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Xer-mediated dimer resolution at the mwr site of the multiresistance plasmid pJHCMW1 is osmoregulated in Escherichia coli containing either the Escherichia coli Xer recombination machinery or Xer recombination elements from K. pneumoniae. In the pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::494775777148f02b7a697a1ccc0b896e
https://doi.org/10.1128/jb.188.8.2812-2820.2006
https://doi.org/10.1128/jb.188.8.2812-2820.2006
Site-specific recombinases XerC and XerD function in the segregation of circular bacterial replicons. In a recombining nucleoprotein complex containing two molecules each of XerC and XerD, coordinated reciprocal switches in recombinase activity ensur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::da28e886ff31f2db77c6cc6085df3fe6
https://doi.org/10.1006/jmbi.2000.3762
https://doi.org/10.1006/jmbi.2000.3762
Chromosome dimers form in bacteria by recombination between circular chromosomes. Resolution of dimers is a highly integrated process involving recombination between dif sites catalysed by the XerCD recombinase, cell division and the integrity of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b48fbf8dbbaac50a575f88e017ba8b24
https://doi.org/10.1046/j.1365-2958.2001.02277.x
https://doi.org/10.1046/j.1365-2958.2001.02277.x
In Xer site-specific recombination, sequential DNA strand exchange reactions are catalyzed by a heterotetrameric complex composed of two recombinases, XerC and XerD. It is demonstrated that XerC and XerD catalytic activity is controlled by an interac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::70e2d357feb7879bb90d557119e67650
https://ora.ox.ac.uk/objects/uuid:071c9c9b-1f02-4fe8-a0df-f806c0fdb743
https://ora.ox.ac.uk/objects/uuid:071c9c9b-1f02-4fe8-a0df-f806c0fdb743
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, vol 110, iss 52
Shimokawa, K; Ishihara, K; Grainge, I; Sherratt, DJ; & Vazquez, M. (2013). FtsK-dependent XerCD-dif recombination unlinks replication catenanes in a stepwise manner. Proceedings of the National Academy of Sciences, 110(52), 20906-20911. doi: 10.1073/pnas.1308450110. UC Davis: Department of Mathematics. Retrieved from: http://www.escholarship.org/uc/item/3079k8f5
Shimokawa, K; Ishihara, K; Grainge, I; Sherratt, DJ; & Vazquez, M. (2013). FtsK-dependent XerCD-dif recombination unlinks replication catenanes in a stepwise manner. Proceedings of the National Academy of Sciences, 110(52), 20906-20911. doi: 10.1073/pnas.1308450110. UC Davis: Department of Mathematics. Retrieved from: http://www.escholarship.org/uc/item/3079k8f5
In Escherichia coli, complete unlinking of newly replicated sister chromosomes is required to ensure their proper segregation at cell division. Whereas replication links are removed primarily by topoisomerase IV, XerC/XerD-dif site-specific recombina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3a5a7bac5fa86f37f8d0075da11548af
https://escholarship.org/uc/item/3079k8f5
https://escholarship.org/uc/item/3079k8f5
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