BMRB Entry 16278
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_anomalous, AVS_full
BMRB Entry DOI: doi:10.13018/BMR16278
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Title: NMR structure of the H103G mutant SO2144 H-NOX domain from Shewanella oneidensis in the Fe(II)CO ligation state PubMed: 19918063
Deposition date: 2009-05-06 Original release date: 2010-05-06
Authors: Erbil, William
Citation: Erbil, W. Kaya; Price, Mark; Wemmer, David; Marletta, Michael. "A structural basis for H-NOX signaling in Shewanella oneidensis by trapping a histidine kinase inhibitory conformation." Proc. Natl. Acad. Sci. U.S.A. 106, 19753-19760 (2009).
Assembly members:
SO2144, polymer, 181 residues, 20453.637 Da.
CMO, non-polymer, 28.010 Da.
HEM, non-polymer, 616.487 Da.
IMD, non-polymer, 69.085 Da.
Natural source: Common Name: Shewanella oneidensis MR-1 Taxonomy ID: 211586 Superkingdom: Bacteria Kingdom: not available Genus/species: Shewanella oneidensis
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
SO2144: MKGIIFNVLEDMVVAQCGMS
VWNELLEKHAPKDRVYVSAK
SYAESELFSIVQDVAQRLNM
PIQDVVKAFGQFLFNGLASR
HTDVVDKFDDFTSLVMGIHD
VIGLEVNKLYHEPSLPHING
QLLPNNQIALRYSSPRRLCF
CAEGLLFGAAQHFQQKIQIS
HDTCMHTGADHCMLIIELQN
D
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 502 |
15N chemical shifts | 167 |
1H chemical shifts | 1149 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | SO2144 | 1 |
2 | CMO | 2 |
3 | HEM | 3 |
4 | IMD | 4 |
Entities:
Entity 1, SO2144 181 residues - 20453.637 Da.
1 | MET | LYS | GLY | ILE | ILE | PHE | ASN | VAL | LEU | GLU | ||||
2 | ASP | MET | VAL | VAL | ALA | GLN | CYS | GLY | MET | SER | ||||
3 | VAL | TRP | ASN | GLU | LEU | LEU | GLU | LYS | HIS | ALA | ||||
4 | PRO | LYS | ASP | ARG | VAL | TYR | VAL | SER | ALA | LYS | ||||
5 | SER | TYR | ALA | GLU | SER | GLU | LEU | PHE | SER | ILE | ||||
6 | VAL | GLN | ASP | VAL | ALA | GLN | ARG | LEU | ASN | MET | ||||
7 | PRO | ILE | GLN | ASP | VAL | VAL | LYS | ALA | PHE | GLY | ||||
8 | GLN | PHE | LEU | PHE | ASN | GLY | LEU | ALA | SER | ARG | ||||
9 | HIS | THR | ASP | VAL | VAL | ASP | LYS | PHE | ASP | ASP | ||||
10 | PHE | THR | SER | LEU | VAL | MET | GLY | ILE | HIS | ASP | ||||
11 | VAL | ILE | GLY | LEU | GLU | VAL | ASN | LYS | LEU | TYR | ||||
12 | HIS | GLU | PRO | SER | LEU | PRO | HIS | ILE | ASN | GLY | ||||
13 | GLN | LEU | LEU | PRO | ASN | ASN | GLN | ILE | ALA | LEU | ||||
14 | ARG | TYR | SER | SER | PRO | ARG | ARG | LEU | CYS | PHE | ||||
15 | CYS | ALA | GLU | GLY | LEU | LEU | PHE | GLY | ALA | ALA | ||||
16 | GLN | HIS | PHE | GLN | GLN | LYS | ILE | GLN | ILE | SER | ||||
17 | HIS | ASP | THR | CYS | MET | HIS | THR | GLY | ALA | ASP | ||||
18 | HIS | CYS | MET | LEU | ILE | ILE | GLU | LEU | GLN | ASN | ||||
19 | ASP |
Entity 2, CMO - C O - 28.010 Da.
1 | CMO |
Entity 3, HEM - C34 H32 Fe N4 O4 - 616.487 Da.
1 | HEM |
Entity 4, IMD - C3 H5 N2 - 69.085 Da.
1 | IMD |
Samples:
sample_1: H-NOX, [U-99% 13C; U-99% 15N], 0.4 0.8 mM; K3PO4 50 mM; DTT 5 mM; glycerol 5%; H2O 90%; D2O 10%; imidazole 10 mM
sample_2: H-NOX, [U-99% 13C; U-99% 15N], 0.4 0.8 mM; K3PO4 50 mM; DTT 5 mM; glycerol 5%; D2O 100%; imidazole 10 mM
sample_3: H-NOX, [U-99% 13C; U-99% 15N], 0.4 0.8 mM; K3PO4 50 mM; DTT 5 mM; glycerol 5%; H2O 90%; D2O 10%; imidazole 10 mM
sample_conditions_1: ionic strength: 50 mM; pH: 7.4; pressure: 1 atm; temperature: 298 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
3D HNCA | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HBHA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D C(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_2 | isotropic | sample_conditions_1 |
3D HCCH-COSY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_3 | isotropic | sample_conditions_1 |
3D 1H-15N TOCSY | sample_3 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_2 | isotropic | sample_conditions_1 |
Software:
X-PLOR NIH, Schwieters, Kuszewski, Tjandra and Clore - refinement
NMR spectrometers:
- Bruker DRX 900 MHz
- Bruker DRX 800 MHz
- Bruker DRX 600 MHz
- Bruker DRX 500 MHz
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts