An inventory of interactors of the human HSP60/HSP10 chaperonin in the mitochondrial matrix space-Reference-Cited by-同舟云学术

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An inventory of interactors of the human HSP60/HSP10 chaperonin in the mitochondrial matrix space

Published:2020-02-14 Issue:3 Volume:25 Page:407-416
ISSN:1355-8145
Container-title:Cell Stress and Chaperones
language:en
Short-container-title:Cell Stress and Chaperones

Author:

Bie Anne Sigaard,Cömert Cagla,Körner Roman,Corydon Thomas J.,Palmfeldt Johan,Hipp Mark S.,Hartl F. Ulrich,Bross Peter^ORCID

Funder

Sundhedsvidenskabelige Fakultet, Aarhus Universitet

Familien Hede Nielsens Fond

Deutscher Akademischer Austauschdienst

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Biochemistry

Link

http://link.springer.com/content/pdf/10.1007/s12192-020-01080-6.pdf

Reference56 articles.

1. Bie AS et al (2016) Effects of a mutation in the HSPE1 gene encoding the mitochondrial co-chaperonin HSP10 and its potential association with a neurological and developmental disorder. Front Mol Biosci 3:65. https://doi.org/10.3389/fmolb.2016.00065

2. Bross P (2015) The Hsp60 Chaperonin. Springer Briefs in Molecular Science. Springer International Publishing, Cham, Switzerland. https://doi.org/10.1007/978-3-319-26088-4

3. Bross P et al (2008) The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo. JBiolChem 283:15694. https://doi.org/10.1074/jbc.M800548200

4. Calvo SE, Clauser KR, Mootha VK (2016) MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins nucleic acids res 44:D1251-D1257. https://doi.org/10.1093/nar/gkv1003

5. Casari G et al (1998) Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease. Cell 93:973–983

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