(Q44897846)

English

Preferential Cu2+ coordination by His96 and His111 induces beta-sheet formation in the unstructured amyloidogenic region of the prion protein

scientific article published on 15 May 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Preferential Cu2+ coordination by His96 and His111 induces beta-sheet formation in the unstructured amyloidogenic region of the prion protein (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

prion protein family

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author name string

Christopher E Jones

1

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Salama R Abdelraheim

2

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

David R Brown

3

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

John H Viles

4

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

language of work or name

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publication date

15 May 2004

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Europe PubMed Central

PubMed publication ID

7 December 2017

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

7 December 2017

279

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

31

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

32018-32027

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Prion diseases and the BSE crisis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Deadly conformations--protein misfolding in prion disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper binding to the prion protein: structural implications of four identical cooperative binding sites

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper stimulates endocytosis of the prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Ablation of the metal ion-induced endocytosis of the prion protein by disease-associated mutation of the octarepeat region

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Expression of prion protein increases cellular copper binding and antioxidant enzyme activities but not copper delivery

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Prion disease: A loss of antioxidant function?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Normal prion protein has an activity like that of superoxide dismutase.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Mapping the functional domain of the prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

NMR solution structure of the human prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

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.M403467200

21 January 2018

Local structural plasticity of the prion protein. Analysis of NMR relaxation dynamics

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Location and properties of metal-binding sites on the human prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper(II) complexes of peptide fragments of the prion protein. Conformation changes induced by copper(II) and the binding motif in C-terminal protein region

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper binding to the octarepeats of the prion protein. Affinity, specificity, folding, and cooperativity: insights from circular dichroism

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Identification of the Cu2+ binding sites in the N-terminal domain of the prion protein by EPR and CD spectroscopy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Molecular features of the copper binding sites in the octarepeat domain of the prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Prion protein devoid of the octapeptide repeat region restores susceptibility to scrapie in PrP knockout mice.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

XAFS study of the high-affinity copper-binding site of human PrP(91-231) and its low-resolution structure in solution

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Role of microglia and host prion protein in neurotoxicity of a prion protein fragment

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper converts the cellular prion protein into a protease-resistant species that is distinct from the scrapie isoform

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper(II)-induced conformational changes and protease resistance in recombinant and cellular PrP. Effect of protein age and deamidation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Strain-specific prion-protein conformation determined by metal ions

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper and zinc binding modulates the aggregation and neurotoxic properties of the prion peptide PrP106-126.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Metal imbalance and compromised antioxidant function are early changes in prion disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Aberrant metal binding by prion protein in human prion disease.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper-catalyzed oxidation of the recombinant SHa(29-231) prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper chelation delays the onset of prion disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper and prion disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Prion and prejudice: normal protein and the synapse

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Metal ions and prion diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Cellular prion protein function in copper homeostasis and redox signalling at the synapse

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper binding in the prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Calculation of protein extinction coefficients from amino acid sequence data

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Three-dimensional structure of ectatomin from Ectatomma tuberculatum ant venom

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Structural implications derived from the analysis of electron paramagnetic resonance spectra of natural and artificial copper proteins.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

pH-dependent migration of copper(II) to the vacant zinc-binding site of zinc-free bovine erythrocyte superoxide dismutase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Modeling of copper(II) sites in proteins based on histidyl and glycyl residues

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Copper binding to the neurotoxic peptide PrP106-126: thermodynamic and structural studies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Contribution of two conserved glycine residues to fibrillogenesis of the 106-126 prion protein fragment. Evidence that a soluble variant of the 106-126 peptide is neurotoxic

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M403467200

21 January 2018

Identifiers

10.1074/JBC.M403467200

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

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