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...
Shranjeno v:
| Principais autores: | , , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
IOP Publishing
2025-01-01
|
| Serija: | Journal of Physics Communications |
| Teme: | |
| Online dostop: | https://doi.org/10.1088/2399-6528/ada985 |
| Oznake: |
Brez oznak, prvi označite!
|