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7DWV

Cryo-EM structure of amyloid fibril formed by familial prion disease-related mutation E196K

Summary for 7DWV
Entry DOI10.2210/pdb7dwv/pdb
EMDB information30887
DescriptorMajor prion protein (1 entity in total)
Functional Keywordsamyloid fibril, protein fibril
Biological sourceHomo sapiens (Human)
Total number of polymer chains6
Total formula weight137978.53
Authors
Primary citationWang, L.Q.,Zhao, K.,Yuan, H.Y.,Li, X.N.,Dang, H.B.,Ma, Y.,Wang, Q.,Wang, C.,Sun, Y.,Chen, J.,Li, D.,Zhang, D.,Yin, P.,Liu, C.,Liang, Y.
Genetic prion disease-related mutation E196K displays a novel amyloid fibril structure revealed by cryo-EM.
Sci Adv, 7:eabg9676-eabg9676, 2021
Cited by
PubMed: 34516876
DOI: 10.1126/sciadv.abg9676
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.07 Å)
Structure validation

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