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Side-chains:
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NOEs:
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Structure from NMR restraints:
Ab initio:
GeNMR
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Flexibility from chemical shifts:
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Chemical shifts re-referencing:
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Flexibility from structure:
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Molecular dynamics:
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Chemical shifts prediction:
From structure:
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CheShift-2- Cα
From sequence:
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Disordered proteins:
MAXOCC
Format conversion & validation:
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From NMR-STAR 3.1
Validate NMR-STAR 3.1
NMR sample preparation:
Protein disorder:
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Protein solubility:
camLILA
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Isotope labeling:
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Solid-state NMR:
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Old 05-09-2018, 03:14 PM
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Default X-ray laser opens new view on Alzheimer's proteins - EurekAlert (press release)

X-ray laser opens new view on Alzheimer's proteins - EurekAlert (press release)



X-ray laser opens new view on Alzheimer's proteins
EurekAlert (press release)
"A major part of our understanding about amyloid fibrils is derived from nuclear magnetic resonance (NMR) and cryo-electron microscopy data," explains Seuring. "When you are working with samples that are as heterogeneous as amyloids, though, and also ...


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