Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells.
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In vitro transport of membrane proteins to peroxisomes by shuttling receptor Pex19pCell-specific subcellular localization of soluble epoxide hydrolase in human tissuesThe membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assemblyThe peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathwayMutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlationCrystal structure of peroxisomal targeting signal-2 bound to its receptor complex Pex7p-Pex21pPex7p translocates in and out of peroxisomes in Saccharomyces cerevisiaeTopogenesis and homeostasis of fatty acyl-CoA reductase 1Cysteine ubiquitination of PTS1 receptor Pex5p regulates Pex5p recycling.The Arabidopsis peroxisomal targeting signal type 2 receptor PEX7 is necessary for peroxisome function and dependent on PEX5.Shuttling mechanism of peroxisome targeting signal type 1 receptor Pex5: ATP-independent import and ATP-dependent export.The membrane peroxin PEX3 induces peroxisome-ubiquitination-linked pexophagy.Proteomic analysis reveals that the Rab GTPase RabE1c is involved in the degradation of the peroxisomal protein receptor PEX7 (peroxin 7).Tail-anchored PEX26 targets peroxisomes via a PEX19-dependent and TRC40-independent class I pathway.Getting a camel through the eye of a needle: the import of folded proteins by peroxisomes.Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata.Molecular mechanisms of import of peroxisome-targeting signal type 2 (PTS2) proteins by PTS2 receptor Pex7p and PTS1 receptor Pex5pL.Assembly of Peroxisomal Membrane Proteins via the Direct Pex19p-Pex3p Pathway.Plasmalogen biosynthesis is spatiotemporally regulated by sensing plasmalogens in the inner leaflet of plasma membranes.Mff functions with Pex11pβ and DLP1 in peroxisomal fissionNew splicing variants of mitochondrial Rho GTPase-1 (Miro1) transport peroxisomes.Functional domains and dynamic assembly of the peroxin Pex14p, the entry site of matrix proteins.Deficiency of a Retinal Dystrophy Protein, Acyl-CoA Binding Domain-containing 5 (ACBD5), Impairs Peroxisomal β-Oxidation of Very-long-chain Fatty Acids.CUL4A-DDB1-Rbx1 E3 ligase controls the quality of the PTS2 receptor Pex7p.Recruiting mechanism of the AAA peroxins, Pex1p and Pex6p, to Pex26p on the peroxisomal membrane.Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotypePeroxisome Dynamics: Molecular Players, Mechanisms, and (Dys)functions
P2860
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P2860
Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
Intracellular localization, fu ...... or, Pex7p, in mammalian cells.
@en
type
label
Intracellular localization, fu ...... or, Pex7p, in mammalian cells.
@en
prefLabel
Intracellular localization, fu ...... or, Pex7p, in mammalian cells.
@en
P2093
P2860
P356
P1476
Intracellular localization, fu ...... or, Pex7p, in mammalian cells.
@en
P2093
Kamran Ghaedi
Satoru Mukai
Yukio Fujiki
P2860
P304
P356
10.1074/JBC.M108635200
P407
P577
2001-12-27T00:00:00Z