| Literature DB >> 3045097 |
Y Kamio1, Y Itoh, Y Terawaki.
Abstract
RepA protein, essential for the replication of plasmid Rts1, was purified, and its binding to mini-Rts1 subregions was examined by a DNase I protection assay. RepA protected the incI and incII iterons, a region immediately upstream of the repA promoter, and a 10-base-pair region located between the most external incII iteron and a GATC box. The protection was less efficient when preheated RepA was used.Entities:
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Year: 1988 PMID: 3045097 PMCID: PMC211463 DOI: 10.1128/jb.170.9.4411-4414.1988
Source DB: PubMed Journal: J Bacteriol ISSN: 0021-9193 Impact factor: 3.490