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1 trix formation and various substrates of the type II secretion system.
2 uter membrane secretin PulD of the bacterial type II secretion system.
3 a(CT)) to enable delivery via the Salmonella type II secretion system.
4 tozoan cells in a process independent of the type II secretion system.
5 nt of the hydrolytic enzymes exported by the type II secretion system.
6 Type IV pilus systems as well as the related Type II secretion system.
7 the assembly of this critical protein in the Type II secretion system.
8 ot/icm-regulated pore-forming toxin, and the type II secretion system.
9 by the extracellular protein secretion (eps) type II secretion system.
10 fibre are conserved; they are related to the type II secretion system.
11 retion across the outer membrane, similar to type II secretion systems.
12 refore likely to be of general importance in type II secretion systems.
13 milarity to the PulD, -F, and -G homologs of type II secretion systems.
15 irulence potential of the S. maltophilia Xps type II secretion system and its StmPr1 and StmPr2 subst
16 S. maltophilia strain K279a encodes the Xps type II secretion system and that Xps promotes rounding,
17 that an lspG mutant that is defective in the type II secretion system and therefore does not secrete
18 ncoding proteins that include members of the type II secretion system and type IV pili, shown to be e
19 MshE-type ATPases associated with bacterial type II secretion system and type IV pilus formation wer
20 estinal colonization, proper function of the type II secretion system, and formation of biofilm matri
21 ncluding XoxF-type alcohol dehydrogenases, a type II secretion system, and proteins without a predict
23 tion, including outer membrane vesicles, the type II secretion system, and the type IV pilus, were di
24 and lspG mutants, which are defective in the type II secretion system, are not defective in the pore-
25 ode proteins homologous to those involved in type II secretion systems, biogenesis of type IV pili, a
28 ejuni include those similar to components of type II secretion systems found in many Gram-negative ba
30 showing that all the core components of the type II secretion system have a structural or sequence o
31 ne proteases to be the substrates of the Xps type II secretion system in S. maltophilia strain K279a.
32 fied serine protease that is secreted by the type II secretion system in Vibrio cholerae, belongs to
34 the activity of enzymes secreted through the type II secretion system, including phospholipase A, lys
35 motif is not present in proteins secreted by type II secretion systems, indicating that this is uniqu
39 nch of the general secretion pathway (Gsp or type II secretion system) is used by several pathogenic
40 sp system is a virulence factor and the only type II secretion system linked to intracellular infecti
45 omplex between two different proteins of the type II secretion system reveals that the N-terminal dom
46 assembly principles and dynamic function of type II secretion system secretins and challenge recent
49 ing diverse virulence factors, including the type II secretion system (T2SS) and type III secretion s
54 at A. nosocomialis M2 possesses a functional type II secretion system (T2SS) that is required for ful
55 Gram-negative bacteria use the multi-protein type II secretion system (T2SS) to selectively transloca
56 ogenic species of Acinetobacter, including a type II secretion system (T2SS), a type VI secretion sys
57 wide array of secretion systems, including a type II secretion system (T2SS), three type III secretio
59 factors produced by Aeromonas hydrophila, a type II secretion system (T2SS)-secreted cytotoxic enter
61 rulence plasmid pO157, which encodes the etp type II secretion system that secretes the genetically l
63 tative pilin genes of the Klebsiella oxytoca type II secretion system with the complete comG locus.
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