ライフサイエンスコーパス: beta-sheet

1 ern consistent with either an alpha helix or beta sheet.

2 phipathic two- or three- strand antiparallel beta sheet.

3 rs, forming a curtain-like membrane-spanning beta-sheet.

4 le to bind MinD, leaving behind a 4-stranded beta-sheet.

5 ge site as an extra beta-strand in a central beta-sheet.

6 strands, can contain a significant amount of beta-sheet.

7 s 30-42, which arranges into an antiparallel beta-sheet.

8 rection between adjacent molecules along the beta-sheet.

9 some binders use unstructured regions and/or beta sheets.

10 ydrophobic interactions holding together the beta-sheets.

11 a-sheets instead of the more common parallel beta-sheets.

12 inclusions specifically enriched in amyloid beta-sheets.

13 nd segment, 15-25 WT, forms non-toxic labile beta-sheets.

14 rdered species and suggested the presence of beta-sheets.

15 drophobic core, and without alpha-helices or beta-sheets.

16 dynamic tendency of all polypeptides to form beta-sheets.

17 structure transformation from alpha-helix to beta-sheets.

18 h monomer composed of 12 alpha-helices and 9 beta-sheets.

19 fiber, whereas BAX was converted entirely to beta-sheets.

20 reported the fibrillation of HN and BAX into beta-sheets.

21 itutions and absence of two peptides and two beta-sheets.

22 ix and ten beta-strands distributed in three beta-sheets.

23 These data suggest that the BARA beta sheet 1 unfolds to directly engage the membrane.

24 Using this mechanism, a BECN1 beta sheet-1 derived peptide activates both PI3KC3 compl

25 cm(-1)), H-bonded parallel- and antiparallel-beta-sheets (1690cm(-1)) and H-bonded beta-turns (1664cm

26 nding takes place at a basic patch on top of beta-sheet A and is different from other heparin-binding

27 mino-terminal segment of the RCL into serpin beta-sheet A as a new strand.

28 Together, basic residues of central beta-sheet A contribute to heparin binding and activatio

29 most likely by insertion of the peptide into beta-sheet A.

30 ons revealed that glycosylation stabilized a beta-sheet adjacent to the N130 GlcNAc and the N-termina

31 ntiparallel manner to form an intermolecular beta-sheet, affect G fusion properties.

32 two-dimensional energy landscape defined by beta-sheet alignment and hydrogen-bonding states, wherea

33 Two-layer beta-sheet amyloid structures predominate, but off-pathw

34 ] and [URE3] are folded in-register parallel beta-sheet amyloids of Sup35p and Ure2p, respectively.

35 ant and dramatic reductions are proposed for beta sheet and alpha helical regions, respectively.

36 ily by dint of its conserved central concave beta sheet and interactions of its dual HxT motif histid

37 Ric-8A binds to the exposed Galpha beta sheet and switch II to stabilize the nucleotide-fre

38 nce of right-hand or left-hand twisted cross-beta sheets and overall fold of the fibril proteins.

39 induced by plasma, particularly contents of beta-sheet and beta-turn.

40 a-helices act as a transient intermediate to beta-sheet and fibril formation of pEAbeta (3-42).

41 fferent secondary structures, including both beta-sheet and helix-forming peptides.

42 a-helical in the cytosol and acquires a more beta-sheet and random coil character in the nucleus.

43 he N-acetyl group interacts with the central beta-sheet and stabilizes the N-terminus and the switch

44 we identify contacts between the assembling beta-sheet and the BamA interior surface that determine

45 important hinge-bbeta region between the PAS beta-sheet and the N-terminal cap helix that in turn des

46 mmetric structure that consists of a central beta-sheet and two alpha-helical bundles.

47 l fold comprising a four strand antiparallel beta-sheet and two helical turns stabilized by a complex

48 structures by intermolecular hydrogen bonded beta-sheets and aggregates.

49 residues at specific positions may stabilize beta-sheets and lower the energy barrier for cross-speci

50 ndary structures of proteins (alpha-helices, beta-sheets and other structures) in EM maps at resoluti

51 ments reduces the formation of parallel IAPP beta-sheets and subsequent nucleation of mature amyloid

52 extended secondary motifs (alpha-helixes and beta-sheets) and intrinsically disordered regions), to f

53 n native proteins are often formed by curved beta sheets, and the ability to control beta-sheet curva

54 eet structures, destabilization of preformed beta-sheets, and suppression of aggregation.

55 f shrimp proteins, including the increase in beta-sheets, and the loss in turns.

56 oid-based with the same in-register parallel beta-sheet architecture as most of the disease-causing h

57 structure between antiparallel and parallel beta-sheet architectures.

58 e theory also predicts that proteins rich in beta-sheets are more collapsible than alpha-helical prot

59 ers that fail to stabilize an intermolecular beta-sheet around a highly divergent beta-strand of the

60 dopts a folded structure in which the native beta-sheet arrangement of the peptide region and global

61 Two antiparallel beta-sheets assemble with symmetric homodimer cross sect

62 crystallography reveals that the macrocyclic beta-sheet assembles to form double-walled nanotubes, wi

63 ces, comparable to those in vivo, by forming beta-sheet assemblies that our data suggest occur via tw

64 o provide non-covalent cross-linking through beta-sheet assembly, reinforced with a polymer backbone

65 the caspase-1 active site, an anti-parallel beta sheet at the caspase-1 L2 and L2' loops bound a hyd

66 TAIL protein that folds into an antiparallel beta-sheet at the A/W interface and presents strong inte

67 hape of the nanostructures or their internal beta-sheet backbone, but must involve accessible adaptiv

68 Furthermore, C(H)2 helical segments, beta-sheets, beta-turns, and random coil regions were le

69 ps and provide evidence that the more global beta-sheet/beta-sheet facial complementarity is a critic

70 ixes alpha3 and alpha4 interact with the Vif beta-sheet (beta2-beta5).

71 ccurs via the formation of an intermolecular beta-sheet between the membrane-proximal (third) Fibrone

72 a novel class of conformationally restricted beta-sheet breaker hybrid peptidomimetics (BSBHps).

73 ting ABAB-type arrangements within assembled beta-sheets, but no direct molecular-level evidence exis

74 onformational transition from random coil to beta-sheet by changing the pH from acidic to alkaline.

75 port the stabilization of a remarkably short beta-sheet by incorporating N-(hydroxy)glycine (Hyg) res

76 are formed from protein chains stacked into beta-sheets by backbone hydrogen bonds, they display dis

77 but TTPA contains an additional antiparallel beta-sheet carrying a lectin-like domain that could be r

78 cal, whereas the N-terminal FP-FPPR exhibits beta-sheet character.

79 In addition, the in-register parallel beta-sheet commonly observed for amyloid fibril structur

80 receding ZPC and following ZPN subdomains by beta-sheet complementation.

81 ers composed of ~ 40 proteins misfolded in a beta-sheet conformation at the membrane surface, as dete

82 ays of incubation, whereas Ac-PHF6 adopted a beta-sheet conformation at the surface of the membrane w

83 ues in the four repeats, indicating a single beta-sheet conformation for the fibril core.

84 We find that residues 11-42 and 69-102 adopt beta-sheet conformation in patient protein fibrils.

85 erized 11 peptides from a T40-IDE digest for beta-sheet conformation, surfactant activity, fibrilliza

86 pentapeptides transform from alpha-helix to beta-sheet conformation.

87 shifts that are indicative of random coil or beta-sheet conformations.

88 ntaining a beta hairpin and an anti-parallel beta sheet consisting of strands from the top and bottom

89 the supramolecular assembly of a macrocyclic beta-sheet containing residues 16-22 of the beta-amyloid

90 ometry and variable levels of intermolecular beta-sheet content in their protein shells.

91 ucture motifs at longer Q-lengths, including beta-sheet content that seems to contribute to the forma

92 te peptide assembly behavior, an increase in beta-sheet content, and patterns of variation in solvent

93 of each oligomer generally exhibit increased beta-sheet content.

94 ed oligomers exhibit a significant amount of beta-sheet content.

95 ted with a loss of alpha-helix and a gain of beta-sheet content.

96 d at 25 degrees C for 18min exhibited higher beta-sheet contents and more chemical bonds such as hydr

97 The alpha-helix and beta-sheet contents decreased, while aggregated beta-she

98 erum albumin, with different alpha-helix and beta-sheet contents.

99 r, these oligomers undergo an alpha-helix to beta-sheet conversion catalyzed by lipid vesicles and di

100 The C-terminus of Galpha is ejected from its beta sheet core, thereby dismantling the GDP binding sit

101 The two faces of the beta-sheet core are hydrophobic and surrounded by the me

102 sducing alpha5-helix of Galpha away from its beta-sheet core.

103 42) tetramer, which comprises a six stranded beta-sheet core.

104 Also, due to the ability of the non-covalent beta-sheet cross-links to reassemble, the hydrogels can

105 eated sheets, whereas Arachnocampa has cross-beta-sheet crystallites within its silk.

106 ifs range from multi-beta-strand barrels, to beta-sheet cups and baskets covered by alpha-helical lid

107 , we investigated the mechanisms controlling beta-sheet curvature by studying the geometry of beta sh

108 match the computational models, showing that beta-sheet curvature can be controlled with atomic-level

109 rved beta sheets, and the ability to control beta-sheet curvature would allow design of binding prote

110 ond beta-strand is organized into a parallel beta-sheet despite the co-existence of an antiparallel b

111 an amphipathic hydrogen-bonded antiparallel beta-sheet dimer that binds chloride anions.

112 twisted beta-sheets with an increased inter-beta-sheet distance and a higher solvent exposure than W

113 d ionic interactions between residues in the beta-sheet domain that reduce the width of the cavity.

114 rated in regions between the alpha-helix and beta-sheet domains.

115 ng the formation of O(L) and elongation into beta-sheets during the formation of O(S).

116 the hydrophilic residues located on the core beta-sheets edges of the oligomers.

117 oherence (HSQC) analyses reveal the 6-strand beta-sheet face of Crabp1 as its Raf-interaction surface

118 These findings are supported by the beta-sheet features observed by FTIR.

119 Injection of small beta-sheet fibril fragments, however, produced the most

120 s to reduce the formation and propagation of beta-sheet fibrillar species could be an important route

121 nformational changes from random coil to its beta-sheet fibrillar states.

122 toxicity peaks, en route to forming nontoxic beta-sheet fibrils.

123 ed to form a large 10-stranded, antiparallel beta-sheet flanked by alpha-helices on each side, repres

124 ackbone aminated peptides that readily adopt beta-sheet folds.

125 well along the pathway toward the 4-stranded beta-sheet form.

126 rimental data demonstrating the reduction of beta-sheet formation by this complex.

127 flavin-T and Congo red binding and increased beta-sheet formation upon heat induction.

128 ugh hydrogen bond formation and inhibits the beta-sheet formation, whereas trimethyl amine oxide itse

129 pitopes cluster on the inner strands of both beta-sheets forming the fibronectin domains.

130 d Cap molecules were conjugated onto a short beta-sheet-forming peptide (Sup35) to yield three differ

131 In the second phase, beta-sheet forms in the polyQ.

132 h just a six-helix bundle and a six-stranded beta-sheet, forms a genome-delivery apparatus and joins

133 s encompassed in a beta-sandwich formed by 2 beta-sheets from the C-terminal domain of MTPalpha.

134 an be used to stabilise a range of different beta-sheet hydrogen bonded architectures.

135 -sheet curvature by studying the geometry of beta sheets in naturally occurring protein structures an

136 ir lack of activity by showing loss of a key beta-sheet in a sequence known as the handle region that

137 scover a similar exchange process across the beta-sheet in GB1 in crystals and in complex with IgG.

138 elements that dock on the C-terminal domain beta-sheet in the dark and unfold in the light to allow

139 despite the co-existence of an antiparallel beta-sheet in the same structure.

140 tially induces opposite motions of the major beta-sheet in this channel mutant.

141 The contents of beta-sheets in dough and disulfide groups in gluten of t

142 Hydrogen-deuterium exchange MS revealed that beta-sheets in NHERF1's PDZ2 domain display lower deuter

143 BSA lost the alpha-helix and gain beta-sheets in the secondary structure during adsorption

144 n that its amyloids are rich in antiparallel beta-sheets instead of the more common parallel beta-she

145 tures where the typical B-D-E immunoglobulin beta-sheet is replaced with an alpha-helix further confi

146 ) fibril consisting of an infinite number of beta-sheet layers.

147 lix and beta-sheet was observed, with higher beta-sheet levels in both pulses dried using CHD.

148 ) at their C-terminal, self-assemble to form beta-sheet like structures upon mixing.

149 Aib-3 yielded peptides 3a-c that preferred a beta-sheet-like conformation.

150 l crystals to thermodynamically stable cross-beta-sheet-like fibrils by a de novo designed heptapepti

151 enon-like intercapsomer joints, and abundant beta-sheet-like mainchain:mainchain intermolecular inter

152 licity, while both parallel and antiparallel beta-sheet-like structures are realized.

153 olving S60, D318, and L320 in the lower body beta-sheets lining the lateral portals.

154 localize to TM1 (V60L), TM2 (G353R), or the beta-sheet linking the TMs to the extracellular ATP bind

155 e of proteins unfolded from alpha-helices to beta-sheets, loops and beta-turns.

156 that one segment, 19-29 S20G, forms pairs of beta-sheets mated by a dry interface that share structur

157 e chain packing interactions within the same beta-sheet may play a critical role in the formation of

158 losed apo conformation, revealing a pivoting beta-sheet mechanism that functions to open and close th

159 Using a standard 3-stranded beta-sheet model, the WW domain, it was found that the p

160 that two complementary pentapeptides from a beta-sheet motif of a protein, being connected to an aro

161 e amino acid interactions in an antiparallel beta-sheet motif.

162 P results in self-assembly of nonaggregating beta-sheet nanofibers with precise structure.

163 inhibitor, Rubicon, was mapped to the first beta sheet of the BECN1 BARA domain and the UVRAG BARA2

164 d homodimer characterized by a large central beta-sheet of 18 strands, extending between two catalyti

165 We also propose that the antiparallel beta-sheet of teixobactin is important for its bioactivi

166 re not observed with TEM, but highly ordered beta-sheets of amyloid secondary structure is identified

167 the C terminus and interactions between the beta-sheets of the Ig domains.

168 We conclude that although the beta-sheet oligomers cause some toxicity, the potent eff

169 random coil structure, evolves into ordered beta-sheet oligomers containing at least 5 strands, and

170 We found that beta-sheet oligomers produce a small but significant los

171 ng from thin peptide films shows features of beta-sheet ordering for both peptides, along with eviden

172 of the experimentally observed antiparallel beta-sheet packing.

173 X-ray crystallographic structure of a cyclic beta-sheet peptide derived from the 19-36 region of medi

174 By altering the beta-sheet peptide graft density and concentration, we c

175 This self-healing polymer-beta-sheet peptide hybrid hydrogel with tailorable mecha

176 Conjugation of beta-sheet peptide motif to the CHP results in self-asse

177 s 11-17 of IAPP (RLANFLV) into a macrocyclic beta-sheet peptide results in a monomeric peptide that d

178 unctionalization of its repeating units with beta-sheet peptides to form a hydrogel, it can easily be

179 lly cross-linked via grafted self-assembling beta-sheet peptides to provide non-covalent cross-linkin

180 Aggron) is necessary and sufficient to seed beta-sheet polymerization, and BiP binding to this Aggro

181 d a beta-sandwich fold, with the face of one beta-sheet possessing the beta-1,3-glucan-binding surfac

182 cleic acids, alteration in the alpha-helical/beta-sheet protein ratio, structural changes in carbohyd

183 cs within the hydration shell than a similar beta-sheet protein, which may contribute to the high pac

184 facial hydration network are observed in the beta-sheet protein.

185 ted here have implications for the design of beta sheet proteins with tunable self-assembling propert

186 he protein surface of both alpha-helical and beta-sheet proteins.

187 A higher proportion of beta sheets, random coils, alpha-helix and beta-turns fo

188 omoted allosteric signaling from the helix 6/beta-sheet region of LRH-1 to the activation function su

189 These results reveal the importance of the beta-sheet region of lysozyme for initiating self-assemb

190 sidues (I476 and V482) were within coiled or beta-sheet regions in domain B distant to the active sit

191 bound cooperatively, but those derived from beta-sheet regions in LF did not, suggesting that an all

192 more efficiently than peptides derived from beta-sheet regions of LF.

193 alline material in which the alpha-helix and beta-sheet regions of the protein are similar to crystal

194 y the increasing formation of intermolecular beta-sheets, revealed by second derivative spectra.

195 flavin T fluorescence, Congo-red binding and beta-sheet rich structures displaying a characteristic c

196 esidues led to the formation of ThT-negative beta-sheet-rich aggregates having high surface hydrophob

197 mble in solution to form ordered, insoluble, beta-sheet-rich amyloid fibrils.

198 heir native-like properties and convert into beta-sheet-rich amyloid-like structures, as indicated by

199 ssembly and further reveal that antiparallel beta-sheet-rich amyloids can be functional forms.

200 Elucidating the role of these beta-sheet-rich fibrils in disease progression is crucia

201 y disordered tau protein into highly ordered beta-sheet-rich fibrils is implicated in the pathogenesi

202 y disordered, monomeric alpha-synuclein into beta-sheet-rich oligomers and fibrils is associated with

203 and self-assembly of the disordered tau into beta-sheet-rich oligomers that subsequently seed fibrill

204 Pvfp-5beta folds as a beta-sheet-rich protein as expected for an epidermal gro

205 e (AD) is characterized by the deposition of beta-sheet-rich, insoluble amyloid beta-peptide (Abeta)

206 n protein (PrP), leading to the formation of beta-sheet-rich, insoluble, and protease-resistant self-

207 s, Mcc naturally exists as two conformers: a beta-sheet-rich, protease-resistant, aggregated, inactiv

208 ion NMR: the full-length protein (6-stranded beta-sheet sandwiched between 4 helices) representing th

209 The characteristic 2D IR features of amyloid beta-sheet secondary structure are created by as few as

210 e elicited antibodies to the peptide and the beta-sheet secondary structure conformation.

211 with glutaraldehyde until it reached a high beta-sheet secondary structure content, and species betw

212 beta-Sheet secondary structure is a common feature of am

213 dies selected to specifically react with the beta-sheet secondary structure of pathological oligomeri

214 Amyloid beta-sheet secondary structure was detected in cataract

215 propagate into fibrils that have a parallel-beta-sheet secondary structure.

216 opy revealed the adoption of a predominantly beta-sheet secondary structure.

217 width of which reflects the curvature of the beta-sheet segment.

218 The beta-sheet self-assembles to form long fibrils with the

219 A new capsule based on a beta-sheet self-assembling cyclic peptide with the abili

220 ils in vitro and is a major signal for cross-beta-sheet self-association of the 49-mer Phe521Leufs pe

221 channel prefers alpha-helical sequences over beta-sheet sequences.

222 on the hierarchic pathway by which distinct beta-sheets sequentially unfold using the unique possibi

223 h revealed that this protein contained three beta-sheets, seven alpha-helices, and coils.

224 tion on dynamics for both an alpha-helix and beta-sheet site of GB1, the immunoglobulin binding domai

225 We observed that hAChE-S beta-sheet species co-localized with Abeta in mature pla

226 on and aggregation, as amyloidogenic hAChE-S beta-sheet species might seed Abeta aggregation.

227 pha-helix and one three-residue antiparallel beta-sheet stabilized by two disulfide bonds.

228 A taxonomy of the oligomer species based on beta-sheet stacking topologies is proposed.

229 ds most of its time trapped in misregistered beta-sheet states connected by weakly bound states twith

230 ser microstructure with increased aggregated beta-sheet structure and a firmer cheese.

231 This protein was designed to lack beta-sheet structure and is competitively inhibited by m

232 l acidic region of Ng peptide pries open the beta-sheet structure between the Ca(2+) binding loops pa

233 ll-known intermolecular in-register parallel beta-sheet structure in the mature fibrils.

234 is distinct from the intermolecular parallel beta-sheet structure observed in mature fibrils.

235 he free sulfhydryl content but increased the beta-sheet structure of gluten.

236 thesize that NUCB1 binds to the common cross-beta-sheet structure of protofibril aggregates to "cap"

237 s the canonical triple-stranded antiparallel beta-sheet structure of WW domains when bound to a two-P

238 that the extracellular sequence of C99 forms beta-sheet structure upon interaction with membrane bila

239 As a result of their distinct beta-sheet structure, 1-108-alphaS fibrils resist incorp

240 ular hydrogen bonding, including an extended beta-sheet structure, as well as aromatic interactions.

241 d interacts with the stalk to form a compact beta-sheet structure.

242 ally recognizes alpha-helical structure over beta-sheet structure.

243 ed further away from the bilayer favored the beta-sheet structure.

244 and cross-seeded lRPT fibrils had a similar beta-sheet structured core, revealed by Raman spectrosco

245 oppositely charged ionic segments that form beta-sheet-structured hydrogel assemblies via polyion co

246 mising attributes and unique features of the beta-sheet-structured PIC hydrogels described here highl

247 ers have a significant degree of native-like beta-sheet structures (35-38%), but with more disordered

248 ually results in the emergence of detectable beta-sheet structures according to thioflavin-T assay.

249 seases contain antiparallel, out-of-register beta-sheet structures and identifies a target for struct

250 peptide-peptoid hybrids form unique parallel beta-sheet structures by self-assembly upon hydrogenatio

251 dynamics in general are more retarded around beta-sheet structures than alpha-helical motifs.

252 4 M), there is an accumulation of random and beta-sheet structures that is mediated by small connecti

253 oncentration, and the amount of antiparallel beta-sheet structures were significantly changed within

254 ta, which demonstrate decreased formation of beta-sheet structures, destabilization of preformed beta

255 tes with other A molecules to form fibrillar beta-sheet structures, is common in nature and widely us

256 loid structure, and UV light induces amyloid beta-sheet structures, linking the presence of amyloid s

257 basic domain contain short alpha-helical or beta-sheet structures.

258 ins are proteins consist of three sequential beta-sheet subdomains that bind to specific carbohydrate

259 hy, we show how a preTCR applies the concave beta-sheet surface of its single variable domain (Vbeta)

260 eutral, Janus, and peptide NPs couple to the beta sheet surfaces of Abeta40 fibrils and only the nega

261 The beta-sheet T7-Pt{100} specificity drives cubic Pt nanocr

262 the concave surface of Ric8A and the Galpha beta-sheet that wraps around the C-terminal part of the

263 The peptide forms amphiphilic parallel beta-sheets that assemble into stacked bilayers with alt

264 try revealed altered packing arrangements of beta-sheets that encompass residues 139 and 186 of PrP(S

265 nformations and that the edge strands in one beta-sheet (the DAGH sheet) are particularly susceptible

266 econdary structure of AAMPs (high portion of beta-sheet), the antimicrobial potency of AAMPs, and the

267 In contrast, beta-sheets, the main secondary structure in cooked past

268 ble through intermolecular hydrogen bonds to beta-sheets thereby placing the azide and alkyne motifs

269 When placed into the turn of a beta-sheet, this leads to a pH switch of folding.

270 necessary for oligomers with an antiparallel beta-sheet to propagate into fibrils that have a paralle

271 emonstrated in this article, the redesign of beta-sheets to contain a global, or local, pH-dependent

272 f subunit interface, altering the packing of beta-sheets to induce changes that lead to asynchronous

273 loid fibrils, just like the well-known cross-beta sheet topology.

274 n, de novo, a series of proteins with curved beta sheets topped with alpha helices.

275 exibility of the TMD in terms of alpha-helix/beta-sheet transitions in model membranes (measured by i

276 a-sheet contents decreased, while aggregated beta-sheet, turns and random coil contents increased as

277 spectroscopy can identify the highly ordered beta-sheets typical of amyloid secondary structure even

278 xplored the effect of bending aromatic amide beta-sheets using building blocks that impart curvature.

279 ure and the presence of both alpha-helix and beta-sheet was observed, with higher beta-sheet levels i

280 ng longer peptide sequences that form stable beta-sheets was found to suppress superstructure formati

281 al segments flanking a central bent aromatic beta-sheet were then synthesized and shown to form well-

282 rdered monomers to alpha-helices and then to beta-sheets when the proteins encounter the cell membran

283 id fibrils (intermolecularly hydrogen-bonded beta-sheets) when the pH is lowered below 4.

284 are highly stable when assembled in parallel beta-sheets, whereas they quickly unfold in antiparallel

285 unique and consists of a CTD coiled around a beta-sheet which makes contacts with the neighboring ARD

286 stinct secondary structures, alpha-helix and beta-sheet, which were exhibited by the peptide.

287 mic transition from the alpha-helices to the beta-sheets, which marks the onset of plastic deformatio

288 quence in the major groove while inserting a beta sheet 'wing' into the adjacent minor groove.

289 ns, each consisting of a mixed five-stranded beta sheet with a defined function.

290 f rhodopsin forms an extended intermolecular beta sheet with the N-terminal beta strands of arrestin.

291 ex is composed of a continuous nine-stranded beta-sheet with four strands from IntS9 and five from In

292 tration, and spontaneously transforms into a beta-sheet with increased concentration.

293 1.79 angstrom revealed a single antiparallel beta-sheet with six conserved cysteine residues forming

294 hitecture which consists of two antiparallel beta-sheets with 7 main strands, packing against each ot

295 8-alphaS fibrils consist of strongly twisted beta-sheets with an increased inter-beta-sheet distance

296 These proteins comprise cylindrical beta-sheets with long extracellular loops and create por

297 are reinforced by formation of intersubunit beta-sheets with N-terminal segments of auxiliary protei

298 ns on the mineral surface and an increase in beta sheets within the protein structure.

299 ecular interaction acting between the paired beta-sheets within Tau fibrils.

300 of the materials and verify the presence of beta-sheets within the hybrid hydrogels.