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Filter Results:

Year

  • 2006 (1)

Author

  • Horton, John (1)
  • Roberts, Richard J. (1)
  • Wilson, Geoffrey G. (1)
  • Yang, Zhe (1)

Subject

  • Chemistry, Biochemistry (1)

Journal

  • Nucleic Acids Research (1)

Author department

  • Biochem: Admin (1)

Search Results for all work with filters:

  • Zhang, Xing
  • Maunus, Robert
  • Cheng, Xiaodong
  • Health Sciences, General

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Article

DNA nicking by HinP1I endonuclease: bending, base flipping and minor groove expansion

by John Horton; Xing Zhang; Robert Maunus; Zhe Yang; Geoffrey G. Wilson; Richard J. Roberts; Xiaodong Cheng

2006

Subjects
  • Chemistry, Biochemistry
  • Health Sciences, General
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Abstract:Close

HinP1I recognizes and cleaves the palindromic tetranucleotide sequence G↓CGC in DNA. We report three structures of HinP1I–DNA complexes: in the presence of Ca2+ (pre-reactive complex), in the absence of metal ion (binary complex) and in the presence of Mg2+ (post-reactive complex). HinP1I forms a back-to-back dimer with two active sites and two DNA duplexes bound on the outer surfaces of the dimer facing away from each other. The 10 bp DNA duplexes undergo protein-induced distortions exhibiting features of A-, B- and Z-conformations: bending on one side (by intercalation of a phenylalanine side chain into the major groove), base flipping on the other side of the recognition site (by expanding the step rise distance of the local base pair to Z-form) and a local A-form conformation between the two central C:G base pairs of the recognition site (by binding of the N-terminal helix in the minor groove). In the pre- and post-reactive complexes, two metals (Ca2+ or Mg2+) are found in the active site. The enzyme appears to cleave DNA sequentially, hydrolyzing first one DNA strand, as seen in the post-reactive complex in the crystalline state, and then the other, as supported by the observation that, in solution, a nicked DNA intermediate accumulates before linearization.
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