Mutational analysis of the bacteriophage P2 Ogr protein: truncation of the carboxy terminus.
- Published Article
Journal of bacteriology
- Publication Date
Dec 01, 1993
The Ogr protein is a 72-residue, zinc-binding transcription factor essential for activation of late gene expression in bacteriophage P2. Analysis of C-terminal truncated proteins generated by stop codon mutagenesis shows that deletion of residues distal to position 51 had negligible effects on Ogr function. More-extensive deletion resulted in unstable products with severely reduced activity. These results, as well as the effects of other mutations in this region, support the idea that the 21 C-terminal residues are not required for transactivation.
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The corresponding record at NLM can be accessed at https://www.ncbi.nlm.nih.gov/pubmed/8244946