Matches in SemOpenAlex for { <https://semopenalex.org/work/W2114804988> ?p ?o ?g. }
- W2114804988 endingPage "e104892" @default.
- W2114804988 startingPage "e104892" @default.
- W2114804988 abstract "The peroxisome is a single membrane-bound organelle in eukaryotic cells involved in lipid metabolism, including β-oxidation of fatty acids. The human genetic disorder X-linked adrenoleukodystrophy (X-ALD) is caused by mutations in the ABCD1 gene (encoding ALDP, a peroxisomal half ATP-binding cassette [ABC] transporter). This disease is characterized by defective peroxisomal β-oxidation and a large accumulation of very long-chain fatty acids in brain white matter, adrenal cortex, and testis. ALDP forms a homodimer proposed to be the functional transporter, whereas the peroxisomal transporter in yeast is a heterodimer comprising two half ABC transporters, Pxa1p and Pxa2p, both orthologs of human ALDP. While the carboxyl-terminal domain of ALDP is engaged in dimerization, it remains unknown whether the same region is involved in the interaction between Pxa1p and Pxa2p.Using a yeast two-hybrid assay, we found that the carboxyl-terminal region (CT) of Pxa2p, but not of Pxa1p, is required for their interaction. Further analysis indicated that the central part of the CT (designated CT2) of Pxa2p was indispensable for its interaction with the carboxyl terminally truncated Pxa1_NBD. An interaction between the CT of Pxa2p and Pxa1_NBD was not detected, but could be identified in the presence of Pxa2_NBD-CT1. A single mutation of two conserved residues (aligned with X-ALD-associated mutations at the same positions in ALDP) in the CT2 of the Pxa2_NBD-CT protein impaired its interaction with Pxa1_NBD or Pxa1_NBD-CT, resulting in a mutant protein that exhibited a proteinase K digestion profile different from that of the wild-type protein. Functional analysis of these mutant proteins on oleate plates indicated that they were defective in transporter function.The CT of Pxa2p is involved in its interaction with Pxa1p and in transporter function. This concept may be applied to human ALDP studies, helping to establish the pathological mechanism for CT-related X-ALD disease." @default.
- W2114804988 created "2016-06-24" @default.
- W2114804988 creator A5006291512 @default.
- W2114804988 creator A5012108080 @default.
- W2114804988 creator A5020098702 @default.
- W2114804988 creator A5031827088 @default.
- W2114804988 creator A5038844374 @default.
- W2114804988 creator A5042301785 @default.
- W2114804988 creator A5048989549 @default.
- W2114804988 creator A5064485654 @default.
- W2114804988 creator A5068688460 @default.
- W2114804988 creator A5079171500 @default.
- W2114804988 date "2014-08-13" @default.
- W2114804988 modified "2023-09-27" @default.
- W2114804988 title "Involvement of the Carboxyl-Terminal Region of the Yeast Peroxisomal Half ABC Transporter Pxa2p in Its Interaction with Pxa1p and in Transporter Function" @default.
- W2114804988 cites W1481406810 @default.
- W2114804988 cites W1509620090 @default.
- W2114804988 cites W1536843212 @default.
- W2114804988 cites W1565953788 @default.
- W2114804988 cites W1971007745 @default.
- W2114804988 cites W1982619578 @default.
- W2114804988 cites W1984048380 @default.
- W2114804988 cites W1986555537 @default.
- W2114804988 cites W1986865985 @default.
- W2114804988 cites W1988695766 @default.
- W2114804988 cites W2002602955 @default.
- W2114804988 cites W2004844038 @default.
- W2114804988 cites W2015577087 @default.
- W2114804988 cites W2022976733 @default.
- W2114804988 cites W2023549144 @default.
- W2114804988 cites W2030756202 @default.
- W2114804988 cites W2033349405 @default.
- W2114804988 cites W2035506170 @default.
- W2114804988 cites W2036885100 @default.
- W2114804988 cites W2037167329 @default.
- W2114804988 cites W2049478377 @default.
- W2114804988 cites W2051608947 @default.
- W2114804988 cites W2053710923 @default.
- W2114804988 cites W2055737079 @default.
- W2114804988 cites W2072956699 @default.
- W2114804988 cites W2073606421 @default.
- W2114804988 cites W2073937441 @default.
- W2114804988 cites W2079075112 @default.
- W2114804988 cites W2082383568 @default.
- W2114804988 cites W2085894877 @default.
- W2114804988 cites W2098906256 @default.
- W2114804988 cites W2101641567 @default.
- W2114804988 cites W2107208925 @default.
- W2114804988 cites W2124230153 @default.
- W2114804988 cites W2135192677 @default.
- W2114804988 cites W2138878645 @default.
- W2114804988 cites W2148385659 @default.
- W2114804988 cites W2154631064 @default.
- W2114804988 cites W2157541965 @default.
- W2114804988 cites W2167246280 @default.
- W2114804988 cites W4233807360 @default.
- W2114804988 doi "https://doi.org/10.1371/journal.pone.0104892" @default.
- W2114804988 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4132065" @default.
- W2114804988 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25118695" @default.
- W2114804988 hasPublicationYear "2014" @default.
- W2114804988 type Work @default.
- W2114804988 sameAs 2114804988 @default.
- W2114804988 citedByCount "6" @default.
- W2114804988 countsByYear W21148049882015 @default.
- W2114804988 countsByYear W21148049882016 @default.
- W2114804988 countsByYear W21148049882017 @default.
- W2114804988 countsByYear W21148049882019 @default.
- W2114804988 countsByYear W21148049882021 @default.
- W2114804988 crossrefType "journal-article" @default.
- W2114804988 hasAuthorship W2114804988A5006291512 @default.
- W2114804988 hasAuthorship W2114804988A5012108080 @default.
- W2114804988 hasAuthorship W2114804988A5020098702 @default.
- W2114804988 hasAuthorship W2114804988A5031827088 @default.
- W2114804988 hasAuthorship W2114804988A5038844374 @default.
- W2114804988 hasAuthorship W2114804988A5042301785 @default.
- W2114804988 hasAuthorship W2114804988A5048989549 @default.
- W2114804988 hasAuthorship W2114804988A5064485654 @default.
- W2114804988 hasAuthorship W2114804988A5068688460 @default.
- W2114804988 hasAuthorship W2114804988A5079171500 @default.
- W2114804988 hasBestOaLocation W21148049881 @default.
- W2114804988 hasConcept C104317684 @default.
- W2114804988 hasConcept C127078168 @default.
- W2114804988 hasConcept C143065580 @default.
- W2114804988 hasConcept C149011108 @default.
- W2114804988 hasConcept C185592680 @default.
- W2114804988 hasConcept C205668238 @default.
- W2114804988 hasConcept C2777150068 @default.
- W2114804988 hasConcept C2779222958 @default.
- W2114804988 hasConcept C44312359 @default.
- W2114804988 hasConcept C501734568 @default.
- W2114804988 hasConcept C55493867 @default.
- W2114804988 hasConcept C86803240 @default.
- W2114804988 hasConceptScore W2114804988C104317684 @default.
- W2114804988 hasConceptScore W2114804988C127078168 @default.
- W2114804988 hasConceptScore W2114804988C143065580 @default.
- W2114804988 hasConceptScore W2114804988C149011108 @default.
- W2114804988 hasConceptScore W2114804988C185592680 @default.
- W2114804988 hasConceptScore W2114804988C205668238 @default.