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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, LACS, SPARTA
BMRB Entry DOI: doi:10.13018/BMR25685
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
XML gzip file.
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Citation: Williamson, Jessica; Cho, Seung-Hyung; Ye, Jiqing; Collet, Jean-Francois; Beckwith, Jonathan; Chou, James. "NMR Structure of the Transmembrane Electron Transporter CcdA" Nat. Struct. Biol. ., .-..
Assembly members:
CcdA, polymer, 208 residues, 20955.492 Da.
Natural source: Common Name: euryarchaeotes Taxonomy ID: 2234 Superkingdom: Archaea Kingdom: not available Genus/species: Archaeoglobus fulgidus
Experimental source: Production method: recombinant technology Host organism: Escherichia coli Vector: pSC124
Data type | Count |
13C chemical shifts | 451 |
15N chemical shifts | 156 |
1H chemical shifts | 158 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | entity | 1 |
Entity 1, entity 208 residues - 20955.492 Da.
Residues 1-10 represent a non-native sequence left over from protease cleavage that removed the N-terminal DsbD fusion protein. The C-terminal HHHHHH is a non-native affinity tag used for purification.
1 | GLY | SER | THR | SER | GLN | GLU | GLN | PRO | THR | ALA | ||||
2 | GLN | LEU | MET | ALA | PHE | ALA | LEU | GLY | ILE | LEU | ||||
3 | SER | VAL | PHE | SER | PRO | ALA | VAL | LEU | PRO | VAL | ||||
4 | VAL | PRO | LEU | ILE | PHE | ALA | GLY | SER | ARG | GLY | ||||
5 | ARG | ALA | LEU | ASP | ALA | PHE | LEU | ILE | VAL | ALA | ||||
6 | GLY | LEU | THR | ILE | SER | MET | LEU | ILE | LEU | GLY | ||||
7 | TYR | THR | ALA | SER | LEU | PHE | PHE | GLY | PHE | PHE | ||||
8 | ARG | VAL | VAL | ALA | MET | LEU | PHE | LEU | LEU | ILE | ||||
9 | PHE | ALA | LEU | ILE | LEU | LEU | SER | ASP | GLU | LEU | ||||
10 | ASP | GLU | LYS | VAL | SER | ILE | PHE | ALA | SER | ARG | ||||
11 | MET | THR | SER | GLY | LEU | SER | TRP | LYS | ILE | GLN | ||||
12 | THR | LEU | PRO | SER | PHE | PHE | PHE | GLY | MET | LEU | ||||
13 | LEU | ALA | PHE | LEU | TRP | LEU | PRO | ALA | ILE | LEU | ||||
14 | PRO | PHE | ALA | GLY | ILE | ALA | ILE | SER | GLN | THR | ||||
15 | LEU | LEU | SER | GLU | ASN | PRO | LEU | VAL | MET | LEU | ||||
16 | SER | TYR | GLY | LEU | GLY | MET | ALA | VAL | THR | ILE | ||||
17 | ALA | ALA | VAL | PHE | LYS | MET | GLY | GLU | LYS | PHE | ||||
18 | VAL | LYS | ALA | ASN | PHE | GLN | LEU | ILE | ARG | LYS | ||||
19 | VAL | THR | GLY | ALA | ILE | VAL | LEU | LEU | TYR | LEU | ||||
20 | ALA | TYR | PHE | ALA | LEU | THR | GLU | VAL | LEU | LEU | ||||
21 | LEU | GLU | HIS | HIS | HIS | HIS | HIS | HIS |
sample_1: CcdA, [U-100% 13C; U-100% 15N; U-80% 2H], 0.8 ± 0.2 mM; MES 20 ± 1 mM; sodium chloride 50 ± 1 mM; dodecylphosphocholine 100 ± 10 mM; H2O 95%; D2O 5%
sample_2: CcdA, [U-100% 13C; U-100% 15N], 0.8 ± 0.2 mM; MES 20 ± 1 mM; sodium chloride 50 ± 1 mM; dodecylphosphocholine, [U-99% 2H], 100 ± 10 mM; H2O 95 ± 10 %; D2O 5 ± 10 %
sample_conditions_1: ionic strength: 0.15 M; pH: 6; pressure: 1 atm; temperature: 273 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N TROSY-HSQC | sample_1 | isotropic | sample_conditions_1 |
3D TROSY HNCA | sample_1 | isotropic | sample_conditions_1 |
3D TROSY HN(CO)CA | sample_1 | isotropic | sample_conditions_1 |
3D TROSY HN(CA)CO | sample_1 | isotropic | sample_conditions_1 |
3D TROSY HNCO | sample_1 | isotropic | sample_conditions_1 |
3D TROSY HNCACB | sample_1 | isotropic | sample_conditions_1 |
2D 1H-15N TROSY-HSQC | sample_2 | isotropic | sample_conditions_1 |
3D 15N-edited NOESY TROSY-HSQC (60 ms mix time) | sample_2 | isotropic | sample_conditions_1 |
3D 15N-edited NOESY TROSY-HSQC (120 ms mix time) | sample_2 | isotropic | sample_conditions_1 |
3D 13C-edited Methyl NOESY (150 ms mix time) | sample_2 | isotropic | sample_conditions_1 |
4D double 15N-edited NOESY (200 ms mix time) | sample_1 | isotropic | sample_conditions_1 |
X-PLOR_NIH v2.38, Schwieters, Kuszewski, Tjandra and Clore - refinement, structure solution
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - data analysis, processing
TOPSPIN v3.0, Bruker Biospin - collection
CCPNMR, CCPN - chemical shift assignment
XEASY, Bartels et al. - chemical shift assignment, data analysis
Download HSQC peak lists in one of the following formats:
CSV: Backbone
or all simulated peaks
SPARKY: Backbone
or all simulated peaks