Central residues in prion protein PrP

Animals Mice Prion Diseases / genetics Prion Proteins / chemistry Prions / pathogenicity Proline Protein Isoforms / genetics Translocation, Genetic
neurodegenerative disease prion prion disease protein misfolding structure-function transgenic mice

Journal

The Journal of biological chemistry
ISSN: 1083-351X
Titre abrégé: J Biol Chem
Pays: United States
ID NLM: 2985121R

Informations de publication

Date de publication:
09 2022
Historique:
received: 09 03 2022
revised: 08 08 2022
accepted: 10 08 2022
pubmed: 17 8 2022
medline: 30 9 2022
entrez: 16 8 2022
Statut: ppublish

Résumé

Conformational conversion of the cellular prion protein, PrP

Identifiants

DOI: 10.1016/j.jbc.2022.102381 PMID: 35973512 PMC: PMC9478402
pubmed: 35973512
pii: S0021-9258(22)00824-9
doi: 10.1016/j.jbc.2022.102381
pmc: PMC9478402
pii:
doi:

Substances chimiques

Prion Proteins 0
Prions 0
Protein Isoforms 0
Proline 9DLQ4CIU6V

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

102381

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interests The authors declare that they have no conflicts of interest with the contents of this article.

Auteurs

Agriani Dini Pasiana (AD)

Division of Molecular Neurobiology, The Institute for Enzyme Research (KOSOKEN), Tokushima University, Tokushima, Japan.

Hironori Miyata (H)

Animal Research Center, School of Medicine, University of Occupational and Environmental Health, Yahatanishi, Kitakyushu, Japan.

Junji Chida (J)

Division of Molecular Neurobiology, The Institute for Enzyme Research (KOSOKEN), Tokushima University, Tokushima, Japan.

Hideyuki Hara (H)

Division of Molecular Neurobiology, The Institute for Enzyme Research (KOSOKEN), Tokushima University, Tokushima, Japan.

Morikazu Imamura (M)

Division of Microbiology, Department of Infectious Diseases, Faculty of Medicine, University of Miyazaki, Kiyotake, Miyazaki, Japan.

Ryuichiro Atarashi (R)

Division of Microbiology, Department of Infectious Diseases, Faculty of Medicine, University of Miyazaki, Kiyotake, Miyazaki, Japan.

Suehiro Sakaguchi (S)

Division of Molecular Neurobiology, The Institute for Enzyme Research (KOSOKEN), Tokushima University, Tokushima, Japan. Electronic address: sakaguchi@tokushima-u.ac.jp.

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Classifications MeSH

questionsmedicales.fr › Eucaryotes › Animaux › Central residues in prion protein PrP
questionsmedicales.fr › Eucaryotes › Animaux › Chordés › Vertébrés › Mammifères › Eutheria › Rodentia › Muridae › Murinae › Souris › Central residues in prion protein PrP
questionsmedicales.fr › Maladies du système nerveux › Maladies neurodégénératives › Maladies à prions › Central residues in prion protein PrP
questionsmedicales.fr › Acides aminés, peptides et protéines › Protéines › Prions › Protéines prion › Central residues in prion protein PrP
questionsmedicales.fr › Acides aminés, peptides et protéines › Protéines › Prions › Central residues in prion protein PrP
questionsmedicales.fr › Acides aminés, peptides et protéines › Acides aminés › Acides aminés cycliques › Imino-acides › Proline › Central residues in prion protein PrP
questionsmedicales.fr › Acides aminés, peptides et protéines › Protéines › Isoformes de protéines › Central residues in prion protein PrP
questionsmedicales.fr › Phénomènes génétiques › Mutagenèse › Translocation génétique › Central residues in prion protein PrP