Plasmid pT181-linked suppressors of the Staphylococcus aureus pcrA3 chromosomal mutation

scientific article

Plasmid pT181-linked suppressors of the Staphylococcus aureus pcrA3 chromosomal mutation is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1128/JB.175.12.3916-3917.1993
P932PMC publication ID204812
P698PubMed publication ID8509346

P2093author name stringIordanescu S
P2860cites workDNA sequencing with chain-terminating inhibitorsQ22066207
Control of pT181 replication II. Mutational analysis.Q33939995
Functional analysis of a palindromic sequence required for normal replication of several staphylococcal plasmidsQ34611752
Single-stranded plasmid DNA in Bacillus subtilis and Staphylococcus aureusQ35599903
Staphylococcus aureus chromosomal mutations that decrease efficiency of Rep utilization in replication of pT181 and related plasmidsQ36180984
In vitro studies of the initiation of staphylococcal plasmid replication. Specificity of RepD for its origin (oriD) and characterization of the Rep-ori tyrosyl ester intermediateQ38341298
The Staphylococcus aureus mutation pcrA3 leads to the accumulation of pT181 replication initiation complexesQ43757108
Purification of pT181-encoded repC protein required for the initiation of plasmid replicationQ44447483
Comparative analysis of five related Staphylococcal plasmidsQ48324751
Complete nucleotide sequence of pT181, a tetracycline-resistance plasmid from Staphylococcus aureusQ48395129
The Inc3B determinant of plasmid pT181. A mutational analysisQ68765366
Specificity of the interactions between the Rep proteins and the origins of replication of Staphylococcus aureus plasmids pT181 and pC221Q69705873
Determination of plasmid copy number by fluorescence densitometryQ70259634
P433issue12
P407language of work or nameEnglishQ1860
P921main subjectStaphylococcus aureusQ188121
P304page(s)3916-3917
P577publication date1993-06-01
P1433published inJournal of BacteriologyQ478419
P1476titlePlasmid pT181-linked suppressors of the Staphylococcus aureus pcrA3 chromosomal mutation
P478volume175