AAA proteases with catalytic sites on opposite membrane surfaces comprise a proteolytic system for the ATP-dependent degradation of inner membrane proteins in mitochondria
about
Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegiaYME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferationA human homologue of Escherichia coli ClpP caseinolytic protease: recombinant expression, intracellular processing and subcellular localizationThe chloroplast ycf3 and ycf4 open reading frames of Chlamydomonas reinhardtii are required for the accumulation of the photosystem I complexMultitasking in the mitochondrion by the ATP-dependent Lon proteaseMgr3p and Mgr1p are adaptors for the mitochondrial i-AAA protease complexProhibitins regulate membrane protein degradation by the m-AAA protease in mitochondria.Peripheral mitochondrial inner membrane protein, Mss2p, required for export of the mitochondrially coded Cox2p C tail in Saccharomyces cerevisiaeA genomewide screen for petite-negative yeast strains yields a new subunit of the i-AAA protease complex.Tim9p, an essential partner subunit of Tim10p for the import of mitochondrial carrier proteins.Translocation of mitochondrially synthesized Cox2 domains from the matrix to the intermembrane space.Regulation of mitochondrial fusion by the F-box protein Mdm30 involves proteasome-independent turnover of Fzo1Regulation of mitochondrial phospholipids by Ups1/PRELI-like proteins depends on proteolysis and Mdm35.Mitochondrial protein quality control: the mechanisms guarding mitochondrial healthHomozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentationStAR enhances transcription of genes encoding the mitochondrial proteases involved in its own degradationEvolutionary conservation in biogenesis of β-barrel proteins allows mitochondria to assemble a functional bacterial trimeric autotransporter protein.Sequential processing of the Toxoplasma apicoplast membrane protein FtsH1 in topologically distinct domains during intracellular traffickingEngineered AAA+ proteases reveal principles of proteolysis at the mitochondrial inner membrane.Protease gene families in Populus and Arabidopsis.Multifunctional Mitochondrial AAA ProteasesChaperone rings in protein folding and degradation.Signaling the mitochondrial unfolded protein response.Proteasome mutants, pre4-2 and ump1-2, suppress the essential function but not the mitochondrial RNase P function of the Saccharomyces cerevisiae gene RPM2.Maintenance of mitochondrial morphology is linked to maintenance of the mitochondrial genome in Saccharomyces cerevisiae.Mitochondrial protein import and the genesis of steroidogenic mitochondriaREXO2 is an oligoribonuclease active in human mitochondria.Mammalian pitrilysin: substrate specificity and mitochondrial targeting.Barth syndrome mutations that cause tafazzin complex lability.Mechanism of the cleavage specificity of Alzheimer's disease gamma-secretase identified by phenylalanine-scanning mutagenesis of the transmembrane domain of the amyloid precursor protein.Sampangine inhibits heme biosynthesis in both yeast and human.Unmasking a temperature-dependent effect of the P. anserina i-AAA protease on aging and development.Multiple roles of the Cox20 chaperone in assembly of Saccharomyces cerevisiae cytochrome c oxidase.Misfolding of mutant adenine nucleotide translocase in yeast supports a novel mechanism of Ant1-induced muscle diseases.The Mitochondrial m-AAA Protease Prevents Demyelination and Hair Greying.Loss of Drosophila i-AAA protease, dYME1L, causes abnormal mitochondria and apoptotic degeneration.Dissecting stop transfer versus conservative sorting pathways for mitochondrial inner membrane proteins in vivoDominant membrane uncoupling by mutant adenine nucleotide translocase in mitochondrial diseases.Translocation and assembly of mitochondrially coded Saccharomyces cerevisiae cytochrome c oxidase subunit Cox2 by Oxa1 and Yme1 in the absence of Cox18.Dynamics of mitochondrial structure during apoptosis and the enigma of Opa1
P2860
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P2860
AAA proteases with catalytic sites on opposite membrane surfaces comprise a proteolytic system for the ATP-dependent degradation of inner membrane proteins in mitochondria
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh
1996年學術文章
@zh-hant
name
AAA proteases with catalytic s ...... brane proteins in mitochondria
@en
type
label
AAA proteases with catalytic s ...... brane proteins in mitochondria
@en
prefLabel
AAA proteases with catalytic s ...... brane proteins in mitochondria
@en
P2093
P2860
P1433
P1476
AAA proteases with catalytic s ...... brane proteins in mitochondria
@en
P2093
P2860
P304
P407
P577
1996-08-01T00:00:00Z