AAA peroxins and their recruiter Pex26p modulate the interactions of peroxins involved in peroxisomal protein import. - Wikidata - awgldk - TriplyDB

AAA peroxins and their recruiter Pex26p modulate the interactions of peroxins involved in peroxisomal protein import.

AAA peroxins and their recruiter Pex26p modulate the interactions of peroxins involved in peroxisomal protein import.

http://www.wikidata.org/entity/Q38305839

about

Alteration of Gene Expression, DNA Methylation, and Histone Methylation in Free Radical Scavenging Networks in Adult Mouse Hippocampus following Fetal Alcohol Exposure.Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6 Nucleotide-dependent assembly of the peroxisomal receptor export complex.Peroxisome biogenesis and human peroxisome-deficiency disorders.Protein transport into peroxisomes: Knowns and unknowns.The PEX1 ATPase Stabilizes PEX6 and Plays Essential Roles in Peroxisome Biology.A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders.Disparate peroxisome-related defects in Arabidopsis pex6 and pex26 mutants link peroxisomal retrotranslocation and oil body utilization.Blue Native PAGE: Applications to Study Peroxisome Biogenesis.Peroxisome Function, Biogenesis, and Dynamics in Plants.The peroxisomal AAA-ATPase Pex1/Pex6 unfolds substrates by processive threading.PEX2:PEX10:PEX12:Ub:PEX5S;L:PEX13:PEX14 binds PEX1:PEX6:PEX26 and ZFAND6 PEX1:PEX6:PEX26:ZFAND6:Ub:PEX5S;L:PEX14:PEX13:PEX2:PEX10:PEX12 dissociates yielding cytosolic Ub:PEX5S;L and membrane PEX14:PEX13:PEX2:PEX10:PEX12 PEX2:PEX10:PEX12:Ub:PEX5L:PEX7:PEX13:PEX14 binds PEX1:PEX6:PEX26 and ZFAND6 PEX1:PEX6:PEX26:ZFAND6 dissociates Ub:PEX5L and PEX7 from PEX14:PEX13:PEX2:PEX10:PEX12 and translocates PEX5L and PEX7 from the peroxisomal membrane to the cytosol Chemically monoubiquitinated PEX5 binds to the components of the peroxisomal docking and export machinery

P2860

Q36005268-08DDF60E-A9CE-4CB5-8965-EC0DE2AE4B4B Q36133280-CAE4FF60-E509-436A-9B1D-8146326CF28F Q36542265-5C23F598-C87F-49AC-AD43-E700AE4795AE Q37670278-490CE24E-585A-4700-A707-03E7FB9D1D7D Q38634873-99901B7F-20E0-4CC0-9762-1B25A37B628C Q38733094-48477C18-B8C5-4809-8F67-C800430D2A81 Q42291746-A604FB08-C3F1-4463-96B1-8B94C62C3B79 Q47821409-14A398F4-5C66-4DB9-8D7D-7EC550C763D5 Q47919789-75C5F5A6-3C0D-4E9B-9807-73A2EF510AA5 Q48208031-0AA94518-A366-49F8-A27A-64AD40F260D2 Q48267632-863B3CA7-C0F6-4474-B27A-EC6F552AD83B Q55217642-C33764EF-1BE2-4D78-995F-A515B4EF31AF Q55217643-A103A28C-6B14-47FE-BC86-D0297ED599D6 Q55217656-5A67EA9A-D25F-4AEE-9885-9D22CDC0196B Q55217658-537401D5-5C82-4156-93CB-82BDE24C0EAE Q58099106-795401BE-6AF4-43BC-AC53-3C69231FE6AD

P2860

AAA peroxins and their recruiter Pex26p modulate the interactions of peroxins involved in peroxisomal protein import.

http://www.wikidata.org/entity/Q38305839

description

2014 nî lūn-bûn

@nan

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

2014年论文

@zh

2014年论文

@zh-cn

name

AAA peroxins and their recruit ...... in peroxisomal protein import.

@en

type

label

AAA peroxins and their recruit ...... in peroxisomal protein import.

@en

prefLabel

AAA peroxins and their recruit ...... in peroxisomal protein import.

@en

P1433

Q38305839-98C0BE0A-B284-42BD-B92B-08924F95E533

P1476

Q38305839-803C5C94-EA45-4327-966D-8E099D6BD7AB

P2093

Q38305839-0A99D8A6-87D7-426F-9E98-A1317DBEA7DD

Q38305839-0E303699-313F-4929-AA9E-35D2616BDCA4

Q38305839-1085C659-43D7-4474-AC13-3111776761C7

Q38305839-18509036-A081-498C-8264-EA8BDEC439C7

P2860

Q38305839-027CD40A-0D8B-4C8D-99FB-96BCBFDA937F

Q38305839-04652A1C-64E5-474F-983C-40573F243B2F

Q38305839-08318887-10F5-4A03-98DC-BB1E4C925D37

Q38305839-095D1033-DB9E-4B78-A06B-FFE58D139189

Q38305839-1AEA75ED-4E1C-4386-84A2-681104129D6E

Q38305839-33F00A7D-0915-48A5-AFBA-F1B6BE61264C

Q38305839-3BCCEAF2-3C95-4F7C-8ED7-78F81974A392

Q38305839-46FEE2E5-495B-4503-86BD-07342C61916E

Q38305839-4F78C45E-86E4-4CCE-8F16-48D3B92DBC2C

Q38305839-6791F55C-A49D-41AB-8905-9EF4264D1C2F

P304

Q38305839-29FBC68D-516E-43D9-B3E5-C6E27909EBDF

P31

Q38305839-F7BEBDFB-49F1-452F-A1FC-0FFABE0968C3

P356

Q38305839-CB237B21-3777-4D8F-9954-A494505EC0E3

P407

Q38305839-83E16449-CC06-4DD3-8CAC-42F2B12DE7DA

P433

Q38305839-E667AA89-9852-4484-9BE2-0FB67D7ECD35

P478

Q38305839-3DCEA1EA-6536-4058-A3B7-B190B2ECC008

P577

Q38305839-0C309F26-029A-4A50-B7DB-75B45F68A855

P698

Q38305839-15804769-207A-41EA-9E3E-120E60D282F0

P932

Q38305839-64536EC3-206A-4A0C-941C-BDDBE735CC9E

P356

JBC.M114.588038

P1433

Journal of Biological Chemistry

P1476

AAA peroxins and their recruit ...... in peroxisomal protein import.

@en

P2093

Naomi Matsumoto

http://www.w3.org/2001/XMLSchema#string

Ryota Takeba

http://www.w3.org/2001/XMLSchema#string

Shigehiko Tamura

http://www.w3.org/2001/XMLSchema#string

Yukio Fujiki

http://www.w3.org/2001/XMLSchema#string

P2860

Identification and characterization of the human orthologue of yeast Pex14p

PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import

Molecular 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, Pex10p

Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction

Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex

Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p

Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis.

Members of the E2D (UbcH5) family mediate the ubiquitination of the conserved cysteine of Pex5p, the peroxisomal import receptor

Two AAA family peroxins, PpPex1p and PpPex6p, interact with each other in an ATP-dependent manner and are associated with different subcellular membranous structures distinct from peroxisomes.

Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation

P304

24336-24346

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1074/JBC.M114.588038

http://www.w3.org/2001/XMLSchema#string

P407

P433

35

http://www.w3.org/2001/XMLSchema#string

P478

289

http://www.w3.org/2001/XMLSchema#string

P577

2014-07-11T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

25016021

http://www.w3.org/2001/XMLSchema#string

P932

4148862

http://www.w3.org/2001/XMLSchema#string