Cargando…
Structural study of the G57W mutant of human gamma-S-crystallin, associated with congenital cataract
PURPOSE: Human γS-crystallin (CrygS) is an important component of the human eye lens nucleus and cortex. The mutation G57W in the molecule is reported to be associated with congenital cataract in children. We compare the conformational features and aggregation properties of the mutant protein G57W w...
Autores principales: | Khan, Ismail, Chandani, Sushil, Balasubramanian, Dorairajan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943855/ https://www.ncbi.nlm.nih.gov/pubmed/27440995 |
Ejemplares similares
-
The Mutation V42M Distorts the Compact Packing of the Human Gamma-S-Crystallin Molecule, Resulting in Congenital Cataract
por: Vendra, Venkata Pulla Rao, et al.
Publicado: (2012) -
Structural analysis of the mutant protein D26G of human γS-crystallin, associated with Coppock cataract
por: Karri, Srinivasu, et al.
Publicado: (2013) -
Structural and aggregation behavior of the human γD-crystallin mutant E107A, associated with congenital nuclear cataract
por: Vendra, Venkata Pulla Rao, et al.
Publicado: (2010) -
Structural Integrity of the Greek Key Motif in βγ-Crystallins Is Vital for Central Eye Lens Transparency
por: Vendra, Venkata Pulla Rao, et al.
Publicado: (2013) -
The genetic landscape of crystallins in congenital cataract
por: Berry, Vanita, et al.
Publicado: (2020)