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1  local expression of this antistaphylococcal peptide antibiotic.
2 a gene-encoded, posttranslationally modified peptide antibiotic.
3 which may enable the discovery of new cyclic peptide antibiotics.
4 de prospection can identify stable, nontoxic peptide antibiotics.
5 foundation for the structure-based design of peptide antibiotics.
6 ly synthesized, posttranslationally modified peptide antibiotics.
7 e involved in the synthesis of polyketide or peptide antibiotics.
8 ed to the polyoxin and nikkomycin nucleoside-peptide antibiotics.
9 esent a large family of ribosomally produced peptide antibiotics.
10 ynthesized and post-translationally modified peptide antibiotics.
11           Lantibiotics are a unique class of peptide antibiotics.
12 pproach to make carbohydrate-modified cyclic peptide antibiotics.
13 elerate rational engineering of nonribosomal peptide antibiotics.
14 human beta-defensins and the design of novel peptide antibiotics.
15  an attractive approach for developing novel peptide antibiotics.
16 n effective approach for preparing selective peptide antibiotics.
17 de a useful template for the design of novel peptide antibiotics.
18 re the best characterized epithelial-derived peptide antibiotics.
19 e reductase inhibitor, an oxazolidinone, two peptide antibiotics, a glycylcycline, and a peptide defo
20                                          The peptide antibiotic albicidin is a DNA topoisomerase inhi
21 osynthetic genes for this subclass of uridyl peptide antibiotics and provide the basis for future mec
22 eptide synthetase (NRPS) proteins to produce peptide antibiotics and siderophores.
23 osporin, cephamycin, fluoroquinolone, penam, peptide antibiotics and tetracycline.
24          D-amino acids are commonly found in peptide antibiotics and the cell wall peptidoglycan of b
25 the production of four chemical compounds, a peptide antibiotic, and carbohydrate catabolism by using
26 g peptide antitumor agents, hormones, cyclic peptide antibiotics, and model proteins.
27  well as in the biosynthesis of menaquinone, peptide antibiotics, and peptide siderophores.
28 a large number of candidate drugs, including peptides, antibiotics, and chemotherapeutic agents.
29 les per second) for three substance classes (peptides, antibiotics, and lipids).
30                                              Peptide antibiotics are an abundant and synthetically tr
31                      Membrane-permeabilizing peptide antibiotics are an underutilized weapon in the b
32                                      Natural peptide antibiotics are part of host innate immunity aga
33                                              Peptide antibiotics are viable alternatives although the
34 entify the thiocillins, a group of thiazolyl peptide antibiotics, as biofilm matrix-inducing compound
35  responsible for the synthesis of the cyclic peptide antibiotic Aureobasidin A (AbA) in Aureobasidium
36 n (a single peptide lantibiotics), and three peptide antibiotics (bacitracin, polymyxin B, and vancom
37 uences and will open prospects for designing peptide antibiotics, biosensors, and new membrane protei
38  intermediates suggest a general strategy in peptide antibiotic biosynthesis.
39 ants of the thiocillin subclass of thiazolyl peptide antibiotics by a cascade of post-translational m
40              In nonribosomal biosynthesis of peptide antibiotics by multimodular synthetases, amino a
41  into microbial secondary metabolism to form peptide antibiotics by specific oxidation, including hyd
42                A member of another family of peptide antibiotics called cathelicidins recently was id
43 cal isolates of Streptococcus mutans produce peptide antibiotics called mutacins.
44 synthesis of the tuberculostatic macrocyclic peptide antibiotic capreomycin IB has been accomplished.
45 emical assignment of the recently discovered peptide antibiotic clovibactin.
46               Extracellular secretion of the peptide antibiotic colicin V (ColV) in Escherichia coli
47 amily and is essential for the export of the peptide antibiotic colicin V.
48         They are members of another class of peptide antibiotics containing aspartate, which when pre
49 ynthesized and post-translationally modified peptide antibiotics containing the characteristic thioet
50  mammalian skin expresses these gene-encoded peptide antibiotics during inflammatory events such as w
51 for the bis-intercalative interaction of the peptide antibiotic echinomycin with DNA.
52 lose similarity to biphenomycins, a class of peptide antibiotics for which the biosynthetic pathway h
53 hicin represents a hydrophobic alpha-helical peptide antibiotic forming voltage-gated ion channels in
54      The human HNP-defensin-1 gene encodes a peptide antibiotic found exclusively in neutrophils and
55 is clue, we identified dynobactin A, a novel peptide antibiotic from Photorhabdus australis containin
56  factor (EF) Tu-GDP and the cyclic thiazolyl peptide antibiotic, GE2270A, has been determined by X-ra
57 ructural approaches, we show that the cyclic-peptide antibiotic GE23077 (GE) binds directly to the ba
58 ical protein PacB, conserved in known uridyl peptide antibiotics gene clusters, has been characterize
59    The non-ribosomal synthesis of the cyclic peptide antibiotic gramicidin S is accomplished by two l
60 eration of a host of D-amino acid-containing peptide antibiotics (gramicidin, actinomycin, bacitracin
61                                              Peptide antibiotic (halocin) preparations from euryarcha
62 or laspartomycins, a family of 11 amino acid peptide antibiotics, has been cloned and sequenced from
63 of cationic steroid antibiotics and cationic peptide antibiotics have been compared.
64                                      Whereas peptide antibiotics have been reported from bacillus spe
65   Previous studies have implicated the novel peptide antibiotic human beta-defensin 1 (hBD-1) in the
66 vivo are shown to constitutively express the peptide antibiotic human beta-defensin type 1 (hBD-1).
67 orial biosynthesis platform to produce novel peptide antibiotics in sufficient quantities for antimic
68 structural diversity of the amphomycin-group peptide antibiotics including the laspartomycins and fri
69        Polymyxin B (PMB), a cyclic, cationic peptide antibiotic, inhibits biological activities of LP
70 ovide templates for designing broad-spectrum peptide antibiotics intended to function in extracellula
71     Synthetic peptides modeled after natural peptide antibiotics interfere with microbial membranes a
72 ring a gene encoding a secreted cathelicidin peptide antibiotic into the airway epithelium grown in a
73 nsiderable number of ribosomally synthesized peptide antibiotics involves the modification of Ser and
74                                         This peptide antibiotic is unique since it is processed from
75  Sensitivity of enteric bacteria to multiple peptide antibiotics is controlled by the single inner me
76 ancomycin, a branched tricyclic glycosylated peptide antibiotic, is a last-line defence against serio
77                      Polymyxin B, a cationic peptide antibiotic, is one of the simplest molecules cap
78 tification and characterization of the lasso peptide antibiotic lariocidin and its internally cyclize
79                                    Synthetic peptide antibiotics may be useful tools in the search fo
80                                      In many peptide antibiotics, modified amino acids are important
81                                    Thiazolyl peptide antibiotic nocathiacin I (1) was converted to no
82 est that the same process used in assembling peptide antibiotics or a yet unidentified mechanism may
83 ysis of the effects of a set of AMPs and the peptide antibiotic polymyxin B (PMB) on the physicochemi
84 lmonella enterica controls resistance to the peptide antibiotic polymyxin B and to several antimicrob
85 nella typhimurium controls resistance to the peptide antibiotic polymyxin B and to several antimicrob
86 henotypes with respect to sensitivity to the peptide antibiotic polymyxin B: classical strains are se
87  Bacitracin is a widely used metal-dependent peptide antibiotic produced by Bacillus subtilis and Bac
88 oesterase, and to create a library of cyclic peptide antibiotic products.
89                                          The peptide antibiotic ramoplanin inhibits bacterial peptido
90 ntibiotics suggest that cationic steroid and peptide antibiotics share mechanistic aspects.
91                                The synthetic peptide antibiotic showed potent activity against differ
92 acking glycolipids are more sensitive to the peptide antibiotic sublancin and are defective in swarmi
93 rent substructure of polycyclic nonribosomal peptide antibiotics such as vancomycin.
94 rn of stereochemistry in residues 1-7 of the peptide antibiotic teixobactin is critical to its extrao
95 efensin 3 (hBD-3) is an inducible epithelial peptide antibiotic that has potent antistaphylococcal ac
96 determination of Novo29 (clovibactin), a new peptide antibiotic that is related to teixobactin and is
97                  Bacitracin is a macrocyclic peptide antibiotic that is widely used as a topical trea
98 report the identification of 2,603 encrypted peptide antibiotics that are encoded in proteins with bi
99  Cathelicidins are a class of small cationic peptide antibiotics that are expressed in skin and in ot
100  beta-defensins are endogenous cysteine-rich peptide antibiotics that are produced either by epitheli
101                 Mutacin 1140 and nisin A are peptide antibiotics that belong to the lantibiotic famil
102                  Lantibiotics are a class of peptide antibiotics that contain one or more thioether b
103          Pacidamycins are a family of uridyl peptide antibiotics that inhibit the translocase MraY, a
104 imics incorporate features of the nucleoside-peptide antibiotics, the polyoxins and the nikkomycins,
105 the response of Streptomyces lividans to the peptide antibiotic thiostrepton, and lesser sequence sim
106 aminobutanoic acid (DAB) is found in several peptide antibiotics, toxins, and biologically active mol
107                                   The uridyl peptide antibiotics (UPAs), of which pacidamycin is a me
108 IV (2) are novel indole-containing thiazolyl peptide antibiotics, which exhibit potent activity again
109 lly encoded and posttranslationally modified peptide antibiotics, which inhibit the growth of other G
110 ctionalized with polymyxin B (PMB), a cyclic peptide antibiotic with high affinity for LPS.
111 tion of the charge cluster of an amphipathic peptide antibiotic with microbial membranes is a salt-se

 
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