Msp1/ATAD1 maintains mitochondrial function by facilitating the degradation of mislocalized tail-anchored proteins
about
The conserved AAA-ATPase Msp1 confers organelle specificity to tail-anchored proteinsMitochondrial protein quality control: the mechanisms guarding mitochondrial healthPrecision therapy for a new disorder of AMPA receptor recycling due to mutations in ATAD1.ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia.Control of mitochondrial biogenesis and function by the ubiquitin-proteasome systemMultifunctional Mitochondrial AAA ProteasesPredicting the targeting of tail-anchored proteins to subcellular compartments in mammalian cells.Evidence for Amino Acid Snorkeling from a High-Resolution, In Vivo Analysis of Fis1 Tail-Anchor Insertion at the Mitochondrial Outer MembraneSpatial and temporal dynamics of the cardiac mitochondrial proteome.Doa1 targets ubiquitinated substrates for mitochondria-associated degradation.Outer membrane protein functions as integrator of protein import and DNA inheritance in mitochondria.Pask integrates hormonal signaling with histone modification via Wdr5 phosphorylation to drive myogenesis.Mitochondrial quality control pathways as determinants of metabolic health.Msp1 Is a Membrane Protein Dislocase for Tail-Anchored Proteins.Assembly of Peroxisomal Membrane Proteins via the Direct Pex19p-Pex3p Pathway.Msp1: patrolling mitochondria for lost proteins.The AAA protein Msp1 mediates clearance of excess tail-anchored proteins from the peroxisomal membrane.Selective sorting and destruction of mitochondrial membrane proteins in aged yeast.Spatial control of lipid droplet proteins by the ERAD ubiquitin ligase Doa10.Thorase variants are associated with defects in glutamatergic neurotransmission that can be rescued by Perampanel.Mitochondrial inner-membrane protease Yme1 degrades outer-membrane proteins Tom22 and Om45.A homozygous ATAD1 mutation impairs postsynaptic AMPA receptor trafficking and causes a lethal encephalopathy.The Plastid and Mitochondrial Peptidase Network in Arabidopsis thaliana: A Foundation for Testing Genetic Interactions and Functions in Organellar Proteostasis.The peroxisomal AAA-ATPase Pex1/Pex6 unfolds substrates by processive threading.Chloroplast Ubiquitin E3 Ligase SP1: Does It Really Function in Peroxisomes?Genomic Deletion at 10q23 in Prostate Cancer: More Than PTEN Loss?A bacteria-derived tail anchor localizes to peroxisomes in yeast and mammalian cells
P2860
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P2860
Msp1/ATAD1 maintains mitochondrial function by facilitating the degradation of mislocalized tail-anchored proteins
description
2014 nî lūn-bûn
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2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2014 թվականի մայիսին հրատարակված գիտական հոդված
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2014年の論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年论文
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name
Msp1/ATAD1 maintains mitochond ...... calized tail-anchored proteins
@ast
Msp1/ATAD1 maintains mitochond ...... calized tail-anchored proteins
@en
Msp1/ATAD1 maintains mitochond ...... calized tail-anchored proteins
@nl
type
label
Msp1/ATAD1 maintains mitochond ...... calized tail-anchored proteins
@ast
Msp1/ATAD1 maintains mitochond ...... calized tail-anchored proteins
@en
Msp1/ATAD1 maintains mitochond ...... calized tail-anchored proteins
@nl
prefLabel
Msp1/ATAD1 maintains mitochond ...... calized tail-anchored proteins
@ast
Msp1/ATAD1 maintains mitochond ...... calized tail-anchored proteins
@en
Msp1/ATAD1 maintains mitochond ...... calized tail-anchored proteins
@nl
P2093
P2860
P356
P1433
P1476
Msp1/ATAD1 maintains mitochond ...... calized tail-anchored proteins
@en
P2093
George K E Umanah
Jared Rutter
Noah Dephoure
Shaida A Andrabi
Valina L Dawson
Yu-Chan Chen
P2860
P304
P356
10.15252/EMBJ.201487943
P407
P577
2014-05-19T00:00:00Z