Unbinding of alpha chain of hemoglobin in sickle and normal structures
Sickle cell disease, a genetic disorder, is caused by a mutation of glutamic acid into valine in β chain of hemoglobin at the sixth residue, resulting in structural change of the entire hemoglobin molecule into a sickle shape. We investigated the atomic level interaction between the α chain (chain A...
Guardado en:
| Autores principales: | , , |
|---|---|
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
IOP Publishing
2025-01-01
|
| Colección: | Journal of Physics Communications |
| Materias: | |
| Acceso en línea: | https://doi.org/10.1088/2399-6528/ada985 |
| Etiquetas: |
Sin Etiquetas, Sea el primero en etiquetar este registro!
|