ライフサイエンスコーパス: cytoplasmic membrane

1 les that originate from invaginations of the cytoplasmic membrane.

2 determine the pH gradient across the E. coli cytoplasmic membrane.

3 access to DNA receptors associated with the cytoplasmic membrane.

4 f a galactopyranoside and an H(+) across the cytoplasmic membrane.

5 pid II during transport across the bacterial cytoplasmic membrane.

6 leton influences fluorescent staining of the cytoplasmic membrane.

7 y electrochemical Na(+) potential across its cytoplasmic membrane.

8 omoting its lipid-mediated attachment to the cytoplasmic membrane.

9 t parallel with FtsZ polymers underneath the cytoplasmic membrane.

10 II, and this complex also forms pores in the cytoplasmic membrane.

11 ty of three enzymes that are embedded in the cytoplasmic membrane.

12 th ubiquinone to pump sodium ions across the cytoplasmic membrane.

13 system is activated by events affecting the cytoplasmic membrane.

14 n bilayers closest in composition to E. coli cytoplasmic membrane.

15 rt of unfolded precursor proteins across the cytoplasmic membrane.

16 transfer to PBP1b after transport across the cytoplasmic membrane.

17 ly folded proteins across the tightly sealed cytoplasmic membrane.

18 and are derived from the OM rather than the cytoplasmic membrane.

19 ructural motif that targets a protein to the cytoplasmic membrane.

20 organisms as they affect the function of the cytoplasmic membrane.

21 h thiolate ligands through a model bacterial cytoplasmic membrane.

22 volved in the flipping of lipid A across the cytoplasmic membrane.

23 y mannosyltransferase enzymes located at the cytoplasmic membrane.

24 inone coupled with proton pumping across the cytoplasmic membrane.

25 ith the negative immune regulator SRFR1 at a cytoplasmic membrane.

26 le transertion of membrane proteins into the cytoplasmic membrane.

27 polysialic acid (NmC PST) is located in the cytoplasmic membrane.

28 ting it without contamination from the inner cytoplasmic membrane.

29 ic pore for transport of NH(4)(+) across the cytoplasmic membrane.

30 actions which include the outer membrane and cytoplasmic membrane.

31 plasm and processed into mature forms on the cytoplasmic membrane.

32 substantial pressure differential across the cytoplasmic membrane.

33 of the topology of these two antennas on the cytoplasmic membrane.

34 ches the protein to the outer leaflet of the cytoplasmic membrane.

35 into helical structures just underneath the cytoplasmic membrane.

36 ituated approximately 200 A away, across the cytoplasmic membrane.

37 ith the stator followed the curvature of the cytoplasmic membrane.

38 inner cell and the negative curvature of the cytoplasmic membrane.

39 omatophores, which form as extensions of the cytoplasmic membrane.

40 ite of synthesis in the cytoplasm across the cytoplasmic membrane.

41 yl-tRNAs to phosphatidylglycerol (PG) in the cytoplasmic membrane.

42 n machine called the divisome that spans the cytoplasmic membrane.

43 involved in translocation of CNF1 across the cytoplasmic membrane.

44 ctopic localization at the inner face of the cytoplasmic membrane.

45 pathway for their insertion into/through the cytoplasmic membrane.

46 n chains are compartmentalized by at least a cytoplasmic membrane.

47 ly enlarged and convoluted, and an energized cytoplasmic membrane.

48 h-like sacculus that surrounds the bacterial cytoplasmic membrane.

49 translocation of the Hsa adhesin across the cytoplasmic membrane.

50 , the TLR2 agonists, from the staphylococcal cytoplasmic membrane.

51 llowed by alpha helices that extend into the cytoplasmic membrane.

52 nt as one molecule for every 91 nm(2) in the cytoplasmic membrane.

53 bly into a functional complex located at the cytoplasmic membrane.

54 s a protective mesh-like sacculus around the cytoplasmic membrane.

55 d dimeric proteins across the tightly sealed cytoplasmic membrane.

56 c oxidase lie on the periplasmic side of the cytoplasmic membrane.

57 e sequence complement on their cell walls or cytoplasmic membranes.

58 tor-containing cargo proteins over bacterial cytoplasmic membranes.

59 tem comprising outer, cytoplasmic, and inner cytoplasmic membranes.

60 taining species can permeate readily through cytoplasmic membranes.

61 ns were shown to accumulate in thylakoid and cytoplasmic membranes.

62 efficient transit through both the outer and cytoplasmic membranes.

63 r at the interface between the thylakoid and cytoplasmic membranes.

64 pids from the outer leaflet of the OM to the cytoplasmic membrane (4) .

65 optimal interactions with the ligand and the cytoplasmic membrane ABC transporter (FepCD), respective

66 ate-responsive, homodimeric NarX sensor, two cytoplasmic membrane alpha-helices delimit the periplasm

67 s also required for the stabilization of the cytoplasmic membrane and as a cofactor for essential enz

68 uclear cyclin D1, which bound ERalpha at the cytoplasmic membrane and augmented AKT phosphorylation (

69 om Escherichia coli resides in the bacterial cytoplasmic membrane and catalyzes the two-electron oxid

70 to extracytoplasmic stresses that damage the cytoplasmic membrane and enable cells to repair their me

71 ids alters the biochemical properties of the cytoplasmic membrane and enables bacteria to adapt to ch

72 Additionally, FraG was located close to the cytoplasmic membrane and in the heterocyst neck, using i

73 Cruzipain is found both on the cytoplasmic membrane and in the internal lysosomal struc

74 Gram-negative bacteria, invagination of the cytoplasmic membrane and inward growth of the peptidogly

75 n transport systems found in the prokaryotic cytoplasmic membrane and is conserved in the thylakoid m

76 (Tat) transports folded proteins across the cytoplasmic membrane and is critical to virulence in Sal

77 r its release from noncentral regions of the cytoplasmic membrane and its subsequent relocation to mi

78 raction of LPS from the outer leaflet of the cytoplasmic membrane and its transport across the cell e

79 ng infection, viral capsids assembled on the cytoplasmic membrane and moved to the surface of the com

80 uire holins and endolysins, which attack the cytoplasmic membrane and peptidoglycan, respectively.

81 chemotactic responses by diffusing into the cytoplasmic membrane and perturbing the structural stabi

82 To fortify their cytoplasmic membrane and protect it from osmotic rupture

83 tly or indirectly interacts with KinD in the cytoplasmic membrane and that this interaction is requir

84 ll as MscK distribute homogeneously over the cytoplasmic membrane and the lateral diffusion of the ch

85 nsports folded proteins across the bacterial cytoplasmic membrane and the plant thylakoid membrane.

86 ports folded proteins across the prokaryotic cytoplasmic membrane and the plant thylakoid membrane.

87 locates folded proteins across the bacterial cytoplasmic membrane and the plant thylakoid membrane.

88 port of folded proteins across the bacterial cytoplasmic membrane and the thylakoid membrane in plant

89 nsports folded proteins across the bacterial cytoplasmic membrane and the thylakoid membranes of plan

90 t relocation of Vipp1 to the vicinity of the cytoplasmic membrane and the thylakoid membranes.

91 l domain of Rz near the outer leaflet of the cytoplasmic membrane and were not allele specific.

92 induce pores, or otherwise permeabilise the cytoplasmic membrane and, as a result, induce cell death

93 sms or receptor-independent diffusion across cytoplasmic membranes and are utilized as nutrients, bui

94 rized the attack of AMPs on Escherichia coli cytoplasmic membranes and directly compared this action

95 rgely responsible for recruitment of pUL7 to cytoplasmic membranes and into the virion tegument.

96 on or blocking of entry mediators, occurs in cytoplasmic membranes and not in cell surface membranes

97 synthesized by enzymes located in the inner (cytoplasmic) membrane and are then translocated to the c

98 NH3 equilibrates across the cytoplasmic membrane, and glutamine synthetase does not

99 ds that accumulated were frequently bound to cytoplasmic membranes, apparently immobilized in interme

100 normally used to translocate proteins across cytoplasmic membranes, are a vast family of natural FPR

101 by a dramatic local outward curvature of the cytoplasmic membrane as it fuses with the phage tail tip

102 Most bacterial exported proteins cross the cytoplasmic membrane as unfolded polypeptides.

103 Cytoplasmic membrane-associated DNA (cmDNA) is a species

104 Importantly, we found there is a special cytoplasmic membrane-associated transcription system in

105 It forms filaments under the cytoplasmic membrane at the division site where, togethe

106 d but not sufficient to compartmentalize the cytoplasmic membrane at the division site.

107 Escherichia coli SecA binds to cytoplasmic membranes at SecYEG high affinity sites and

108 c myristoylation and Src localization to the cytoplasmic membrane, attenuating Src-mediated oncogenic

109 inked precursors at the inner surface of the cytoplasmic membrane before being translocated across th

110 drial membrane potential, the development of cytoplasmic membrane blebs containing high levels of rea

111 s tropism for mononuclear phagocytes forming cytoplasmic membrane-bound microcolonies called morulae.

112 l to several respiratory pathways is CymA, a cytoplasmic membrane-bound tetraheme c-type cytochrome t

113 e MS4A2, MS4A2(trunc) did not traffic to the cytoplasmic membrane but instead was associated with the

114 teobacteria, might hydrolyze DOP outside the cytoplasmic membrane, but the former could also transpor

115 for energy production and biogenesis of the cytoplasmic membrane, but they also enhance cellular sig

116 tion to Fe(2+) prior to traversal across the cytoplasmic membrane by FeoAB.

117 into a proto-ring structure, tethered to the cytoplasmic membrane by FtsA and ZipA.

118 nked PG precursor called lipid II across the cytoplasmic membrane by interfering with the activity of

119 ery and that RNase II is associated with the cytoplasmic membrane by its amino-terminal amphipathic h

120 ipheral membrane protein, is anchored to the cytoplasmic membrane by the 21 amino acids of its C-term

121 ell division protein FtsZ is anchored to the cytoplasmic membrane by the action of the bitopic membra

122 ns, such as PAO1, AlgU is sequestered to the cytoplasmic membrane by the anti-sigma factor MucA that

123 Within 30 s of permeabilization of the cytoplasmic membrane by the cationic AMP CM15 [combining

124 tigated the physical properties of bacterial cytoplasmic membranes by applying the method of micropip

125 show penetration of the ARMAN cell wall and cytoplasmic membranes by protuberances extended from cel

126 ition to distinguishing invaginations of the cytoplasmic membrane (CM) and interconnected vesicular s

127 In Escherichia coli, the integral cytoplasmic membrane (CM) proteins TonB, ExbB, and ExbD

128 r structures, others are found nearer to the cytoplasmic membrane (CM), often forming interconnected

129 lar filaments along the inner surface of the cytoplasmic membrane (CM).

130 action center (RC), which is embedded in the cytoplasmic membrane (CM).

131 y virions leading to their accumulation in a cytoplasmic membrane compartment.

132 ribosome radial distributions extend to the cytoplasmic membrane, consistent with the transertion hy

133 ive Escherichia coli to demonstrate that its cytoplasmic membrane contains microdomains with distinct

134 the proton gradient across the cell wall and cytoplasmic membrane controls Mg(2+) transport into the

135 oxvirus double-stranded DNA genome occurs in cytoplasmic membrane-delimited factories.

136 We observed immediate cytoplasmic membrane depolarization, not seen with enter

137 cquire their final envelopes by budding into cytoplasmic membranes derived from the trans-Golgi netwo

138 found that deltaT prevented ionophore-caused cytoplasmic membrane disruption, which may account for i

139 d proteins that accumulate harmlessly in the cytoplasmic membrane during the infection cycle until su

140 Analysis of cytoplasmic membrane fatty acids (CMFAs) in acid-adapted

141 how this sulfur is activated and crosses the cytoplasmic membrane for further oxidation to sulfite by

142 ial flippase that translocates it across the cytoplasmic membrane for PG polymerization is unclear.

143 All positive-sense RNA viruses modify host cytoplasmic membranes for viral replication complex form

144 d SrtA mutants that are loosely bound to the cytoplasmic membrane form high-molecular-weight complexe

145 scribed the isolation of a virion-associated cytoplasmic membrane fraction from HSV-infected cells.

146 HtaB and HmuT were detected primarily in the cytoplasmic membrane fraction regardless of the growth m

147 ges in lateral tension in the bilayer of the cytoplasmic membrane generated by rapid water flow into

148 lae (h-caveolae) form by budding in from the cytoplasmic membrane, generating a membrane domain with

149 transport, implying the existence of another cytoplasmic membrane Hn transporter.

150 used to transport folded proteins across the cytoplasmic membrane in bacteria and archaea and across

151 etory and outer membrane proteins across the cytoplasmic membrane in bacteria.

152 the outer membrane or cell wall and (b) the cytoplasmic membrane in case of a cytoplasmic location o

153 RNA processing and decay and tethers to the cytoplasmic membrane in Escherichia coli; however, the f

154 y dissipating the proton motive force of the cytoplasmic membrane in P. aeruginosa.

155 pendent protein translocation pathway across cytoplasmic membranes in bacteria.

156 lipoproteins cover the outer leaflet of the cytoplasmic membrane, in contrast to the rare outer memb

157 are phage-encoded proteins that connect the cytoplasmic membrane (inner membrane, IM) and the OM.

158 endent outer membrane receptor (PcuB), and a cytoplasmic membrane-integral protein (PcuE).

159 ains the so-called common region (CR) at the cytoplasmic/membrane interface still has the ability to

160 rerequisite for its translocation across the cytoplasmic membrane into the bacterial periplasm.

161 d proteins are first translocated across the cytoplasmic membrane into the inner wall zone.

162 ome single-stranded RNA viruses remodel host cytoplasmic membranes into specialized organelles.

163 Protein translocation across the bacterial cytoplasmic membrane is an essential process catalyzed p

164 Protein translocation across the cytoplasmic membrane is an essential process in all bact

165 The bacterial cytoplasmic membrane is composed of roughly equal propor

166 adial extension of ribosomes and RNAP to the cytoplasmic membrane is consistent with the hypothesis o

167 nstrated that the proton motive force of the cytoplasmic membrane is critical.

168 that controlled AsIII trafficking across the cytoplasmic membrane is important to a process understoo

169 ings strongly suggest that disruption of the cytoplasmic membrane is not the growth-halting mechanism

170 The cytoplasmic membrane is probably the most important phys

171 ation of the amphipathic lipid II across the cytoplasmic membrane is required for subsequent incorpor

172 Val-4830-Val-4841) that lies parallel to the cytoplasmic membrane leaflet.

173 ter membrane is much faster than through the cytoplasmic membrane, likely reflecting the effectivenes

174 EsaE has a dual cytoplasmic/membrane localization, and membrane-bound Es

175 idase (COX) and quinol oxidase (Cyd) and the cytoplasmic membrane-localized alternative respiratory t

176 c access without the toxicity of nonspecific cytoplasmic membrane lysis.

177 enerate holes in the cell wall through which cytoplasmic membrane material protrudes and is released

178 Through these openings, cytoplasmic membrane material protrudes into the extrace

179 regulate gene expression whereas Set-beta at cytoplasmic membranes may regulate unique cofactors, inc

180 teins, members of which reside in either the cytoplasmic membrane (NfsD, -E, and -G) or outer membran

181 hrinkage, resembling the constriction of the cytoplasmic membrane, occurs at ZipA densities higher th

182 Effector domains of MARTX toxins cross the cytoplasmic membrane of a host cell through a putative p

183 cantly stronger capacity to permeabilize the cytoplasmic membrane of Bacillus megaterium than theroma

184 hinery transports folded proteins across the cytoplasmic membrane of bacteria and the thylakoid membr

185 ates transport of folded proteins across the cytoplasmic membrane of bacteria and the thylakoid membr

186 tegration of most membrane proteins into the cytoplasmic membrane of bacteria occurs co-translational

187 osphatidylglycerol (PG) to form aa-PG in the cytoplasmic membrane of bacteria.

188 ation of a galactoside and a H(+) across the cytoplasmic membrane of Escherichia coli (galactoside/H(

189 Galactoside/H(+) symport across the cytoplasmic membrane of Escherichia coli is catalyzed by

190 proton-coupled zinc transporter found in the cytoplasmic membrane of Escherichia coli.

191 through a protein-conducting channel in the cytoplasmic membrane of eubacteria.

192 er anionic lipids in a mixture mimicking the cytoplasmic membrane of Gram-negative bacteria, as measu

193 vestigated the MBH protein purified from the cytoplasmic membrane of hoxR mutant cells.

194 his protein was found to be expressed on the cytoplasmic membrane of human monocytes.

195 Surrounding the cytoplasmic membrane of most bacteria, the peptidoglycan

196 or-3 protein localizes asymmetrically on the cytoplasmic membrane of neoblasts, and the ratio of asym

197 anslocating fully folded proteins across the cytoplasmic membrane of prokaryotes and the thylakoid me

198 stem translocates folded proteins across the cytoplasmic membrane of prokaryotes and the thylakoid me

199 that surrounds the inner cell but not in the cytoplasmic membrane of the outer cell.

200 Holins form pores in the cytoplasmic membranes of bacteria for the primary purpos

201 phosphate-linked oligosaccharides across the cytoplasmic membranes of bacteria.

202 obial peptides (AMPs) directly attacking the cytoplasmic membranes of Escherichia coli spheroplasts.

203 The drug interacts with the cytoplasmic membranes of Gram-positive pathogens, causin

204 ransport of fully folded proteins across the cytoplasmic membranes of many bacteria and the chloropla

205 rt of the molecular ion across the outer and cytoplasmic membranes of the Gram-negative bacteria is r

206 meshwork that is localized between adjacent cytoplasmic membranes of the myelin sheath.

207 nic pathway for protein secretion across the cytoplasmic membrane or insertion of integral membrane p

208 itive bacteria, CPS linkage is to either the cytoplasmic membrane or the cell wall.

209 targeting delivers proteins to the bacterial cytoplasmic membrane or to the eukaryotic endoplasmic re

210 cells is by causing a profound defect in the cytoplasmic membrane permeability barrier.

211 icity in a psp null strain and the extent of cytoplasmic membrane permeability to large molecules.

212 ne proteins that are translocated across the cytoplasmic membrane primarily by the Sec general secret

213 ta suppressed, whereas Set-beta localized to cytoplasmic membranes promoted neurite growth in rodent

214 In this study, we have discovered that the cytoplasmic membrane protease FtsH is involved in this p

215 TonB-dependent transducer (PSPTO_1206) and a cytoplasmic membrane protein (PSPTO_2145), which is loca

216 cterized were lambda Rz and Rz1, an integral cytoplasmic membrane protein and an outer membrane lipop

217 isulfide bonds into substrates, and then the cytoplasmic membrane protein DsbB reoxidizes DsbA's cyst

218 ognized by IcsA requires the activity of the cytoplasmic membrane protein insertase YidC.

219 Except for TolQRA, no cytoplasmic membrane protein is essential for cytotoxici

220 Expression of the cytoplasmic membrane protein RipA is required for Franci

221 The lambda holin, or S105, is a small cytoplasmic membrane protein that controls the timing of

222 We show that as a cytoplasmic membrane protein, ASIC1 is also associated w

223 rom cytoplasmic thioredoxin-1 (Trx1) via the cytoplasmic membrane protein, DsbD.

224 tween integral (PspBC) and peripheral (PspA) cytoplasmic membrane proteins and a soluble transcriptio

225 In Escherichia coli, cytoplasmic membrane proteins ExbB and ExbD couple the p

226 Current data suggest that cytoplasmic membrane proteins ExbB and ExbD harness pmf

227 Cytoplasmic membrane proteins ExbB and ExbD harness the

228 Cytoplasmic membrane proteins ExbB and ExbD of the Esche

229 In Escherichia coli, cytoplasmic membrane proteins ExbB and ExbD promote conf

230 The cytoplasmic membrane proteins harvest and transmit the p

231 proteins B (PspB) and C (PspC) are integral cytoplasmic membrane proteins involved in inducing the Y

232 The cytoplasmic membrane proteins PspB and PspC are critical

233 The cytoplasmic membrane proteins PspB and PspC were propose

234 In contrast, PspA associates with the cytoplasmic membrane proteins PspBC during inducing cond

235 PspB and PspC are cytoplasmic membrane proteins required for stress-depend

236 Escherichia coli TonB system consists of the cytoplasmic membrane proteins TonB, ExbB, and ExbD and m

237 The TonB system couples cytoplasmic membrane proton motive force (pmf) to active

238 The TonB system couples cytoplasmic membrane proton motive force to TonB-gated o

239 e transporters using energy derived from the cytoplasmic membrane proton motive force.

240 In gram-negative bacteria, the cytoplasmic membrane proton-motive force energizes the a

241 D of the Escherichia coli TonB system couple cytoplasmic membrane protonmotive force (pmf) to TonB.

242 e point mutation, E613R, introduced into the cytoplasmic membrane-proximal "wedge" domain of CD45 is

243 aking unmediated diffusion of NH3 across the cytoplasmic membrane rate-limiting for cell growth in a

244 , at least in part through the disruption of cytoplasmic membrane related functions, and that resista

245 h SecA2 drives export of proteins across the cytoplasmic membrane remains poorly understood.

246 -nm lipid bilayer of both outer membrane and cytoplasmic membrane resolved in 3D reconstructions, pro

247 ane, hydrophilic outer membrane, and outer + cytoplasmic membrane, respectively.

248 integral membrane proteins of the bacterial cytoplasmic membrane responsible for biosynthesis of pep

249 -transducing protein that is anchored in the cytoplasmic membrane, resulted in a fivefold larger valu

250 , predicted to export the protein beyond the cytoplasmic membrane, resulted in loss of functional tra

251 ddenly trigger to cause lethal damage to the cytoplasmic membrane, resulting in the cessation of resp

252 NEs and nuclear morphology, with coincident cytoplasmic membrane sheet accumulation.

253 led cytochrome bd 1 ubiquinol oxidase in the cytoplasmic membrane show that CpcA-PEB and CpcA-PCB are

254 pesvirus-4 perturbs B cell signaling using a cytoplasmic/membrane shuttling factor that nucleates the

255 tion by the terminal oxidases located at the cytoplasmic membrane significantly affects the activitie

256 gression by guiding the targeted delivery of cytoplasmic membrane stores to the cell surface through

257 ely with no contamination from lipids of the cytoplasmic membrane, such as phosphatidylglycerol.

258 target some proteins for insertion into the cytoplasmic membrane, suggested that FtsEX might contrib

259 transmembrane segment 2 (TM2) and TM3 on the cytoplasmic membrane surface.

260 aeroides is initiated at indentations of the cytoplasmic membrane, termed UPB.

261 exes are organized in extended arrays in the cytoplasmic membrane that allow bacteria to respond to c

262 are unclear, as these cells possess a single cytoplasmic membrane that is surrounded by a thick cell

263 al cell wall, forming a meshwork outside the cytoplasmic membrane that maintains cell shape and preve

264 the formation of a signaling complex at the cytoplasmic membrane that responds to environmental Pi l

265 e RNA virus is the modification of host cell cytoplasmic membranes that serve as sites of viral RNA s

266 ion and folding of proteins in the bacterial cytoplasmic membrane, the chloroplast thylakoid membrane

267 In the cytoplasmic membrane, the Hup transporter was specific f

268 serine, an acidic lipid prevalent in various cytoplasmic membranes, thereby enhancing the lipid speci

269 d by the association of FtsZ polymers to the cytoplasmic membrane through the membrane-tethering FtsA

270 all, heptameric lesions, or pinholes, in the cytoplasmic membrane, thus initiating lysis.

271 ssential for maintaining self-renewal on the cytoplasmic membrane to cope with low ligand levels outs

272 ansduces the protonmotive force (pmf) of the cytoplasmic membrane to drive active transport by high-a

273 ia uses the proton motive force (PMF) of the cytoplasmic membrane to energize active transport of nut

274 ems transduce the proton motive force of the cytoplasmic membrane to energize substrate transport thr

275 owth halts does the peptide permeabilize the cytoplasmic membrane to GFP and the small dye Sytox Gree

276 ectron transfer from the quinone pool in the cytoplasmic membrane to terminal reductase enzymes locat

277 er translocates virulence factors across the cytoplasmic membrane to the cell wall, cell surface, and

278 bacteria and expel toxic molecules from the cytoplasmic membrane to the medium.

279 and suggest that energy transduced from the cytoplasmic membrane to the outer membrane by TolA could

280 ples the translocation of protons across the cytoplasmic membrane to the synthesis or hydrolysis of A

281 Of the tol genes that function in the cytoplasmic membrane translocon, colE1 requires tolA and

282 a previously uncharacterized iron-repressed cytoplasmic membrane transporter system, fbpABC, that is

283 anonical holins accumulate harmlessly in the cytoplasmic membrane until they suddenly trigger to form

284 ese robust reconstituted proteoliposomes and cytoplasmic membrane vesicles have revealed that the num

285 when assessed in their native environment of cytoplasmic membrane vesicles.

286 otein that is attached to the outside of the cytoplasmic membrane via a covalent diacylglycerol ancho

287 Association of PflB with the cytoplasmic membrane was shown to be FocA dependent and

288 ison, vesicles representing all parts of the cytoplasmic membrane were captured by expressing a Tar v

289 tions of the outer permeability barriers and cytoplasmic membranes were found to be dependent on grow

290 No defects in the transport of capsids to cytoplasmic membranes were observed, but the wrapping of

291 the proper integration of the enzyme at the cytoplasmic membrane, which is mediated by the extended

292 roteins form a macromolecular complex at the cytoplasmic membrane, which we have purified and charact

293 microscopy shows that FtsH1 is mainly in the cytoplasmic membrane, while the remaining FtsH proteins

294 Most bacteria surround their cytoplasmic membrane with a net-like, elastic heteropoly

295 Bacteria surround their cytoplasmic membrane with an essential, stress-bearing p

296 period and then trigger to permeabilize the cytoplasmic membrane with lethal holes; thus, terminatin

297 d with a signal peptide securing them to the cytoplasmic membrane with the lipoprotein domain in the

298 d that RipA has a unique topology within the cytoplasmic membrane, with the N and C termini in the cy

299 Sec pathway to transport proteins across the cytoplasmic membrane, with the SecA ATPase playing a cen

300 The resultant bacterial ghosts contain cytoplasmic membrane within bacteria-shaped peptidoglyca