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8CE0

N-terminal domain of human apolipoprotein E

Summary for 8CE0
Entry DOI10.2210/pdb8ce0/pdb
DescriptorMaltodextrin-binding protein,Apolipoprotein E, GLYCEROL (3 entities in total)
Functional Keywordsapolipoprotein e, n-terminal domain, lipid transport
Biological sourceEscherichia coli
More
Total number of polymer chains1
Total formula weight75209.97
Authors
Marek, M.,Nemergut, M. (deposition date: 2023-02-01, release date: 2023-07-19, Last modification date: 2024-06-19)
Primary citationNemergut, M.,Marques, S.M.,Uhrik, L.,Vanova, T.,Nezvedova, M.,Gadara, D.C.,Jha, D.,Tulis, J.,Novakova, V.,Planas-Iglesias, J.,Kunka, A.,Legrand, A.,Hribkova, H.,Pospisilova, V.,Sedmik, J.,Raska, J.,Prokop, Z.,Damborsky, J.,Bohaciakova, D.,Spacil, Z.,Hernychova, L.,Bednar, D.,Marek, M.
Domino-like effect of C112R mutation on ApoE4 aggregation and its reduction by Alzheimer's Disease drug candidate.
Mol Neurodegener, 18:38-38, 2023
Cited by
PubMed Abstract: Apolipoprotein E (ApoE) ε4 genotype is the most prevalent risk factor for late-onset Alzheimer's Disease (AD). Although ApoE4 differs from its non-pathological ApoE3 isoform only by the C112R mutation, the molecular mechanism of its proteinopathy is unknown.
PubMed: 37280636
DOI: 10.1186/s13024-023-00620-9
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.75 Å)
Structure validation

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