| Literature DB >> 3129311 |
M Granger-Schnarr1, P Oertel, M Schnarr.
Abstract
Using site-directed mutagenesis of the lexA gene we have changed the amino acid Ala-84 of the LexA repressor for a cysteine. The reason for this change was the striking homology between LexA and UmuD and the comparable size of the two amino acid side chains. Using an in vivo repression/induction assay it is shown that the LexA-Cys-84 mutant remains inducible by mitomycin C and UV irradiation essentially in the same way as the wild-type repressor.Entities:
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Year: 1988 PMID: 3129311 DOI: 10.1016/0014-5793(88)80866-4
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124