The presence of valine at residue 129 in human prion protein accelerates amyloid formation. (Q46464219)

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11 January 2020

title

The presence of valine at residue 129 in human prion protein accelerates amyloid formation (English)

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11 January 2020

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3

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11 January 2020

Petra Disterer

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11 January 2020

William James

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11 January 2020

author name string

Ilia Baskakov

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11 January 2020

Michael Shaw

4

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11 January 2020

Andrew Gill

5

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11 January 2020

Abdessamad Tahiri-Alaoui

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11 January 2020

language of work or name

English

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publication date

8 April 2005

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11 January 2020

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11 January 2020

volume

579

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11 January 2020

issue

12

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11 January 2020

page(s)

2589-2596

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Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

11 January 2020

cites work

1 reference

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Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

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Aminoacid polymorphism in human prion protein and age at death in inherited prion disease

21 January 2018

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Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease

21 January 2018

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

21 January 2018

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Pathway complexity of prion protein assembly into amyloid

21 January 2018

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Methionine 129 variant of human prion protein oligomerizes more rapidly than the valine 129 variant: implications for disease susceptibility to Creutzfeldt-Jakob disease.

21 January 2018

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Rapid formation of amyloid from alpha-monomeric recombinant human PrP in vitro

21 January 2018

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

21 January 2018

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Prion protein NMR structure and familial human spongiform encephalopathies

21 January 2018

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The residue 129 polymorphism in human prion protein does not confer susceptibility to Creutzfeldt-Jakob disease by altering the structure or global stability of PrPC.

21 January 2018

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The peculiar nature of unfolding of the human prion protein

21 January 2018

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Synthetic mammalian prions

21 January 2018

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Novel proteinaceous infectious particles cause scrapie

21 January 2018

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Competing intrachain interactions regulate the formation of beta-sheet fibrils in bovine PrP peptides.

21 January 2018

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In vitro conversion of full-length mammalian prion protein produces amyloid form with physical properties of PrP(Sc).

21 January 2018

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Protein conformational prediction

21 January 2018

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Thermodynamic beta-sheet propensities measured using a zinc-finger host peptide.

21 January 2018

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

21 January 2018

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Binding of prion protein to lipid membranes and implications for prion conversion

21 January 2018

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Unusual property of prion protein unfolding in neutral salt solution

21 January 2018

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RNA molecules stimulate prion protein conversion

21 January 2018

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DNA-induced partial unfolding of prion protein leads to its polymerisation to amyloid

21 January 2018

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Molecular biology of prion diseases

21 January 2018

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Autocatalytic conversion of recombinant prion proteins displays a species barrier

21 January 2018

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Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.

21 January 2018

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BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein

21 January 2018

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The same prion strain causes vCJD and BSE

21 January 2018

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Impact of the tail and mutations G131V and M129V on prion protein flexibility

21 January 2018

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