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1 usly assembles into amyloid fibrils of cross-beta sheet structure.
2 inal monomer, contain substantial amounts of beta sheet structure.
3 pha-helical conformation to one dominated by beta-sheet structure.
4 ntacts; a prominent alpha-helix supports the beta-sheet structure.
5 main participate in the in-register parallel beta-sheet structure.
6 ontaining approximately 5-nm-long regions of beta-sheet structure.
7 ntrolled by the region that acquires a cross-beta-sheet structure.
8 red 3(1)-helical conformation and an ordered beta-sheet structure.
9 ally recognizes alpha-helical structure over beta-sheet structure.
10 ) and A53T-alphaSyn(2SS) take on significant beta-sheet structure.
11 h-molecular weight species and adoption of a beta-sheet structure.
12 ists of at least 78% alpha-helix with little beta-sheet structure.
13 nsignificant presence of an alpha-helical or beta-sheet structure.
14 tion were associated with the development of beta-sheet structure.
15 high percentage of random coil and possibly beta-sheet structure.
16 s 25-27 A wide protofilaments having a cross beta-sheet structure.
17 rmolecular beta-sheets, which form the cross-beta-sheet structure.
18 T, suggesting that they contain an organised beta-sheet structure.
19 large unilamellar vesicles (LUV), adopting a beta-sheet structure.
20 ial fibrinogen was mainly contributed by the beta-sheet structure.
21 rapidly displayed CD spectra consistent with beta-sheet structure.
22 e peptides in register in H-bonded, parallel beta-sheet structure.
23 e conversion is associated with formation of beta-sheet structure.
24 y NMR to contain a substantial population of beta-sheet structure.
25 in each of these species contains a similar beta-sheet structure.
26 n by the propensity of this sequence to form beta-sheet structure.
27 nd an intermolecular aggregation of extended beta-sheet structure.
28 protein self-association or a conversion to beta-sheet structure.
29 hile X-ray crystallography revealed only 17% beta-sheet structure.
30 ure, into a disease specific isoform rich in beta-sheet structure.
31 ies of the folding mechanism of this unusual beta-sheet structure.
32 on of ABri are required for the formation of beta-sheet structure.
33 t in a stable monomeric form that is rich in beta-sheet structure.
34 This band is assigned to the parallel beta-sheet structure.
35 nt to specify and stabilize the single-layer beta-sheet structure.
36 ifting from a predominantly alpha-helical to beta-sheet structure.
37 helical structure and formation of extensive beta-sheet structure.
38 amyloid proteins because of their extensive beta-sheet structure.
39 hift from a predominantly alpha-helical to a beta-sheet structure.
40 hthalene-8-sulphonic acid and lack extensive beta-sheet structure.
41 at of bacterial porins, indicating extensive beta-sheet structure.
42 ichroism showed that OmpG contains largely a beta-sheet structure.
43 protein, suggesting partial unfolding of the beta-sheet structure.
44 posite phase with oxygen, is consistent with beta-sheet structure.
45 pected, the protein exhibits a predominantly beta-sheet structure.
46 -helical, the stable intermediate is rich in beta-sheet structure.
47 al content of the wild type, while retaining beta-sheet structure.
48 sense, form compact, fibrillar solids with a beta-sheet structure.
49 natural tendency of each variant to acquire beta-sheet structure.
50 C strands of the four-stranded V1/V2 domain beta-sheet structure.
51 conformation upon aggregation and gain some beta-sheet structure.
52 ta) proteins with parallel in-register cross-beta-sheet structure.
53 d interacts with the stalk to form a compact beta-sheet structure.
54 ntramolecular disulfides stabilize a largely beta-sheet structure.
55 helix secondary structure and an increase in beta-sheet structure.
56 gregation into oligomers and fibrils rich in beta-sheet structure.
57 completely engaged in protective-presumably beta-sheet-structure.
58 sistent with the formation of folded dimeric beta-sheet structures.
59 icantly red-shifted for the two antiparallel beta-sheet structures.
60 serve to nucleate the formation of extended beta-sheet structures.
61 in turn stability and formation of extended beta-sheet structures.
62 as high propensity to assemble as aggregated beta-sheet structures.
63 mation of extended, linear preprotofibrillar beta-sheet structures.
64 eta species and induced a rapid formation of beta-sheet structures.
65 Protein chains coil into alpha-helices and beta-sheet structures.
66 of very slow rates of rearrangement of their beta-sheet structures.
67 stos coating proteins contain high levels of beta-sheet structures.
68 lus of these highly ordered, hydrogen-bonded beta-sheet structures.
70 ually results in the emergence of detectable beta-sheet structures according to thioflavin-T assay.
71 is sufficient to nucleate some antiparallel beta-sheet structure; addition of beta-capping units and
72 he occurrence of new bands due to aggregated beta-sheet structures, all of which indicate protein den
73 hange including a reduction in the extent of beta sheet structures and an increase in coil-turn confo
74 domains and indicate a parallel in-register beta-sheet structure and a general loss of native confor
75 s is generally accompanied by an increase in beta-sheet structure and a propensity to aggregate into
76 d proteins characterized by a specific cross-beta-sheet structure and are typically associated with n
77 (N)-CH(3) and CH(3)-CH(3) NOEs confirmed the beta-sheet structure and assisted in the positioning of
79 the assembly of the extended strands into a beta-sheet structure and confirmed the assignment of the
80 P fibril is held together by hydrogen bonded beta-sheet structure and contribute to the understanding
81 Consistent with this, similar changes in beta-sheet structure and decreases in in vitro methylati
83 This fibril core has an in-register parallel beta-sheet structure and does not include the Q-rich, pr
84 proteins of known structure, lacks extensive beta-sheet structure and does not traverse the outer mem
86 knowledge, unstable aggregates of Abeta with beta-sheet structure and fibrous morphology have not bee
87 this variant has a reduced tendency to form beta-sheet structure and forms deposits with much less s
89 ne-inserted conformation of PrP is richer in beta-sheet structure and has a disruptive effect on the
91 tion from an alpha-helical conformation to a beta-sheet structure and oligomerization of huPrP90-231
92 t pre-nucleation intermediates sample intra- beta-sheet structure and place bounds on the possible nu
94 of the data indicates that the formation of beta-sheet structure and protein oligomerization likely
95 nonbranched polymeric proteins with a cross beta-sheet structure and the ability to alter the optica
96 a-sandwich core of the domain, disrupted the beta-sheet structure and the loop-sheet-helix motif.
97 two "Hao" amino acids that help template the beta-sheet structure and the two delta-linked ornithine
99 ed by increases in intra- and intermolecular beta-sheet structures and a decrease in random coil and
100 l environment, with nonlocal interactions in beta-sheet structures and alpha-helical structures domin
102 assuming an equilibrium between antiparallel beta-sheet structures and conformations in which the C-t
103 seases contain antiparallel, out-of-register beta-sheet structures and identifies a target for struct
104 of peptides containing Hfl in the context of beta-sheet structures and may be useful in interpreting
105 activators promote a mixture of unfolded and beta-sheet structures and rapidly form large aggregates,
106 s tend to form gels (due to the formation of beta-sheet structures) and, as a result, are not readily
107 ibril surfaces bound Congo red, a marker for beta sheet structures, and exhibited a slow linear backg
108 c fibril morphology, a significant amount of beta-sheet structure, and exhibited green birefringence
109 yptophan at position 66, has a predominantly beta-sheet structure, and is less stable than the wild t
110 erent molecules lead to a disturbance of the beta-sheet structure, and polymorphism in ssNMR spectra
111 of alpha-syn shows strong tendencies to form beta-sheet structures, and deletion of this region has b
112 le of being prions form parallel in-register beta-sheet structures, and our data indicate the same co
114 ised 3-fold hollow model with a more regular beta-sheet structure are in much better agreement with t
115 ls containing a mixture of alpha-helical and beta-sheet structures are formed at higher concentration
117 d to lipids, (KIGAKI)3-NH2 did indeed form a beta-sheet structure as evidenced by Fourier transform i
118 re, BoNT/A in aqueous solution has about 47% beta-sheet structure as revealed by infrared spectroscop
119 natured state show evidence of some residual beta-sheet structure as well as other band components no
120 as been refolded into both alpha-helical and beta-sheet structures as well as various intermediates i
121 e binding and contain a characteristic cross-beta sheet structure, as revealed by x-ray scattering.
122 accompanied a conformational conversion to a beta-sheet structure, as judged with circular dichroism
123 ular hydrogen bonding, including an extended beta-sheet structure, as well as aromatic interactions.
124 particularly important for the formation of beta-sheet structures, as the polypeptide chain searches
125 DPPG (7/3 mol ratio) adopted an antiparallel beta-sheet structure at all surface pressures studied >
132 l acidic region of Ng peptide pries open the beta-sheet structure between the Ca(2+) binding loops pa
133 t both variants have an in-register parallel beta-sheet structure, both in the fully hydrated form an
134 -oligomer is not preceded by precursors with beta-sheet structure but by a partially unfolded clearly
135 denosine triphosphate induces disassembly of beta-sheet structures but not the alpha-helical contents
136 CD spectra consistent with anticipated major beta-sheet structures but underwent spectral changes upo
137 ied YapV passenger is functional and rich in beta-sheet structure, but lacks a approximately 20 kDa C
139 FOs are soluble at 100,000 x g, rich in beta-sheet structures, but yet bind weakly to thioflavin
141 fibrils containing the in-register, parallel beta-sheet structure commonly found in WT-Abeta40 fibril
142 the mutation site and in spatially adjacent beta-sheet structures comprising the hydrophobic core.
143 Amyloids, protein aggregates with a cross beta-sheet structure, contribute to inflammation in debi
144 nvironment further perturbed and some of the beta-sheet structure converted to disordered structure.
146 content of teleost osteocalcin increases and beta-sheet structure decreases upon calcium binding, sim
147 n be induced to form either alpha-helical or beta-sheet structure depending on its concentration and
148 ne fusion, adopts either an alpha-helical or beta-sheeted structure depending on the cholesterol conc
149 it forms either a beta-solenoid or a stacked beta-sheet structure, depending on the integrity of the
150 -UV CD studies show that the small amount of beta-sheet structure developed by hIAPP(8-37) 3xP after
152 rgoes a spontaneous conversion to oligomeric beta-sheet structure even in the absence of guanidine HC
154 ed fibril bundles have indicated an extended beta-sheet structure for Alzheimer's beta-amyloid fibril
155 re2p fibrils support an in-register parallel beta-sheet structure for the PD core of Ure2p fibrils.
157 ons, suggesting that an in-register parallel beta-sheet structure formed by the C-terminal end may be
159 ongo red and thioflavin T), and antiparallel beta-sheet structure (Fourier transform infrared spectro
160 instead of the formation of alpha-helical or beta-sheet structures, group 1 LEA proteins retain a hig
161 ies of amino acids to form alpha-helical and beta-sheet structures has been important in clarifying s
162 arallel dimer, which is close to the amyloid beta-sheet structure, has fewer interpeptide hydrogen bo
164 rtion of disulfide bridges on the surface of beta-sheet structures have implications for enhancing th
165 oppositely charged ionic segments that form beta-sheet-structured hydrogel assemblies via polyion co
167 olecular template and turn units that induce beta-sheet structure in a heptapeptide strand that forms
169 ate forms during the lag phase with parallel beta-sheet structure in a region that is ultimately a pa
171 anged in a rigid conformation, and confirm a beta-sheet structure in an assigned stretch of three ami
172 partially parallel, arrangement for cystatin beta-sheet structure in mature amyloids and propose a mo
175 se two regions promote aggregation and adopt beta-sheet structure in the fibrils, and may also do so
178 antagonist, SQ29,548, could induce more of a beta-sheet structure in the TP than that of the agonist,
179 actions account for the in-register parallel beta-sheet structure in Ure2p(10)(-)(39) fibrils and tha
180 tide system, which forms stable antiparallel beta-sheet structure in water, is destabilized in urea s
182 central core of Abeta consists of a parallel beta-sheet structure in which identical residues on adja
185 SFHILLINleSAQSLLVPSIIFILAYSLK) formed stable beta-sheet structures in both sodium dodecyl sulfate mic
190 At the same time, when protofilaments form, beta-sheet structure increases to about 54% from the app
191 (FTIR) amide I band shows that antiparallel beta-sheet structure increases with syneresis in the tau
195 lpha-helical conformation into an oligomeric beta-sheet structure is about 50 times faster than that
197 among proteins, which suggests that parallel beta-sheet structure is not stabilized by such disulfide
199 of a prion domain further suggests that the beta-sheet structure is of the parallel in-register type
200 ay scattering data indicate that much of the beta-sheet structure is retained in acidic solution and
201 NMR structure reveals that the native Pin WW beta-sheet structure is retained upon incorporating a st
206 ation is an increase in the frequency of the beta-sheet structure, leading to hydrogen bonding betwee
208 These results, in the context of a primarily beta-sheet structure, led us to build detailed models of
209 fectious amyloid has an in-register parallel beta-sheet structure, like that of the S. cerevisiae Ure
210 suggesting that the formation of a specific beta-sheet structure may be required for the peptide to
212 similar to those described for antiparallel beta-sheet structure observed in protein X-ray crystal s
213 ion algorithms indicate that the majority of beta-sheet structure occurs in the p53 core DNA binding
214 t side-chain ordering in a key region of the beta-sheet structure occurs on a slower time scale than
215 However, a time-dependent transition to beta-sheet structure occurs upon addition of both urea a
217 fibrils have the characteristic antiparallel beta-sheet structure of amyloid fibrils, as measured by
219 the clearest evidence yet that the intrinsic beta-sheet structure of an in vitro Abeta aggregate depe
221 chanism that involves through-H-bonds of the beta-sheet structure of Az, likely also those in the Cu
223 teraction of a collagen beta-strand with the beta-sheet structure of Fn modules seen in the high reso
224 l increase in stability was observed for the beta-sheet structure of hGHbp which included sites dista
225 thesize that NUCB1 binds to the common cross-beta-sheet structure of protofibril aggregates to "cap"
230 lpha-helix and the parallel and antiparallel beta-sheet structures of alanine polypeptides are analyz
231 h very high sequence identity can form cross-beta-sheet structures of sufficient stringency for incor
232 sferred to corresponding larger oligopeptide beta-sheet structures of up to five strands of eight res
235 (nonselective peptides) or an intermolecular beta-sheet structure only able to permeabilize DMPG vesi
238 mising attributes and unique features of the beta-sheet-structured PIC hydrogels described here highl
239 acid sequence may not participate in a rigid beta-sheet structure, possibly including portions of the
240 his difference may be due to a predominantly beta-sheet structure present in RBP in contrast to the a
241 lsE's native and non-native superhelical and beta-sheet structures readily occur (pH 7, 20 degrees C)
242 een the consensus components, we show that a beta sheet structured region separating the consensus el
243 PIN1 WW domain, a 34-residue three-stranded beta-sheet structure, removes a favorable electrostatic
244 redominates in the normal PrP isoform into a beta-sheet structure resistant to proteinase K (PK).
245 intermediates proceed to convert into stable beta-sheet structured species and maintain their stackin
248 nsisting of a centrally located six-stranded beta-sheet structure surrounding the C-terminal alpha-he
249 ding protein (IFABP) primarily comprises two beta-sheet structures surrounding a large internal cavit
251 olded in Tris buffer contained slightly less beta-sheet structure than detergent-folded Msp(Fl); both
255 IF protein, these two binding regions form a beta-sheet structure that includes the MIF oxidoreductas
256 forms have a mixed parallel and antiparallel beta-sheet structure that is different from fibrils whic
257 R-S-S-TTR)(1) retaining a stable 16-stranded beta-sheet structure that is equivalent to the dimer not
259 easurements showed that Crp4 has an expected beta-sheet structure that is not evident in the pro-Crp4
260 beta (11-25) fibrils are clearly composed of beta-sheet structure that is observable as striations ac
261 0-19), encompasses the A strand of the inner beta-sheet structure that lines the thyroid hormone bind
262 opts a compact, three-stranded, antiparallel beta-sheet structure that mediates protein-protein inter
263 c16-AHL(3)K(3)-CO(2)H, capable of forming a beta-sheet structure that propagates into larger fibrous
264 consistent with formation of triple-stranded beta-sheet structures that assemble into two-dimensional
265 heterogeneous, containing both antiparallel beta-sheet structures that can grow into full fibrils as
266 fold in CDCl3 solution to form well-defined beta-sheet structures that dimerize through parallel bet
268 infrared spectra are attributed primarily to beta-sheet structures, these findings indicate that the
270 esults indicate that an in-register parallel beta-sheet structure underlies the [PSI(+)] prion phenom
271 NAC in solution altered from random coil to beta-sheet structure upon ageing, a process that has pre
273 luble fibrillar aggregates with antiparallel beta-sheet structure upon incubation at physiological te
274 that the extracellular sequence of C99 forms beta-sheet structure upon interaction with membrane bila
275 de (hIAPP) that is known to misfold into the beta-sheet structure upon interaction with membranes.
277 leavage, likely reflecting the extent of the beta-sheet structure, varies mostly as a function of the
279 on of PrP from alpha-helical structures into beta-sheet structures was confirmed by circular dichrois
281 GAKI)(3)-NH(2), designed to form amphipathic beta-sheet structure when bound to lipid bilayers, posse
282 IGAKI-NH(2) was designed to form amphiphilic beta-sheet structures when bound to lipid bilayers.
283 non-inhibitory peptides, readily formed high beta-sheet structures when placed under the conditions o
284 It is known that the fibrils have a cross-beta-sheet structure where main chain hydrogen bonding o
285 ther neurodegenerative diseases have a cross beta-sheet structure, where main chain hydrogen bonding
286 to TMDs three and six assumed predominantly beta-sheet structures, whereas those corresponding to TM
287 erstand the topological properties of larger beta-sheet structures which frequently contain four-stra
288 ar dichroism suggest that eIF4H has a mostly beta-sheet structure, which appears similar to other RNA
289 that the aggregate adopts a fibrillar double beta-sheet structure, which is formed by packing the RT-
290 egates undergo structure rearrangements into beta-sheet structures, which are able to recruit monomer
291 into unstructured Abeta aggregates with some beta-sheet structures, which could prevent both the prim
292 1 and [Gly(6)]ccTP 1a exhibited well-ordered beta-sheet structures, while the less constrained [Gly(6
293 gle cross-beta unit is then a double-layered beta-sheet structure with a hydrophobic core and one hyd
294 The protein is dominated by an open alpha/beta-sheet structure with a prominent V-shaped cleft: Ad
295 esponding to the G helix forms a hyperstable beta-sheet structure with its strands oriented perpendic
298 ly reported, support an in-register parallel beta-sheet structure, with one Rnq1 molecule per 0.47-nm
299 e gKDelta31-68 mutation spans a well-defined beta-sheet structure within the amino terminus of gK, wh
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