ライフサイエンスコーパス: periplasmic protein

1 heme domain of NapC has been expressed as a periplasmic protein.

2 ng of molybdate and other anions to the ModA periplasmic protein.

3 Fvs was confirmed by competitive ELISA using periplasmic protein.

4 partner (prey) as a soluble, epitope-tagged, periplasmic protein.

5 rminal domain of RseA interacts with RseB, a periplasmic protein.

6 electron acceptors for oxidative folding of periplasmic proteins.

7 cotemporally with the cysteine-rich doublet periplasmic proteins.

8 tect against the acid-induced aggregation of periplasmic proteins.

9 grobacterium as are VirJ and ChvE, two known periplasmic proteins.

10 TAA autotransport is assisted by additional periplasmic proteins.

11 ect donor of disulfides to newly synthesized periplasmic proteins.

12 n antibiotics, as well as a tendency to leak periplasmic proteins.

13 ethods generally employed in the recovery of periplasmic proteins.

14 in general, found on the precursors of other periplasmic proteins.

15 r of the glycan to serine residues of select periplasmic proteins.

16 oth BBB26 and BBB27 are membrane-associated, periplasmic proteins.

17 d signaling pathways, and other membrane and periplasmic proteins.

18 id extrusion was accelerated strongly by the periplasmic protein AcrA in the presence of Mg2+, and at

19 owed translocation of erythromycin and small periplasmic proteins across the outer membrane.

20 I), a type II membrane protein (AlgJ), and a periplasmic protein (AlgF).

21 e uronic acids, as does a mutant lacking the periplasmic protein AlgK.

22 ylase (PSBT) is translationally fused to the periplasmic proteins alkaline phosphatase and maltose-bi

23 ntified traK, which is predicted to encode a periplasmic protein, among positive prey plasmids.

24 cpxP gene encodes a small, stress-combative periplasmic protein and is the most strongly induced mem

25 now found that endogenous CtpA is a soluble periplasmic protein and that a ctpA null mutant has spec

26 RseB is a periplasmic protein and was found to co-purify with the

27 ctionation experiments showed that MreC is a periplasmic protein and, as assayed by immunofluorescenc

28 ner membrane pore-forming protein), VirB9 (a periplasmic protein), and VirB7 (an outer membrane-assoc

29 ects cells to synthesize an apparently novel periplasmic protein, and ribB is a homolog of the Escher

30 the second predicted to encode a 12, 000-Da periplasmic protein, and the third (cyp) encoding cytoch

31 The periplasmic protein ApbE was identified through the anal

32 NAs encoding outer-membrane, cytoplasmic and periplasmic proteins are distributed throughout the cyto

33 n the periplasm, including whether accessory periplasmic proteins are involved in translocation to th

34 teins are well buffered against such swings, periplasmic proteins are not.

35 cate that the T. pallidum GlpQ ortholog is a periplasmic protein associated predominantly with the sp

36 superfamilies of proteins, RND, ABC, or MF; periplasmic proteins belonging to the membrane fusion pr

37 Production of the periplasmic protein beta-lactamase (Bla) does not inhibi

38 The precursor polypeptides of periplasmic proteins binding seven types of redox cofact

39 ain, two protective antigens were found: the periplasmic protein, bp26, and the chaperone protein, tr

40 AlgG and AlgK may be part of a periplasmic protein complex, or scaffold, that guides al

41 t the VPI-encoded Orf4 is a predicted 34-kDa periplasmic protein containing a zinc metalloprotease mo

42 We discovered that the periplasmic protein CsgC was a highly effective inhibito

43 We show here that the periplasmic protein CusB from the Cus copper/silver effl

44 The periplasmic protein CusF, as a part of the CusCFBA efflu

45 n calorimetry, we have demonstrated that two periplasmic proteins, CusF and CusB, of the Escherichia

46 Penicillin G acylase is a periplasmic protein, cytoplasmically expressed as a prec

47 Maltose-binding protein (MBP), a soluble periplasmic protein, delivers maltose to the MalFGK(2) t

48 lex of the prokaryotic histidine permease, a periplasmic protein-dependent ABC transporter, is compos

49 ia gonorrhoeae has been proposed to encode a periplasmic protein-dependent iron transport system.

50 ctive-site cysteines of the Escherichia coli periplasmic protein disulfide bond isomerase (DsbC) are

51 While DsbD transfers reducing potential to periplasmic protein disulfide bond isomerases and to the

52 In Escherichia coli, the periplasmic protein disulfide isomerase, DsbC, is mainta

53 It reoxidizes DsbA, the periplasmic protein disulfide oxidant, using the oxidizi

54 Biochemical studies have shown that the periplasmic protein disulfide oxidoreductase DsbC can is

55 cans ccmG gene indicates that it codes for a periplasmic protein-disulphide oxidoreductase; the prese

56 a coli disulfide bond formation pathway, the periplasmic protein DsbA introduces disulfide bonds into

57 richia coli is responsible for oxidizing the periplasmic protein DsbA, which forms disulfide bonds in

58 tion in Escherichia coli is catalyzed by the periplasmic protein DsbA.

59 The Escherichia coli periplasmic protein DsbC is active both in vivo and in v

60 and 34kDa were both identified as a putative periplasmic protein encoded by the C. jejuni NCTC 11168

61 TrbB, a periplasmic protein encoded by the conjugative plasmid F

62 of enteropathogenic Escherichia coli GfcC, a periplasmic protein encoded by the gfc operon, which is

63 We show that L. pneumophila periplasmic protein EnhC, which is uniquely required for

64 The periplasmic protein FepB of Escherichia coli is a compon

65 The periplasmic protein FlhE is a member of the flhBAE opero

66 e cell envelope and activates genes encoding periplasmic protein folding and degrading factors.

67 activating the expression of genes encoding periplasmic protein folding and trafficking factors that

68 Improved understanding of the bacterial periplasmic protein folding machinery may assist in high

69 Little is known about either the process of periplasmic protein folding or how information concernin

70 /c mice vaccinated with six salt-extractable periplasmic protein fractions (Brucella cell surface pro

71 nvestigating the subcellular localization of periplasmic proteins have been hampered by problems with

72 V. cholerae encodes three putative periplasmic proteins, here denoted ShyA, ShyB, and ShyC,

73 tudied further and found to encode a soluble periplasmic protein important for XcpQ localization to t

74 posttranslational folding intermediates of a periplasmic protein in which the protein and DsbA, a per

75 tion of SecA completely blocks the export of periplasmic proteins in vivo.

76 olated were found to overexpress one or more periplasmic proteins including OsmY, Ivy, DppA, OppA, an

77 val of the outer membrane by spheroplasting, periplasmic proteins, including any unbound epitope-tagg

78 Periplasmic proteins, including SodCII, are released and

79 n gene ftsZ; and genes encoding membrane and periplasmic proteins, including the osmotically inducibl

80 heterologously expressed outer membrane and periplasmic proteins into bacterial vesicles.

81 nas aeruginosa, actively secrete a subset of periplasmic proteins into their surrounding medium.

82 ermined the crystal structure of apo-CusF, a periplasmic protein involved in copper and silver resist

83 ession of catabolic enzymes and envelope and periplasmic proteins is regulated by pH.

84 he KpsD protein, previously believed to be a periplasmic protein, is an outer membrane protein involv

85 SodCII is protease sensitive, and like other periplasmic proteins, it is released by osmotic shock.

86 ently small at genes encoding cytoplasmic or periplasmic proteins (K(S) < 0.09).

87 membrane exit duct of the TolC family, and a periplasmic protein known as the adaptor.

88 ough uses a larger number of cytoplasmic and periplasmic proteins linked in three intertwining pathwa

89 studies with deletion mutants implicate the periplasmic protein LptA, the cytosolic protein LptB, an

90 ts the transcription factor AlgU, and by the periplasmic protein MucB.

91 the disulfide oxidoreductase DsbA, a soluble periplasmic protein, nonspecifically transfers a disulfi

92 coli nutrient transporters as well as IM and periplasmic proteins normally used to maintain cell wall

93 The B subunit of heat-labile enterotoxin, a periplasmic protein of Escherichia coli has an internal

94 DsbC is a periplasmic protein of Escherichia coli that was previou

95 SurA, a periplasmic protein of Escherichia coli, has sequence si

96 Here, we show that a periplasmic protein of the bacterial oligonucleotide/oli

97 Previous studies showed that AcrA, a periplasmic protein of the membrane fusion protein famil

98 n demonstrated to induce the expression of a periplasmic protein of unknown function, Spy.

99 compassing 90% inner- and outer-membrane and periplasmic proteins of Escherichia coli.

100 iii) the transfer of the O-acetyl group to a periplasmic protein or to alginate.

101 and SDS but did not nonspecifically release periplasmic proteins or VirE2 truncated of its secretion

102 to be specifically involved in the repair of periplasmic proteins oxidized by hypochlorous acid.

103 Two of the genes encode the soluble periplasmic proteins PcoA and PcoC.

104 The predicted gene products are periplasmic proteins (PcuA, PcuC, and PcuD), a TonB-depe

105 me fusion between the leader sequence of the periplasmic protein PeIB and the mature FlgH sequence, w

106 eta-1,6-N-acetyl-D-glucosamine (PNAG) by the periplasmic protein PgaB is required for polysaccharide

107 depends on dedicated chain length regulator periplasmic proteins (polysaccharide co-polymerases, PCP

108 ia utilize chaperone proteins that stabilize periplasmic proteins, preventing their precipitation.

109 nzymes (DhaKLM, GapA, TnaA, HisC, and HisD), periplasmic proteins (ProX, OppA, DegQ, MalB, and MglB),

110 es and chaperones exhibit important roles in periplasmic protein quality control and stress responses

111 on was located in the dsbA gene coding for a periplasmic protein required for disulfide bond formatio

112 TcpQ is a predicted periplasmic protein required for TCP biogenesis.

113 r membrane or its synthesis as an unanchored periplasmic protein resulted in constitutive activation

114 tivation of a second negative regulator, the periplasmic protein RseB, is also required for sigma(E)

115 he cmeR mutant, Cj0561c (encoding a putative periplasmic protein) showed the greatest increase in exp

116 DsbG is one of the first periplasmic proteins shown to have general chaperone act

117 lated, but functionally distinct, classes of periplasmic proteins specifically bind carbohydrate liga

118 rane proteins such as PhoE and LamB and some periplasmic proteins such as maltose-binding protein, in

119 membrane sigma(E) antisigma factor; RseB, a periplasmic protein that binds to the periplasmic face o

120 cpxP specifies a periplasmic protein that can combat the lethal phenotype

121 We show that FlhE is a periplasmic protein that co-purifies with flagellar basa

122 n reaction is now known to be catalyzed by a periplasmic protein that contains a covalently bound hem

123 A, which inhibits AlgU activity, and MucB, a periplasmic protein that negatively controls AlgU.

124 xin MqsR degrades YgiS mRNA, which encodes a periplasmic protein that promotes deoxycholate uptake an

125 in Gram-negative bacterial pathogens is the periplasmic protein that shuttles heme between outer and

126 We found 10 cysteine-containing periplasmic proteins that are substrates of the disulfid

127 as wild-type cells, and does not synthesize periplasmic proteins that normally accumulate during sul

128 YycI and YycH are two membrane-anchored periplasmic proteins that regulate the essential Bacillu

129 nct cellular receptors, the F' pilus and the periplasmic protein TolA.

130 requires the toxin-coregulated pilus and the periplasmic protein TolA.

131 ty to the N-terminal domain of the prevalent periplasmic protein TolB.

132 included metabolic enzymes (GatY and AckA), periplasmic proteins (TolC, HdeA, and OmpA), and redox e

133 gh FepA are energy-dependent, relying on the periplasmic protein TonB to interact with FepA.

134 y, herein named virulence and stress-related periplasmic protein (VisP), on binding to the sugar moie

135 37 degrees C, whereas synthesis of a 66-kDa periplasmic protein was increased at the higher temperat

136 ires SurA in vivo, while the folding of four periplasmic proteins was independent of SurA.

137 id) genes encoding putative lipoproteins and periplasmic proteins were preferentially expressed in en

138 Two pH-dependent periplasmic proteins were redox modulators: Tpx (acid-in

139 reduced and mercury-bound forms of merP, the periplasmic protein, which binds Hg(II) and transfers it

140 er, an outer membrane channel protein, and a periplasmic protein, which together coordinate efflux fr

141 idocalcisome function impacts trafficking of periplasmic proteins, which can then feed back on the tr

142 pH-dependent clusters included envelope and periplasmic proteins, which directly experience external

143 g protein (RBP) is a sugar-binding bacterial periplasmic protein whose function is associated with a

144 eron with a gene encoding a small, predicted periplasmic protein with an unknown function, ygiW.

145 lysaccharide, the fourth subunit, BcsZ, is a periplasmic protein with endo-beta-1,4-glucanase activit

146 We present evidence that SurA, a periplasmic protein with peptidyl-prolyl isomerase activ

147 A and Cjj0382, we found that they are stable periplasmic proteins with an apparent heme-dependent per

148 ponent systems composed of membrane-spanning periplasmic proteins with histidine kinase, phosphoaccep

149 The discovery of T. pallidum periplasmic proteins with potentially defined functions

150 entification of a previously uncharacterized periplasmic protein, YbcL, encoded by UPEC that contribu

151 -GMP production by YfiN was repressed by the periplasmic protein YfiR, and deletion of yfiR promoted