ライフサイエンスコーパス: barrel

1 s of adjacent subunits and an internal alpha-barrel.

2 an open cavity of the C-terminal FBXO31 beta-barrel.

3 bilayer and assemble into a 168-strand beta-barrel.

4 and from the reactions that occur inside the barrel.

5 closed pocket at the centre of the lipocalin barrel.

6 it is an 18-stranded, not 16-stranded, beta-barrel.

7 es that yield an 88-strand pore-forming beta-barrel.

8 extracellular loops within the forming beta-barrel.

9 lular loop, to the lumen of the forming beta-barrel.

10 , with the ligands paneling the sides of the barrels.

11 ic structures resembling cylindrins and beta-barrels.

12 d by a major capsid protein bearing two beta-barrels.

13 ortex, but did not affect the segregation of barrels.

14 fruity characteristics in vinegars from wood barrels.

15 ptal area, the cell-sparse region separating barrels.

16 cing residues observed in transmembrane beta-barrels.

17 te, eventually innervating non-corresponding barrels.

18 different countries matured in the same oak barrels.

19 ains and C-terminal membrane-integrated beta-barrels.

20 a home to oil sands deposits of 1.7 trillion barrels.

21 (betaalpha)8 triosephosphate isomerase (TIM) barrel, a canonical [4Fe-4S] cluster binds SAM in close

22 We show that the lumen of the barrel accepts 21 mutations to functional polar residues

23 ) the surprisingly pervasive double-Psi beta-barrel active-site configuration among different nucleic

24 analysis revealed that freshly-distilled and barrel-aged spirits were differentiated by their megasti

25 s 2012 and 2013 was performed during the oak barrel ageing process.

26 e proteins are composed of a C-terminal beta-barrel and a different number of N-terminal POTRA domain

27 We find that, although barrel and clam-shell drops have different shapes, these

28 lex) mediates subsequent folding of the beta-barrel and its integration into the target membrane.

29 mA is present, indicating that both the beta-barrel and polypeptide transport-associated (POTRA) doma

30 o induce movement of the beta-strands of the barrel and promote insertion of the nascent OMP.

31 of retinotopic organization that extend into barrel and retrosplenial cortices.

32 operativity and stability of the folded beta-barrel and that the thermodynamic contributions of the l

33 pendent asymmetric distortions of the VDAC-1 barrel and the displacement of particular charged amino

34 , suggesting that lateral gating of the BamA barrel and/or hybrid barrel formation is not required, a

35 Short-tailed opossums lack barrels and septa in S1 but show active whisking behavio

36 During wine aging in barrels, antioxidant molecules from wood, such as ellagi

37 263, I299, and F387) were located in the TIM barrel around the active site in domain A, and two resid

38 fic structure with characteristics of a beta-barrel arrangement that we named beta-barrel pore-formin

39 ribe the motions of the residues of the beta-barrel as a collective rocking of low amplitude and of h

40 host organism, and confirms the (betaalpha)8 barrel as an inherently evolvable protein scaffold.

41 t are believed to be less important for beta-barrel assembly in vitro Here, we experimentally measure

42 beta-signal motif required for assisted beta-barrel assembly in vivo but are believed to be less impo

43 These two systems are the beta-barrel assembly machine (BAM) complex and the translocat

44 ponents interact with the two essential beta-barrel assembly machine (Bam) components, BamA and BamD.

45 alton five-component complex called the beta-barrel assembly machinery (BAM) complex has been implica

46 The beta-barrel assembly machinery (BAM) is a approximately 203 k

47 The beta-barrel assembly machinery (BAM) is a conserved multicomp

48 livery by periplasmic chaperones to the beta-barrel assembly machinery (BAM), which catalyzes OMP ins

49 eginning to understand, mediated by the beta-barrel assembly machinery (BAM).

50 d folded into the outer membrane by the beta-barrel assembly machinery (BAM).

51 dditionally, the effective rate for the beta-barrel assembly machinery complex necessary for physiolo

52 force for assembly independently of the beta-barrel assembly machinery.

53 h a cooperative mechanism involving the beta-barrel assembly machinery.

54 nd provide mechanistic insight into the beta-barrel assembly pathway that enables the rapid deploymen

55 the beta-signal motif are vital for in vitro barrel assembly, because they exhibit a side chain-speci

56 trands, and the loops extending out the beta-barrel at both N-terminus and C-terminus, which is disti

57 esel to be 1.14 (80% CI, 0.67-2.15) and 1.22 barrel/barrel (80% CI, 0.71-2.29), respectively, 13% of

58 o oil price, ranging from 20000 wells at $30/barrel (bbl) oil to 97000 wells at $100/bbl oil.

59 Deaths from barrel bombs were overwhelmingly civilian rather than op

60 Of 7566 deaths from barrel bombs, 7351 (97.2%) were civilians, of whom 2007

61 ocyte processes are structurally confined by barrel boundaries in the mouse, by the border of primary

62 y adopt beta-barrel structures and that beta-barrels can be formed by folding an out-of-register beta

63 glucosyl-1,6-deoxynojirimycin revealed a TIM barrel catalytic domain that contains a deep substrate-b

64 The nonameric assembly reveals a long beta-barrel channel spanning the length of the complex that,

65 FapF forms a trimer of gated beta-barrel channels in which opening is regulated by a helic

66 ioning for three structurally different beta-barrel channels: voltage-dependent anion channel from ou

67 enance of projection topology from different barrel columns in the BC, albeit with target-specific pr

68 and a P1 domain, which forms a squashed beta-barrel consisting of six antiparallel beta-strands simil

69 Spirits aged in oak barrels contain higher amounts, but megastigmatrienones

70 The barrel core is fastened by three layers of hydrophobic r

71 on is that between L5B neurons in the rodent barrel cortex (BC) and the posterior medial nucleus of t

72 On the example of rat barrel cortex (vS1), we illustrate that retrograde trace

73 so sends information directly to the sensory barrel cortex (vS1).

74 imaging to assess tactile defensiveness and barrel cortex activity in young and adult Fmr1 knock-out

75 ing and that this involves both whiskers and barrel cortex activity.

76 nal, bilateral whisker representation in the barrel cortex and activation of distinct cortical loci f

77 ates of the connectivity of layer 4 (L4) rat barrel cortex and numerical simulations of this circuit

78 al for normal synaptic dynamics in the mouse barrel cortex and sensory function.

79 his theory is supported by simulations of L4 barrel cortex during spontaneous and stimulus-evoked con

80 pharmacogenetic activation of PV+INs in the barrel cortex during stress.

81 dissimilarity suggests that some aspects of barrel cortex function may not generalize to tactile pro

82 t all three major interneuron classes in the barrel cortex integrate both feedforward and feedback in

83 Barrel cortex layer IV spiny stellate cells (bSCs) are t

84 vivo two-photon calcium imaging of layer 2/3 barrel cortex neurons expressing GCaMP6s, we found no di

85 tion processing in adapting and non-adapting barrel cortex neurons, and that eventual deficits in inh

86 e sensory evoked population responses in the barrel cortex of aged transgenic (Tg) mice and of age-ma

87 Here, we show that pyramidal neurons in the barrel cortex of BC1 knock out (KO) mice display larger

88 rease GABAAreceptor-mediated response in the barrel cortex of mice with compromised Met signaling.

89 luate whisker sensory evoked activity in the barrel cortex of mice.

90 Here, we show that in the whisker-related barrel cortex of neonatal rats, spontaneous whisker move

91 Here, we show that, in the whisker-related barrel cortex of neonatal rats, spontaneous whisker move

92 ion evoked abnormal sensory responses in the barrel cortex of Tg mice.

93 structural and functional impairments in the barrel cortex of the Bird mouse line, a popular animal m

94 e spike frequency adaptation - split layer 5 barrel cortex pyramidal neurons into two clusters: one o

95 y and sharpen the response of neurons in the barrel cortex to incoming sensory input signals.

96 ion on gene expression in the adult male rat barrel cortex were investigated using RNA sequencing.

97 n on gene expression in the adult female rat barrel cortex were investigated using RNA sequencing.

98 r (L) 5 pyramidal neurons (PNs) in the mouse barrel cortex, and such spine loss closely associates wi

99 t reorganization of synaptic circuits in the barrel cortex, as well as diminished spatial and associa

100 ell as a lack of L2/3 neuronal adaptation in barrel cortex, during whisker stimulation.

101 tone on whisker-evoked NVC responses in rat barrel cortex, measured by cerebral blood flow (CBF) and

102 microscopy (EM) analysis, performed in mouse barrel cortex, showed that the proposed method has low f

103 Layer (L) 4 excitatory neurons in the barrel cortex, the major target of the somatosensory tha

104 nctionally comparable to changes in the male barrel cortex, where changes in genes related to morphol

105 in the developing primary somatosensory (S1) barrel cortex.

106 efficiently triggered bursts of activity in barrel cortex.

107 ivity is roughly topographic but weak in the barrel cortex.

108 s in the ventroposteromedial, as well as the barrel cortex.

109 U.S. pipelines (capacity greater than 100000 barrels/day) to estimate the variability of GHG emission

110 dependent protein changes include asymmetric barrel distortion, its interaction with the membrane, an

111 e demonstrate that cross-linking of the BamA barrel does not affect tOmpA folding kinetics in 1,2-dim

112 d archaellin monomer has two domains, a beta-barrel domain and a long, mildly kinked alpha-helix tail

113 al subunits that together form a single beta-barrel domain and an extracellular coiled-coil ("passeng

114 ted to form between the most C-terminal beta-barrel domain and the catalytic core domain of tTG.

115 es the beta-strands within the (beta/alpha)8-barrel domain and the linked active site loops that are

116 Further, conformational shifts in the barrel domain lead to opening of the exit pore and rearr

117 By mutating conserved residues in the beta-barrel domain of this protein, we generated three assemb

118 uter membrane proteins (OMPs) contain a beta barrel domain that serves as a membrane anchor, but the

119 This activity is located in the BamA beta-barrel domain, but is greater when full-length BamA is p

120 rane beta-barrels that can also identify the barrel domain, predict the topology and identify the ori

121 etween the first and last strand of the TamA barrel domain, providing the first experimental evidence

122 ng of an N-terminal "RxxxR" motif and a beta-barrel domain, represents a prototype c-di-GMP receptor.

123 Located within the mu1 jelly roll beta barrel domain, which is a known regulator of ISVP* forma

124 MS) domain and a C-terminal 16-stranded beta-barrel domain.

125 Toc75, followed by a membrane-spanning beta-barrel domain.

126 hange (V403A) within the mu1 jelly roll beta barrel domain.

127 minal extension, methyltransferase, and beta-barrel domains is stabilized by the dimerization arm of

128 h DNA must travel, such as the alpha-helical barrel domains of P22 portal proteins and T7 proteins th

129 ses the conserved methyltransferase and beta-barrel domains, an N-terminal extension, and a dimerizat

130 bstrate OMPs may not be threaded through the barrel during biogenesis.

131 20 amino acids using the transmembrane beta-barrel E. coli PagP as a scaffold protein.

132 The barrel end opposite the HlyIIC-core has a positively cha

133 Such alpha-helix barrels engineered from peptides could find applications

134 In that experiment, the (betaalpha)8 barrel enzyme HisA was under selection for two functions

135 phobicity scale using the transmembrane beta-barrel Escherichia coli OmpLA as a scaffold protein.

136 I: impact site, primary somatosensory cortex barrel field (S1BF), and a remote region.

137 ory nucleus preluding the enlargement of the barrel-field.

138 ucture as primary forces in defining the TIM barrel fitness landscape and suggest that fitness landsc

139 DddY catalytic domain adopts a typical beta-barrel fold and contains two conserved cupin motifs.

140 Toc75 is predicted to have a beta-barrel fold consisting of an N-terminal intermembrane sp

141 CteB has the (beta/alpha)6-TIM barrel fold that is characteristic of radical SAM enzyme

142 The beta-barrel fold with a central molecular pocket is similar a

143 Viperin contains a partial (betaalpha)6-barrel fold with a disordered N-terminal extension (resi

144 cture, VP24 consists of a nine-stranded beta-barrel fold with mostly antiparallel beta-strands, and t

145 in, which adopts the typical jelly-roll beta-barrel fold, and a P1 domain, which forms a squashed bet

146 xpectedly, the structures reveal a truncated barrel fold, wherein binding of large peptide substrates

147 nelles mitochondria and plastids have a beta-barrel fold.

148 s of secondary structure, fastening the beta-barrel fold.

149 lytic domain that displays an (alpha/alpha)6 barrel-fold.

150 model consistent with these findings is that barrel folding by the Bam complex begins in the periplas

151 in Cabernet Sauvignon wines macerated in oak barrels for a year was studied.

152 dues at the C terminus of transmembrane beta-barrels form the beta-signal motif required for assisted

153 eral gating of the BamA barrel and/or hybrid barrel formation is not required, at least for the assem

154 he fabrication of monodisperse transmembrane barrels formed from short synthetic peptides has not bee

155 ystal structure of UvsY in four similar open-barrel heptameric assemblies and provide structural and

156 velop into discrete, concentrated patches in barrel hollows, and the complexity of the dendritic bran

157 pecific neural modules called barreloids and barrels in the contralateral thalamus and cortex represe

158 These modules are called "barrels" in layer 4 of the primary somatosensory cortex.

159 OEP40 protein forms a high conductance beta-barrel ion channel with subconductant states in planar l

160 In the center of the barrel is a deep pocket, which, based on mutagenesis dat

161 barreloids with their corresponding cortical barrels is critical for processing of vibrissal sensory

162 te topology prediction of transmembrane beta-barrels is still an open question.

163 dues localized to the ends of the heptameric barrel-like CP structure that occlude substrate entry po

164 The barrel-like distribution of cohesin complexes surroundin

165 ha/beta region and a C-terminal twisted beta barrel-like domain.

166 he FliW monomer reveal a novel, minimal beta-barrel-like fold.

167 philin-1 interacted directly with the RuvbL1 barrel-like structure near the opening of the central ch

168 -beta4-alphaB-beta5, that come together in a barrel-like structure.

169 Super-resolution imaging of Nup188 shows two barrel-like structures with dimensions and organization

170 These assemblies typically adopt barrel-like structures, with the ligands paneling the si

171 posed of a separate extended network of beta-barrel-like tetramers.

172 n a closed state that prevents access to the barrel lumen, which indicates substrate OMPs may not be

173 while a solid carbon electrode in the other barrel measures the local concentration and flux of the

174 CSE genes and associated enzyme activity in barrel medic (Medicago truncatula, dicot, Leguminosae),

175 channel-1 (VDAC1) is a highly regulated beta-barrel membrane protein that mediates transport of ions

176 ic resonance spectra for both VDAC-1, a beta-barrel membrane protein, and the G-protein-coupled recep

177 is applicable to both alpha-helical and beta-barrel membrane proteins of diverse architectures with o

178 ter membrane channels known to date are beta-barrel membrane proteins, including the abundant voltage

179 Five barrel modalities were used; three polyphenol indices (I

180 ter strands, the promoter-guided assembly of barrels modified with 12 left- or right-handed tethers i

181 Thus, despite the absence of barrels, most receptive field properties were similar to

182 strate-binding domain consisting of two beta-barrel motifs, whereas cyclin D1 binds to FBXO31 by tuck

183 e the efficacy of this approach using a beta-barrel MP, outer membrane protein F (OmpF), in short-cha

184 nvestigated the dendritic differentiation of barrel neurons and individual thalamocortical axon (TCA)

185 e with respect to the integral membrane beta-barrel of BamA to induce movement of the beta-strands of

186 peptide-binding proteins (OBPs) and the beta-barrel of BamA.

187 hrough a 'lateral gating' motion of the beta-barrel of BamA.

188 24% reductions in the CO2 emissions on a per barrel of crude oil processed) can be achieved in a medi

189 The approach is applied to the dynamic beta-barrel of SOD1, associated with pathologic aggregation i

190 tion strands, allowing them to form the beta-barrel of the channel.

191 arginine residue near the middle of the beta barrel of the Escherichia coli OMPs OmpLA and EspP creat

192 One barrel of the probe is filled with electrolyte and the m

193 sulted in the accidental release of millions barrels of crude oil into the Gulf of Mexico.

194 ) accident released an estimated 4.1 million barrels of oil and 10(10) mol of natural gas into the Gu

195 il and bitumen deposits amount to 9 trillion barrels of oil distributed in over 280 basins around the

196 n oil spill released approximately 4 million barrels of oil into the GOM, with severe ecosystem and e

197 spill resulted in the release of millions of barrels of oil into the Gulf of Mexico, and some marsh s

198 studies reveal rapid depletion of many beta-barrel OM proteins from JB-95-treated E. coli, consisten

199 ugh interactions of JB-95 with selected beta-barrel OM proteins, including BamA and LptD as shown by

200 a foggy environment, water drops with either barrel or clam-shell shapes are capable of self-running

201 mainly assemblies of type Pt8L4, which adopt barrel- or gyrobifastigium-like structures.

202 cies that possess whiskers lack the modular "barrel" organization found in the primary somatosensory

203 Ail is an eight-stranded beta-barrel outer membrane protein with four extracellular lo

204 beta-Barrel outer membrane proteins (OMPs) are found in the o

205 mplex responsible for the biogenesis of beta-barrel outer membrane proteins (OMPs) in Gram-negative b

206 s such as the tip of a glass pipet, a double-barrel pipet, and a freestanding silicon nitride membran

207 onomeric subunit structure leading to a beta-barrel pore approximately 10 nm long and 1.6-2.5 nm wide

208 s of VDAC proteins show a wide beta-stranded barrel pore, with its N-terminal alpha-helix (N-alpha) b

209 a beta-barrel arrangement that we named beta-barrel pore-forming Abeta42 oligomers (betaPFOsAbeta42).

210 ipid bilayer, resulting in an irregular beta-barrel pore.

211 addition to cholesterol, to form giant beta-barrel pores in host membranes.

212 rotein PelB with a predicted C-terminal beta-barrel porin localizes to the outer membrane, and propos

213 rotein translocases drive the import of beta-barrel precursor proteins into the mitochondrial outer m

214 to the unassisted folding of the model beta-barrel protein PagP.

215 f the filamentous hemagglutinin adhesin beta-barrel protein transporter solubilized by n-Octyl beta-D

216 nd structure were explored using a model TIM barrel protein, indole-3-glycerol phosphate synthase (IG

217 wed the folding of the Escherichia coli beta-barrel protein, LptD, with its lipoprotein plug, LptE.

218 rization of hydration dynamics around a beta-barrel protein, rat liver fatty acid-binding protein (rL

219 RcsF exists in complexes with beta-barrel proteins (OMPs) allowing it to adopt a transmembr

220 transmembrane region of outer membrane beta-barrel proteins (OMPs) by combining an empirical energy

221 genesis of mitochondrial outer membrane beta-barrel proteins (SAM/TOB) complex and controls the shape

222 Transmembrane beta-barrel proteins (TMBs) serve a multitude of essential ce

223 ng antibiotics that specifically target beta-barrel proteins and the integrity of the Gram-negative O

224 o obtaining evidence that at least some beta-barrel proteins begin to fold before they interact with

225 ey interaction sites within clusters of beta-barrel proteins in the OM.

226 The assembly of beta-barrel proteins into membranes is mediated by an evoluti

227 e Bam complex promotes the insertion of beta-barrel proteins into the bacterial outer membrane, but i

228 The Bam complex assembles beta-barrel proteins into the outer membrane (OM) of Gram-neg

229 M promotes the folding and insertion of beta-barrel proteins into the outer membrane via a poorly und

230 rerequisite for membrane integration of beta-barrel proteins is burial of the extracellular loops wit

231 oneous predictions on non-transmembrane beta-barrel proteins.

232 transporters form homodimers, with each beta-barrel protomer tightly capped by SusD.

233 Wood barrels provided more aroma complexity than glass contai

234 nding of the leader peptide in the catalytic barrel rather than the N-terminal domain.

235 rization arose preferentially in the whisker barrel region of parietal sensory cortex.

236 asing the pH of the solution destabilize the barrel region, the central part of vault particles, and

237 ops (linking the C and D strands of the beta-barrel), replacing the depression known as the canyon, f

238 that most wild-type neurons were located in barrel rings encircling thalamocortical axon (TCA) clust

239 nylbenzene core, as pivotal moieties for the barrel-rosette ion channel formation, and the activity o

240 A theoretical model of the supramolecular barrel-rosette, favored by a network of intermolecular h

241 rface for optimal stability of the PagP beta-barrel scaffold.

242 s into UpaG assembly, we show that UpaG beta-barrel segments fold into a trimeric structure in the pe

243 Among these are lipocalins, ubiquitous barrel-shaped proteins that sequester small, typically h

244 This 16-cell barrel-shaped structure surrounds an opening between epi

245 Centrioles are small barrel-shaped structures that form centrosomes and cilia

246 MSM0273 is a pentameric beta-barrel shell protein that likely plugs the vertex of the

247 terminal UPF0261 domain and a C-terminal TIM-barrel signal transduction (TBST) domain.

248 ure of which is a dodecamer of (beta/alpha)8 barrels, similar to the majority of its homologs.

249 cal activity across a range of species; from barrel-specific blood flow in the rodent somatosensory c

250 The giant barrel sponge, Xestospongia muta, is a high microbial ab

251 lecular dynamics simulation of the archetype barrel-stave alamethicin (alm) pore in a 1,2-dioleoyl-sn

252 ween molecular models of AMP actions such as barrel-stave pore formation, toroidal pore formation, an

253 ion was initialized with 20 peptides in four barrel-stave pores in a fully hydrated 1-palmitoyl-2-ole

254 Barrel-stave pores were identified by uniform frequency

255 Uniquely, the data showed that barrel-stave-forming peptides such as alamethicin are no

256 eaved to form VP2 and VP4, so the 'VP2' beta-barrel structure is complemented with a unique extended

257 l decoherence because of the protective beta-barrel structure that encapsulates the fluorophore in th

258 rel structure, whereas the latter displays a barrel structure with a distorted square orthobicupola g

259 lpha/beta)8 triose-phosphate isomerase (TIM) barrel structure with a highly conserved active site.

260 alysis indicated that Der p 13 adopts a beta-barrel structure with a predominately apolar pocket repr

261 ntegral transmembrane proteins assume a beta-barrel structure, and their assembly is catalyzed by the

262 The former adopts a pentagonal barrel structure, whereas the latter displays a barrel s

263 n to autofluorescent FPs is their tight beta-barrel structure, which provides the rigidity and chemic

264 the partial barrel to form an overall closed barrel structure.

265 oligomers of these fragments may adopt beta-barrel structures and that beta-barrels can be formed by

266 we studied the assembly of an essential beta-barrel substrate for the Bam complex, BamA.

267 nderstood because no stable partially folded barrel substrates have been characterized.

268 nding peptides on opposite sides of its beta-barrel supports the fabrication of protein-capped ZnS:Mn

269 mersed in the lipid bilayer, while the inner barrel surface is highly charged.

270 The apolar outer barrel surface with large sidechains is immersed in the

271 aximum SDF value of 30.36%, were as follows: barrel temperature, 129 degrees C; feed moisture, 15%; a

272 cessed in a single-screw extruder at various barrel temperatures (X1; 115-135 degrees C), feed moistu

273 GFP is a beta barrel that can be divided into 11 strands.

274 show that the pore is most probably a helix barrel that contains eight D4 peptides arranged in paral

275 ular structures: a 60-stranded vertical beta-barrel that forms a large inner channel encircled by two

276 tDIR6 as an eight-stranded antiparallel beta-barrel that forms a trimer with spatially well-separated

277 ogy prediction method for transmembrane beta-barrels that can also identify the barrel domain, predic

278 Membrane nanopores-hollow nanoscale barrels that puncture biological or synthetic membranes-

279 h activity flows sequentially from visual to barrel then to hindlimb somatosensory; the second princi

280 (residues 285-362) that bridges the partial barrel to form an overall closed barrel structure.

281 not take place locally but require the SOD1 barrel to unfold globally.

282 ructural motifs range from multi-beta-strand barrels, to beta-sheet cups and baskets covered by alpha

283 r these compounds were observed depending on barrel toasting, wine matrix and their interactions.

284 Scaling up experiments in 12L barrels verified findings from small scale in 100mL flas

285 residues on the interior of the nascent beta-barrel wall with residues in one of the extracellular lo

286 vated neuronal network within the responsive barrel was unchanged, as characterized by c-Fos upregula

287 s as a cheaper alternative to expensive wood barrels was recently permitted in Europe, which led to a

288 Barrels were equipped with windows to measure the oxygen

289 different containers (glass, oak and cherry barrels) were determined by gas chromatography-olfactome

290 etely de novo and thermostable alpha-helical barrel, which comprises seven helices arranged around an

291 revealed a domain-like insertion into a TIM-barrel, which might serve as a flexible lid for the acti

292 the targeted synthesis of pentagonal Pt10L5 barrels, which are formed in nearly quantitative yields.

293 atches differs from cortical modules such as barrels, which scale with brain size.

294 of the VtrA/VtrC heterodimer reveals a beta-barrel with a hydrophobic inner chamber.

295 process involving closure of the ends of the barrel with release from the Bam components.

296 This domain includes a cupin-like beta-barrel with the ligand-binding site buried at its centre

297 phenomenon was significantly more marked in barrels with a higher IP and medium grain.

298 Identical barrels with different toastings (medium toasting, mediu

299 modular design for PNTs using alpha-helical barrels with tunable internal cavities as building block

300 ostrocaudal extent and area of the activated barrel without altering its identity.

301 epresentations and doubling of the number of barrels without changes in the size of S1.