Biosynthetic tailoring of microcin E492m: post-translational modification affords an antibacterial siderophore-peptide conjugate.
about
HUMAN MICROBIOTA. Small molecules from the human microbiotaThe bacterial chemical repertoire mediates metabolic exchange within gut microbiomesPseudouridine Monophosphate Glycosidase: A New Glycosidase MechanismIsolation and characterization of two members of the siderophore-microcin family, microcins M and H47Targeting virulence: salmochelin modification tunes the antibacterial activity spectrum of β-lactams for pathogen-selective killing of Escherichia coli.Analysis of carbohydrates and glycoconjugates by matrix-assisted laser desorption/ionization mass spectrometry: an update for 2007-2008.Genome mining for ribosomally synthesized natural productsRibosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature.Microcins in action: amazing defence strategies of Enterobacteria.Microcin e492 amyloid formation is retarded by posttranslational modification.Total (bio)synthesis: strategies of nature and of chemists.Natural products as mediators of disease.Syntheses of Siderophore-Drug Conjugates Using a Convergent Thiol-Maleimide SystemFollow the leader: the use of leader peptides to guide natural product biosynthesis.How nature morphs peptide scaffolds into antibioticsDefining the mode of action of tetramic acid antibacterials derived from Pseudomonas aeruginosa quorum sensing signals.Ribosomal peptide natural products: bridging the ribosomal and nonribosomal worlds.Microbial manipulation of the amyloid fold.Biosynthetic considerations of triscatechol siderophores framed on serine and threonine macrolactone scaffolds.Whole-Genome Sequence of the Microcin E492-Producing Strain Klebsiella pneumoniae RYC492.The production in vivo of microcin E492 with antibacterial activity depends on salmochelin and EntF.Antibiotics and specialized metabolites from the human microbiota.Major gene-regulatory mechanisms operating in ribosomally synthesized and post-translationally modified peptide (RiPP) biosynthesis.Dual substrate-controlled kinase activity leads to polyphosphorylated lasso peptides.The Ferric uptake regulator (Fur) and iron availability control the production and maturation of the antibacterial peptide microcin E492
P2860
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P2860
Biosynthetic tailoring of microcin E492m: post-translational modification affords an antibacterial siderophore-peptide conjugate.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Biosynthetic tailoring of micr ...... siderophore-peptide conjugate.
@en
type
label
Biosynthetic tailoring of micr ...... siderophore-peptide conjugate.
@en
prefLabel
Biosynthetic tailoring of micr ...... siderophore-peptide conjugate.
@en
P2093
P2860
P356
P1476
Biosynthetic tailoring of micr ...... siderophore-peptide conjugate.
@en
P2093
Alexander Koglin
Christopher T Walsh
Elizabeth M Nolan
Michael A Fischbach
P2860
P304
14336-14347
P356
10.1021/JA074650F
P407
P577
2007-10-31T00:00:00Z