Related references
Note: Only part of the references are listed.Systematic approaches to identify E3 ligase substrates
Mary Iconomou et al.
BIOCHEMICAL JOURNAL (2016)
Peroxisome homeostasis: Mechanisms of division and selective degradation of peroxisomes in mammals
Masanori Honsho et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2016)
Assembly, maintenance and dynamics of peroxisomes Preface
Ralf Erdmann
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2016)
Human disorders of peroxisome metabolism and biogenesis
Hans R. Waterham et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2016)
53BP1 and USP28 mediate p53 activation and G1 arrest after centrosome loss or extended mitotic duration
Franz Meitinger et al.
JOURNAL OF CELL BIOLOGY (2016)
Trim37-deficient mice recapitulate several features of the multi-organ disorder Mulibrey nanism
Kaisa M. Kettunen et al.
BIOLOGY OPEN (2016)
ATM functions at the peroxisome to induce pexophagy in response to ROS
Jiangwei Zhang et al.
NATURE CELL BIOLOGY (2015)
Distinct Modes of Ubiquitination of Peroxisome-targeting Signal Type 1 ( PTS1) Receptor Pex5p Regulate PTS1 Protein Import
Kanji Okumoto et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
Peroxisomal Atg37 binds Atg30 or palmitoyl-CoA to regulate phagophore formation during pexophagy
Taras Y. Nazarko et al.
JOURNAL OF CELL BIOLOGY (2014)
TRIM37 is a new histone H2A ubiquitin ligase and breast cancer oncoprotein
Sanchita Bhatnagar et al.
NATURE (2014)
PEX5, the Shuttling Import Receptor for Peroxisomal Matrix Proteins, Is a Redox-Sensitive Protein
Oksana Apanasets et al.
TRAFFIC (2014)
Discovering Regulators of Centriole Biogenesis through siRNA-Based Functional Genomics in Human Cells
Fernando R. Balestra et al.
DEVELOPMENTAL CELL (2013)
Phosphorylation of mitophagy and pexophagy receptors coordinates their interaction with Atg8 and Atg11
Jean-Claude Farre et al.
EMBO REPORTS (2013)
Peroxisomes take shape
Jennifer J. Smith et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2013)
A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11β gene
Merel S. Ebberink et al.
JOURNAL OF MEDICAL GENETICS (2012)
Peroxisome assembly: matrix and membrane protein biogenesis
Changle Ma et al.
JOURNAL OF CELL BIOLOGY (2011)
Cysteine Ubiquitination of PTS1 Receptor Pex5p Regulates Pex5p Recycling
Kanji Okumoto et al.
TRAFFIC (2011)
Detection of Protein Ubiquitination
Yeun Su Choo et al.
Jove-Journal of Visualized Experiments (2009)
Predicted mouse peroxisome-targeted proteins and their actual subcellular locations
Yumi Mizuno et al.
BMC BIOINFORMATICS (2008)
Members of the E2D (UbcH5) family mediate the ubiquitination of the conserved cysteine of Pex5p, the peroxisomal import receptor
Claudia P. Grou et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Ubiquitination of mammalian pex5p, the peroxisomal import receptor
Andreia F. Carvalho et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
A conserved cysteine is essential for Pex4p-dependent ubiquitination of the peroxisomal import receptor Pex5p
Chris Williams et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Ubiquitination of the peroxisomal import receptor Pex5p is required for its recycling
Harald W. Platta et al.
JOURNAL OF CELL BIOLOGY (2007)
Peroxisomal matrix protein receptor ubiquitination and recycling
Sven Thoms et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2006)
Peroxisome biogenesis disorders
Steven J. Steinberg et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2006)
Peroxisomes and oxidative stress
Michael Schrader et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2006)
Dynamics of the peroxisomal import cycle of PpPex20p:: ubiquitin-dependent localization and regulation
S Léon et al.
JOURNAL OF CELL BIOLOGY (2006)
TRIM37 defective in mulibrey nanism is a novel RING finger ubiquitin E3 ligase
J Kallijärvi et al.
EXPERIMENTAL CELL RESEARCH (2005)
Ubiquitination of the peroxisomal targeting signal type 1 receptor, Pex5p, suggests the presence of a quality control mechanism during peroxisomal matrix protein import
JAKW Kiel et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Mulibrey nanism: clinical features and diagnostic criteria
N Karlberg et al.
JOURNAL OF MEDICAL GENETICS (2004)
A novel splice site mutation in the TRIM37 gene causes Mulibrey Nanism iin a Turkish family with phenotypic heterogeneity
P Jagiello et al.
HUMAN MUTATION (2003)
Intracellular localization of proteasomes
C Wójcik et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2003)
The TRIM37 gene encodes a peroxisomal RING-B-box-coiled-coil protein:: Classification of mulibrey nanism as a new peroxisomal disorder
J Kallijärvi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
The di-aromatic pentapeptide repeats of the human peroxisome import receptor PEX5 are separate high affinity binding sites for the peroxisomal membrane protein PEX14
J Saidowsky et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p•PTS2 protein complex into peroxisomes via its initial docking site, Pex14p
H Otera et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism
K Avela et al.
NATURE GENETICS (2000)