BMRB Entry 16032
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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/BMR16032
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Title: Nav1.2 C-terminal EF-Hand Domain PubMed: 19129176
Deposition date: 2008-11-15 Original release date: 2009-01-20
Authors: Miloushev, Vesselin; Levine, Joshua; Arbing, Mark; Hunt, John; Pitt, Geoff; Palmer, Arthur
Citation: Miloushev, Vesselin; Levine, Joshua; Arbing, Mark; Hunt, John; Pitt, Geoff; Palmer, Arthur. "Solution structure of the NaV1.2 C-terminal EF-hand domain." J. Biol. Chem. 284, 6446-6454 (2009).
Assembly members:
NaV1.2 C-terminal EF-hand domain, polymer, 129 residues, 12130.777 Da.
Natural source: Common Name: Humans Taxonomy ID: 9606 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Homo sapiens
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
NaV1.2 C-terminal EF-hand domain: MGSSHHHHHHSSGLVPRGSH
MASENFSVATEESAEPLSED
DFEMFYEVWEKFDPDATQFI
EFAKLSDFADALDPPLLIAK
PNKVQLIAMDLPMVSGDRIH
CLDILFAFTKRVLGESGEMD
ALRIQMEER
- assigned_chemical_shifts
- conformer_family_coord_set
Data type | Count |
13C chemical shifts | 344 |
15N chemical shifts | 101 |
1H chemical shifts | 751 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | NaV1.2 C-terminal EF-hand domain | 1 |
Entities:
Entity 1, NaV1.2 C-terminal EF-hand domain 129 residues - 12130.777 Da.
1 | MET | GLY | SER | SER | HIS | HIS | HIS | HIS | HIS | HIS | ||||
2 | SER | SER | GLY | LEU | VAL | PRO | ARG | GLY | SER | HIS | ||||
3 | MET | ALA | SER | GLU | ASN | PHE | SER | VAL | ALA | THR | ||||
4 | GLU | GLU | SER | ALA | GLU | PRO | LEU | SER | GLU | ASP | ||||
5 | ASP | PHE | GLU | MET | PHE | TYR | GLU | VAL | TRP | GLU | ||||
6 | LYS | PHE | ASP | PRO | ASP | ALA | THR | GLN | PHE | ILE | ||||
7 | GLU | PHE | ALA | LYS | LEU | SER | ASP | PHE | ALA | ASP | ||||
8 | ALA | LEU | ASP | PRO | PRO | LEU | LEU | ILE | ALA | LYS | ||||
9 | PRO | ASN | LYS | VAL | GLN | LEU | ILE | ALA | MET | ASP | ||||
10 | LEU | PRO | MET | VAL | SER | GLY | ASP | ARG | ILE | HIS | ||||
11 | CYS | LEU | ASP | ILE | LEU | PHE | ALA | PHE | THR | LYS | ||||
12 | ARG | VAL | LEU | GLY | GLU | SER | GLY | GLU | MET | ASP | ||||
13 | ALA | LEU | ARG | ILE | GLN | MET | GLU | GLU | ARG |
Samples:
13C-15N: entity, [U-99% 13C; U-99% 15N], 0.5 ± 0.05 mM; glycine, [D5-98%], 100 ± 10 mM; TRIS, [D11-98 %], 20 ± 2 mM; EDTA, [D16-98%], 0.1 ± 0.01 mM; D2O, [U-99% 2H], 10 ± 1 %; DTT, [D10-98%], 1 ± 0.1 mM; NaN3 0.02 ± 0.002 %
10%13-C: entity, [U-10% 13C; U-99% 15N], 0.5 ± 0.05 mM; glycine, [D5-98%], 100 ± 10 mM; TRIS, [D11-98 %], 20 ± 2 mM; EDTA, [D16-98%], 0.1 ± 0.01 mM; D2O, [U-99% 2H], 10 ± 1 %; DTT, [D10-98%], 1 ± 0.1 mM; NaN3 0.02 ± 0.002 %
phage: entity, [U-99% 13C; U-99% 15N], 0.5 ± 0.05 mM; glycine, [D5-98%], 100 ± 10 mM; TRIS, [D11-98 %], 20 ± 2 mM; EDTA, [D16-98%], 0.1 ± 0.01 mM; D2O, [U-99% 2H], 10 ± 1 %; DTT, [D10-98%], 1 ± 0.1 mM; NaN3 0.02 ± 0.002 %; pF1 phage 15 ± 1 mg
sample_conditions: ionic strength: 0.1 M; pH: 7.4; pressure: 1.0 atm; temperature: 290.5 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
3D HNCO | 13C-15N | isotropic | sample_conditions |
3D HNCA | 13C-15N | isotropic | sample_conditions |
3D HN(CO)CA | 13C-15N | isotropic | sample_conditions |
3D HN(CA)CO | 13C-15N | isotropic | sample_conditions |
3D HNCACB | 13C-15N | isotropic | sample_conditions |
3D CBCA(CO)NH | 13C-15N | isotropic | sample_conditions |
3D HCCH-TOCSY | 13C-15N | isotropic | sample_conditions |
3D HBHA(CO)NH | 13C-15N | isotropic | sample_conditions |
3D 1H-15N NOESY | 13C-15N | isotropic | sample_conditions |
3D 1H-13C NOESY | 13C-15N | isotropic | sample_conditions |
2D 1H-13C HSQC | 10%13-C | isotropic | sample_conditions |
3D HCACO | phage | anisotropic | sample_conditions |
2D IPAP HSQC | phage | anisotropic | sample_conditions |
3D quant HNCO | phage | anisotropic | sample_conditions |
3D CCa HNCO | phage | anisotropic | sample_conditions |
Software:
NMRPipe v2.4, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
SPARKY v3.110, Goddard - chemical shift assignment, peak picking
ARIA v2.2, Linge, O, . - initial structure solution
CNS v1.2, Brunger, Adams, Clore, Gros, Nilges and Read - initial structure solution
X-PLOR NIH v2.18, Schwieters, Kuszewski, Tjandra and Clore - refinement, structure solution
NMR spectrometers:
- Bruker DRX 600 MHz
- Bruker Avance 600 MHz
- Bruker Avance 800 MHz
- Bruker Avance 700 MHz
Related Database Links:
PDB | |
DBJ | BAA92594 BAC27748 BAC30078 BAG63295 BAK62861 |
EMBL | CAA27287 CAA46438 CAA68735 CAB85895 |
GB | AAA18895 AAA67695 AAB22226 AAG53412 AAG53413 |
PIR | S29185 |
PRF | 1204264B |
REF | NP_001035232 NP_001035233 NP_001075145 NP_001075146 NP_001092768 |
SP | P04775 P08104 Q99250 Q9NY46 |
TPG | DAA32692 DAA32708 DAA32709 DAA32710 DAA32711 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts