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«Uridine Diphosphate N-Acetylmuramic Acid

Below is an extended Uridine Diphosphate N-Acetylmuramic Acid research listing. Click here to return to the Uridine Diphosphate N-Acetylmuramic Acid main in depth entry.

Recent Publications on Uridine Diphosphate N-Acetylmuramic Acid:

Isolation of temperature-sensitive mutations in murC of Staphylococcus aureus.
Enzymes in the bacterial peptidoglycan biosynthesis pathway are important...
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11th July, 2008
Graduate School of Pharmaceutical Sciences, The University of Tokyo,
Staphylococcus aureus MurC participates in L-alanine recognition via histidine 343, a conserved motif in the shallow hydrophobic pocket.
UDP-N-acetylmuramic acid:L-alanine ligase that is encoded by the murC...
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24th June, 2008
Laboratory of Microbiology, Graduate School of Pharmaceutical Sciences,
Characterization of tRNA-dependent peptide bond formation by MurM in the synthesis of Streptococcus pneumoniae peptidoglycan.
MurM is an aminoacyl ligase that adds l-serine or l-alanine as the first...
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31st May, 2008
Departments of Biological Sciences and Chemistry, University of Warwick,
Elucidation of the antimicrobial mechanism of mutacin 1140.
Mutacin 1140 and nisin A are peptide antibiotics that belong to the...
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29th May, 2008
Department of Biological Sciences, Mississippi State University,
An Arabidopsis homolog of the bacterial peptidoglycan synthesis enzyme MurE has an essential role in chloroplast development.
Enzymes encoded by bacterial MurE genes catalyze the ATP-dependent...
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20th May, 2008
Graduate School of Science and Technology, Kumamoto University, Kumamoto
The biosynthesis of peptidoglycan lipid-linked intermediates.
The biosynthesis of bacterial cell wall peptidoglycan is a complex process...
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16th May, 2008
Laboratoire des Enveloppes Bacteriennes et Antibiotiques, Institut de
Molecular mechanism of target recognition by subtilin, a class I lanthionine antibiotic.
The increasing resistance of human pathogens to conventional antibiotics...
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30th April, 2008
School of Biomedical Sciences, University of Nottingham, Nottingham NG7
Optimization of UDP-N-acetylmuramic acid synthesis. 24th April, 2008
Drug Discovery Department, Lek Pharmaceuticals, Verovikova 57, 1526
Expanding role of lipid II as a target for lantibiotics.
Lipid II is an essential cell-wall precursor required for the growth and...
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6th December, 2007
Utrecht University, Department of Medicinal Chemistry & Chemical Biology,
Adenosine phosphonate inhibitors of lipid II: alanyl tRNA ligase MurM from Streptococcus pneumoniae.
Adenosine and 2'-deoxyadenosine phosphonate transition state analogues act...
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6th December, 2007
Department of Chemistry, University of Warwick, Coventry CV4 7AL, UK.
Transmembrane transport of peptidoglycan precursors across model and bacterial membranes.
Translocation of the peptidoglycan precursor Lipid II across the...
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6th December, 2007
Department Biochemistry of Membranes, Bijvoet Centre, Utrecht University,
The tubulin homologue FtsZ contributes to cell elongation by guiding cell wall precursor synthesis in Caulobacter crescentus.
The tubulin homologue FtsZ is well known for its essential function in...
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6th December, 2007
Department of Molecular, Cellular, and Developmental Biology, and
Cell wall growth during elongation and division: one ring to bind them?
The role of the cell division protein FtsZ in bacterial cell wall (CW)...
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6th December, 2007
Molecular Microbiology, Institute for Molecular Cell Biology, Vrije
Synthesis of bicyclic alkene-/alkane-bridged nisin mimics by ring-closing metathesis and their biochemical evaluation as lipid II binders: toward the design of potential novel antibiotics.
This report describes the design, synthesis, and biochemical evaluation of...
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30th October, 2007
Medicinal Chemistry & Chemical Biology, Utrecht Institute for
Cell envelope stress induced by the bacteriocin Lcn972 is sensed by the Lactococcal two-component system CesSR.
The non-pore-forming bacteriocin lactococcin 972 (Lcn972) inhibits the...
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31st May, 2007
Instituto de Productos Lacteos de Asturias, IPLA-CSIC. Apdo. 85. 33300
 

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