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1 nisms that could enable engineering of novel non-ribosomal peptide synthetases.
2 otryptophan represents a novel substrate for non-ribosomal peptide synthetases.
3 umarate:coenzyme A ligases, luciferases, and non-ribosomal peptide synthetases.
4              Here we report an unprecedented non-ribosomal peptide synthetase activity that both asse
5 mproved substrate specificity prediction for non-ribosomal peptide synthetase adenylation domains bas
6 ly strict substrate specificities of related non-ribosomal peptide synthetase adenylation enzymes.
7           In an unprecedented convergence of non-ribosomal peptide synthetase and polyketide synthase
8 is synthesized in part by enzymes resembling non-ribosomal peptide synthetases and that the ABC trans
9                                              Non-ribosomal peptide synthetases are assembly line bios
10                                              Non-ribosomal peptide synthetases are giant enzymes comp
11                                              Non-ribosomal peptide synthetases are important enzymes
12             Modular polyketide synthases and non-ribosomal peptide synthetases are molecular assembly
13 ynthase to a separate carrier protein, and a non-ribosomal peptide synthetase condensation domain con
14       Flavopeptins are synthesized through a non-ribosomal peptide synthetase containing a terminal N
15     Curacin A is a polyketide synthase (PKS)-non-ribosomal peptide synthetase-derived natural product
16         Secondary metabolites synthesized by non-ribosomal peptide synthetases display diverse and co
17 key enzyme was identified, the non-canonical non-ribosomal peptide synthetase Fub8.
18        Gliotoxin, a major product of the gli non-ribosomal peptide synthetase gene cluster, is strong
19 tations that upregulate transcription of the non-ribosomal peptide synthetase gene required for nidul
20 e diversification of polyketide synthase and non-ribosomal peptide synthetase genes from two newly de
21                               We studied the non-ribosomal peptide synthetase genes involved in A2197
22               Individual inactivation of the non-ribosomal peptide synthetase genes, xcnA and xcnK, a
23  non-ribosomal peptide and hybrid polyketide-non-ribosomal peptide synthetases, including those respo
24                                            A non-ribosomal peptide synthetase-independent siderophore
25  suggests that AcsD and other members of the non-ribosomal peptide synthetase-independent siderophore
26                       PMI0229-0239 encodes a non-ribosomal peptide synthetase-independent siderophore
27 diction software, TxtB was identified as the non-ribosomal peptide synthetase module specific for 4-n
28 ached to CmaD through the actions of CmaA, a non-ribosomal peptide synthetase module, and CmaE, an un
29 Thaxtomin A is produced by the action of two non-ribosomal peptide synthetase modules (TxtA and TxtB)
30 cluding the expected polyketide synthase and non-ribosomal peptide synthetase modules and tailoring g
31 escribe the structures of two different holo-non-ribosomal peptide synthetase modules, each revealing
32 n this model, VbsS, which is similar to many non-ribosomal peptide synthetase multienzymes, has a cen
33 iously identified but experimentally elusive non-ribosomal peptide synthetase (NRPS) and NRPS-polyket
34 elating cyclic hexapeptides are assembled by non-ribosomal peptide synthetase (NRPS) enzymes remains
35 ge of an L-Pro-L-Trp dipeptide from the MalG non-ribosomal peptide synthetase (NRPS) followed by reve
36  are biosynthesized by a single multi-domain non-ribosomal peptide synthetase (NRPS) gene cluster.
37 e approach were applied to the known PKS and non-ribosomal peptide synthetase (NRPS) gene clusters in
38 hotransferase self-resistance gene (vph) and non-ribosomal peptide synthetase (NRPS) gene probes ampl
39    The initial stages of the pathway involve non-ribosomal peptide synthetase (NRPS) mediated assembl
40                          CrpD-M2 is a unique non-ribosomal peptide synthetase (NRPS) module comprised
41 tion of specialized metabolites derived from non-ribosomal peptide synthetase (NRPS) or polyketide sy
42 been proposed to require only the two-module non-ribosomal peptide synthetase (NRPS) peramine synthet
43 study, we determined the function of a novel non-ribosomal peptide synthetase (NRPS) system carried b
44                        The EpoB protein is a non-ribosomal peptide synthetase (NRPS) that catalyzes f
45 ve combination of polyketide synthase (PKS), non-ribosomal peptide synthetase (NRPS), and shikimate p
46                                              Non-ribosomal peptide synthetases (NRPS) and polyketide
47                     The initiation module of non-ribosomal peptide synthetases (NRPS) selects and act
48     In vitro assays reveal two single-module non-ribosomal peptide synthetases (NRPs) that incorporat
49 -CoA synthetases, the adenylation domains of non-ribosomal peptide synthetases (NRPS), and firefly lu
50  production in five Aspergillus species, the non-ribosomal peptide synthetases (NRPS).
51  The peptide backbone of PVD is assembled by non-ribosomal peptide synthetases (NRPSs) and modified b
52                                              Non-ribosomal peptide synthetases (NRPSs) are megaenzyme
53                                              Non-ribosomal peptide synthetases (NRPSs) are modular en
54                                              Non-Ribosomal Peptide Synthetases (NRPSs) assemble a div
55 ide-derived natural products are produced by non-ribosomal peptide synthetases (NRPSs) in an assembly
56 teins termed polyketide synthases (PKSs) and non-ribosomal peptide synthetases (NRPSs) that contain r
57 y, the nocardicin A gene cluster encodes two non-ribosomal peptide synthetases (NRPSs), NocA and NocB
58 natural products are produced by multidomain non-ribosomal peptide synthetases (NRPSs).
59 egonmycins were also shown to originate from non-ribosomal peptide synthetases (NRPSs).
60 ring the biosynthesis of natural products by non-ribosomal peptide synthetases (NRPSs).
61 ical protein and has no sequence homology to non-ribosomal peptide synthetase or bacterial cyclodipep
62 and peptide-polyketide siderophores involves non-ribosomal peptide synthetase, polyketide synthase an
63  organization of the nos synthetase, a mixed non-ribosomal peptide synthetase-polyketide synthase, is
64  mutations in ausA, encoding the aureusimine non-ribosomal peptide synthetase, reduced S. aureus cyto
65  Here we show that communication between two non-ribosomal peptide synthetase subunits responsible fo
66 osynthetic gene clusters for uncharacterised non-ribosomal peptide synthetases, suggesting a high div
67                                          The non-ribosomal peptide synthetase that synthesizes HC-tox
68 s are synthesized from a classically derived non-ribosomal peptide synthetase tripeptide (from delta-
69                     The most common BGCs are non-ribosomal peptide synthetases, type 1 polyketide syn
70 und that expression of nrps1 which encodes a non-ribosomal peptide synthetase was elevated in the omp
71 ding the structural basis for catalysis with non-ribosomal peptide synthetases will facilitate bioeng
72 ed by the action of polyketide synthases and non-ribosomal peptide synthetases with unusual domain st