Biochemistry of mammalian peroxisomes revisited

RJA Wanders, HR Waterham - Annu. Rev. Biochem., 2006 - annualreviews.org
In this review, we describe the current state of knowledge about the biochemistry of
mammalian peroxisomes, especially human peroxisomes. The identification and …

Distribution and physiology of ABC-type transporters contributing to multidrug resistance in bacteria

J Lubelski, WN Konings… - … and molecular biology …, 2007 - Am Soc Microbiol
Membrane proteins responsible for the active efflux of structurally and functionally unrelated
drugs were first characterized in higher eukaryotes. To date, a vast number of transporters …

Large‐scale mapping of human protein–protein interactions by mass spectrometry

RM Ewing, P Chu, F Elisma, H Li, P Taylor… - Molecular systems …, 2007 - embopress.org
Mapping protein–protein interactions is an invaluable tool for understanding protein
function. Here, we report the first large‐scale study of protein–protein interactions in human …

The Arabidopsis thaliana ABC protein superfamily, a complete inventory

R Sánchez-Fernández, TGE Davies… - Journal of Biological …, 2001 - ASBMB
We describe the first complete inventory of ATP-binding cassette (ABC) proteins from a
multicellular organism, the model plant Arabidopsis thaliana. By the application of several …

The Arabidopsis pxa1 Mutant Is Defective in an ATP-Binding Cassette Transporter-Like Protein Required for Peroxisomal Fatty Acid β-Oxidation

BK Zolman, ID Silva, B Bartel - Plant Physiology, 2001 - academic.oup.com
Peroxisomes are important organelles in plant metabolism, containing all the enzymes
required for fatty acid β-oxidation. More than 20 proteins are required for peroxisomal …

ABCD1 mutations and the X‐linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations

S Kemp, A Pujol, HR Waterham, BM Van Geel… - Human …, 2001 - Wiley Online Library
Abstract X‐linked adrenoleukodystrophy (X‐ALD) is caused by mutations in the ABCD1
gene, which encodes a peroxisomal ABC half‐transporter (ALDP) involved in the import of …

[HTML][HTML] Coexpression of ATP-binding cassette proteins ABCG5 and ABCG8 permits their transport to the apical surface

GA Graf, WP Li, RD Gerard, I Gelissen… - The Journal of …, 2002 - Am Soc Clin Investig
Mutations in either ATP-binding cassette (ABC) G5 or ABCG8 cause sitosterolemia, an
autosomal recessive disorder of sterol trafficking. To determine the site of action of ABCG5 …

Role of ATP‐binding cassette transporters in brain lipid transport and neurological disease

WS Kim, CS Weickert, B Garner - Journal of neurochemistry, 2008 - Wiley Online Library
The brain is lipid‐rich compared to other organs and although previous studies have
highlighted the importance of ATP‐binding cassette (ABC) transporters in the regulation of …

The genetic landscape of X-linked adrenoleukodystrophy: inheritance, mutations, modifier genes, and diagnosis

C Wiesinger, FS Eichler, J Berger - The application of clinical …, 2015 - Taylor & Francis
X-linked adrenoleukodystrophy (X-ALD) is caused by mutations in the ABCD1 gene
encoding a peroxisomal ABC transporter. In this review, we compare estimates of incidence …

[HTML][HTML] Peroxisomal ABC transporters: structure, function and role in disease

M Morita, T Imanaka - Biochimica et Biophysica Acta (BBA)-Molecular Basis …, 2012 - Elsevier
ATP-binding cassette (ABC) transporters belong to one of the largest families of membrane
proteins, and are present in almost all living organisms from eubacteria to mammals. They …