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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR16249
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
XML gzip file.
RDF gzip file.
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Citation: Hagn, Franz; Eisoldt, Lukas; Hardy, John; Vendrely, Charlotte; Coles, Murray; Scheibel, Thomas; Kessler, Horst. "A conserved spider silk domain acts as a molecular switch that controls fibre assembly." Nature 465, 239-242 (2010).
PubMed: 20463741
Assembly members:
NR3, polymer, 140 residues, 13329.825 Da.
Natural source: Common Name: spiders Taxonomy ID: 45920 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Araneus Diadematus
Experimental source: Production method: recombinant technology Host organism: Escherichia coli Vector: pET28a
Data type | Count |
13C chemical shifts | 517 |
15N chemical shifts | 148 |
1H chemical shifts | 860 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | NR3,chain_1 | 1 |
2 | NR3,chain_2 | 1 |
Entity 1, NR3,chain_1 140 residues - 13329.825 Da.
1 | MET | ALA | SER | MET | THR | GLY | GLY | GLN | GLN | MET | |
2 | GLY | ARG | GLY | SER | MET | GLY | ALA | ALA | SER | ALA | |
3 | ALA | VAL | SER | VAL | GLY | GLY | TYR | GLY | PRO | GLN | |
4 | SER | SER | SER | ALA | PRO | VAL | ALA | SER | ALA | ALA | |
5 | ALA | SER | ARG | LEU | SER | SER | PRO | ALA | ALA | SER | |
6 | SER | ARG | VAL | SER | SER | ALA | VAL | SER | SER | LEU | |
7 | VAL | SER | SER | GLY | PRO | THR | ASN | GLN | ALA | ALA | |
8 | LEU | SER | ASN | THR | ILE | SER | SER | VAL | VAL | SER | |
9 | GLN | VAL | SER | ALA | SER | ASN | PRO | GLY | LEU | SER | |
10 | GLY | CYS | ASP | VAL | LEU | VAL | GLN | ALA | LEU | LEU | |
11 | GLU | VAL | VAL | SER | ALA | LEU | VAL | SER | ILE | LEU | |
12 | GLY | SER | SER | SER | ILE | GLY | GLN | ILE | ASN | TYR | |
13 | GLY | ALA | SER | ALA | GLN | TYR | THR | GLN | MET | VAL | |
14 | GLY | GLN | SER | VAL | ALA | GLN | ALA | LEU | ALA | GLY |
sample_1: NR3, [U-99% 13C; U-99% 15N], 1 mM; sodium phosphate 10 mM; trifluoroethanol 1%; H2O 95%; D2O 5%
sample_2: NR30.6 1 mM; H2O 95%; D2O 5%
sample_3: NR3, [U-99% 13C; U-99% 15N], 1 mM; NR3 1 mM; H2O 95%; D2O 5%
sample_4: NR3, [U-99% 15N], 0.2 1 mM; H2O 95%; D2O 5%
sample_conditions_1: ionic strength: 0.02 M; pH: 6.0; pressure: 1 atm; temperature: 298 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_4 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D HNCA | sample_1 | isotropic | sample_conditions_1 |
3D HNCACB | sample_1 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HN(CO)CA | sample_1 | isotropic | sample_conditions_1 |
3D HN(CA)CO | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
3D HNHA | sample_4 | isotropic | sample_conditions_1 |
3D HNHB | sample_4 | isotropic | sample_conditions_1 |
3D CCH-COSY | sample_1 | isotropic | sample_conditions_1 |
3D C(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_4 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_1 | isotropic | sample_conditions_1 |
3D CNH NOESY | sample_1 | isotropic | sample_conditions_1 |
3D NNH NOESY | sample_4 | isotropic | sample_conditions_1 |
3D CCH NOESY | sample_1 | isotropic | sample_conditions_1 |
2D 1H-1H NOESY | sample_2 | isotropic | sample_conditions_1 |
filtered NOESY | sample_3 | isotropic | sample_conditions_1 |
TOPSPIN v1.3, Bruker Biospin - processing
SPARKY v3.11, Goddard - peak picking
PASTA v0.1, Kessler and Gemmecker - chemical shift assignment
TALOS v9.4, Cornilescu, Delaglio and Bax - data analysis
X-PLOR NIH, Schwieters, Kuszewski, Tjandra and Clore - structure solution
ProcheckNMR, Laskowski and MacArthur - data analysis
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