Purification of a Recombinant Human PEX1/PEX6 AAA+ ATPase Complex from HEK293TT Cells
Author:
Publisher
Springer US
Link
https://link.springer.com/content/pdf/10.1007/978-1-0716-3048-8_25
Reference18 articles.
1. Pedrosa AG, Francisco T, Bicho D, Dias AF, Barros-Barbosa A, Hagmann V, Dodt G, Rodrigues TA, Azevedo JE (2018) Peroxisomal monoubiquitinated PEX5 interacts with the AAA ATPases PEX1 and PEX6 and is unfolded during its dislocation into the cytosol. J Biol Chem 293(29):11553–11563. https://doi.org/10.1074/jbc.RA118.003669
2. Francisco T, Rodrigues TA, Dias AF, Barros-Barbosa A, Bicho D, Azevedo JE (2017) Protein transport into peroxisomes: knowns and unknowns. BioEssays 39(10). https://doi.org/10.1002/bies.201700047
3. Argyriou C, D'Agostino MD, Braverman N (2016) Peroxisome biogenesis disorders. Transl Sci Rare Dis 1(2):111–144. https://doi.org/10.3233/TRD-160003
4. Ebberink MS, Mooijer PA, Gootjes J, Koster J, Wanders RJ, Waterham HR (2011) Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder. Hum Mutat 32(1):59–69. https://doi.org/10.1002/humu.21388
5. Waterham HR, Ebberink MS (2012) Genetics and molecular basis of human peroxisome biogenesis disorders. Biochim Biophys Acta 1822(9):1430–1441. https://doi.org/10.1016/j.bbadis.2012.04.006
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