| scholarly article | Q13442814 |
| P50 | author | Stephane Betzi | Q55117889 |
| Huijong Han | Q58869810 | ||
| P2093 | author name string | Ernst Schönbrunn | |
| Yan Yang | |||
| Sanne H Olesen | |||
| Jin-Yi Zhu | |||
| Frank Marsilio | |||
| P2860 | cites work | MolProbity: all-atom structure validation for macromolecular crystallography | Q24649111 |
| MurA (MurZ), the enzyme that catalyzes the first committed step in peptidoglycan biosynthesis, is essential in Escherichia coli | Q24671787 | ||
| Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination | Q26778405 | ||
| Role of the loop containing residue 115 in the induced-fit mechanism of the bacterial cell wall biosynthetic enzyme MurA | Q27621570 | ||
| Structural basis for the interaction of the fluorescence probe 8-anilino-1-naphthalene sulfonate (ANS) with the antibiotic target MurA | Q27622627 | ||
| Comparative X-ray analysis of the un-liganded fosfomycin-target murA | Q27622761 | ||
| A new view of the mechanisms of UDP-N-acetylglucosamine enolpyruvyl transferase (MurA) and 5-enolpyruvylshikimate-3-phosphate synthase (AroA) derived from X-ray structures of their tetrahedral reaction intermediate states | Q27642065 | ||
| ??? | Q27748883 | ||
| Crystal structure of UDP-N-acetylglucosamine enolpyruvyl transferase from Haemophilus influenzae in complex with UDP-N-acetylglucosamine and fosfomycin | Q27649770 | ||
| Evidence of kinetic control of ligand binding and staged product release in MurA (enolpyruvyl UDP-GlcNAc synthase)-catalyzed reactions | Q27658111 | ||
| The Fungal Product Terreic Acid Is a Covalent Inhibitor of the Bacterial Cell Wall Biosynthetic Enzyme UDP- N -Acetylglucosamine 1-Carboxyvinyltransferase (MurA), | Q27660525 | ||
| 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 | ||
| Coot: model-building tools for molecular graphics | Q27860505 | ||
| Version 1.2 of the Crystallography and NMR system | Q27860583 | ||
| Improved R-factors for diffraction data analysis in macromolecular crystallography | Q27860992 | ||
| The CCP4 suite: programs for protein crystallography | Q27861090 | ||
| Recent advances in the formation of the bacterial peptidoglycan monomer unit | Q28204307 | ||
| Automatic processing of rotation diffraction data from crystals of initially unknown symmetry and cell constants | Q29546524 | ||
| The mechanism of action of fosfomycin (phosphonomycin) | Q34214482 | ||
| Evidence that the fosfomycin target Cys115 in UDP-N-acetylglucosamine enolpyruvyl transferase (MurA) is essential for product release | Q37866109 | ||
| A novel inhibitor that suspends the induced fit mechanism of UDP-N-acetylglucosamine enolpyruvyl transferase (MurA). | Q42647502 | ||
| Studies on the conformational changes in the bacterial cell wall biosynthetic enzyme UDP-N-acetylglucosamine enolpyruvyltransferase (MurA). | Q42680309 | ||
| UDP-N-acetylmuramic acid (UDP-MurNAc) is a potent inhibitor of MurA (enolpyruvyl-UDP-GlcNAc synthase). | Q45307734 | ||
| The unusual binding mode of cnicin to the antibacterial target enzyme MurA revealed by X-ray crystallography | Q46450774 | ||
| 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 | ||
| Lysine 22 in UDP-N-Acetylglucosamine Enolpyruvyl Transferase fromEnterobacter cloacaeIs Crucial for Enzymatic Activity and the Formation of Covalent Adducts with the Substrate Phosphoenolpyruvate and the Antibiotic Fosfomycin† | Q57978316 | ||
| 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 | ||
| Evidence that the reaction of the UDP-N-acetylglucosamine 1-carboxyvinyltransferase proceeds through the O-phosphothioketal of pyruvic acid bound to Cys115 of the enzyme | Q72709263 | ||
| A protein antibiotic in the phage Qbeta virion: diversity in lysis targets | Q74087194 | ||
| P433 | issue | 16 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cell biology | Q7141 |
| P304 | page(s) | 12657-67 | |
| P577 | publication date | 2012-04-13 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Functional Consequence of Covalent Reaction of Phosphoenolpyruvate with UDP-N-acetylglucosamine 1-Carboxyvinyltransferase (MurA) | |
| P478 | volume | 287 |
| Q28547100 | Antimicrobial Susceptibility and Molecular Mechanisms of Fosfomycin Resistance in Clinical Escherichia coli Isolates in Mainland China |
| Q51773259 | Computed insight into a peptide inhibitor preventing the induced fit mechanism of MurA enzyme from Pseudomonas aeruginosa. |
| Q89620800 | Cyclic AMP-CRP Modulates the Cell Morphology of Klebsiella pneumoniae in High-Glucose Environment |
| Q91675209 | Design, synthesis and evaluation of biological activities of some novel anti-TB agents with bio-reducible functional group |
| Q99631291 | Development and Clinical Application of Phosphorus-Containing Drugs |
| Q37335513 | Development of a one-pot assay for screening and identification of Mur pathway inhibitors in Mycobacterium tuberculosis |
| Q90189782 | Fosfomycin Resistance in Escherichia coli Isolates from South Korea and in vitro Activity of Fosfomycin Alone and in Combination with Other Antibiotics |
| Q39071416 | Fosfomycin: Mechanism and Resistance |
| Q27677278 | Heteroresistance to Fosfomycin Is Predominant in Streptococcus pneumoniae and Depends on the murA1 Gene |
| Q43190887 | Inhibitory mechanism of the Qβ lysis protein A2. |
| Q45278217 | MurA as a primary target of tulipalin B and 6-tuliposide B. |
| Q57470806 | Reaching toward underexplored targets in antibacterial drug design |
| Q27670812 | Structural and Functional Characterization of NikO, an Enolpyruvyl Transferase Essential in Nikkomycin Biosynthesis |
| Q36319020 | Structural and functional features of enzymes of Mycobacterium tuberculosis peptidoglycan biosynthesis as targets for drug development. |
| Q45325569 | Structures of Qβ virions, virus-like particles, and the Qβ-MurA complex reveal internal coat proteins and the mechanism of host lysis. |
Search more.