(Q44174343)

English

Disease-associated F198S mutation increases the propensity of the recombinant prion protein for conformational conversion to scrapie-like form

scientific article published on 7 October 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Disease-associated F198S mutation increases the propensity of the recombinant prion protein for conformational conversion to scrapie-like form (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

prion protein family

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author name string

David L Vanik

1

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Witold K Surewicz

2

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

language of work or name

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publication date

7 October 2002

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Europe PubMed Central

PubMed publication ID

30 November 2017

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

30 November 2017

277

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

50

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

49065-49070

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

The Ninth Datta Lecture. Molecular biology of transmissible spongiform encephalopathies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Prion diseases of humans and animals: their causes and molecular basis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Transmissible spongiform encephalopathies and prion protein interconversions

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Novel proteinaceous infectious particles cause scrapie

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Transmissible spongiform encephalopathies, amyloidoses and yeast prions: common threads?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

[URE3] as an altered URE2 protein: evidence for a prion analog in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Mad cows meet psi-chotic yeast: the expansion of the prion hypothesis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Evidence for the prion hypothesis: induction of the yeast [PSI+] factor by in vitro- converted Sup35 protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Separation and properties of cellular and scrapie prion proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Thermal stability and conformational transitions of scrapie amyloid (prion) protein correlate with infectivity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Fluorometric determination of amyloid fibrils in vitro using the fluorescent dye, thioflavin T1.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Unfolding free energy changes determined by the linear extrapolation method. 1. Unfolding of phenylmethanesulfonyl alpha-chymotrypsin using different denaturants

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Aggregation and fibrillization of the recombinant human prion protein huPrP90-231.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

On the mechanism of alpha-helix to beta-sheet transition in the recombinant prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Folding of prion protein to its native alpha-helical conformation is under kinetic control

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Structural clues to prion replication

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Familial mutations and the thermodynamic stability of the recombinant human prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

NMR solution structure of the human prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Crystal structure of the human prion protein reveals a mechanism for oligomerization

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Prion protein NMR structure and familial human spongiform encephalopathies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Amyloid fibril formation and protein misassembly: a structural quest for insights into amyloid and prion diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

A role for destabilizing amino acid replacements in light-chain amyloidosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Partially folded intermediates as critical precursors of light chain amyloid fibrils and amorphous aggregates.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Differences between the prion protein and its homolog Doppel: a partially structured state with implications for scrapie formation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Cell-free formation of protease-resistant prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Chaperone-supervised conversion of prion protein to its protease-resistant form

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Sulfated glycans and elevated temperature stimulate PrP(Sc)-dependent cell-free formation of protease-resistant prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Local cooperativity in the unfolding of an amyloidogenic variant of human lysozyme

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Human prion proteins expressed in Escherichia coli and purified by high-affinity column refolding

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Membrane environment alters the conformational structure of the recombinant human prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Extremely rapid folding of the C-terminal domain of the prion protein without kinetic intermediates

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Structural mobility of the human prion protein probed by backbone hydrogen exchange

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Kinetic intermediate in the folding of human prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M207511200

21 January 2018

Identifiers

10.1074/JBC.M207511200

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

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