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Redox-sensing transcriptional repressor Rex
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创建时间：
2024-03-27
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Comparison of previously identified Ihk/Irr regulated genes [25] with differentially expressed genes of intracellular wildtype bacteria at 2h pi.
aMicroarray array data. bGene expression in wildtype and irr-deficient S. pyogenes strains was determined at both early and late exponential growth phase, indicated by EE and LE resp. Genes that show
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PrrA target genes identified by ChIP-seq and gene expression analysis of R. sphaeroides cells.
aChromosomal locations of start and stop of ChIP-seq peaks. bFold enrichment of PrrA-myc ChIP over control myc antibody ChIP in WT control. cRegulatory role of PrrA on target operons based on change i
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Expression data from E. coli cells overexpressing GraL for long periods of time. Escherichia coli
While studying greA expression, we noted presence of an intrinsic terminator in the leader region of greA mRNA transcript. We found this terminator to be quite efficient both in vivo and in vitro. Thi
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High-confidence CRP binding sites on the ETEC H10407 chromosome identified by ChIP-seq.
aChomosome coordinate of the ChIP-seq peak in H10407. Underlined text indicates that the ChIP-seq peak maps to sequence that is not conserved in E. coli K-12. bCRP binding site sequence predicted by M
NIAID Data Ecosystem60
Data_Sheet_1_“Urate and NOX5 Control Blood Digestion in the Hematophagous Insect Rhodnius prolixus”.PDF
Low levels of reactive oxygen species (ROS) are now recognized as essential players in cell signaling. Here, we studied the role of two conserved enzymes involved in redox regulation that play a criti
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