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Chemical shift assignments for the parallel in-register D23N Iowa Mutant Beta Amyloid Fibrils
Authors
Sgourakis, N., Qiang, W.
Assembly
D23N parallel
Entity
1. D23N parallel (polymer, Thiol state: not present), 26 monomers, 2648.126 Da Detail

QKLVFFAENV GSNKGAIIGL MVGGVV


Formula weight
2648.126 Da
Source organism
Homo sapiens
Exptl. method
NMR
Refine. method
Rosetta refinement
Data set
assigned_chemical_shifts
Chem. Shift Complete
Sequence coverage: 80.8 %, Completeness: 51.3 %, Completeness (bb): 78.1 % Detail

Polymer type: polypeptide(L)

Total13C
All51.3 % (59 of 115)51.3 % (59 of 115)
Backbone78.1 % (57 of 73)78.1 % (57 of 73)
Sidechain30.2 % (19 of 63)30.2 % (19 of 63)
Aromatic 0.0 % (0 of 10) 0.0 % (0 of 10)
Methyl20.0 % (4 of 20)20.0 % (4 of 20)

1. D23N Abeta

QKLVFFAENV GSNKGAIIGL MVGGVV

Sample

Solvent system solid, Temperature 298 K, pH 7.4


#NameIsotope labelingTypeConcentration
1D23N_Abeta[U-100% 13C; U-100% 15N]25.0 ~ 100.0 uM

Protein Blocks Logo
Calculated from 5 models in PDB: 2MPZ, Strand ID: A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X, Y, Z Detail


Release date
2015-04-19
Citation
Modeling an in-register, parallel "iowa" aβ fibril structure using solid-state NMR data from labeled samples with rosetta
Sgourakis, N., Yau, W., Qiang, W.
Structure (2015), 23, 216-227, PubMed 25543257 , DOI 10.1016/j.str.2014.10.022 ,
Related entities 1. D23N parallel, : 1 : 1 : 88 : 16 entities Detail
Interaction partners 1. D23N parallel, : 2 interactors Detail
Experiments performed 3 experiments Detail
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