Identification of proximal sites for unwound DNA substrate inEscherichia colitopoisomerase I with oxidative crosslinking-Reference-Cited by-同舟云学术

Identification of proximal sites for unwound DNA substrate inEscherichia colitopoisomerase I with oxidative crosslinking

Published:2016-12-20 Issue:1 Volume:591 Page:28-38
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:FEBS Lett

Author:

Cheng Bokun¹,Zhou Qingxuan²³,Weng Liwei⁴,Leszyk John D.⁵,Greenberg Marc M.⁴,Tse-Dinh Yuk-Ching²³

Affiliation:

1. Department of Biochemistry and Molecular Biology; New York Medical College; Valhalla NY USA

2. Department of Chemistry and Biochemistry; Florida International University; Miami FL USA

3. Biomolecular Sciences Institute; Florida International University; Miami FL USA

4. Department of Chemistry; Johns Hopkins University; Baltimore MD USA

5. Department of Biochemistry and Molecular Pharmacology and Proteomics and Mass Spectrometry Facility; University of Massachusetts Medical School; Worcester MA USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Reference49 articles.

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3. New mechanistic and functional insights into DNA topoisomerases;Chen;Annu Rev Biochem,2013

4. An increase in negative supercoiling in bacteria reveals topology-reacting gene clusters and a homeostatic response mediated by the DNA topoisomerase I gene;Ferrandiz;Nucleic Acids Res,2016

5. Homeostatic regulation of supercoiling sensitivity coordinates transcription of the bacterial genome;Blot;EMBO Rep,2006

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