Differential modes of DNA binding by mismatch uracil DNA glycosylase from Escherichia coli: implications for abasic lesion processing and enzyme communication in the base excision repair pathway-Reference-Cited by-同舟云学术

Differential modes of DNA binding by mismatch uracil DNA glycosylase from Escherichia coli: implications for abasic lesion processing and enzyme communication in the base excision repair pathway

Published:2010-11-26 Issue:7 Volume:39 Page:2593-2603
ISSN:1362-4962
Container-title:Nucleic Acids Research
language:en
Short-container-title:

Author:

Grippon Seden,Zhao Qiyuan,Robinson Tom,Marshall Jacqueline J. T.,O’Neill Rory J.,Manning Hugh,Kennedy Gordon,Dunsby Christopher,Neil Mark,Halford Stephen E.,French Paul M. W.,Baldwin Geoff S.

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/39/7/2593/16783108/gkq913.pdf

Reference38 articles.

1. The base excision repair pathway;Seeberg;Trends Biochem. Sci.,1995

2. A new class of uracil-DNA glycosylases related to human thymine-DNA glycosylase;Gallinari;Nature,1996

3. Crystal structure of a G:T/U mismatch-specific DNA glycosylase: mismatch recognition by complementary-strand interactions;Barrett;Cell,1998

4. 3,N(4)-ethenocytosine, a highly mutagenic adduct, is a primary substrate for Escherichia coli double-stranded uracil-DNA glycosylase and human mismatch-specific thymine-DNA glycosylase;Saparbaev;Proc. Natl Acad. Sci. USA,1998

5. Mismatch uracil glycosylase from Escherichia coli: a general mismatch or a specific DNA glycosylase?;O’Neill;J. Biol. Chem.,2003

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