Structure of peptide deformylase and identification of the substrate binding site
about
Antibiotic Activity and Characterization of BB-3497, a Novel Peptide Deformylase InhibitorCrystal structure of type II peptide deformylase from Staphylococcus aureusStructural variation and inhibitor binding in polypeptide deformylase from four different bacterial speciesCrystal structure of OxyC, a cytochrome P450 implicated in an oxidative C-C coupling reaction during vancomycin biosynthesisThe crystal structure of the periplasmic domain of the Escherichia coli membrane protein insertase YidC contains a substrate binding cleftStructure and Activity of Human Mitochondrial Peptide Deformylase, a Novel Cancer TargetUnderstanding the highly efficient catalysis of prokaryotic peptide deformylases by shedding light on the determinants specifying the low activity of the human counterpartIron center, substrate recognition and mechanism of peptide deformylaseEukaryotic peptide deformylases. Nuclear-encoded and chloroplast-targeted enzymes in ArabidopsisPeptide deformylase in Staphylococcus aureus: resistance to inhibition is mediated by mutations in the formyltransferase geneLigand-induced changes in the structure and dynamics of Escherichia coli peptide deformylasePeptide deformylase as a target for new generation, broad spectrum antimicrobial agents.Resistance of Streptococcus pneumoniae to deformylase inhibitors is due to mutations in defB.N-alkyl urea hydroxamic acids as a new class of peptide deformylase inhibitors with antibacterial activityPeptide deformylase: a target for novel antibiotics?The crystal structure of mitochondrial (Type 1A) peptide deformylase provides clear guidelines for the design of inhibitors specific for the bacterial forms.Zinc is the metal cofactor of Borrelia burgdorferi peptide deformylase.Peptide deformylase--a promising therapeutic target for tuberculosis and antibacterial drug discovery.Mapping the surface of Escherichia coli peptide deformylase by NMR with organic solvents.Formyl-methionine as a degradation signal at the N-termini of bacterial proteins.A slow, tight-binding inhibitor of the zinc-dependent deacetylase LpxC of lipid A biosynthesis with antibiotic activity comparable to ciprofloxacin.External nickel inhibits epithelial sodium channel by binding to histidine residues within the extracellular domains of alpha and gamma subunits and reducing channel open probability.Crystal structure of methylenetetrahydromethanopterin reductase (Mer) in complex with coenzyme F420: Architecture of the F420/FMN binding site of enzymes within the nonprolyl cis-peptide containing bacterial luciferase family.Virtual Screening Approach of Bacterial Peptide Deformylase Inhibitors Results in New Antibiotics.
P2860
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P2860
Structure of peptide deformylase and identification of the substrate binding site
description
1998 nî lūn-bûn
@nan
1998 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Structure of peptide deformylase and identification of the substrate binding site
@ast
Structure of peptide deformylase and identification of the substrate binding site
@en
Structure of peptide deformylase and identification of the substrate binding site
@nl
type
label
Structure of peptide deformylase and identification of the substrate binding site
@ast
Structure of peptide deformylase and identification of the substrate binding site
@en
Structure of peptide deformylase and identification of the substrate binding site
@nl
prefLabel
Structure of peptide deformylase and identification of the substrate binding site
@ast
Structure of peptide deformylase and identification of the substrate binding site
@en
Structure of peptide deformylase and identification of the substrate binding site
@nl
P2093
P2860
P356
P1476
Structure of peptide deformylase and identification of the substrate binding site
@en
P2093
P2860
P304
P356
10.1074/JBC.273.19.11413
P407
P577
1998-05-08T00:00:00Z