Nucleation-dependent conformational conversion of the Y145Stop variant of human prion protein: structural clues for prion propagation. (Q36348186)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14519851%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

title

Nucleation-dependent conformational conversion of the Y145Stop variant of human prion protein: structural clues for prion propagation (English)

1 reference

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19 December 2019

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1

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19 December 2019

author name string

Nilesh R Maiti

2

1 reference

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19 December 2019

Eric M Jones

3

1 reference

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19 December 2019

Krystyna A Surewicz

4

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19 December 2019

David L Vanik

5

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19 December 2019

Witold K Surewicz

6

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19 December 2019

language of work or name

English

0 references

publication date

30 September 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14519851%20AND%20SRC:MED&resulttype=core&format=json

Proceedings of the National Academy of Sciences of the United States of America

19 December 2019

published in

1 reference

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19 December 2019

volume

100

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19 December 2019

issue

21

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19 December 2019

page(s)

12069-12074

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Domain organization and structure-function relationship of the HET-s prion protein of Podospora anserina

19 December 2019

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30 September 2017

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30 September 2017

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NMR solution structure of the human prion protein

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Overexpression of nonconvertible PrPc delta114-121 in scrapie-infected mouse neuroblastoma cells leads to trans-dominant inhibition of wild-type PrP(Sc) accumulation

30 September 2017

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

30 September 2017

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Self-seeded fibers formed by Sup35, the protein determinant of [PSI+], a heritable prion-like factor of S. cerevisiae.

30 September 2017

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Recombinant scrapie-like prion protein of 106 amino acids is soluble

30 September 2017

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Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

30 September 2017

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Perturbation of the secondary structure of the scrapie prion protein under conditions that alter infectivity

30 September 2017

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Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro

30 September 2017

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Molecular characteristics of a protease-resistant, amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein

30 September 2017

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A single hamster PrP amino acid blocks conversion to protease-resistant PrP in scrapie-infected mouse neuroblastoma cells.

30 September 2017

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Novel proteinaceous infectious particles cause scrapie

30 September 2017

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New insight into protein secondary structure from resolution-enhanced infrared spectra

30 September 2017

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30 September 2017

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A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice

30 September 2017

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

29 June 2018

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Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state

29 June 2018

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Prion domain initiation of amyloid formation in vitro from native Ure2p

29 June 2018

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A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform

29 June 2018

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

29 June 2018

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Novel polymorphisms in the caprine PrP gene: a codon 142 mutation associated with scrapie incubation period

29 June 2018

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29 June 2018

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29 June 2018

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29 June 2018

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29 June 2018

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29 June 2018

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21 January 2018

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NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).

21 January 2018

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Neurotoxicity of a prion protein fragment

21 January 2018

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Conformational transitions in peptides containing two putative alpha-helices of the prion protein.

21 January 2018

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A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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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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Cell-free formation of protease-resistant prion protein.

21 January 2018

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Locally disordered conformer of the hamster prion protein: a crucial intermediate to PrPSc?

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele

21 January 2018

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Specific inhibition of in vitro formation of protease-resistant prion protein by synthetic peptides

21 January 2018

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Kinetic intermediate in the folding of human prion protein

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/14519851

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.2033281100

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14519851%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

0 references

1 reference

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19 December 2019

PubMed publication ID

14519851

1 reference