k BSEcausing prion Prion protein. Computer model of the prion protein responsible for causing the diseases BSE bovine spongiform encephalopathy in cows and CJD CreutzfeldtJakob disease in humans. It is a mutated form of a normal cell protein PrP. This prion comprises spiralling alpha helices orange and straight beta sheets green. The C and N represent the carbon and nitrogen ends of the amino acid structure respectively. Both BSE and CJD are brainwasting disorders characterised by progressive dementia and a rapid deterioration in coordination, leading inevitably to death. Stock Photo - Afloimages
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BSE causing prion Prion protein. Computer model of the prion protein responsible for causing the diseases BSE  bovine spongiform encephalopathy  in cows and CJD  Creutzfeldt Jakob disease  in humans. It is a mutated form of a normal cell protein  PrP . This prion comprises spiralling alpha helices  orange  and straight beta sheets  green . The C and N represent the carbon and nitrogen ends of the amino acid structure respectively. Both BSE and CJD are brain wasting disorders characterised by progressive dementia and a rapid deterioration in co ordination, leading inevitably to death.
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BSE-causing prion

Prion protein. Computer model of the prion protein responsible for causing the diseases BSE (bovine spongiform encephalopathy) in cows and CJD (Creutzfeldt-Jakob disease) in humans. It is a mutated form of a normal cell protein (PrP). This prion comprises spiralling alpha helices (orange) and straight beta sheets (green). The C and N represent the carbon and nitrogen ends of the amino acid structure respectively. Both BSE and CJD are brain-wasting disorders characterised by progressive dementia and a rapid deterioration in co-ordination, leading inevitably to death.

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