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9ERO

CTE type III tau filament from vacuolar tauopathy

Summary for 9ERO
Entry DOI10.2210/pdb9ero/pdb
Related9ERM
EMDB information19928
DescriptorMicrotubule-associated protein tau (1 entity in total)
Functional Keywordstau filament, cte type iii, vacuolar tauopathy, protein fibril
Biological sourceHomo sapiens (human)
Total number of polymer chains10
Total formula weight459198.71
Authors
Qi, C.,Scheres, H.W.S.,Goedert, M. (deposition date: 2024-03-24, release date: 2024-05-29, Last modification date: 2024-07-24)
Primary citationQi, C.,Kobayashi, R.,Kawakatsu, S.,Kametani, F.,Scheres, S.H.W.,Goedert, M.,Hasegawa, M.
Tau filaments with the chronic traumatic encephalopathy fold in a case of vacuolar tauopathy with VCP mutation D395G.
Acta Neuropathol, 147:86-86, 2024
Cited by
PubMed Abstract: Dominantly inherited mutation D395G in the gene encoding valosin-containing protein causes vacuolar tauopathy, a type of behavioural-variant frontotemporal dementia, with marked vacuolation and abundant filamentous tau inclusions made of all six brain isoforms. Here we report that tau inclusions were concentrated in layers II/III of the frontotemporal cortex in a case of vacuolar tauopathy. By electron cryomicroscopy, tau filaments had the chronic traumatic encephalopathy (CTE) fold. Tau inclusions of vacuolar tauopathy share this cortical location and the tau fold with CTE, subacute sclerosing panencephalitis and amyotrophic lateral sclerosis/parkinsonism-dementia complex, which are believed to be environmentally induced. Vacuolar tauopathy is the first inherited disease with the CTE tau fold.
PubMed: 38758288
DOI: 10.1007/s00401-024-02741-x
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.9 Å)
Structure validation

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