| scholarly article | Q13442814 |
| P2093 | author name string | Bush K | |
| Foleno BD | |||
| Baum EZ | |||
| Webb GC | |||
| Montenegro DA | |||
| Licata L | |||
| Turchi I | |||
| P2860 | cites work | 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 |
| Comparative study of fosfomycin activity in Mueller-Hinton media and in tissues | Q71829315 | ||
| Detection and characterization of a phospholactoyl-enzyme adduct in the reaction catalyzed by UDP-N-acetylglucosamine enolpyruvoyl transferase, MurZ | Q72160243 | ||
| Kinetics, stoichiometry, and identification of the reactive thiolate in the inactivation of UDP-GlcNAc enolpyruvoyl transferase by the antibiotic fosfomycin | Q72160246 | ||
| Critical evaluation of the research docking program for the CASP2 challenge | Q74252623 | ||
| MurA (MurZ), the enzyme that catalyzes the first committed step in peptidoglycan biosynthesis, is essential in Escherichia coli | Q24671787 | ||
| Role of the loop containing residue 115 in the induced-fit mechanism of the bacterial cell wall biosynthetic enzyme MurA | Q27621570 | ||
| Crystal structure of UDP-N-acetylglucosamine enolpyruvyltransferase, the target of the antibiotic fosfomycin | Q27733409 | ||
| Structure of UDP-N-acetylglucosamine enolpyruvyl transferase, an enzyme essential for the synthesis of bacterial peptidoglycan, complexed with substrate UDP-N-acetylglucosamine and the drug fosfomycin | Q27734363 | ||
| Cloning and sequencing of Escherichia coli murZ and purification of its product, a UDP-N-acetylglucosamine enolpyruvyl transferase | Q33202551 | ||
| Two active forms of UDP-N-acetylglucosamine enolpyruvyl transferase in gram-positive bacteria | Q33601835 | ||
| In vitro susceptibility testing procedures for fosfomycin tromethamine | Q33744499 | ||
| Emergence of fosfomycin-resistant isolates of Shiga-like toxin-producing Escherichia coli O26 | Q33976610 | ||
| Multiple mechanisms of action for inhibitors of histidine protein kinases from bacterial two-component systems | Q33977169 | ||
| The mechanism of action of fosfomycin (phosphonomycin) | Q34214482 | ||
| Intracellular steps of bacterial cell wall peptidoglycan biosynthesis: enzymology, antibiotics, and antibiotic resistance | Q34541598 | ||
| Fosfomycin resistance protein (FosA) is a manganese metalloglutathione transferase related to glyoxalase I and the extradiol dioxygenases | Q36855782 | ||
| Studies on the conformational changes in the bacterial cell wall biosynthetic enzyme UDP-N-acetylglucosamine enolpyruvyltransferase (MurA). | Q42680309 | ||
| Plasmid-encoded fosfomycin resistance in bacteria isolated from the urinary tract in a multicentre survey | Q48044137 | ||
| A fast flexible docking method using an incremental construction algorithm. | Q52298930 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Escherichia coli | Q25419 |
| P304 | page(s) | 3182-3188 | |
| P577 | publication date | 2001-11-01 | |
| P1433 | published in | Antimicrobial Agents and Chemotherapy | Q578004 |
| P1476 | title | Identification and characterization of new inhibitors of the Escherichia coli MurA enzyme | |
| P478 | volume | 45 |
| Q24564306 | 1,2-dithiole-3-ones as potent inhibitors of the bacterial 3-ketoacyl acyl carrier protein synthase III (FabH) |
| Q42647502 | A novel inhibitor that suspends the induced fit mechanism of UDP-N-acetylglucosamine enolpyruvyl transferase (MurA). |
| Q88906095 | Adaptation to the coupling of glycolysis to toxic methylglyoxal production in tpiA deletion strains of Escherichia coli requires synchronized and counterintuitive genetic changes |
| Q92647920 | Cell wall peptidoglycan in Mycobacterium tuberculosis: An Achilles' heel for the TB-causing pathogen |
| Q33793074 | Challenges of antibacterial discovery |
| Q28539823 | Cloning, expression and characterization of UDP-N-acetylglucosamine enolpyruvyl transferase (MurA) from Wolbachia endosymbiont of human lymphatic filarial parasite Brugia malayi |
| Q30895039 | Combinatorial enzymatic assay for the screening of a new class of bacterial cell wall inhibitors |
| Q38420842 | Comprehensive structural and functional characterization of Mycobacterium tuberculosis UDP-NAG enolpyruvyl transferase (Mtb-MurA) and prediction of its accurate binding affinities with inhibitors |
| Q51773259 | Computed insight into a peptide inhibitor preventing the induced fit mechanism of MurA enzyme from Pseudomonas aeruginosa. |
| Q38807273 | Coprinuslactone protects the edible mushroom Coprinus comatus against biofilm infections by blocking both quorum-sensing and MurA. |
| Q37081699 | Cytoplasmic steps of peptidoglycan biosynthesis |
| Q36175676 | Differential antibacterial properties of the MurA inhibitors terreic acid and fosfomycin |
| Q35713880 | Fatty acid biosynthesis as a target for novel antibacterials |
| Q41812492 | Fosfomycin enhances the active transport of tobramycin in Pseudomonas aeruginosa |
| Q34882983 | Glutathione transferases in bacteria. |
| Q48022320 | Identification of druggable targets for Acinetobacter baumannii via subtractive genomics and plausible inhibitors for MurA and MurB. |
| Q30152646 | Inhibition of the MurA enzyme in Fusobacterium nucleatum by potential inhibitors identified through computational and in vitro approaches |
| Q38035171 | Inhibitors targeting on cell wall biosynthesis pathway of MRSA. |
| Q45278217 | MurA as a primary target of tulipalin B and 6-tuliposide B. |
| Q36052586 | Parasite plastids: approaching the endgame |
| Q37810971 | Peptidoglycan biosynthesis machinery: a rich source of drug targets |
| Q34107220 | Purification, characterization, and identification of novel inhibitors of the beta-ketoacyl-acyl carrier protein synthase III (FabH) from Staphylococcus aureus |
| Q39383708 | Resistance mechanism to an uncompetitive inhibitor of a single-substrate, single-product enzyme: a study of Helicobacter pylori glutamate racemase |
| Q26859841 | Resistance to antibiotics targeted to the bacterial cell wall |
| Q37912224 | Screening strategies for discovery of antibacterial natural products |
| Q47106726 | Structural evidence for the covalent modification of FabH by 4,5-dichloro-1,2-dithiol-3-one (HR45). |
| Q41031126 | Structural insight into the binding of C60-derivatives with enoyl-pyruvate transferase from Helicobacter pylori |
| Q53603346 | Structure-based optimization of MurF inhibitors. |
| Q34568935 | The bacterial cell wall as a source of antibacterial targets |
| Q42079513 | Toxin ζ reversible induces dormancy and reduces the UDP-N-acetylglucosamine pool as one of the protective responses to cope with stress |
| Q34151913 | Transcriptomic and proteomic analyses of the Aspergillus fumigatus hypoxia response using an oxygen-controlled fermenter |
| Q37913126 | UDP-N-acetylglucosamine enolpyruvyl transferase as a potential target for antibacterial chemotherapy: recent developments |
| Q38070780 | Viable screening targets related to the bacterial cell wall. |
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