Presequence-dependent folding ensures MrpL32 processing by the m-AAA protease in mitochondria. - sprookjes - yvandenbroek - TriplyDB

Presequence-dependent folding ensures MrpL32 processing by the m-AAA protease in mitochondria.

Presequence-dependent folding ensures MrpL32 processing by the m-AAA protease in mitochondria.

http://www.wikidata.org/entity/Q41786453

about

Mgr2 promotes coupling of the mitochondrial presequence translocase to partner complexes.Role of the AAA protease Yme1 in folding of proteins in the intermembrane space of mitochondria.Mitochondrial Quality Control in Cardiac Diseases Mitochondrial protein quality control: the mechanisms guarding mitochondrial health YME1L degradation reduces mitochondrial proteolytic capacity during oxidative stress Plus ça change - evolutionary sequence divergence predicts protein subcellular localization signals Multifunctional Mitochondrial AAA Proteases Loss of the m-AAA protease subunit AFG₃L₂ causes mitochondrial transport defects and tau hyperphosphorylation.Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies.Dissecting stop transfer versus conservative sorting pathways for mitochondrial inner membrane proteins in vivo Dislocation by the m-AAA protease increases the threshold hydrophobicity for retention of transmembrane helices in the inner membrane of yeast mitochondria.Mitochondrial quality control and communications with the nucleus are important in maintaining mitochondrial function and cell health.Mitochondrial protein quality control in health and disease.Mitochondrial quality control: a matter of life and death for neurons.Mitochondrial protein homeostasis.Import of ribosomal proteins into yeast mitochondria.The versatility of the mitochondrial presequence processing machinery: cleavage, quality control and turnover.Early complex I assembly defects result in rapid turnover of the ND1 subunit.The role of Lon-mediated proteolysis in the dynamics of mitochondrial nucleic acid-protein complexes.Mitochondrial inner membrane protease promotes assembly of presequence translocase by removing a carboxy-terminal targeting sequence.Molecular insights into the m-AAA protease-mediated dislocation of transmembrane helices in the mitochondrial inner membrane.Metalloproteases of the Inner Mitochondrial Membrane.Identification of a Degradation Signal Sequence within Substrates of the Mitochondrial i-AAA Protease.Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species.m-AAA proteases, mitochondrial calcium homeostasis and neurodegeneration.

P2860

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P2860

Presequence-dependent folding ensures MrpL32 processing by the m-AAA protease in mitochondria.

http://www.wikidata.org/entity/Q41786453

description

2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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2011年论文

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2011年论文

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name

Presequence-dependent folding ...... -AAA protease in mitochondria.

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type

label

Presequence-dependent folding ...... -AAA protease in mitochondria.

@en

prefLabel

Presequence-dependent folding ...... -AAA protease in mitochondria.

@en

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P1433

The EMBO Journal

P1476

Presequence-dependent folding ...... -AAA protease in mitochondria.

@en

P2093

Carmelina Petrungaro

http://www.w3.org/2001/XMLSchema#string

Florian Bonn

http://www.w3.org/2001/XMLSchema#string

Jan Riemer

http://www.w3.org/2001/XMLSchema#string

Takashi Tatsuta

http://www.w3.org/2001/XMLSchema#string

Thomas Langer

http://www.w3.org/2001/XMLSchema#string

P2860

Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

High resolution structure of the large ribosomal subunit from a mesophilic eubacterium

The YTA10-12 complex, an AAA protease with chaperone-like activity in the inner membrane of mitochondria.

Import of proteins into yeast mitochondria: the purified matrix processing protease contains two subunits which are encoded by the nuclear MAS1 and MAS2 genes

The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria.

Superoxide dismutase activity is essential for stationary phase survival in Saccharomyces cerevisiae. Mitochondrial production of toxic oxygen species in vivo.

Role of the ABC transporter Mdl1 in peptide export from mitochondria.

Manganese activation of superoxide dismutase 2 in the mitochondria of Saccharomyces cerevisiae.

Extended N-terminal sequencing of proteins of the large ribosomal subunit from yeast mitochondria.

P304

2545-2556

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scholarly article

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10.1038/EMBOJ.2011.169

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13

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30

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2011-05-24T00:00:00Z

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51163478

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21610694

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3155303

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