Molecular organization in site-specific recombination: the catalytic domain of bacteriophage HP1 integrase at 2.7 A resolution

Cell. 1997 Apr 18;89(2):227-37. doi: 10.1016/s0092-8674(00)80202-0.

Abstract

HP1 integrase promotes site-specific recombination of the HP1 genome into that of Haemophilus influenzae. The isolated C-terminal domain (residues 165-337) of the protein interacts with the recombination site and contains the four catalytic residues conserved in the integrase family. This domain represents a novel fold consisting principally of well-packed alpha helices, a surface beta sheet, and an ordered 17-residue C-terminal tail. The conserved triad of basic residues and the active-site tyrosine are contributed by a single monomer and occupy fixed positions in a defined active-site cleft. Dimers are formed by mutual interactions of the tail of one monomer with an adjacent monomer; this orients active-site clefts antiparallel to each other.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Bacteriophages / genetics
  • Binding Sites
  • Dimerization
  • Integrases / chemistry*
  • Models, Molecular
  • Molecular Sequence Data
  • Protein Conformation*
  • Recombinant Fusion Proteins / chemistry
  • Recombination, Genetic
  • Sequence Analysis

Substances

  • Recombinant Fusion Proteins
  • HP1 integrase
  • Integrases