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 language | English |
|---|---|
| Pages (from-to) | 1630-1633 |
| Number of pages | 4 |
| Journal | Journal of Structural Biology |
| Volume | 56 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 31 Dec 2000 |
Keywords
- bacterial protein
- colicin immunity proteins
- amino acid substitution
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