(Q31979097)

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Prion protein fragments spanning helix 1 and both strands of beta sheet (residues 125-170) show evidence for predominantly helical propensity by CD and NMR.

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Europe PubMed Central

PubMed publication ID

5 July 2017

Prion protein fragments spanning helix 1 and both strands of beta sheet (residues 125-170) show evidence for predominantly helical propensity by CD and NMR. (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

prion protein family

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Landon M

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Europe PubMed Central

PubMed publication ID

5 July 2017

author name string

Sharman GJ

1

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Europe PubMed Central

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5 July 2017

Kenward N

2

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Europe PubMed Central

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5 July 2017

Williams HE

3

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Europe PubMed Central

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5 July 2017

Mayer RJ

5

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Europe PubMed Central

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5 July 2017

Searle MS

6

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5 July 2017

publication date

1 January 1998

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5 July 2017

Folding & design

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5 July 2017

3

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Europe PubMed Central

PubMed publication ID

5 July 2017

5

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Europe PubMed Central

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5 July 2017

313-320

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Europe PubMed Central

PubMed publication ID

5 July 2017

Prion diseases and the BSE crisis

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Prion protein peptides induce alpha-helix to beta-sheet conformational transitions

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Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

1 reference

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Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease

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Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome

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Theoretical studies of sequence effects on the conformational properties of a fragment of the prion protein: implications for scrapie formation

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Unaltered susceptibility to BSE in transgenic mice expressing human prion protein

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Human prion diseases

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Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid

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Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

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NMR structure of the mouse prion protein domain PrP(121-231)

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Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform

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Prion (PrPSc)-specific epitope defined by a monoclonal antibody

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Calculation of protein conformation from circular dichroism

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Secondary structure of proteins through circular dichroism spectroscopy

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Aromatic side-chain contribution to far-ultraviolet circular dichroism of helical peptides and its effect on measurement of helix propensities

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Improvement of z Filters and Purging Pulses by the Use of Zero-Quantum Dephasing in Inhomogeneous B1 or B0 Fields

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Intrinsic phi, psi propensities of amino acids, derived from the coil regions of known structures

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Relationship between nuclear magnetic resonance chemical shift and protein secondary structure

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The chemical shift index: a fast and simple method for the assignment of protein secondary structure through NMR spectroscopy

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7 January 2021

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Analysis of main chain torsion angles in proteins: prediction of NMR coupling constants for native and random coil conformations

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7 January 2021

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Origin of β-Hairpin Stability in Solution: Structural and Thermodynamic Analysis of the Folding of a Model Peptide Supports Hydrophobic Stabilization in Water

1 reference

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7 January 2021

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Folding of peptide fragments comprising the complete sequence of proteins

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Local conformations of peptides representing the entire sequence of bovine pancreatic trypsin inhibitor and their roles in folding

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Formation of a hydrophobic cluster in denatured bovine pancreatic trypsin inhibitor.

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High helicity of peptide fragments corresponding to beta-strand regions of beta-lactoglobulin observed by 2D-NMR spectroscopy.

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Native-like beta-hairpin structure in an isolated fragment from ferredoxin: NMR and CD studies of solvent effects on the N-terminal 20 residues.

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Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible

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10.1016/S1359-0278(98)00043-1

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Europe PubMed Central

PubMed publication ID

5 July 2017

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24 November 2022

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PubMed publication ID

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Europe PubMed Central

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5 July 2017

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