Cargando…
The Impairment of TorsinA's Binding to and Interactions With Its Activator: An Atomistic Molecular Dynamics Study of Primary Dystonia
Primary dystonia's prolonged muscle contractions and the associated abnormal postures and twisting movements remain incurable. Genetic mutation/deletion of GAG from TorsonA's gene resulting in ΔE303 (which weakens the binding between TorsinA and its activator, such as LULL1) primarily caus...
Autor principal: | Salawu, Emmanuel O. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048259/ https://www.ncbi.nlm.nih.gov/pubmed/30042949 http://dx.doi.org/10.3389/fmolb.2018.00064 |
Ejemplares similares
-
Resolving the TorsinA Oligomerization Conundrum: The Glycan Hypothesis
por: Fercher, Christian, et al.
Publicado: (2020) -
Structures of TorsinA and its disease-mutant complexed with an activator reveal the molecular basis for primary dystonia
por: Demircioglu, F Esra, et al.
Publicado: (2016) -
TorsinA and the TorsinA-Interacting Protein Printor Have No Impact on Endoplasmic Reticulum Stress or Protein Trafficking in Yeast
por: Valastyan, Julie S., et al.
Publicado: (2011) -
Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia
por: Pratt, Drew, et al.
Publicado: (2016) -
Intracellular complexes of the early-onset torsion dystonia-associated AAA+ ATPase TorsinA
por: Li, Hui, et al.
Publicado: (2014)