Cloning and characterization of the gene encoding the human peroxisomal assembly protein Pex3p
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Peroxisome synthesis in the absence of preexisting peroxisomesIdentification of peroxisomal proteins by using M13 phage protein VI phage display: molecular evidence that mammalian peroxisomes contain a 2,4-dienoyl-CoA reductasePEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesisMolecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10pDefective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group GTopogenesis of peroxisomal membrane protein requires a short, positively charged intervening-loop sequence and flanking hydrophobic segments. study using human membrane protein PMP34Multiple distinct targeting signals in integral peroxisomal membrane proteinsTwo different targeting signals direct human peroxisomal membrane protein 22 to peroxisomesPEX19 is a predominantly cytosolic chaperone and import receptor for class 1 peroxisomal membrane proteinsCharacterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of TRP-104 IN Pex3p as a critical residue for the interactionThe membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assemblyStructural basis for docking of peroxisomal membrane protein carrier Pex19p onto its receptor Pex3pThe peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathwayPEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.The peroxin pex3p initiates membrane assembly in peroxisome biogenesisHuman pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequencesPeroxisome biogenesis in mammalian cellsOptogenetic control of molecular motors and organelle distributions in cells.Insights into Peroxisome Function from the Structure of PEX3 in Complex with a Soluble Fragment of PEX19Saccharomyces cerevisiae pex3p and pex19p are required for proper localization and stability of peroxisomal membrane proteinsGenomic organization, expression analysis, and chromosomal localization of the mouse PEX3 gene encoding a peroxisomal assembly proteinPeroxisome biogenesis and peroxisome biogenesis disorders.M-LP, Mpv17-like protein, has a peroxisomal membrane targeting signal comprising a transmembrane domain and a positively charged loop and up-regulates expression of the manganese superoxide dismutase gene.Probing intracellular motor protein activity using an inducible cargo trafficking assay.PEX11 promotes peroxisome division independently of peroxisome metabolismInhibitors of COPI and COPII do not block PEX3-mediated peroxisome synthesis.Pex17p is required for import of both peroxisome membrane and lumenal proteins and interacts with Pex19p and the peroxisome targeting signal-receptor docking complex in Pichia pastoris.Peroxisome biogenesis and human peroxisome-deficiency disorders.Emerging role of the endoplasmic reticulum in peroxisome biogenesis.A stretch of positively charged amino acids at the N terminus of Hansenula polymorpha Pex3p is involved in incorporation of the protein into the peroxisomal membrane.De novo peroxisome biogenesis: Evolving concepts and conundrums.Investigations of human myosin VI targeting using optogenetically controlled cargo loading.The role of conserved PEX3 regions in PEX19-binding and peroxisome biogenesis.Assembly of Peroxisomal Membrane Proteins via the Direct Pex19p-Pex3p Pathway.Human Peroxin PEX3 Is Co-translationally Integrated into the ER and Exits the ER in Budding Vesicles.Intra-ER sorting of the peroxisomal membrane protein Pex3 relies on its luminal domain.Hansenula polymorpha Pex3p is a peripheral component of the peroxisomal membrane.Removal of Pex3p is an important initial stage in selective peroxisome degradation in Hansenula polymorpha.Peroxisomal ascorbate peroxidase resides within a subdomain of rough endoplasmic reticulum in wild-type Arabidopsis cells.The import competence of a peroxisomal membrane protein is determined by Pex19p before the docking step.
P2860
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P2860
Cloning and characterization of the gene encoding the human peroxisomal assembly protein Pex3p
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Cloning and characterization o ...... xisomal assembly protein Pex3p
@ast
Cloning and characterization o ...... xisomal assembly protein Pex3p
@en
Cloning and characterization o ...... xisomal assembly protein Pex3p
@en-gb
Cloning and characterization o ...... xisomal assembly protein Pex3p
@nl
type
label
Cloning and characterization o ...... xisomal assembly protein Pex3p
@ast
Cloning and characterization o ...... xisomal assembly protein Pex3p
@en
Cloning and characterization o ...... xisomal assembly protein Pex3p
@en-gb
Cloning and characterization o ...... xisomal assembly protein Pex3p
@nl
prefLabel
Cloning and characterization o ...... xisomal assembly protein Pex3p
@ast
Cloning and characterization o ...... xisomal assembly protein Pex3p
@en
Cloning and characterization o ...... xisomal assembly protein Pex3p
@en-gb
Cloning and characterization o ...... xisomal assembly protein Pex3p
@nl
P2093
P2860
P1433
P1476
Cloning and characterization o ...... xisomal assembly protein Pex3p
@en
P2093
A A Roscher
A Holzinger
S Kammerer
P2860
P356
10.1016/S0014-5793(98)00557-2
P407
P577
1998-06-05T00:00:00Z