance role by unlinking chromosome multimers, but their mechanism of action has remained structurally uncharacterized. Here, we present two high-resolution structures of Helicobacter pylori XerH with its recombination site DNA difH, representing pre-cleavage and post-cleavage synaptic intermediates in the recombination pathway. The structures reveal that activation of DNA strand cleavage and rejoining involves large conformational changes and DNA bending, suggesting how interaction with the cell division protein FtsK may license recombination at the septum. Together with biochemical and in vivo analysis, our structures also reveal how a small sequence asymmetry in difH defines protein conformation in the synaptic complex and orchestrates the order of DNA strand exchanges. Our results provide insights into the catalytic mechanism of Xer recombination and a model for regulation of recombination activity during cell division. Structural snapshots of Xer recombination reveal activation by synaptic complex remodeling and DNA bending.,Bebel A, Karaca E, Kumar B, Stark WM, Barabas O Elife. 2016 Dec 23;5. pii: e19706. doi: 10.7554/eLife.19706. PMID:28009253[2] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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