Site information for: PerR in species Streptococcus pyogenes; genome accession: NC

Transcription Factor Binding Site Information

dbxref: CollecTF:EXPSITE_0000c8c0
Genome: Streptococcus pyogenes - NC_002737.1
TF: PerR [UniProtKB:Q9A1M6, view regulon]

Supporting Evidence

Binding site	Location	Publication	Experimental techniques used	Curation
CGATAATGATTCTAA	- [1260072, 1260086]	15612930	Experimental technique details qPCR [quantitative real-time] (ECO:0005660) qPCR [quantitative real-time] - ECO:0005660 Quantitative PCR (or quantitative real time polymerase chain reaction) is a modification of the conventional PCR reaction used to amplify and simultaneously quantify a targeted DNA molecule. In its more standard incarnation, a inactive fluorescent dye is added to the PCR mix. This dye is activated upon binding double-stranded DNA; as the PCR iterates, there is more and more dsDNA and therefore more fluorescence intensity. -	531

Regulated genes

Regulated genes for each binding site are displayed below. Gene regulation diagrams show binding sites, positively-regulated genes, negatively-regulated genes, both positively and negatively regulated genes, genes with unspecified type of regulation. For each indvidual site, experimental techniques used to determine the site are also given.

Gene	Locus tag	Description
dpr	SPy_1531	peroxide resistance protein
SPy_1530	SPy_1530	hypothetical protein
glcK	SPy_1529	glucose kinase
SPy_1528	SPy_1528	hypothetical protein
SPy_1532	SPy_1532	hypothetical protein
SPy_1533	SPy_1533	ribosomal RNA large subunit methyltransferase N
SPy_1534	SPy_1534	hypothetical protein