ライフサイエンスコーパス: pleated sheet

1 eight-stranded cup-shaped anti-parallel beta-pleated sheet.

2 are predicted to have a high content of beta-pleated sheet.

3 structural element of the antiparallel beta-pleated sheet.

4 osed of two three-stranded antiparallel beta-pleated sheets.

5 peptide (Abeta), which forms fibrils of beta-pleated sheets.

6 oximately perpendicular to the faces of beta-pleated sheets.

7 und-B (PiB) binds with high affinity to beta-pleated sheet aggregates of the amyloid-beta (Abeta) pep

8 amyloid-beta or phosphorylated tau in a beta-pleated sheet amyloid configuration.

9 r more alpha-helices, a middle layer of beta-pleated sheet and a top layer formed by segments of the

10 ucture of this protein has considerable beta-pleated sheet and is very compact.

11 sed of 27 +/- 3% alpha-helix, 20 +/- 3% beta-pleated sheet, and 53 +/- 3% coil.

12 beta-hairpin conformation and extended beta-pleated sheet assembly have been characterized by single

13 lular and filamentous structure rich in beta-pleated sheets, Biondi ring tangles might attract the ad

14 ructure, must undergo a transition to a beta-pleated sheet by a mechanism shared by other lipoprotein

15 formations into soluble, macromolecular beta-pleated-sheet complexes without any covalent modificatio

16 ties in vivo when it adopts a fibrillar beta-pleated sheet conformation.

17 t rather seemed to be directed toward a beta-pleated sheet conformational epitope expressed by AL and

18 Significance for controlling beta-pleated-sheet content during thermal processing of bioma

19 Beta-pleated-sheet crystals are among the most stable of prot

20 ng, and the accepted paradigm, was that beta-pleated-sheet crystals in the dry solid state were so st

21 llar crystals of synthetic polymers and beta-pleated-sheet crystals is confirmed.

22 rn that assumption and demonstrate that beta-pleated-sheet crystals melt directly from the solid stat

23 t reversible thermal melting of protein beta-pleated-sheet crystals, exemplified by silk fibroin.

24 In addition, the 2 beta-pleated sheet-derived peptides and the alpha1-derived pe

25 In particular, the 2 beta-pleated sheet-derived peptides covering residues 91 to 1

26 e sites are thought to be important for beta-pleated sheet formation.

27 rmation into insoluble cell-deleterious beta-pleated-sheet motifs.

28 -beta-strand turn of the three-stranded beta-pleated sheet of beta2m.

29 ) polymers that self-assemble into nanoscale pleated sheets of hairpin RNA, which in turn form sponge

30 support the changing of the alpha-helix/beta-pleated sheets ratio in protein structure analysis.

31 The pleated sheet region of the leucine-rich G-protein-coupl

32 ve and below peptide planes of internal beta-pleated sheet residues in five globular proteins.

33 proteins, we observe the formation of alpha-pleated sheet secondary structure, which was first propo

34 ere we show that this gB fragment forms beta-pleated sheets, self-assembles into fibrils that are thi

35 s are discussed, namely tight (occludin) and pleated-sheet septate (neurexin IV).

36 forms in the peripheral nervous system where pleated-sheet septate junctions bond cells of the nascen

37 structural analogs of the BBB are occlusive (pleated-sheet) septate and tight junctions between perin

38 that tear lipocalins have a predominant beta-pleated sheet structure (44%) that is essentially retain

39 ansthyretin and beta(2)-microglobulin, alpha-pleated sheet structure formed over the strands that are

40 We propose that the formation of alpha-pleated sheet structure may be a common conformational t

41 1-42) into the neurotoxic amyloid-like, beta-pleated sheet structure, and instead encourages folding

42 hosphorylated, and nor did they contain beta-pleated sheet structure.

43 dyes that bind specifically to crossed beta-pleated sheet structures (eg, Congo red, Thioflavin S).

44 that the trimers were formed mainly of beta-pleated sheet structures in detergent micelles.

45 its, the ABri peptide adopts aggregated beta-pleated sheet structures, similar to those formed by the

46 omain is characterized by 10 strands of beta-pleated sheet that form two distinct layers which lie ne

47 In PD, alpha-syn misfolds into multimeric b-pleated sheets that aggregate in neurons (Lewy Bodies/ne

48 iders produce viscid silk consisting of beta-pleated sheets, whereas Arachnocampa has cross-beta-shee

49 nsists of a single twisted antiparallel beta-pleated sheet with Greek-key topology.