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GtrS and GltR form a two-component system: the central role of 2-ketogluconate in the expression of exotoxin A and glucose catabolic enzymes inPseudomonas aeruginosa

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1460-2075.1995.tb00039.xopenalex-snapshot
A common switch in activation of the response regulators NtrC and PhoB: phosphorylation induces dimerization of the receiver modules.
inferredcites →https://doi.org/10.1007/s004380050729openalex-snapshot
Characterization of ptxS, a Pseudomonas aeruginosa gene which interferes with the effect of the exotoxin A positive regulatory gene, ptxR
inferredcites →https://doi.org/10.1007/springerreference_225126openalex-snapshot
Ventilator-Associated Pneumonia
inferredcites →https://doi.org/10.1016/0022-2836(89)90131-9openalex-snapshot
Signal transduction in the phosphate regulon of Escherichia coli involves phosphotransfer between PhoR and PhoB proteins
inferredcites →https://doi.org/10.1016/0167-4781(93)90149-8openalex-snapshot
Analysis of the mRNA structure of the Pseudomonas putida TOL meta fission pathway operon around the transcription initiation point, the xylTE and the xylFJ regions
inferredcites →https://doi.org/10.1016/0378-1119(89)90369-7openalex-snapshot
A dual-labeling method for identifying differentially expressed genes: use in the identification of cDNA clones that hybridize to RNAs whose abundance in tomato flowers is potentially regulated by gibberellins
inferredcites →https://doi.org/10.1016/j.febslet.2012.07.031openalex-snapshot
Analysis of solvent tolerance in Pseudomonas putida DOT‐T1E based on its genome sequence and a collection of mutants
inferredcites →https://doi.org/10.1016/j.ijmm.2008.08.003openalex-snapshot
Pseudomonas exotoxin A: From virulence factor to anti-cancer agent
inferredcites →https://doi.org/10.1016/j.jiph.2009.08.003openalex-snapshot
Urinary tract infections caused by Pseudomonas aeruginosa: A minireview
inferredcites →https://doi.org/10.1016/j.jmb.2007.12.004openalex-snapshot
Hierarchical Binding of the TodT Response Regulator to Its Multiple Recognition Sites at the tod Pathway Operon Promoter
inferredcites →https://doi.org/10.1016/j.mib.2010.01.005openalex-snapshot
Diversity of structure and function of response regulator output domains
inferredcites →https://doi.org/10.1016/s0021-9258(17)39227-xopenalex-snapshot
Multiple forms of the CheB methylesterase in bacterial chemosensing.
inferredcites →https://doi.org/10.1016/s0021-9258(19)89485-1openalex-snapshot
Subunit composition and domain structure of the Spo0A sporulation transcription factor of Bacillus subtilis
inferredcites →https://doi.org/10.1016/s1369-5274(00)00070-9openalex-snapshot
Two-component and phosphorelay signal transduction
inferredcites →https://doi.org/10.1021/bi00170a008openalex-snapshot
Phosphorylation-dependent binding of the chemotaxis signal molecule CheY to its phosphatase, CheZ
inferredcites →https://doi.org/10.1046/j.1365-2958.1996.6251337.xopenalex-snapshot
Isolation and characterization of a Pseudomonas aeruginosa gene, ptxR, which positively regulates exotoxin A production
inferredcites →https://doi.org/10.1073/pnas.72.6.2284openalex-snapshot
NAD-dependent inhibition of protein synthesis by Pseudomonas aeruginosa toxin,.
inferredcites →https://doi.org/10.1073/pnas.89.11.5088openalex-snapshot
Phosphorylation of nitrogen regulator I of Escherichia coli induces strong cooperative binding to DNA essential for activation of transcription.
inferredcites →https://doi.org/10.1073/pnas.90.19.8787openalex-snapshot
Phosphorylation-dependent binding of a signal molecule to the flagellar switch of bacteria.
inferredcites →https://doi.org/10.1074/jbc.m109.014555openalex-snapshot
Regulation of Glucose Metabolism in Pseudomonas
inferredcites →https://doi.org/10.1093/dnares/4.2.161openalex-snapshot
Compilation of All Genes Encoding Two-component Phosphotransfer Signal Transducers in the Genome of Escherichia coli
inferredcites →https://doi.org/10.1093/emboj/17.5.1385openalex-snapshot
Activation of the yeast SSK2 MAP kinase kinase kinase by the SSK1 two‐component response regulator
inferredcites →https://doi.org/10.1093/nar/17.16.6545openalex-snapshot
A simple method for site-directed mutagenesis using the polymerase chain reaction
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a122817openalex-snapshot
Phosphorylation of a Bacterial Activator Protein, OmpR, by a Protein Kinase, EnvZ, Results in Stimulation of Its DNA-Binding Ability1
inferredcites →https://doi.org/10.1093/protein/10.6.673openalex-snapshot
Prediction of transmembrane alpha-helices in prokaryotic membrane proteins: the dense alignment surface method
inferredcites →https://doi.org/10.1094/mpmi-19-0250openalex-snapshot
Organic Acids, Sugars, and l -Tryptophane in Exudates of Vegetables Growing on Stonewool and Their Effects on Activities of Rhizosphere Bacteria
inferredcites →https://doi.org/10.1097/01.mlg.0000172036.82897.d4openalex-snapshot
Mucosal Biofilm Formation on Middle‐Ear Mucosa in a Nonhuman Primate Model of Chronic Suppurative Otitis Media
inferredcites →https://doi.org/10.1099/mic.0.056127-0openalex-snapshot
A novel host-responsive sensor mediates virulence and type III secretion during Pseudomonas aeruginosa–host cell interactions
inferredcites →https://doi.org/10.1099/mic.0.2007/011577-0openalex-snapshot
Regulation of Pseudomonas aeruginosa ptxR by Vfr
inferredcites →https://doi.org/10.1111/j.1365-2958.1991.tb00774.xopenalex-snapshot
Modular structure of Fix J: homology of the transcriptional activator domain with the ‐35 binding domain of sigma factors
inferredcites →https://doi.org/10.1111/j.1365-2958.1996.tb02636.xopenalex-snapshot
The activation of PhoB by acetylphosphate
inferredcites →https://doi.org/10.1111/j.1751-7915.2007.00013.xopenalex-snapshot
Microcalorimetry: a response to challenges in modern biotechnology
inferredcites →https://doi.org/10.1126/science.275.5306.1658openalex-snapshot
Unusual Oligomerization Required for Activity of NtrC, a Bacterial Enhancer-Binding Protein
inferredcites →https://doi.org/10.1128/iai.38.3.1296-1298.1982openalex-snapshot
Loss of virulence associated with absence of flagellum in an isogenic mutant of Pseudomonas aeruginosa in the burned-mouse model
inferredcites →https://doi.org/10.1128/iai.62.3.897-903.1994openalex-snapshot
Characterization of Pseudomonas aeruginosa mutants that are deficient in exotoxin A synthesis and are altered in expression of regA, a positive regulator of exotoxin A
inferredcites →https://doi.org/10.1128/jb.00203-07openalex-snapshot
Convergent Peripheral Pathways Catalyze Initial Glucose Catabolism inPseudomonas putida: Genomic and Flux Analysis
inferredcites →https://doi.org/10.1128/jb.00520-10openalex-snapshot
Compartmentalized Glucose Metabolism in Pseudomonas putida Is Controlled by the PtxS Repressor
inferredcites →https://doi.org/10.1128/jb.00679-07openalex-snapshot
Simultaneous Catabolite Repression between Glucose and Toluene Metabolism in Pseudomonas putida Is Channeled through Different Signaling Pathways
inferredcites →https://doi.org/10.1128/jb.01726-07openalex-snapshot
A Set of Activators and Repressors Control Peripheral Glucose Pathways in Pseudomonas putida To Yield a Common Central Intermediate
inferredcites →https://doi.org/10.1128/jb.170.10.4477-4483.1988openalex-snapshot
Kinetics of toxA and regA mRNA accumulation in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.171.12.6782-6790.1989openalex-snapshot
Regulator and enzyme specificities of the TOL plasmid-encoded upper pathway for degradation of aromatic hydrocarbons and expansion of the substrate range of the pathway
inferredcites →https://doi.org/10.1128/jb.174.4.1428-1431.1992openalex-snapshot
The central domain of Rhizobium leguminosarum DctD functions independently to activate transcription
inferredcites →https://doi.org/10.1128/jb.178.20.6064-6066.1996openalex-snapshot
A two-component response regulator, gltR, is required for glucose transport activity in Pseudomonas aeruginosa PAO1
inferredcites →https://doi.org/10.1128/jb.185.16.4755-4763.2003openalex-snapshot
In Vivo and In Vitro Evidence that TtgV Is the Specific Regulator of the TtgGHI Multidrug and Solvent Efflux Pump of Pseudomonas putida
inferredcites →https://doi.org/10.1146/annurev.biochem.69.1.183openalex-snapshot
Two-Component Signal Transduction
inferredcites →https://doi.org/10.1164/ajrccm.165.7.2105078openalex-snapshot
Ventilator-associated Pneumonia
inferredcites →https://doi.org/10.1371/journal.pone.0039390openalex-snapshot
Genes for Carbon Metabolism and the ToxA Virulence Factor in Pseudomonas aeruginosa Are Regulated through Molecular Interactions of PtxR and PtxS
inferredcites →https://doi.org/10.1371/journal.pone.0055731openalex-snapshot
Root Exudation of Phytochemicals in Arabidopsis Follows Specific Patterns That Are Developmentally Programmed and Correlate with Soil Microbial Functions
inferredcites →https://doi.org/10.1517/14728220903454988openalex-snapshot
Pseudomonas aeruginosa biofilm infections in cystic fibrosis: insights into pathogenic processes and treatment strategies

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Glucose-Induced Enhanced Virulence in Strains of Multidrug-Resistant Pseudomonas aeruginosa Isolated from Diabetic Patients
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Engineering glucose metabolism for enhanced muconic acid production in Pseudomonas putida KT2440
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