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1 onents and the TssF and TssG proteins of the type VI secretion system.
2 ivered into competing bacterial cells by the type VI secretion system.
3 l width of the Hcp1 hexamer of P. aeruginosa type VI secretion system.
4 nding and new insights into the effectors of Type VI secretion system.
5 It also shares features with the type VI secretion systems.
6 phenotypes for markers of both type III and type VI secretion systems.
7 d valine-glycine repeat protein G genes from type VI secretion systems.
8 plasm of eukaryotic host cells via Type I or Type VI secretion systems.
9 ropose that these genes encode a prototypic "type VI" secretion system.
10 we and others have shown that one of these, type VI secretion system 5 (T6SS-5), is required for vir
11 nduced via an unknown mechanism by bacterial type VI secretion system 5 (T6SS-5), which is an essenti
12 Interestingly, acidic conditions induced a type VI secretion system and a putative nonheme catalase
13 ce, and its genome contains genes encoding a type VI secretion system and several factors that may pa
15 ed serine protease htrA, and components of a type VI secretion system, but the genome does not harbor
16 anisms: they repress expression of the large type VI secretion system cluster through base pairing an
18 light microscopy reveals that sheaths of the type VI secretion system cycle between assembly, quick c
20 risubalbicans were identified, including the type VI secretion system effector Hcp1, suggesting that
22 regulated secretion island I (HSI-I)-encoded type VI secretion system (H1-T6SS) of Pseudomonas aerugi
23 a and find that gene PA2374, proximal to the type VI secretion system H3 (H3-T6SS), functions synergi
24 the dispersin translocator Aat, and the Aai type VI secretion system, have been found to be regulate
25 mA negatively and include genes encoding the type VI secretion system HSI-I, which has been implicate
26 ultiple and new conformations of the dynamic type VI secretion system in the crowded interior of Myxo
27 accharide production and upregulation of the type VI secretion system; in turn, it repressed the type
28 cellular self-intoxication through an active type VI secretion system, indicating a mechanism for exp
31 Thus, the genes encoding the VAS-related, type VI secretion system likely play an important conser
33 Here we show that protein secretion by the type VI secretion system of Vibrio cholerae requires the
34 modifications that influence sensitivity to Type VI secretion system peptidoglycan endopeptidases an
35 tail-derived bacterial apparatuses, such as type VI secretion systems, Photorhabdus virulence casset
36 the expression of FPI genes, which encode a Type VI secretion system required for intramacrophage gr
37 port a model in which the contraction of the type VI secretion system sheath provides the energy need
39 lation of genes, including components of the type VI secretion system (T6SS) and alginate biosyntheti
40 tsiV3, encoding immunity to a bacteriocidal type VI secretion system (T6SS) effector VgrG3, exhibite
42 We recently delineated the importance of a type VI secretion system (T6SS) gene cluster in the viru
62 he B728a genome shares homology to the novel type VI secretion system (T6SS) locus recently described
64 ctors mediating substrate recognition by the type VI secretion system (T6SS) of Gram-negative bacteri
67 how how killing adjacent competitors via the Type VI secretion system (T6SS) precipitates phase separ
68 ains sequenced to date harbour genes for the type VI secretion system (T6SS) that translocates effect
69 se rapid contraction of a long sheath of the type VI secretion system (T6SS) to deliver effectors int
73 c bacterial interactions as effectors of the type VI secretion system (T6SS) translocation apparatus;
76 the most widespread is the newly recognized Type VI secretion system (T6SS) which is composed of 15-
78 ms of interbacterial antagonism, such as the type VI secretion system (T6SS), a multiprotein needle-l
80 s three genetic architectures (GA1-3) of the type VI secretion system (T6SS), an effector delivery pa
81 cluding a type II secretion system (T2SS), a type VI secretion system (T6SS), autotransporter, and ou
82 emonstrated that a secreted component of the type VI secretion system (T6SS), haemolysin co-regulated
83 ms of interbacterial antagonism, such as the type VI secretion system (T6SS), have not been defined i
84 to various forms of attacks mediated by the type VI secretion system (T6SS), P1vir phage, and polymy
91 Recent studies have shown that the cluster 1 type VI secretion system (T6SS-1) expressed by this orga
92 pathogens was dependent on the activity of a type VI secretion system (T6SS-1) that functions downstr
93 usion requires the function of the cluster 5 type VI secretion system (T6SS-5) and its associated val
101 animal and plant-associated proteobacteria, type VI secretion systems (T6SSs) are potentially capabl
103 f Pseudomonas aeruginosa PAO1 contains three type VI secretion systems (T6SSs) called H1-, H2-, and H
108 deria pseudomallei K96243 genome encodes six type VI secretion systems (T6SSs), but little is known a
109 ions including membrane transport from which type VI secretion systems were in particular upregulated
110 inding protein, and vasK, a component of the type VI secretion system, were also found to exhibit som
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