Peroxisome synthesis in the absence of preexisting peroxisomes
about
Identification of peroxisomal proteins by using M13 phage protein VI phage display: molecular evidence that mammalian peroxisomes contain a 2,4-dienoyl-CoA reductasePEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein importPEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesisIdentification and characterization of HAOX1, HAOX2, and HAOX3, three human peroxisomal 2-hydroxy acid oxidasesDefective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group GIn vitro transport of membrane proteins to peroxisomes by shuttling receptor Pex19pRequirement for microtubules and dynein motors in the earliest stages of peroxisome biogenesisThe 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 pathwayPEX3 functions as a PEX19 docking factor in the import of class I peroxisomal membrane proteinsThe origin and maintenance of mammalian peroxisomes involves a de novo PEX16-dependent pathway from the ERPEX11alpha is required for peroxisome proliferation in response to 4-phenylbutyrate but is dispensable for peroxisome proliferator-activated receptor alpha-mediated peroxisome proliferationPEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.The peroxin pex3p initiates membrane assembly in peroxisome biogenesisCrosstalk between mitochondria and peroxisomesPeroxisome biogenesis in mammalian cellsPlant peroxisomes: biogenesis and functionInsights into Peroxisome Function from the Structure of PEX3 in Complex with a Soluble Fragment of PEX19Saccharomyces cerevisiae PTS1 receptor Pex5p interacts with the SH3 domain of the peroxisomal membrane protein Pex13p in an unconventional, non-PXXP-related manner.The biochemistry of peroxisomal beta-oxidation in the yeast Saccharomyces cerevisiae.Endoplasmic reticulum-associated secretory proteins Sec20p, Sec39p, and Dsl1p are involved in peroxisome biogenesis.Pex30p, Pex31p, and Pex32p form a family of peroxisomal integral membrane proteins regulating peroxisome size and number in Saccharomyces cerevisiae.Yeast peroxisomes multiply by growth and division.Saccharomyces cerevisiae pex3p and pex19p are required for proper localization and stability of peroxisomal membrane proteinsCatalase-less peroxisomes. Implication in the milder forms of peroxisome biogenesis disorderDynamin-like protein 1 is involved in peroxisomal fissionConstruction of a natural panel of 11p11.2 deletions and further delineation of the critical region involved in Potocki-Shaffer syndromeRegulation of peroxisomal lipid metabolism by catalytic activity of tumor suppressor H-rev107The peroxisome: still a mysterious organelleSimultaneous live-imaging of peroxisomes and the ER in plant cells suggests contiguity but no luminal continuity between the two organellesPeroxisomal remnant structures in Hansenula polymorpha Pex5 cells can develop into normal peroxisomes upon induction of the PTS2 protein amine oxidase.Glycosome biogenesis in trypanosomes and the de novo dilemma.Yarrowia lipolytica cells mutant for the PEX24 gene encoding a peroxisomal membrane peroxin mislocalize peroxisomal proteins and accumulate membrane structures containing both peroxisomal matrix and membrane proteins.Inactivation of the endoplasmic reticulum protein translocation factor, Sec61p, or its homolog, Ssh1p, does not affect peroxisome biogenesis.Peroxisome biogenesis and peroxisome biogenesis disorders.Newly born peroxisomes are a hybrid of mitochondrial and ER-derived pre-peroxisomes.How peroxisomes arise.The life cycle of the peroxisome.Protein translocation machineries of peroxisomes.
P2860
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P2860
Peroxisome synthesis in the absence of preexisting peroxisomes
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Peroxisome synthesis in the absence of preexisting peroxisomes
@ast
Peroxisome synthesis in the absence of preexisting peroxisomes
@en
Peroxisome synthesis in the absence of preexisting peroxisomes
@en-gb
Peroxisome synthesis in the absence of preexisting peroxisomes
@nl
type
label
Peroxisome synthesis in the absence of preexisting peroxisomes
@ast
Peroxisome synthesis in the absence of preexisting peroxisomes
@en
Peroxisome synthesis in the absence of preexisting peroxisomes
@en-gb
Peroxisome synthesis in the absence of preexisting peroxisomes
@nl
prefLabel
Peroxisome synthesis in the absence of preexisting peroxisomes
@ast
Peroxisome synthesis in the absence of preexisting peroxisomes
@en
Peroxisome synthesis in the absence of preexisting peroxisomes
@en-gb
Peroxisome synthesis in the absence of preexisting peroxisomes
@nl
P2860
P921
P356
P1476
Peroxisome synthesis in the absence of preexisting peroxisomes
@en
P2093
P2860
P304
P356
10.1083/JCB.144.2.255
P407
P577
1999-01-25T00:00:00Z