The crystal structures of four peptide deformylases bound to the antibiotic actinonin reveal two distinct types: a platform for the structure-based design of antibacterial agents (Q27639382)

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English	The crystal structures of four peptide deformylases bound to the antibiotic actinonin reveal two distinct types: a platform for the structure-based design of antibacterial agents	scientific article

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scholarly article

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The crystal structures of four peptide deformylases bound to the antibiotic actinonin reveal two distinct types: a platform for the structure-based design of antibacterial agents (English)

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crystal structure

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2

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Thierry Meinnel

9

object named as

Thierry Meinnel

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Carmela Giglione

object named as

Carmela Giglione

3

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author name string

Jean-Pierre Guilloteau

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Véronique Blanc

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Alain Dupuy

5

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Miline Chevrier

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Patricia Gil

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Alain Famechon

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Vincent Mikol

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publication date

26 July 2002

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Journal of Molecular Biology

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320

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5

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951-62

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Methionine as translation start signal: a review of the enzymes of the pathway in Escherichia coli.

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On the release of the formyl group from nascent protein

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Deformylation and protein biosynthesis

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Protein chain initiation and deformylation in B. subtilis homogenates

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Interplay of Methionine tRNAs with Translation Elongation Factor Tu and Translation Initiation Factor 2 inEscherichia coli

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Characterization of the Thermus thermophilus locus encoding peptide deformylase and methionyl-tRNA(fMet) formyltransferase

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Peptide deformylase in Staphylococcus aureus: resistance to inhibition is mediated by mutations in the formyltransferase gene

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Peptide deformylase as an antibacterial drug target: target validation and resistance development

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Identification of eukaryotic peptide deformylases reveals universality of N-terminal protein processing mechanisms

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Distinctive features of the two classes of eukaryotic peptide deformylases

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Peptide deformylase as a target for new generation, broad spectrum antimicrobial agents

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Peptide deformylase: a target for novel antibiotics?

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Deformylase as a novel antibacterial target.

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Enzymatic properties of Escherichia coli peptide deformylase

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Isolation and crystallization of functionally competent Escherichia coli peptide deformylase forms containing either iron or nickel in the active site

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Control of peptide deformylase activity by metal cations

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Characterization of cobalt(II)-substituted peptide deformylase: function of the metal ion and the catalytic residue Glu-133.

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Actinonin: an Antibiotic Substance produced by an Actinomycete

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7 January 2021

Studies concerning the antibiotic actinonin. Part I. The constitution of actinonin. A natural hydroxamic acid with antibiotic activity

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Actinonin, a naturally occurring antibacterial agent, is a potent deformylase inhibitor

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Mapping of the active site zinc ligands of peptide deformylase.

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Substrate recognition and selectivity of peptide deformylase. Similarities and differences with metzincins and thermolysin

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7 January 2021

Solution structure of nickel-peptide deformylase

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https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900549-1

7 January 2021

The C-terminal domain of peptide deformylase is disordered and dispensable for activity

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7 January 2021

Structure-function relationships within the peptide deformylase family. Evidence for a conserved architecture of the active site involving three conserved motifs and a metal ion.

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Crystals of peptide deformylase from Plasmodium falciparum reveal critical characteristics of the active site for drug design

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Iron center, substrate recognition and mechanism of peptide deformylase

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Crystal Structure of the Escherichia coli Peptide Deformylase,

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Peptide deformylase of eukaryotic protists: a target for new antiparasitic agents?

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7 January 2021

Resistance of Streptococcus pneumoniae to deformylase inhibitors is due to mutations in defB.

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YkrB is the main peptide deformylase in Bacillus subtilis, a eubacterium containing two functional peptide deformylases

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Organellar peptide deformylases: universality of the N-terminal methionine cleavage mechanism.

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Design and Synthesis of Substrate Analogue Inhibitors of Peptide Deformylase†

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7 January 2021

Antibiotic Activity and Characterization of BB-3497, a Novel Peptide Deformylase Inhibitor

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7 January 2021

Resistance to anti-peptide deformylase drugs

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In vitro activities of peptide deformylase inhibitors against gram-positive pathogens

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On the size of the active site in proteases. I. Papain

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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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Processing of X-ray diffraction data collected in oscillation mode

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The CCP4 suite: programs for protein crystallography

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[27] Maximum-likelihood heavy-atom parameter refinement for multiple isomorphous replacement and multiwavelength anomalous diffraction methods.

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Improved methods for building protein models in electron density maps and the location of errors in these models

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Peptide deformylase as an emerging target for antiparasitic agents

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Multiple sequence alignment with Clustal X

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PROMOTIF--a program to identify and analyze structural motifs in proteins

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Identifiers

10.1016/S0022-2836(02)00549-1

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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