ライフサイエンスコーパス: export apparatus

1 apparatus) and sipB (a substrate of the SPI1 export apparatus).

2 flagellar rotor switch complex and flagellar export apparatus.

3 membrane proteins that compose the so-called export apparatus.

4 on of the protein is linked to the flagellar export apparatus.

5 he switching of substrate specificity of the export apparatus.

6 revealing features of the rotor, stator and export apparatus.

7 ponents are exported by a flagellum-specific export apparatus.

8 Cia proteins are secreted from the flagellar export apparatus.

9 mplex consisting of the C-ring, MS-ring, and export apparatus.

10 were still recruited to assemble the type I export apparatus.

11 s a member of the flagellum-specific protein export apparatus.

12 FlhB, a component of the type III flagellar export apparatus.

13 oplasmic component of the type III flagellar export apparatus.

14 ponents of the Salmonella type III flagellar export apparatus.

15 odes a protein that is exported via the SPI1 export apparatus.

16 asion proteins secreted by the SPI1 type III export apparatus.

17 required for the assembly or function of the export apparatus.

18 lves feedback from the assembly point to the export apparatus.

19 scB-L proteins of the yersiniae Yop type III export apparatus.

20 h other components in the flagellum-specific export apparatus.

21 nal signal sequence that targets them to the export apparatus.

22 at a site that eventually loads the nuclear export apparatus.

23 FliJ is a general component of the flagellar export apparatus and has a chaperone-like activity for b

24 rved of the membrane-bound components of the export apparatus and has not been annotated for any of t

25 the needle complex base is initiated at the export apparatus and that, in the absence of export appa

26 ts of the inner membrane-localized flagellar export apparatus and the FlgSR two-component regulatory

27 uction of or signaling between the flagellar export apparatus and the FlgSR two-component regulatory

28 tor), spaS (a component of the SPI1 type III export apparatus) and sipB (a substrate of the SPI1 expo

29 ssociated needle complex, the inner membrane export apparatus, and a large cytoplasmic sorting platfo

30 with novel features in the flagellar C ring, export apparatus, and stator.

31 Six of the components of the export apparatus are integral membrane proteins and are

32 Two modes of action within the flagellar export apparatus are proposed, in which the motor perfor

33 ir interactions with other components of the export apparatus are unclear.

34 pression or a typical defect in the flagella export apparatus as there was no class III gene downregu

35 ctural components of the MS ring, switch and export apparatus, as well as the genes encoding both Fli

36 Here, we show that components of the export apparatus associate intimately with the needle co

37 to the C ring and thus the membrane-embedded export apparatus beyond.

38 lar interactions of the internalized SpaPQR 'export apparatus' complex, which is intimately encapsula

39 rast, the secretin SctC (YscC) and the major export apparatus component SctV (YscV) display minimal e

40 We also show that InvA, a critical export apparatus component, forms a multiring cytoplasmi

41 basal body proteins, the flagellar type III export apparatus components FliO, FliP, FliQ, FliR, FlhA

42 We show the precise location of the core export apparatus components within the injectisome and b

43 export apparatus and that, in the absence of export apparatus components, there is a significant redu

44 The export apparatus consists of a transmembrane PMF-driven

45 The membrane-embedded part of the flagellar export apparatus contains five essential proteins: FlhA,

46 We propose that the flagellar export apparatus contains FliP and FliR and that this ap

47 a gene encoding a component of the flagella export apparatus, eliminated lipase but not protease or

48 es with or works downstream of the flagellar export apparatus-FlgSR pathway to influence sigma(54)-de

49 ain of the largest membrane component of the export apparatus, FlhA; although small deletions in FliJ

50 a protein that is believed to be part of the export apparatus for flagellum assembly and which is hom

51 n or another protein that uses the flagellar export apparatus for localization or both.

52 hether the flagellar apparatus serves as the export apparatus for the Cia proteins.

53 The export apparatus for this process is poorly understood.

54 arily related to bacterial flagellar protein export apparatuses (fT3SSs), which are essential for fla

55 ation of components of the flagellar protein export apparatus has been indirect.

56 is linked to and downstream of the flagellar export apparatus in a regulatory cascade that terminates

57 em (T3SS) chaperones pilot substrates to the export apparatus in a secretion-competent state, and are

58 We propose a model for the flagellar export apparatus in which FlhA and FlhB and the other fo

59 e locations of five proteins involved in the export apparatus including FliI, whose position below th

60 srupting certain components of the flagellar export apparatus inhibited transcription of the RpoN reg

61 wo of its proteins; that the RNA capping and export apparatus is a hollow cylinder, which probably se

62 liI from hydrolysing ATP until the flagellar export apparatus is competent to link this hydrolysis to

63 cient delivery to membrane components of the export apparatus is discussed.

64 Here we show that the Legionella export apparatus is localized to the bacterial poles, as

65 re discussed, and a model of FlhA within the export apparatus is presented.

66 demonstrate here that the type III secretion export apparatus is required for the assembly of the nee

67 ment of their cytoplasmic and inner membrane export apparatuses is much less clear.

68 howed that FlhA interacts with several other export apparatus membrane proteins.

69 ns among several components of the flagellar export apparatus of Salmonella were studied using affini

70 describe a high-resolution structure of the export apparatus of the Salmonella type III secretion sy

71 Considering that the flagellar export apparatuses of Escherichia coli and Salmonella sp

72 in which at least the FlhA component of the export apparatus physically interacts with the MS ring w

73 and FliJ) of the type III flagellar protein export apparatus, plus the cytoplasmic domains (FlhAC an

74 The export apparatus processively transported flagellar prot

75 Mutants with incomplete flagellar export apparatuses produced wild-type levels of FlgS and

76 s to be required for wild-type levels of the export apparatus protein FlhA in the membrane.

77 One of the export apparatus proteins, FlhB, regulates the substrate

78 the F(1) ATPase motor, within the flagellar export apparatus remains unclear.

79 FliH is a soluble component of the flagellar export apparatus that binds to the ATPase FliI, and nega

80 some is the needle complex, which houses the export apparatus that serves as a gate for the passage o

81 nvolves the synthesis of a dedicated protein export apparatus that subsequently transports other flag

82 liI mutants of C. jejuni that form flagellar export apparatuses that are secretion incompetent, we de

83 naceous components of the protein import and export apparatuses, the lipids found within plastid memb

84 The pre-inhibitor is cleaved by the protein export apparatus to a putative pro-inhibitor that is fur

85 gether with a membrane protein, FlhB, of the export apparatus to mediate the switching of export subs

86 the bacterial flagellum, a specific protein export apparatus utilizes ATP and proton motive force (P

87 In this study, the flagellum export apparatus was shown to function also as a secreti

88 agellar proteins are exported via a type III export apparatus which, in part, consists of the membran

89 FlhA is a component of the flagellar protein export apparatus, with an integral membrane domain encom