scholarly article | Q13442814 |
P356 | DOI | 10.1016/J.YMBEN.2018.05.012 |
P698 | PubMed publication ID | 29842925 |
P50 | author | Bernhard Palsson | Q4894212 |
Troy E Sandberg | Q56994240 | ||
Elizabeth Brunk | Q57219165 | ||
Adam M. Feist | Q89604738 | ||
Richard Szubin | Q114338580 | ||
Ying Hefner | Q114338583 | ||
Douglas McCloskey | Q114563005 | ||
P2093 | author name string | Sibei Xu | |
P2860 | cites work | Intermediates in the transformation of phosphonates to phosphate by bacteria | Q24618411 |
Hypothetical functions of toxin-antitoxin systems | Q24675719 | ||
Three-dimensional crystal structure of the transcription factor PhoB receiver domain | Q27766453 | ||
Oxidative DNA damage: mechanisms, mutation, and disease | Q28182969 | ||
Glyoxalase I--structure, function and a critical role in the enzymatic defence against glycation | Q28187673 | ||
Glyoxalase II: molecular characteristics, kinetics and mechanism | Q28261914 | ||
Principles of c-di-GMP signalling in bacteria | Q29615333 | ||
Identification and characterization of new inhibitors of the Escherichia coli MurA enzyme | Q31016009 | ||
Endogenous morphine levels are increased in sepsis: a partial implication of neutrophils | Q33526332 | ||
Benzothioxalone derivatives as novel inhibitors of UDP-N-acetylglucosamine enolpyruvyl transferases (MurA and MurZ). | Q33699586 | ||
Recruitment of genes and enzymes conferring resistance to the nonnatural toxin bromoacetate | Q33710466 | ||
Role of IscX in iron-sulfur cluster biogenesis in Escherichia coli | Q33776550 | ||
Global regulation by the seven-component Pi signaling system | Q34099835 | ||
DNA damage and oxygen radical toxicity | Q34172435 | ||
Advanced glycation end-products: a review | Q34196489 | ||
Evolution of Escherichia coli to 42 °C and subsequent genetic engineering reveals adaptive mechanisms and novel mutations | Q34201864 | ||
Genome-wide PhoB binding and gene expression profiles reveal the hierarchical gene regulatory network of phosphate starvation in Escherichia coli. | Q34448182 | ||
Tempo and mode of genome evolution in a 50,000-generation experiment | Q34535938 | ||
Advanced glycation end products: sparking the development of diabetic vascular injury | Q34555042 | ||
Use of adaptive laboratory evolution to discover key mutations enabling rapid growth of Escherichia coli K-12 MG1655 on glucose minimal medium | Q34747829 | ||
Age of inoculum strongly influences persister frequency and can mask effects of mutations implicated in altered persistence | Q35096460 | ||
Oxidative damage to DNA: formation, measurement and biochemical features. | Q35592841 | ||
Advanced glycation end products and vascular inflammation: implications for accelerated atherosclerosis in diabetes. | Q35860982 | ||
Genomewide overexpression screen for fosfomycin resistance in Escherichia coli: MurA confers clinical resistance at low fitness cost | Q35941216 | ||
Does the Transcription Factor NemR Use a Regulatory Sulfenamide Bond to Sense Bleach? | Q36086174 | ||
Sesquiterpene lactones are potent and irreversible inhibitors of the antibacterial target enzyme MurA. | Q54456599 | ||
Characterization of a Cys115 to Asp substitution in the Escherichia coli cell wall biosynthetic enzyme UDP-GlcNAc enolpyruvyl transferase (MurA) that confers resistance to inactivation by the antibiotic fosfomycin. | Q54590227 | ||
Evidence for a fourteen-gene, phnC to phnP locus for phosphonate metabolism in Escherichia coli. | Q54654469 | ||
Characterization of an iron sensitive Mud1 mutant in E. coli lacking the ribonucleotide reductase subunit B2 | Q69823208 | ||
Protein cross-linking by the Maillard reaction. Isolation, characterization, and in vivo detection of a lysine-lysine cross-link derived from methylglyoxal | Q71245770 | ||
Identification of N2-(1-carboxyethyl)guanine (CEG) as a guanine advanced glycosylation end product | Q72403672 | ||
Deficient nucleotide excision repair increases base-pair substitutions but decreases TGGC frameshifts induced by methylglyoxal in Escherichia coli | Q77874858 | ||
Reactions of methylglyoxal with nucleic acids | Q77920888 | ||
Interplay between genetic regulation of phosphate homeostasis and bacterial virulence | Q36147512 | ||
Decreased expression of type 1 fimbriae by a pst mutant of uropathogenic Escherichia coli reduces urinary tract infection | Q36211098 | ||
Manganese import is a key element of the OxyR response to hydrogen peroxide in Escherichia coli | Q37418527 | ||
MqsR, a crucial regulator for quorum sensing and biofilm formation, is a GCU-specific mRNA interferase in Escherichia coli. | Q37431140 | ||
The PhoU protein from Escherichia coli interacts with PhoR, PstB, and metals to form a phosphate-signaling complex at the membrane. | Q37713140 | ||
Advanced glycation end products. | Q37887379 | ||
Adaptive laboratory evolution -- principles and applications for biotechnology | Q38118393 | ||
sigmaS, a major player in the response to environmental stresses in Escherichia coli: role, regulation and mechanisms of promoter recognition. | Q38193405 | ||
Ribonucleotide reductases: essential enzymes for bacterial life. | Q38210214 | ||
Network of protein-protein interactions among iron-sulfur cluster assembly proteins in Escherichia coli | Q38289718 | ||
Induction of the sufA operon encoding Fe-S assembly proteins by superoxide generators and hydrogen peroxide: involvement of OxyR, IHF and an unidentified oxidant-responsive factor | Q38343869 | ||
Escherichia coli toxin/antitoxin pair MqsR/MqsA regulate toxin CspD. | Q38346935 | ||
Transcriptional analysis of the pst operon of Escherichia coli | Q38360005 | ||
An array of Escherichia coli clones over-expressing essential proteins: a new strategy of identifying cellular targets of potent antibacterial compounds | Q38505082 | ||
Defining the growth conditions and promoter-proximal DNA sequences required for activation of gene expression by CreBC in Escherichia coli. | Q38608942 | ||
Methylglyoxal, an endogenous aldehyde, crosslinks DNA polymerase and the substrate DNA. | Q39097246 | ||
Development of a whole-cell assay for peptidoglycan biosynthesis inhibitors | Q39651496 | ||
Identification of a mutation in the pst-phoU operon that reduces pathogenicity of an Escherichia coli strain causing septicemia in pigs | Q39823802 | ||
MID Max: LC-MS/MS Method for Measuring the Precursor and Product Mass Isotopomer Distributions of Metabolic Intermediates and Cofactors for Metabolic Flux Analysis Applications | Q40213227 | ||
Methylglyoxal toxicity in mammals | Q40678654 | ||
Gene regulation by phosphate in enteric bacteria | Q40875648 | ||
The iron-binding CyaY and IscX proteins assist the ISC-catalyzed Fe-S biogenesis in Escherichia coli. | Q41645273 | ||
The alternative aerobic ribonucleotide reductase of Escherichia coli, NrdEF, is a manganese-dependent enzyme that enables cell replication during periods of iron starvation | Q42020372 | ||
An alternative route for recycling of N-acetylglucosamine from peptidoglycan involves the N-acetylglucosamine phosphotransferase system in Escherichia coli | Q42154162 | ||
Toxins Hha and CspD and small RNA regulator Hfq are involved in persister cell formation through MqsR in Escherichia coli | Q42155399 | ||
Integrated stress response of Escherichia coli to methylglyoxal: transcriptional readthrough from the nemRA operon enhances protection through increased expression of glyoxalase I. | Q42201400 | ||
The uncharacterized transcription factor YdhM is the regulator of the nemA gene, encoding N-ethylmaleimide reductase | Q42406816 | ||
Expression analysis of the nrdHIEF operon from Escherichia coli. Conditions that trigger the transcript level in vivo | Q42502019 | ||
Phenyl thiazolyl urea and carbamate derivatives as new inhibitors of bacterial cell-wall biosynthesis | Q43835367 | ||
Oxidative damage of DNA by the reaction of amino acid with methylglyoxal in the presence of Fe(III) | Q44643558 | ||
A suf operon requirement for Fe-S cluster assembly during iron starvation in Escherichia coli | Q44854381 | ||
Latent pathway activation and increased pathway capacity enable Escherichia coli adaptation to loss of key metabolic enzymes | Q44915385 | ||
Modeling Method for Increased Precision and Scope of Directly Measurable Fluxes at a Genome-Scale | Q46101177 | ||
Bacterial toxin YafQ is an endoribonuclease that associates with the ribosome and blocks translation elongation through sequence-specific and frame-dependent mRNA cleavage | Q46125112 | ||
Metabolic flux analysis of Escherichia coli in glucose-limited continuous culture. II. Dynamic response to famine and feast, activation of the methylglyoxal pathway and oscillatory behaviour | Q46368004 | ||
Identification of DNA adducts of methylglyoxal | Q46987843 | ||
Ribonucleoside diphosphate reductase. Purification of the two subunits, proteins B1 and B2. | Q47790520 | ||
Endoribonuclease type II toxin-antitoxin systems: functional or selfish? | Q50900124 | ||
Epistasis and allele specificity in the emergence of a stable polymorphism in Escherichia coli. | Q51463292 | ||
2-Aminotetralones: novel inhibitors of MurA and MurZ. | Q52852098 | ||
Evidence for the transport of zinc(II) ions via the pit inorganic phosphate transport system in Escherichia coli. | Q54059264 | ||
Membrane homeostasis requires intact pst in extraintestinal pathogenic Escherichia coli. | Q54394783 | ||
Expression of the PitA phosphate/metal transporter of Escherichia coli is responsive to zinc and inorganic phosphate levels. | Q54412898 | ||
Escherichia coli dinJ-yafQ genes act as a toxin-antitoxin module. | Q54447623 | ||
P921 | main subject | mutation | Q42918 |
Escherichia coli | Q25419 | ||
P304 | page(s) | 82-93 | |
P577 | publication date | 2018-05-26 | |
P1433 | published in | Metabolic Engineering | Q6822334 |
P1476 | title | Adaptation to the coupling of glycolysis to toxic methylglyoxal production in tpiA deletion strains of Escherichia coli requires synchronized and counterintuitive genetic changes | |
P478 | volume | 48 |
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Q60938695 | How adaptive evolution reshapes metabolism to improve fitness: recent advances and future outlook |
Q58122460 | Identification of growth-coupled production strains considering protein costs and kinetic variability |
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