BMRB Entry 25518
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                Entry in NMR Restraints Grid
                Validation report in NRG-CING
            Chem Shift validation:  AVS_full
BMRB Entry DOI: doi:10.13018/BMR25518
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Title: Atomic-resolution structure of alpha-synuclein fibrils PubMed: 27018801
Deposition date: 2015-03-04 Original release date: 2016-03-15
Authors: Tuttle, Marcus; Comellas, Gemma; Nieuwkoop, Andrew; Covell, Dustin; Berthold, Deborah; Kloepper, Kathryn; Courtney, Joseph; Kim, Jae; Schwieters, Charles; Lee, Virginia; George, Julia; Rienstra, Chad
Citation: Tuttle, Marcus; Comellas, Gemma; Nieuwkoop, Andrew; Covell, Dustin; Berthold, Deborah; Kloepper, Kathryn; Courtney, Joseph; Kim, Jae; Barclay, Alexander; Kendall, Amy; Wan, William; Stubbs, Gerald; Schwieters, Charles; Lee, Virginia; George, Julia; Rienstra, Chad. "Solid-state NMR structure of a pathogenic fibril of full-length human {alpha}-Synuclein" Nature Struc. Mol. Biol. 23, 409-415 (2016).
Assembly members:
alpha-synuclein, polymer, 140 residues,   14476.245 Da.
Natural source: Common Name: Human Taxonomy ID: 9606 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Homo sapiens
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
alpha-synuclein: MDVFMKGLSKAKEGVVAAAE
KTKQGVAEAAGKTKEGVLYV
GSKTKEGVVHGVATVAEKTK
EQVTNVGGAVVTGVTAVAQK
TVEGAGSIAAATGFVKKDQL
GKNEEGAPQEGILEDMPVDP
DNEAYEMPSEEGYQDYEPEA
- assigned_chemical_shifts
 
| Data type | Count | 
| 13C chemical shifts | 135 | 
| 15N chemical shifts | 39 | 
Additional metadata:
Assembly:
| Entity Assembly ID | Entity Name | Entity ID | 
|---|---|---|
| 1 | strand_1 | 1 | 
| 2 | strand_2 | 1 | 
| 3 | strand_3 | 1 | 
| 4 | strand_4 | 1 | 
| 5 | strand_5 | 1 | 
| 6 | strand_6 | 1 | 
| 7 | strand_7 | 1 | 
| 8 | strand_8 | 1 | 
| 9 | strand_9 | 1 | 
| 10 | strand_10 | 1 | 
Entities:
Entity 1, strand_1 140 residues - 14476.245 Da.
| 1 | MET | ASP | VAL | PHE | MET | LYS | GLY | LEU | SER | LYS | |
| 2 | ALA | LYS | GLU | GLY | VAL | VAL | ALA | ALA | ALA | GLU | |
| 3 | LYS | THR | LYS | GLN | GLY | VAL | ALA | GLU | ALA | ALA | |
| 4 | GLY | LYS | THR | LYS | GLU | GLY | VAL | LEU | TYR | VAL | |
| 5 | GLY | SER | LYS | THR | LYS | GLU | GLY | VAL | VAL | HIS | |
| 6 | GLY | VAL | ALA | THR | VAL | ALA | GLU | LYS | THR | LYS | |
| 7 | GLU | GLN | VAL | THR | ASN | VAL | GLY | GLY | ALA | VAL | |
| 8 | VAL | THR | GLY | VAL | THR | ALA | VAL | ALA | GLN | LYS | |
| 9 | THR | VAL | GLU | GLY | ALA | GLY | SER | ILE | ALA | ALA | |
| 10 | ALA | THR | GLY | PHE | VAL | LYS | LYS | ASP | GLN | LEU | |
| 11 | GLY | LYS | ASN | GLU | GLU | GLY | ALA | PRO | GLN | GLU | |
| 12 | GLY | ILE | LEU | GLU | ASP | MET | PRO | VAL | ASP | PRO | |
| 13 | ASP | ASN | GLU | ALA | TYR | GLU | MET | PRO | SER | GLU | |
| 14 | GLU | GLY | TYR | GLN | ASP | TYR | GLU | PRO | GLU | ALA | 
Samples:
sample_1: alpha-synuclein, [U-100% 13C; U-100% 15N], 66 % w/w; H2O 34 % w/w
sample_2: alpha-synuclein, [U-100% 13C 1,3-Glycerol; U-100% 15N], 66 % w/w; H2O 34 % w/w
sample_3: alpha-synuclein, [U-100% 13C 2-Glycerol; U-100% 15N], 66 % w/w; H2O 34 % w/w
sample_4: alpha-synuclein, [U-25% 13C; U-25% 15N], 66 % w/w; H2O 34 % w/w
sample_5: alpha-synuclein, [U-25% 13C 1,3-Glycerol; natural abundance N][natural abundance C13, U-50% N15], 66 % w/w; H2O 34 % w/w
sample_6: alpha-synuclein, [U-25% 13C 2-Glycerol; natural abundance N][natural abundance C13, U-50% N15], 66 % w/w; H2O 34 % w/w
Adamantane: Adamantane 90 % w/w; KBr 10 % w/w
sample_conditions_1: pH: 7; pressure: 1 atm; temperature controller setting: 273 K
Experiments:
| Name | Sample | Sample state | Sample conditions | 
|---|---|---|---|
| Cross Polarization C1D | Adamantane | solid | sample_conditions_1 | 
| 3D NCACX | sample_1 | solid | sample_conditions_1 | 
| 3D NCOCX | sample_1 | solid | sample_conditions_1 | 
| 3D CANCO | sample_1 | solid | sample_conditions_1 | 
| 2D CC DARR | sample_1 | solid | sample_conditions_1 | 
| 2D CC DARR | sample_2 | solid | sample_conditions_1 | 
| 3D NCOCX | sample_2 | solid | sample_conditions_1 | 
| 2D NC TEDOR | sample_2 | solid | sample_conditions_1 | 
| 2D CC DARR | sample_2 | solid | sample_conditions_1 | 
| 2D CC DARR | sample_2 | solid | sample_conditions_1 | 
| 3D NCOCX | sample_2 | solid | sample_conditions_1 | 
| 2D CC DARR | sample_3 | solid | sample_conditions_1 | 
| 3D NCACX | sample_3 | solid | sample_conditions_1 | 
| 2D CC DARR | sample_3 | solid | sample_conditions_1 | 
| 2D NC TEDOR | sample_3 | solid | sample_conditions_1 | 
| 2D CC DARR | sample_3 | solid | sample_conditions_1 | 
| 3D NCACX | sample_3 | solid | sample_conditions_1 | 
| 2D NC TEDOR | sample_4 | solid | sample_conditions_1 | 
| 2D NC TEDOR | sample_5 | solid | sample_conditions_1 | 
| 2D CC DARR | sample_6 | solid | sample_conditions_1 | 
| 2D ChhC | sample_6 | solid | sample_conditions_1 | 
Software:
X-PLOR_NIH v2.33.4, Schwieters, Kuszewski, Tjandra and Clore - geometry optimization, refinement, structure solution
SPARKY v3, T. D. Goddard and D. G. Kneller, SPARKY 3, University of California, San Francisco - data visualization, manual analysis
NMR spectrometers:
- Agilent VNMRS 750 MHz
 - Agilent InfinityPlus 600 MHz
 - Agilent VNMRS 500 MHz