Structure and mechanism of human ABC transporters

A Alam, KP Locher - Annual Review of Biophysics, 2023 - annualreviews.org
ABC transporters are essential for cellular physiology. Humans have 48 ABC genes
organized into seven distinct families. Of these genes, 44 (in five distinct families) encode for …

[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 …

Structural basis of substrate recognition and translocation by human very long-chain fatty acid transporter ABCD1

ZP Chen, D Xu, L Wang, YX Mao, Y Li… - Nature …, 2022 - nature.com
Human ABC transporter ABCD1 transports very long-chain fatty acids from cytosol to
peroxisome for β-oxidation, dysfunction of which usually causes the X-linked …

[HTML][HTML] The peroxisome: an update on mysteries

M Islinger, S Grille, HD Fahimi, M Schrader - Histochemistry and cell …, 2012 - Springer
Peroxisomes contribute to several crucial metabolic processes such as β-oxidation of fatty
acids, biosynthesis of ether phospholipids and metabolism of reactive oxygen species …

[HTML][HTML] Peroxisomal metabolite and cofactor transport in humans

S Chornyi, L IJlst, CWT van Roermund… - Frontiers in cell and …, 2021 - frontiersin.org
Peroxisomes are membrane-bound organelles involved in many metabolic pathways and
essential for human health. They harbor a large number of enzymes involved in the different …

Peroxisomal ABC transporters: an update

A Tawbeh, C Gondcaille, D Trompier… - International Journal of …, 2021 - mdpi.com
ATP-binding cassette (ABC) transporters constitute one of the largest superfamilies of
conserved proteins from bacteria to mammals. In humans, three members of this family are …

A novel bile acid biosynthesis defect due to a deficiency of peroxisomal ABCD3

S Ferdinandusse, G Jimenez-Sanchez… - Human molecular …, 2015 - academic.oup.com
ABCD3 is one of three ATP-binding cassette (ABC) transporters present in the peroxisomal
membrane catalyzing ATP-dependent transport of substrates for metabolic pathways …

The role of ELOVL1 in very long‐chain fatty acid homeostasis and X‐linked adrenoleukodystrophy

R Ofman, IME Dijkstra, CWT van Roermund… - EMBO molecular …, 2010 - embopress.org
Abstract X‐linked adrenoleukodystrophy (X‐ALD) is caused by mutations in the ABCD1
gene encoding the peroxisomal ABC transporter adrenoleukodystrophy protein (ALDP). X …

Differential substrate specificities of human ABCD1 and ABCD2 in peroxisomal fatty acid β-oxidation

CWT van Roermund, WF Visser, L IJlst… - … et Biophysica Acta (BBA …, 2011 - Elsevier
The gene mutated in X-linked adrenoleukodystrophy (X-ALD) codes for the HsABCD1
protein, also named ALDP, which is a member of the superfamily of ATP-binding cassette …

[HTML][HTML] Metabolic perturbations in pregnant rats exposed to low-dose perfluorooctanesulfonic acid: An integrated multi-omics analysis

G Yu, J Wang, Y Liu, T Luo, X Meng, R Zhang… - Environment …, 2023 - Elsevier
Emerging epidemiological evidence has linked per-and polyfluoroalkyl substances (PFAS)
exposure could be linked to the disturbance of gestational glucolipid metabolism, but the …