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...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
IOP Publishing
2025-01-01
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| Series: | Journal of Physics Communications |
| Subjects: | |
| Online Access: | https://doi.org/10.1088/2399-6528/ada985 |
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