Cargando…
Analysis of the dominant mutation N188T of human connexin46 (hCx46) using concatenation and molecular dynamics simulation
Connexins (Cx) are proteins that form cell‐to‐cell gap junction channels. A mutation at position 188 in the second extracellular loop (E2) domain of hCx46 has been linked to an autosomal dominant zonular pulverulent cataract. As it is dominantly inherited, it is possible that the mutant variant affe...
Autores principales: | Schadzek, Patrik, Stahl, Yannick, Preller, Matthias, Ngezahayo, Anaclet |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487695/ https://www.ncbi.nlm.nih.gov/pubmed/31034164 http://dx.doi.org/10.1002/2211-5463.12624 |
Ejemplares similares
-
Concatenation of Human Connexin26 (hCx26) and Human Connexin46 (hCx46) for the Analysis of Heteromeric Gap Junction Hemichannels and Heterotypic Gap Junction Channels
por: Schadzek, Patrik, et al.
Publicado: (2018) -
Data of the molecular dynamics simulations of mutations in the human connexin46 docking interface
por: Schadzek, Patrik, et al.
Publicado: (2016) -
Mutations of CX46/CX50 and Cataract Development
por: Shi, Yumeng, et al.
Publicado: (2022) -
The Connexin46 Mutant, Cx46T19M, Causes Loss of Gap Junction Function and Alters Hemi-channel Gating
por: Tong, Jun-Jie, et al.
Publicado: (2014) -
The Bioactive Phenolic Agents Diaryl Ether CVB2-61 and Diarylheptanoid CVB4-57 as Connexin Hemichannel Blockers
por: Dierks, Anne, et al.
Publicado: (2022)