ライフサイエンスコーパス: periplasmic

1 the only Ln-proteins identified to date are periplasmic.

2 e, although BoMan26A and BoGal36A are likely periplasmic.

3 CsgE is a periplasmic accessory protein that plays a crucial role

4 Unexpectedly, the periplasmic adaptor protein CusB is a key metal-sensing

5 mplex machinery comprised of outer membrane, periplasmic adaptor, and inner membrane protein componen

6 -ATPase proton pump efflux that dissociates periplasmic AGP-Ca(2+) resulting in a Ca(2+) influx that

7 Co-incubation of BoMan26B and the periplasmic alpha-galactosidase BoGal36A increased the r

8 Using SHG, we quantify periplasmic and cytoplasmic accumulations separately in

9 nduced displacement of an alpha helix in the periplasmic and transmembrane domains, but it is unknown

10 y which OprM is activated via opening of its periplasmic aperture through a concerted interaction wit

11 novel Hechtian oscillator that integrates a periplasmic arabinogalactan glycoprotein-calcium (AGP-Ca

12 rface endo-1,6-beta-glucanase, BT3312, and a periplasmic beta-glucosidase that targets primarily 1,6-

13 o results show that MtrE can be regulated by periplasmic binding events and that the interaction betw

14 or that, together with its integral membrane periplasmic binding partner ToxS, is conserved across th

15 h-throughput method relies upon the thiamine periplasmic binding protein (TBP) from Escherichia coli

16 Here, we show that the periplasmic binding protein CeuE of Campylobacter jejuni

17 In Campylobacter jejuni the periplasmic binding protein CeuE, an integral part of th

18 orescence spectroscopy showed that MatC, the periplasmic binding protein from this system, binds to l

19 the TonB-dependent transporter MbnT and the periplasmic binding protein MbnE.

20 e pathogenicity and are mediated through the periplasmic binding protein NspS and the transmembrane b

21 Uptake is facilitated by high-affinity periplasmic binding proteins (PBPs) that bind cargo in t

22 The contribution of periplasmic binding proteins forming part of amino acid

23 structures and ligand binding affinities of periplasmic binding proteins from bacterial phosphite an

24 the potential for using genetically encoded periplasmic binding proteins such as RBP to measure meta

25 cholerae, and other bacteria with homologous periplasmic binding proteins.

26 nts and imported into the bacterial cell via periplasmic-binding proteins (PBPs) and ABC-transporters

27 ng cavity in LptFG that moves LPS to the Lpt periplasmic bridge.

28 N-terminal domain on the cell surface and a periplasmic C-terminal domain.

29 ght-transmembrane helix fold that supports a periplasmic carbon-nitrogen hydrolase domain containing

30 esent crystal structures revealing the MCR-1 periplasmic, catalytic domain to be a zinc metalloprotei

31 d the lateral gate, the plug domain, and the periplasmic cavity of SecY.

32 formation in which an aromatic belt near the periplasmic channel exit seals the transporter in a rest

33 (SilP), an effluxer complex (SilCFBA) and a periplasmic chaperon of Ag(+) (SilE).

34 RND) system) and of a putative Cu(+)-binding periplasmic chaperone and the unusual presence of two cy

35 SurA is a conserved ATP-independent periplasmic chaperone involved in the biogenesis of oute

36 s thought to explain the essentiality of the periplasmic chaperone LolA and its OM receptor LolB that

37 The periplasmic chaperone network ensures the biogenesis of

38 We identified the PCuA C-like periplasmic chaperone PccA and analyzed its contribution

39 asmic protein stability over external pH and periplasmic chaperone protection mechanisms, and 3) chan

40 Additionally, the periplasmic chaperone Skp contributes to yciB dcrB mutan

41 The periplasmic chaperone SurA plays a key role in outer mem

42 HdeA is a periplasmic chaperone that is rapidly activated upon shi

43 ved chaperone-usher (CU) pathway, in which a periplasmic chaperone works together with an outer membr

44 We find that some periplasmic chaperones function primarily as quality-con

45 of membrane thickness, the Escherichia coli periplasmic chaperones Skp and SurA, and BamA, the centr

46 apidly and were effectively engaged by fewer periplasmic chaperones than their urea-denatured counter

47 gram-negative bacteria involves delivery by periplasmic chaperones to the beta-barrel assembly machi

48 e through the Sec-translocon for delivery to periplasmic chaperones, for example SurA, which prevent

49 of the pilus and then taken up by binding to periplasmic ComEA, acting as a Brownian ratchet to preve

50 DNA uptake to the periplasmic compartment requires a DNA-uptake pilus and

51 lls), but owing to the smaller volume of the periplasmic compartment, its concentration in the cytopl

52 he 1.56 angstrom resolution structure of the periplasmic complex of the C-terminal CSS domain (CCSSD)

53 enhancing factor that we identify as AcrA, a periplasmic component of RND efflux pumps.

54 brane efflux protein TolC and with PstS, the periplasmic component of the ABC transporter complex (Ps

55 , the structure, assembly and roles of other periplasmic components remain enigmatic, limiting our kn

56 ia acquire phosphate (P(i)) by maintaining a periplasmic concentration below environmental levels.

57 ux kinetics through the determination of its periplasmic concentrations by quantitation of the first

58 cal BAM pathway, while formation of a stable periplasmic conformer involves an export-related, foldin

59 The periplasmic conversion of ferribactin to pyoverdine is e

60 Finally I suggest that the periplasmic conversion of nutrients acquired across the

61 femtomolar affinities and transfer it to the periplasmic copper metallochaperone CueP.

62 al envelope-restricts the expression of this periplasmic copper resistance protein solely to cells en

63 thanotrophs, including proteins that contain periplasmic copper-A chaperone (PCu(A)C) domains.

64 u and the high-affinity CcoI feeds Cu into a periplasmic Cu relay system required for cbb(3) -Cox bio

65 ane transporters, whereas CopR/S responds to periplasmic Cu(+) Analysis of DeltacopR and DeltacueR mu

66 a CopR regulon composed of genes involved in periplasmic Cu(+) homeostasis and its putative DNA recog

67 Periplasmic CueO was readily activated by the addition o

68 is consistent with MbnE's proposed role as a periplasmic CuMbn transporter.

69 on flow from sulfide to oxygen that involves periplasmic cytochromes, yet-unidentified conductive per

70 Expression of the chimeric periplasmic-cytoplasmic MalE-LacZ72-47 protein is an his

71 Cytochrome c nitrite reductase (ccNiR) is a periplasmic, decaheme homodimeric enzyme that catalyzes

72 pilus docked to the OM without an associated periplasmic density.

73 y, nickel import ATP-binding protein (NikE), periplasmic dipeptide transport protein (DppA), and oute

74 DddY is the only known periplasmic DMSP lyase and is present in beta-, gamma-,

75 velocity depends on the concentration of the periplasmic DNA-binding protein ComE, indicating that Co

76 and produced a soluble version of AcrB [AcrB periplasmic domain (AcrBper)], which is highly congruent

77 o 190) is essential for viability, while the periplasmic domain (residues 191 to 586) is dispensable.

78 d LptG are composed of a beta-jellyroll-like periplasmic domain and six alpha-helical segments in the

79 How the inner membrane protein YejM with its periplasmic domain changes membrane properties remains u

80 The EnvC-FtsX periplasmic domain complex has a 1-to-2 stoichiometry wi

81 r supported by results showing that the ToxR periplasmic domain contributed to indole-mediated increa

82 e pbgADelta191-586 mutant (in which the PbgA periplasmic domain from residues 191 to 586 is deleted).

83 esent the 2.1 angstrom structure of the FtsX periplasmic domain in complex with its periplasmic partn

84 ish that RcsF interacts with the C-terminal, periplasmic domain of OmpA, not with the N-terminal beta

85 pair in which the electron transfer from the periplasmic domain of ScsB (n-ScsB) to ScsC is thermodyn

86 Thirteen protomers form a large periplasmic domain of six stacked rings and a secretin d

87 rotein allows the interaction of ComH with a periplasmic domain of the inner-membrane channel ComEC,

88 A 1.7 angstrom crystal structure of the periplasmic domain of the RsbU protein from C. trachomat

89 se requires that at least one subunit of the periplasmic domain of the Tsr homodimer (pTsr) has an in

90 intra-chain disulfide bond in the C-terminal periplasmic domain of ToxR (dbToxRp).

91 PelB, a membrane-embedded porin with a large periplasmic domain predicted to contain 19 tetratricopep

92 ToxRp to have a higher affinity for the ToxS periplasmic domain than the non-disulfide bonded conform

93 2 gene product contains a ~200-aa N-terminal periplasmic domain that is anchored in the membrane by t

94 This process was dependent on the ToxR periplasmic domain, suggesting that indole was a ToxR ag

95 e, malate and oxaloacetate bound to the RsbU periplasmic domain.

96 y homologous to the V. parahaemolyticus VtrA periplasmic domain.

97 f a membrane domain on which sits a globular periplasmic domain.

98 intermolecular disulphide bonds in the TcpP periplasmic domain.

99 th bound metal ions in the structure of YejM periplasmic domain.

100 rane 'insertase' YidC - contacts BAM through periplasmic domains of SecDF and YidC, ensuring efficien

101 The crystal structure of the periplasmic domains of the VtrA/VtrC heterodimer reveals

102 erwhelming structural similarity between the periplasmic domains of two YejM homologues with hydrolas

103 The periplasmic domains of YidC and SecD are poised at the p

104 mains drives opening and closing of the MacB periplasmic domains via concerted movements of the secon

105 f Ca(2+) with a wide-open pore and remodeled periplasmic domains, including increased contacts betwee

106 thought to interact through their respective periplasmic domains, ToxRp and ToxSp.

107 eveal the functionality of the LptF and LptG periplasmic domains.

108 ible densities corresponding to the HAMP and periplasmic domains.

109 d transmembrane beta-barrel connected to two periplasmic domains.

110 ailable atomic structures of cytoplasmic and periplasmic domains.

111 hydrophobic cavity toward the transporter's periplasmic domains.Lipopolysaccharides (LPS) are synthe

112 These sub-complexes consist of the periplasmic embellished P- and L-rings, and bend the mem

113 ogical membrane, lipid molecules occupy this periplasmic exit and prevent water flux in the transport

114 The channel's periplasmic exit is sealed by detergent molecules that b

115 , with its catalytic cavity connected to the periplasmic exit of the TM domain.

116 embedded cavity with a lateral opening and a periplasmic exit.

117 The periplasmic/extra-cytoplasmic targets of penicillin are

118 dant outer membrane lipoprotein, Lpp, at the periplasmic face of the inner membrane leads to lethal i

119 and structural rearrangement of CsgA at the periplasmic face of the secretion machinery.

120 ncharacterized helical membrane domain and a periplasmic facing soluble domain.

121 ate that the double labeling of sites on the periplasmic-facing surface of BtuB is possible using a d

122 mic cytochromes, yet-unidentified conductive periplasmic fibers, and periplasmic oxygen reduction.

123 Whereas periplasmic FlaF binds the surface layer (S-layer), the

124 ease bacterium Borrelia burgdorferi has 7-11 periplasmic flagella (PF) that arise from the cell poles

125 gy with hook-shaped ends and the presence of periplasmic flagella (PF) with pronounced spontaneous su

126 investigated the role played by T. denticola periplasmic flagella (PF), unique motility organelles of

127 ernal flagellated bacteria, spirochetes have periplasmic flagella (PF).

128 th one or two flat curves, and have 10 to 14 periplasmic flagella inserted at each cell end.

129 ike flagella of other bacteria, spirochetes' periplasmic flagella possess a complex structure called

130 pathogenicity; indeed, spirochaete flagella (periplasmic flagella) reside and rotate within the perip

131 hete, and motility, which is provided by its periplasmic flagella, is critical for every part of the

132 eri is a highly motile spirochete due to its periplasmic flagella.

133 ious important functions to the spirochete's periplasmic flagellar assembly and rotation.

134 b0326+ cells, leading us to rename BB0326 as periplasmic flagellar collar protein A or FlcA.

135 high torque needed to power the spirochete's periplasmic flagellar motors.

136 lated bacteria, spirochetes possess a unique periplasmic flagellar structure called the collar.

137 pathogen, Campylobacter jejuni, possesses a periplasmic formate dehydrogenase and two terminal oxida

138 equent electron transfer could proceed via a periplasmic formate dehydrogenase and/or hydrogenase, al

139 ct with MexB directly, and that it opens its periplasmic gate by forming a complex.

140 Introduction of mutations in the periplasmic gate lead to the formation of a channel that

141 the first two crystal structures of soluble periplasmic globular domain of PbgA from S. typhimurium

142 The mechanism involves PbgA's periplasmic globular region (residues 245 to 586), but t

143 first high resolution crystal structures of periplasmic glucose-binding protein fromPseudomonas puti

144 have developed probes based on the bacterial periplasmic glutamate/aspartate binding protein with eit

145 rprising discovery that the Escherichia coli periplasmic glycerol-3-phosphate (G3P)-binding protein U

146 are consistent with the conclusion that the periplasmic half-channel is more easily protonated in a

147 es acidification through protonation of CpxA periplasmic histidine residues, and upregulates the fabA

148 ToxR requires its operon partner ToxS, a periplasmic integral membrane protein, for full activity

149 dhesion proteins of the outer membrane via a periplasmic interaction platform, which presumably invol

150 Both the ATPase activity of FtsEX and its periplasmic interaction with EnvC are required for amida

151 Both the ATPase activity of FtsEX and its periplasmic interaction with EnvC are required for resis

152 hybrid system was successfully used to study periplasmic interactions.

153 In Methylorubrum extorquens AM1, the periplasmic lanthanide-dependent methanol dehydrogenase

154 flet of the inner membrane is flipped to the periplasmic leaflet by MsbA, an ATP-binding cassette tra

155 rane on a lipid anchor and reoriented to the periplasmic leaflet by the channel-forming WzmWzt ABC tr

156 s identify a lipid A-binding motif along the periplasmic leaflet of the inner membrane.

157 binds deep inside MsbA at the height of the periplasmic leaflet, establishing extensive hydrophilic

158 Here, we report the structure of the periplasmic ligand-binding domain (LBD) of the transmemb

159 from the nitrilase domain interacts with the periplasmic lipid leaflet, forming an interfacial entran

160 a gene, virJ, that codes for a protein with periplasmic localization that is involved in the intrace

161 Specifically, we show that the D1 periplasmic loop and a conserved tyrosine are essential

162 Two helices located in a periplasmic loop between two transmembrane helices conta

163 ach, we demonstrate that LpqN interacts with periplasmic loop domains of the MmpL3 and MmpL11 transpo

164 ng binds and the other located in the second periplasmic loop of DsbB, which interacts with DsbA.

165 tutions in transmembrane domains 2 and 8 and periplasmic loops of MurJ could be cross-linked with hom

166 er contains 12 transmembrane helices and two periplasmic loops that suggest a plausible pathway for s

167 kinetic and genetic specificities of various periplasmic lyases which dictate glycosaminoglycan metab

168 alF-MalG; a homodimeric ATPase, MalK2; and a periplasmic maltose receptor, MalE.

169 in modifications are well characterized, the periplasmic maturation steps are far from understood.

170 o communicate conformational changes between periplasmic, membrane, and cytoplasmic regions.

171 An ABC transporter with a periplasmic metallo-aminopeptidase domain forms a sensor

172 de two routes for methylamine oxidation: the periplasmic methylamine dehydrogenase (MaDH) and the cyt

173 tric and electronic structure of the E. coli periplasmic molybdenum-dependent methionine sulfoxide re

174 MS also identified candidate partners for periplasmic MOSP, including TDE1658, a spirochete-specif

175 d by a localized 16-mer stoichiometry in the periplasmic-most coupling domain of the otherwise 15-mer

176 of a respiratory arsenate reductase (arrA), periplasmic nitrate reductase (napA) and membrane-bound

177 iated growth inhibition, whereas all but the periplasmic nitrite reductase NrfA provide protection ag

178 e Escherichia coli K-12 nrf operon encodes a periplasmic nitrite reductase, the expression of which i

179 ulfofustis deltaproteobacterium, including a periplasmic NTD fused to the conventional ligand-binding

180 particularly involving Ca(2+) modulation and periplasmic NTDs.

181 It involves two proteins: a periplasmic one, MsrP, previously named YedY, carrying o

182 itrosoglutathione (GSNO) in vitro However, a periplasmic or extracellular denitrosylase has not been

183 f accumulated P(i) pairs could influence the periplasmic osmolarity of marine bacteria.

184 DsbA acts as the periplasmic oxidant of periplasmic substrate proteins.

185 actin, and their fluorophore is generated by periplasmic oxidation and cyclization reactions of d-tyr

186 NOX family and involved in the reduction of periplasmic oxidized proteins.

187 Here we report that the putative periplasmic oxidoreductase PvdO of Pseudomonas fluoresce

188 dentified conductive periplasmic fibers, and periplasmic oxygen reduction.

189 ccumulation in the periplasm we propose that periplasmic P(i) anions pair with chemiosmotic cations o

190 The periplasmic P(i) can be gradually imported into the cyto

191 single H(+)-driven stator have only the core periplasmic P- and L-rings; those with dual H(+)-driven

192 Although only the soluble, periplasmic part of AcrB binds and exports the ligands,

193 ch is highly congruent in structure with the periplasmic part of the full-length protein, and is capa

194 ne relies on the piston-type movement of the periplasmic part of TM2.

195 FtsX periplasmic domain in complex with its periplasmic partner, EnvC.

196 ia coli, a proteolytic system comprising the periplasmic PDZ-protease Prc and the lipoprotein adaptor

197 C transporter that regulates the activity of periplasmic peptidoglycan amidases via its interaction w

198 lation of EnvC and its downstream control of periplasmic peptidoglycan amidases.

199 hey operate efficiently without compromising periplasmic plasticity.

200 upon cellular demand while still maintaining periplasmic plasticity; this could be broadly relevant t

201 , with one open and one closed cytosolic and periplasmic portal.

202 he predatory behaviour of two strains of the periplasmic predator B. bacteriovorus and of the epibiot

203 Here, examining the invasive bacterial periplasmic predator Bdellovibrio bacteriovorus, we repo

204 -competent, they were slowly degraded by the periplasmic protease DegP.

205 ies have established the essentiality of the periplasmic protease MarP for Mtb to survive in acidifie

206 Here, we identify CtpA as a periplasmic protease that is responsible for the regulat

207 e receptor for c-di-GMP, LapD, and a cognate periplasmic protease, LapG.

208 ed by LapD, a c-di-GMP receptor, and LapG, a periplasmic protease, which together control whether Lap

209 from the inner membrane and places it onto a periplasmic protein bridge through a poorly understood m

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

211 Here, we find that the periplasmic protein FlaG and the association with its pa

212 We also document that the periplasmic protein PA0808, heretofore of unknown functi

213 are important for efficient transport of the periplasmic protein proPhoA.

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

215 omponents, the membrane protein ScsB and the periplasmic protein ScsC.

216 e lipid fatty acid composition, 2) change in periplasmic protein stability over external pH and perip

217 eipA encodes a soluble periplasmic protein that adopts an unusual eight-strande

218 uter membrane MlaA-OmpC/F complex, a soluble periplasmic protein, MlaC, and the inner membrane ATPase

219 idely conserved but poorly understood 20 kDa periplasmic protein.

220 Fvs was confirmed by competitive ELISA using periplasmic protein.

221 Degradation of periplasmic proteins (Deg)/high temperature requirement

222 Two general groups - metalloproteins and periplasmic proteins - show enrichment of their antioxid

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

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

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

226 energy to synthesizing ATP-binding cassette periplasmic proteins that bind substrates.

227 n protein, connecting MmpL transporters with periplasmic proteins, and provide general insight into t

228 electron acceptors for oxidative folding of periplasmic proteins.

229 dergoing oxidative stress impairs folding of periplasmic proteins.

230 Here we identify the protein ComH as the periplasmic receptor for the transforming DNA during nat

231 ant predators can replicate unusually in the periplasmic region between the peptidoglycan wall and th

232 uorimetry showed interaction of the isolated periplasmic region of McpX (McpX(PR) and McpX34-306 ) wi

233 olves association of the plug helices in the periplasmic region of the MotB dimer into a parallel coi

234 that link the outer membrane to the aqueous periplasmic region.

235 s with most of the transmembrane helices and periplasmic regions of SecY, with a clustering of intera

236 rganized into an outer membrane cap (OMC), a periplasmic ring (PR) and a stalk.

237 features of the outer membrane cap (OMC) and periplasmic ring (PR).

238 brane core complex (OMCC), 17-fold symmetric periplasmic ring complex (PRC), and central stalk.

239 cterial flagellar motor, including two novel periplasmic ring structures, and the stator ring harbori

240 sought to determine whether PelB serves as a periplasmic scaffold that recruits other components of t

241 s direct interactions with transmembrane and periplasmic segments, as well as peripheral interactions

242 The absence of a periplasmic sensing domain suggested that PilS may sense

243 experiments uncover a model in which direct periplasmic sensing of LPS by PbgA coordinates the biosy

244 hosphatase domain but also contains a unique periplasmic sensor domain that is expected to control th

245 tion of osmotic upshift does not require its periplasmic sensor domain.

246 Previously overlooked N-terminal periplasmic sensor domains were detected in the well-cha

247 he interfacial metal-binding sites in CusS's periplasmic sensor domains, prior to ATP binding and aut

248 nts and belongs to the dCache superfamily of periplasmic sensor domains.

249 SagS harbours a periplasmic sensory HmsP, and phosphorelay HisKA and Rec

250 The TM2 helix further extends on the periplasmic side into the alpha6-helix of the sensory PA

251 At the end of the cycle, the periplasmic side is expected to open to release drugs.

252 polysaccharides (LPS) are synthesized at the periplasmic side of the inner membrane of Gram-negative

253 within the lumen of an OmpF subunit from the periplasmic side of the membrane, a binding mode reminis

254 The nitrilase domain is located on the periplasmic side of the membrane, with its catalytic cav

255 e cytoplasmic side and the other open to the periplasmic side with substrate bound.

256 AmpDh2 is a periplasmic soluble enzyme with the former anchored to t

257 cific and high-affinity binding of zinc by a periplasmic solute-binding protein (SBP).

258 at rod length is limited by the width of the periplasmic space between the inner and outer membranes.

259 d that their small size and relatively large periplasmic space might enable them to outcompete other

260 y coexpressing 3 recombinant proteins in the periplasmic space of Escherichia coli-an antibody clone,

261 This protein, localized in the periplasmic space of the mycobacterial cell wall, was sh

262 ginosa when delivered to or expressed in the periplasmic space of this organism.

263 ansports these components across the aqueous periplasmic space separating the two membranes.

264 cetes, including a defined outer membrane, a periplasmic space that can be greatly enlarged and convo

265 ecules can be taken up and accumulate in the periplasmic space through unclear mechanisms.

266 of moving Braun's lipoprotein (BLP) from the periplasmic space to the outer membrane of E. coli, via

267 ipids are exported from the cytoplasm to the periplasmic space via the mycobacterial membrane protein

268 asmic flagella) reside and rotate within the periplasmic space(2-11).

269 hich polar substrates move directly into the periplasmic space, PpF1 TodX and CymD direct their hydro

270 te channels of sufficient length to span the periplasmic space.

271 e channel, followed by diffusion towards the periplasmic space.

272 oth inner and outer membranes separated by a periplasmic space.

273 anslocation across the two membranes and the periplasmic space.

274 transport for drug entry into the bacterial periplasmic space.

275 ap around the cell body, confined within the periplasmic space.

276 bel single or paired cysteines that face the periplasmic space.

277 ytoplasm, a cytoplasmic disc and dome, and a periplasmic stem.

278 ssential component of TRAP transporters is a periplasmic substrate binding protein (SBP).

279 DsbA acts as the periplasmic oxidant of periplasmic substrate proteins.

280 Periplasmic substrate-binding proteins (SBPs) bind to th

281 , which is able to bind both Hep and HS, and periplasmic sulfatases reveal the major specificity dete

282 For example, we discover a trans-periplasmic supercomplex comprising subunits of the Bam

283 ve to oxidative metabolism enabled by higher periplasmic superoxide defense.

284 During this process, the periplasmic thiol-disulfide oxidoreductase DsbA is thoug

285 onstrate that signaling also occurs from the periplasmic to the extracellular surface in BtuB.

286 Moreover, mutants in the periplasmic Ton box that are transport-defective alter t

287 ngements to the structural adjustment of the periplasmic TonB-binding motif.

288 ther proteobacteria that we termed PtaA for "periplasmic transaminase A" An in-frame-deleted ptaA mut

289 In silico analyses indicated a periplasmic transaminase in fluorescent pseudomonads and

290 verdine-producing bacteria, its catalysis of periplasmic transaminations is most likely a general too

291 Its biosynthesis requires periplasmic transpeptidation reactions, which construct

292 us influenzae use tripartite ATP-independent periplasmic transporters (TRAPs) to scavenge sialic acid

293 proteins, including overwhelmingly abundant periplasmic transporters for nutrient acquisition and pr

294 The tripartite ATP-independent periplasmic (TRAP) transporters are a widespread class o

295 OSP in TDE exists as outer membrane (OM) and periplasmic trimeric conformers; PelB-MOSP, in contrast,

296 the fluorophore is known to be driven by the periplasmic tyrosinase PvdP.

297 e inner membrane, the T2SS has a much longer periplasmic vestibule and it has a short-lived flexible

298 that this discrepancy can be resolved if the periplasmic volume decreases as the cell wall becomes so

299 ow alterations of cell wall stiffness affect periplasmic volume regulation.

300 The length of Braun's lipoprotein determines periplasmic width by tethering the outer membrane to the