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1 oaded with toxic cargo before assembling the secretion apparatus.
2 es are predicted to encode a type IV-related secretion apparatus.
3 they are responsible for the formation of a secretion apparatus.
4 iae possess genes that may encode a type III secretion apparatus.
5 (SPI1), that encode components of a type III secretion apparatus.
6 tion of Yops by the plasmid-encoded type III secretion apparatus.
7 oteins targeted to plant cells by a type III secretion apparatus.
8 g EsaE in targeting the EsaDG complex to the 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 ign of drugs targeting this highly prevalent secretion apparatus.
12 ted to the host cell cytoplasm by a type III secretion apparatus.
13 els the accessibility of the location to the secretion apparatus.
14 cifically and efficiently transported by the secretion apparatus.
15 ichia coli (EPEC) is exported via a type III secretion apparatus.
16 , which may be assembly intermediates of the secretion apparatus.
17 proteins secreted by a specialized type III secretion apparatus.
18 des components of a sec-independent type III secretion apparatus.
19 imensional structures of the fully assembled secretion apparatus.
20 oteins mediate polar localization of the Tad secretion apparatus.
21 these proteins are assembled into the active secretion apparatus.
22 r architecture and biogenesis of the Dot/Icm secretion apparatus.
23 s well as components of the flagellar type 3 secretion apparatus.
24 nscription to the activation of the type III secretion apparatus.
25 r protein translocation through the type III secretion apparatus.
26 are thought to form part of an extracellular secretion apparatus.
27 orted from the cell via a dedicated Type III secretion apparatus.
28 l tested cargo proteins through the cellular secretion apparatus.
29 roximity to each other, likely surrounding a secretion apparatus.
30 participate in recruiting the complex to the secretion apparatus.
31 of the cargo-conducting part of the type-III secretion apparatus.
32 omologous to the Legionella/Coxiella Type IV secretion apparatus.
33 responses into host cells through a type III secretion apparatus.
34 r proteins into plant cells using a type III secretion apparatus.
35 to direct heterologous proteins to the CsgG secretion apparatus.
36 of a type IVB system, the Legionella Dot/Icm secretion apparatus.
37 ions of the individual components of the Tad secretion apparatus.
38 aeruginosa to assemble a functional type III secretion apparatus.
39 ole in the assembly of the H. pylori type IV secretion apparatus.
40 ld that recruits other components of the PEL secretion apparatus.
41 of Pseudomonas aeruginosa encodes a protein secretion apparatus.
42 nteraction with structural components of the secretion apparatus.
43 g the YopN-chaperone complex to the type III secretion apparatus.
44 g the activity of the L. pneumophila type IV secretion apparatus.
45 we lack details on the architecture of this secretion apparatus.
46 ciates with this complex to form the type IV secretion apparatus.
47 domains that specifically target them to the secretion apparatus.
48 are necessary for an efficiently functioning secretion apparatus.
49 que perspective on the role of this critical secretion apparatus.
50 the assembly of the flagellum and the pilus secretion apparatus.
51 hagosome trafficking mediated by the type IV secretion apparatus.
52 into eukaryotic cells by the SPI-1 type III secretion apparatus.
53 of substrates or the assembly of the type IV secretion apparatus.
54 Thus, RalF is a substrate of the Dot/Icm secretion apparatus.
55 ranslocated proteins in type III and type IV secretion apparatuses.
56 ar multiple motifs associated with bacterial secretion apparatuses.
57 extracellular virulence factors, the type II secretion apparatus, a stationary-phase sigma factor (si
58 tumefaciens VirB proteins assemble a type IV secretion apparatus and a T-pilus for secretion of DNA a
59 h encode proteins that are secreted via this secretion apparatus and are required for bacterial entry
60 SS), virulence determinants that include the secretion apparatus and associated secretion substrates.
61 ical pattern of expression in which a set of secretion apparatus and regulatory genes is constitutive
62 s (ORFs), including components of a type III secretion apparatus and secreted molecules involved in t
64 ssociated protein that is a component of the secretion apparatus and that it is necessary for the eff
65 ssion of the structural genes for a type III secretion apparatus and the effectors secreted by that a
66 s recent findings on the organization of the secretion apparatus and the role of its various componen
67 he host cell cytoplasm requires the type III secretion apparatus and the secreted proteins EspA and E
68 le-forming pili (BFP), intimin, the type III secretion apparatus and the secreted proteins EspA, EspB
69 s thought to be localized at the base of the secretion apparatus and to participate in the recognitio
70 tial chaperone, a potential component of the secretion apparatus, and a hypothetical peptide with pro
71 ein is an essential component of the dot/icm secretion apparatus, and that a conserved mechanism of h
72 membrane adhesin called intimin, a type III secretion apparatus, and the EspA and EspB secreted prot
73 uires cell contact-dependent delivery by the secretion apparatus, and thus their export is highly rep
74 ture and molecular components of the rhoptry secretion apparatus, and to the current conceptual frame
76 ng the structural components of the type III secretion apparatus are conserved among bacterial specie
77 cation required the function of the type III secretion apparatus, as an S. typhimurium strain carryin
78 diated by a virulence (vir)-specific type IV secretion apparatus assembled from 11 VirB proteins and
79 died the role of a putative type III protein secretion apparatus (Bsa) in the interaction between B.
80 3 paralogous region that lacks genes for the secretion apparatus but encodes EsxR and EsxS, apparent
81 own about the assembly and structure of this secretion apparatus, but the InvG protein is essential a
85 e plasmid, encodes an indispensable type III secretion apparatus component, required for both Ipa tra
90 gram-negative pathogens, encodes a type III secretion apparatus dedicated to the release of virulenc
91 ion in switch complex and flagellum-specific secretion apparatus deletion mutants blocked for flagell
92 to be secreted independently of the type III secretion apparatus encoded by genes located within the
93 is dependent upon the extracellular protein secretion apparatus encoded by the eps gene locus of Vib
96 mammalian host cells by means of a type III secretion apparatus, encoded by the pathogenicity island
97 tructures are exported through a specialized secretion apparatus energized by the proton gradient.
98 ighboring bacterial competitors by a Type VI secretion apparatus, eventually leading to cell lysis an
100 tumefaciens VirB proteins assemble a type IV secretion apparatus for the transfer of DNA and proteins
102 ling of the central channel in the flagellar secretion apparatus from a closed to an open conformatio
103 ytoplasmically localized LcrG blocks the Yop secretion apparatus from the cytoplasmic side and that L
105 injected into host cells through a type III secretion apparatus, functions as an effector molecule t
106 DotL, a critical component of the Dot/Icm secretion apparatus, functions as the type IV coupling p
107 However, certain essential components of the secretion apparatus have diverged to such a degree as to
108 the "secretin" of the extracellular protein secretion apparatus), (ii) in a hydG-like gene (encodes
109 entified 15 loci that are part of a type III secretion apparatus in B. bronchiseptica and three secre
110 machinery in single-cell organisms like the secretion apparatus in bacteria and Toxoplasma gondii, a
112 e bacterial flagellum contains a specialized secretion apparatus in its base that pumps certain prote
113 stems to shut down energy-expensive type III secretion apparatus in response to specific environmenta
117 1 (Salmonella pathogenicity island) type III secretion apparatus is known to require the transcriptio
118 ion of extracellular proteins via a type III secretion apparatus is necessary for the formation of at
119 iae RyhB include those encoding the type III secretion apparatus, its secreted effectors, and specifi
121 zed airway epithelial cells via the type III secretion apparatus leads to release of Ca stored in the
123 he switch complex and the flagellum-specific secretion apparatus, no protein was detected in a strain
124 otein secretion by the extracellular protein secretion apparatus occurred in the absence of both TonB
126 e insights into the function of the type III secretion apparatus of EPEC and the functions of the Esp
127 putative type III translocation proteins and secretion apparatus of P. aeruginosa were required for t
128 ssion of type III genes would then replenish secretion apparatus on vegetative RBs and serve as a sou
129 s a distinct chromosomal locus, the Yersinia secretion apparatus pathogenicity island (YSA PI) that e
131 rocolitica chromosome that encode a type III secretion apparatus plus two associated putative regulat
132 II secretion by blocking the entrance to the secretion apparatus prior to contact with mammalian cell
133 om the chlamydial vacuole through a type III secretion apparatus results in efflux of K(+) through gl
134 edicted to be components of a membrane-bound secretion apparatus similar to type IV conjugal transfer
135 PscJ protein, a structural component of the secretion apparatus, suggesting that cytotoxins are inje
138 t physiologic role for the Shigella type III secretion apparatus (T3SA) in mediating phagosomal escap
139 previously demonstrated that the type three secretion apparatus (T3SA) proteins IpaB and IpaD are pr
141 port, we establish that the Inv-Spa type III secretion apparatus target invasin SipB is necessary and
142 Bacterial flagella contain a specialized secretion apparatus that functions to deliver the protei
144 ella pneumophila Dot/Icm system is a type IV secretion apparatus that transfers bacterial proteins in
145 Legionnaires' disease, expresses a type IVB secretion apparatus that translocates bacterial proteins
146 the bacterial Dot/Icm system, a multiprotein secretion apparatus that translocates proteins from the
147 observed for the components of the type III secretion apparatus, the Ces chaperones, and the Ler reg
148 ex choreography of the substrate through the secretion apparatus, the molecular mechanism of the type
149 of PA103, we demonstrated that the type III secretion apparatus, the type III-secreted effector ExoU
150 with the activation of the Shigella type III secretion apparatus, thus evidencing injectisome activit
151 opathogenic Escherichia coli uses a type III secretion apparatus to deliver proteins essential for pa
152 paE and CpaC components of the pili-specific secretion apparatus to one pole of the predivisional cel
153 ella flexneri requires a functional type III secretion apparatus to serve as a conduit for injecting
154 c side of the injectisome, reprogramming the secretion apparatus to stop secretion of the needle prot
155 a needle-like protein assembly, the type III secretion apparatus, to inject virulence factors into ta
156 burst of protein secretion via its type III secretion apparatus (TTSA) as an initial step in cellula
160 roteins of the type II extracellular protein secretion apparatus undergo two consecutive post-transla
161 ught to physically block the entrance to the secretion apparatus until an appropriate signal is recei
162 injects invasin proteins through a type III secretion apparatus upon contacting the host cell, which
163 e the function of this chromosomally-encoded secretion apparatus, we created an in frame deletion of
164 which encodes an essential component of the secretion apparatus, were also significantly attenuated.
166 ence that P. aeruginosa possesses a type III secretion apparatus which is required for the export of
167 roteins into host cells through the type III secretion apparatus, which is comprised of a basal body,
168 ein LcrV for proper function of the type III secretion apparatus, which is crucial for virulence.
169 es direct effector proteins to a needle-like secretion apparatus, which then delivers the effector pr
170 ing domain of PelB localizes PelA to the PEL secretion apparatus within the periplasm and that this m