Cargando…
The Role of Protein Denaturation Energetics and Molecular Chaperones in the Aggregation and Mistargeting of Mutants Causing Primary Hyperoxaluria Type I
Primary hyperoxaluria type I (PH1) is a conformational disease which result in the loss of alanine:glyoxylate aminotransferase (AGT) function. The study of AGT has important implications for protein folding and trafficking because PH1 mutants may cause protein aggregation and mitochondrial mistarget...
Autores principales: | Mesa-Torres, Noel, Fabelo-Rosa, Israel, Riverol, Debora, Yunta, Cristina, Albert, Armando, Salido, Eduardo, Pey, Angel L. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3796444/ https://www.ncbi.nlm.nih.gov/pubmed/24205397 http://dx.doi.org/10.1371/journal.pone.0071963 |
Ejemplares similares
-
Molecular Recognition of PTS-1 Cargo Proteins by Pex5p: Implications for Protein Mistargeting in Primary Hyperoxaluria
por: Mesa-Torres, Noel, et al.
Publicado: (2015) -
Protein Homeostasis Defects of Alanine-Glyoxylate Aminotransferase: New Therapeutic Strategies in Primary Hyperoxaluria Type I
por: Pey, Angel L., et al.
Publicado: (2013) -
Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1
Publicado: (1990) -
Phosphorylation of Thr9 Affects the Folding Landscape of the N-Terminal Segment of Human AGT Enhancing Protein Aggregation of Disease-Causing Mutants
por: Neira, Jose L., et al.
Publicado: (2022) -
Inhibition of alanine:glyoxylate aminotransferase 1 dimerization is a
prerequisite for its peroxisome-to-mitochondrion mistargeting in primary
hyperoxaluria type 1
Publicado: (1996)