Structural basis for DNA recognition and processing by UvrB

被引:88
|
作者
Truglio, JJ
Karakas, E
Rhau, B
Wang, H
DellaVecchia, MJ
Van Houten, B
Kisker, C [1 ]
机构
[1] SUNY Stony Brook, Dept Pharmacol Sci, Stony Brook, NY 11794 USA
[2] Natl Inst Environm Hlth Sci, Lab Mol Genet, US Natl Inst Hlth, Res Triangle Pk, NC 27709 USA
[3] Univ Wurzburg, Inst Struct Biol, Rudolf Virchow Ctr Expt Biomed, D-97078 Wurzburg, Germany
关键词
D O I
10.1038/nsmb1072
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA-damage recognition in the nucleotide excision repair ( NER) cascade is a complex process, operating on a wide variety of damages. UvrB is the central component in prokaryotic NER, directly involved in DNA-damage recognition and guiding the DNA through repair synthesis. We report the first structure of a UvrB-double-stranded DNA complex, providing insights into the mechanism by which UvrB binds DNA, leading to formation of the preincision complex. One DNA strand, containing a 3' overhang, threads behind a beta-hairpin motif of UvrB, indicating that this motif inserts between the strands of the double helix, thereby locking down either the damaged or undamaged strand. The nucleotide directly behind the beta-hairpin is flipped out and inserted into a small, highly conserved pocket in UvrB.
引用
收藏
页码:360 / 364
页数:5
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