Structure of the bacteriophage Mu transposase core: a common structural motif for DNA transposition and retroviral integration

Cell. 1995 Jul 28;82(2):209-20. doi: 10.1016/0092-8674(95)90308-9.

Abstract

The crystal structure of the core domain of bacteriophage Mu transposase, MuA, has been determined at 2.4 A resolution. The first of two subdomains contains the active site and, despite very limited sequence homology, exhibits a striking similarity to the core domain of HIV-1 integrase, which carries out a similar set of biochemical reactions. It also exhibits more limited similarity to other nucleases, RNase H and RuvC. The second, a beta barrel, connects to the first subdomain through several contacts. Three independent determinations of the monomer structure from two crystal forms all show the active site held in a similar, apparently inactive configuration. The enzymatic activity of MuA is known to be activated by formation of a DNA-bound tetramer of the protein. We propose that the connections between the two subdomains may be involved in the cross-talk between the active site and the other domains of the transposase that controls the activity of the protein.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Bacteriophage mu / enzymology*
  • Crystallography, X-Ray / methods
  • DNA Nucleotidyltransferases / chemistry*
  • DNA, Viral / chemistry*
  • DNA, Viral / metabolism*
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / metabolism
  • HIV-1 / enzymology
  • Integrases
  • Models, Molecular
  • Molecular Sequence Data
  • Nucleotidyltransferases / chemistry*
  • Nucleotidyltransferases / metabolism*
  • Protein Structure, Secondary*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Retroviridae / genetics*
  • Sequence Homology, Amino Acid
  • Transposases
  • Virus Integration*

Substances

  • DNA, Viral
  • DNA-Binding Proteins
  • Recombinant Proteins
  • DNA Nucleotidyltransferases
  • Integrases
  • Nucleotidyltransferases
  • Transposases