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Crystallization of the cytotoxic domain of a ribosome-inactivating colicin in complex with its immunity protein

Stephen Carr, Daniel Walker, Richard James, Colin Kleanthous, Andrew M. Hemmings

Research output: Contribution to journalArticlepeer-review

Abstract

The complex between the ribonuclease domain of the ribosome-inactivating colicin E3 and its protein inhibitor, the cognate immunity Im3, has been crystallized and preliminary X-ray characterization has been performed. Single crystals of the 1:1 complex were grown from hanging-drop vapour-diffusion experiments using 2-propanol as a precipitant. The space group is P3(1)21 or P3(2)21, with unit-cell parameters a = b = 93.7, c = 76.2 A. When cryocooled, these crystals diffract to a resolution of 2.4 A. A search for suitable conventional heavy-atom derivatives was unsuccessful and so Im3 mutants containing engineered cysteine or methionine residues have been produced for mercury soaks and selenomethionine-labelling experiments, respectively.
Original languageEnglish
Pages (from-to)1630-1633
Number of pages4
JournalJournal of Structural Biology
Volume56
Issue number12
DOIs
Publication statusPublished - 31 Dec 2000

Keywords

  • bacterial protein
  • colicin immunity proteins
  • amino acid substitution

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