In sickle cell hemoglobin (HbS) glutamic acid in position 6 (in beta chain) is mutated to valine. This change allows the deoxygenated form of the hemoglobin to stick to each other as seen (PDB entry=2hbs) more details...
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2006-07-16T19:35:57Z Giac83 272x600 (107934 Bytes) {{Information| |Description=In sickle cell hemoglobin (HbS) glutamic acid in position 6 (in beta chain) is mutated to valine. This change allows the deoxygenated form of the hemoglobin to stick to each other as seen (PDB entr
{{Information |Description=In sickle cell hemoglobin (HbS) glutamic acid in position 6 (in beta chain) is mutated to valine. This change allows the deoxygenated form of the hemoglobin to stick to each other as seen (PDB entry=2hbs) [http://www.pdb.org/pdb
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