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1 orm the protein translocating element of the Tat system.
2 Pmut3* exported to the periplasm through the Tat system.
3 ated that Mycobacterium smegmatis contains a TAT system.
4 but not because of reversion to a functional TAT system.
5 nal recognition particle (SRP), and Delta pH/Tat systems.
6 ly, with 24% dissymmetry in a triazatruxene (TAT) system.
7 s introduce the twin-arginine translocation (Tat) systems.
9 cent progress on the characterization of the Tat system and critically discuss the structure and oper
10 The pectin lyase, PnlH, is exported by the Tat system and is somehow targeted to the outer membrane
11 highlight the remarkable flexibility of the Tat system and its potential for studying and engineerin
14 ansported to the periplasm of E. coli by the tat system, and the corresponding B polypeptides of CT,
16 pan from this Tat(BC) fusion inactivates the Tat system but does not affect assembly of the core comp
17 assembly cycle could explain how the DeltapH/Tat system can assemble translocases to accommodate fold
20 A and tatC encode components of a functional Tat system capable of exporting characteristic Tat subst
26 strate that the twin arginine translocation (Tat) system contributes to bacterial resistance to catio
29 several virulence factors that depend on the TAT system for proper export to the periplasm, outer mem
33 ve important consequences for the use of the Tat system in biotechnology applications where high leve
36 between the mechanistically distinct Sec and Tat systems in the assembly of a single integral membran
37 demonstrate the functional activity of these Tat systems in vivo, since expression of the tatABC oper
38 000 is a multifactorial process and that the Tat system is an important virulence determinant of this
39 m of membrane integration of proteins by the Tat system is fundamentally distinct from that employed
41 biological membranes, the DeltapH-dependent/Tat system is unusual in its sole reliance upon the tran
43 richia coli twin-arginine protein transport (Tat) system is a molecular machine dedicated to the tran
44 ylakoid twin arginine protein translocation (Tat) system is thought to have a multivalent receptor co
45 tA, the protein-translocating element of the Tat system, is a small transmembrane protein that assemb
49 scherichia coli twin arginine translocation (Tat) system mediates Sec-independent export of protein p
50 The twin-arginine protein translocation (Tat) system mediates transport of folded proteins across
51 functioning in alternative respiration, the TAT system of A. tumefaciens is an important virulence d
56 ylakoid twin arginine protein translocation (Tat) system operates by a cyclical mechanism in which pr
57 plasm using the twin-arginine translocation (Tat) system, or fused to an integral plasma membrane pro
58 e action of the twin-arginine translocation (Tat) system propose that substrates bind initially to th
64 eins), is based on the unique ability of the Tat system to efficiently cotranslocate noncovalent comp
65 we utilized the twin arginine translocation (tat) system to produce fluorescent CT chimeras, as well
80 hat the thylakoid twin-arginine translocase (Tat) system transports folded proteins in a unidirection
81 scherichia coli twin-arginine translocation (Tat) system transports fully folded and assembled protei
82 he mechanism and capabilities of the E. coli Tat system using green fluorescent protein (GFP) fused t
85 ins through the twin-arginine translocation (Tat) system, we screened a collection of E. coli mutant
86 y mutations affecting the PrsDE (Type I) and TAT systems were observed to affect the growth phenotype
88 tionally to the twin-arginine translocation (Tat) system which transports folded substrates across th