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1 of the cargo-conducting part of the type-III secretion apparatus.
2 ign of drugs targeting this highly prevalent secretion apparatus.
3 es are predicted to encode a type IV-related secretion apparatus.
4 they are responsible for the formation of a secretion apparatus.
5 iae possess genes that may encode a type III secretion apparatus.
6 (SPI1), that encode components of a type III secretion apparatus.
7 tion of Yops by the plasmid-encoded type III secretion apparatus.
8 oteins targeted to plant cells by a type III secretion apparatus.
9 e predicted to be components of the invasion secretion apparatus.
10 S1 may be required for interaction with the secretion apparatus.
11 ted to the host cell cytoplasm by a type III secretion apparatus.
12 els the accessibility of the location to the secretion apparatus.
13 cifically and efficiently transported by the secretion apparatus.
14 ichia coli (EPEC) is exported via a type III secretion apparatus.
15 , which may be assembly intermediates of the secretion apparatus.
16 proteins secreted by a specialized type III secretion apparatus.
17 des components of a sec-independent type III secretion apparatus.
18 oteins mediate polar localization of the Tad secretion apparatus.
19 these proteins are assembled into the active secretion apparatus.
20 s well as components of the flagellar type 3 secretion apparatus.
21 nscription to the activation of the type III secretion apparatus.
22 r protein translocation through the type III secretion apparatus.
23 ld that recruits other components of the PEL secretion apparatus.
24 are thought to form part of an extracellular secretion apparatus.
25 orted from the cell via a dedicated Type III secretion apparatus.
26 l tested cargo proteins through the cellular secretion apparatus.
27 roximity to each other, likely surrounding a secretion apparatus.
28 we lack details on the architecture of this secretion apparatus.
29 participate in recruiting the complex to the secretion apparatus.
30 omologous to the Legionella/Coxiella Type IV secretion apparatus.
31 responses into host cells through a type III secretion apparatus.
32 r proteins into plant cells using a type III secretion apparatus.
33 to direct heterologous proteins to the CsgG secretion apparatus.
34 of a type IVB system, the Legionella Dot/Icm secretion apparatus.
35 ions of the individual components of the Tad secretion apparatus.
36 aeruginosa to assemble a functional type III secretion apparatus.
37 ole in the assembly of the H. pylori type IV secretion apparatus.
38 of Pseudomonas aeruginosa encodes a protein secretion apparatus.
39 nteraction with structural components of the secretion apparatus.
40 g the YopN-chaperone complex to the type III secretion apparatus.
41 g the activity of the L. pneumophila type IV secretion apparatus.
42 ciates with this complex to form the type IV secretion apparatus.
43 domains that specifically target them to the secretion apparatus.
44 are necessary for an efficiently functioning secretion apparatus.
45 que perspective on the role of this critical secretion apparatus.
46 the assembly of the flagellum and the pilus secretion apparatus.
47 g EsaE in targeting the EsaDG complex to the secretion apparatus.
48 hagosome trafficking mediated by the type IV secretion apparatus.
49 into eukaryotic cells by the SPI-1 type III secretion apparatus.
50 of substrates or the assembly of the type IV secretion apparatus.
51 Thus, RalF is a substrate of the Dot/Icm secretion apparatus.
52 ranslocated proteins in type III and type IV secretion apparatuses.
53 ar multiple motifs associated with bacterial secretion apparatuses.
54 extracellular virulence factors, the type II secretion apparatus, a stationary-phase sigma factor (si
55 tumefaciens VirB proteins assemble a type IV secretion apparatus and a T-pilus for secretion of DNA a
56 h encode proteins that are secreted via this secretion apparatus and are required for bacterial entry
57 ical pattern of expression in which a set of secretion apparatus and regulatory genes is constitutive
58 s (ORFs), including components of a type III secretion apparatus and secreted molecules involved in t
60 ssociated protein that is a component of the secretion apparatus and that it is necessary for the eff
61 ssion of the structural genes for a type III secretion apparatus and the effectors secreted by that a
62 s recent findings on the organization of the secretion apparatus and the role of its various componen
63 he host cell cytoplasm requires the type III secretion apparatus and the secreted proteins EspA and E
64 le-forming pili (BFP), intimin, the type III secretion apparatus and the secreted proteins EspA, EspB
65 tial chaperone, a potential component of the secretion apparatus, and a hypothetical peptide with pro
66 ein is an essential component of the dot/icm secretion apparatus, and that a conserved mechanism of h
67 membrane adhesin called intimin, a type III secretion apparatus, and the EspA and EspB secreted prot
68 uires cell contact-dependent delivery by the secretion apparatus, and thus their export is highly rep
70 ng the structural components of the type III secretion apparatus are conserved among bacterial specie
71 cation required the function of the type III secretion apparatus, as an S. typhimurium strain carryin
72 diated by a virulence (vir)-specific type IV secretion apparatus assembled from 11 VirB proteins and
73 died the role of a putative type III protein secretion apparatus (Bsa) in the interaction between B.
74 own about the assembly and structure of this secretion apparatus, but the InvG protein is essential a
78 e plasmid, encodes an indispensable type III secretion apparatus component, required for both Ipa tra
83 gram-negative pathogens, encodes a type III secretion apparatus dedicated to the release of virulenc
84 ion in switch complex and flagellum-specific secretion apparatus deletion mutants blocked for flagell
85 to be secreted independently of the type III secretion apparatus encoded by genes located within the
86 is dependent upon the extracellular protein secretion apparatus encoded by the eps gene locus of Vib
89 mammalian host cells by means of a type III secretion apparatus, encoded by the pathogenicity island
90 tructures are exported through a specialized secretion apparatus energized by the proton gradient.
91 ighboring bacterial competitors by a Type VI secretion apparatus, eventually leading to cell lysis an
92 tumefaciens VirB proteins assemble a type IV secretion apparatus for the transfer of DNA and proteins
94 ling of the central channel in the flagellar secretion apparatus from a closed to an open conformatio
95 ytoplasmically localized LcrG blocks the Yop secretion apparatus from the cytoplasmic side and that L
97 injected into host cells through a type III secretion apparatus, functions as an effector molecule t
98 DotL, a critical component of the Dot/Icm secretion apparatus, functions as the type IV coupling p
99 However, certain essential components of the secretion apparatus have diverged to such a degree as to
100 the "secretin" of the extracellular protein secretion apparatus), (ii) in a hydG-like gene (encodes
101 entified 15 loci that are part of a type III secretion apparatus in B. bronchiseptica and three secre
102 machinery in single-cell organisms like the secretion apparatus in bacteria and Toxoplasma gondii, a
104 e bacterial flagellum contains a specialized secretion apparatus in its base that pumps certain prote
105 stems to shut down energy-expensive type III secretion apparatus in response to specific environmenta
109 1 (Salmonella pathogenicity island) type III secretion apparatus is known to require the transcriptio
110 ion of extracellular proteins via a type III secretion apparatus is necessary for the formation of at
111 iae RyhB include those encoding the type III secretion apparatus, its secreted effectors, and specifi
113 zed airway epithelial cells via the type III secretion apparatus leads to release of Ca stored in the
115 he switch complex and the flagellum-specific secretion apparatus, no protein was detected in a strain
116 otein secretion by the extracellular protein secretion apparatus occurred in the absence of both TonB
118 e insights into the function of the type III secretion apparatus of EPEC and the functions of the Esp
119 putative type III translocation proteins and secretion apparatus of P. aeruginosa were required for t
120 ssion of type III genes would then replenish secretion apparatus on vegetative RBs and serve as a sou
121 s a distinct chromosomal locus, the Yersinia secretion apparatus pathogenicity island (YSA PI) that e
123 rocolitica chromosome that encode a type III secretion apparatus plus two associated putative regulat
124 II secretion by blocking the entrance to the secretion apparatus prior to contact with mammalian cell
125 om the chlamydial vacuole through a type III secretion apparatus results in efflux of K(+) through gl
126 edicted to be components of a membrane-bound secretion apparatus similar to type IV conjugal transfer
127 PscJ protein, a structural component of the secretion apparatus, suggesting that cytotoxins are inje
130 t physiologic role for the Shigella type III secretion apparatus (T3SA) in mediating phagosomal escap
131 previously demonstrated that the type three secretion apparatus (T3SA) proteins IpaB and IpaD are pr
133 port, we establish that the Inv-Spa type III secretion apparatus target invasin SipB is necessary and
134 Bacterial flagella contain a specialized secretion apparatus that functions to deliver the protei
136 ella pneumophila Dot/Icm system is a type IV secretion apparatus that transfers bacterial proteins in
137 Legionnaires' disease, expresses a type IVB secretion apparatus that translocates bacterial proteins
138 the bacterial Dot/Icm system, a multiprotein secretion apparatus that translocates proteins from the
139 observed for the components of the type III secretion apparatus, the Ces chaperones, and the Ler reg
140 ex choreography of the substrate through the secretion apparatus, the molecular mechanism of the type
141 of PA103, we demonstrated that the type III secretion apparatus, the type III-secreted effector ExoU
142 with the activation of the Shigella type III secretion apparatus, thus evidencing injectisome activit
143 opathogenic Escherichia coli uses a type III secretion apparatus to deliver proteins essential for pa
144 paE and CpaC components of the pili-specific secretion apparatus to one pole of the predivisional cel
145 ella flexneri requires a functional type III secretion apparatus to serve as a conduit for injecting
146 c side of the injectisome, reprogramming the secretion apparatus to stop secretion of the needle prot
147 a needle-like protein assembly, the type III secretion apparatus, to inject virulence factors into ta
148 burst of protein secretion via its type III secretion apparatus (TTSA) as an initial step in cellula
152 roteins of the type II extracellular protein secretion apparatus undergo two consecutive post-transla
153 ught to physically block the entrance to the secretion apparatus until an appropriate signal is recei
154 injects invasin proteins through a type III secretion apparatus upon contacting the host cell, which
155 e the function of this chromosomally-encoded secretion apparatus, we created an in frame deletion of
156 which encodes an essential component of the secretion apparatus, were also significantly attenuated.
158 ence that P. aeruginosa possesses a type III secretion apparatus which is required for the export of
159 roteins into host cells through the type III secretion apparatus, which is comprised of a basal body,
160 ein LcrV for proper function of the type III secretion apparatus, which is crucial for virulence.
161 es direct effector proteins to a needle-like secretion apparatus, which then delivers the effector pr
162 ing domain of PelB localizes PelA to the PEL secretion apparatus within the periplasm and that this m
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