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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_anomalous, AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR16929
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
XML gzip file.
RDF gzip file.
All files associated with the entry
Citation: Pan, Yun-Ru; Lou, Yuan-Chao; Seven, Alpay; Rizo, Josep; Chen, Chinpan. "NMR Structure and Calcium-Binding Properties of the Tellurite Resistance Protein TerD from Klebsiella pneumoniae." J. Mol. Biol. 405, 1188-1201 (2011).
PubMed: 21112337
Assembly members:
TerD, polymer, 200 residues, 21558.7 Da.
CA, non-polymer, 40.078 Da.
Natural source: Common Name: K. pneumoniae Taxonomy ID: 573 Superkingdom: Bacteria Kingdom: not available Genus/species: Klebsiella pneumoniae
Experimental source: Production method: recombinant technology Host organism: Escherichia coli Vector: BL 21 DE3
Data type | Count |
13C chemical shifts | 806 |
15N chemical shifts | 203 |
1H chemical shifts | 1209 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | TerD | 1 |
2 | CA | 2 |
Entity 1, TerD 200 residues - 21558.7 Da.
1 | MET | SER | VAL | SER | LEU | SER | LYS | GLY | GLY | ASN | |
2 | VAL | SER | LEU | SER | LYS | THR | ALA | PRO | SER | MET | |
3 | LYS | ASN | VAL | LEU | VAL | GLY | LEU | GLY | TRP | ASP | |
4 | ALA | ARG | SER | THR | ASP | GLY | GLN | ASP | PHE | ASP | |
5 | LEU | ASP | ALA | SER | ALA | PHE | LEU | LEU | ALA | ALA | |
6 | ASN | GLY | LYS | VAL | ARG | GLY | ASP | ALA | ASP | PHE | |
7 | ILE | PHE | TYR | ASN | ASN | LEU | LYS | SER | ALA | ASP | |
8 | GLY | SER | VAL | THR | HIS | THR | GLY | ASP | ASN | ARG | |
9 | THR | GLY | GLU | GLY | ASP | GLY | ASP | ASP | GLU | SER | |
10 | LEU | LYS | ILE | LYS | LEU | ASP | ALA | VAL | PRO | GLY | |
11 | ASP | VAL | ASP | LYS | ILE | ILE | PHE | VAL | VAL | THR | |
12 | ILE | HIS | ASP | ALA | GLN | ALA | ARG | ARG | GLN | SER | |
13 | PHE | GLY | GLN | VAL | SER | GLY | ALA | PHE | ILE | ARG | |
14 | LEU | VAL | ASN | ASP | ASP | ASN | GLN | THR | GLU | VAL | |
15 | ALA | ARG | TYR | ASP | LEU | THR | GLU | ASP | ALA | SER | |
16 | THR | GLU | THR | ALA | MET | LEU | PHE | GLY | GLU | LEU | |
17 | TYR | ARG | HIS | ASN | GLY | GLU | TRP | LYS | PHE | ARG | |
18 | ALA | VAL | GLY | GLN | GLY | TYR | ALA | GLY | GLY | LEU | |
19 | ALA | SER | VAL | CYS | ALA | GLN | TYR | GLY | ILE | ASN | |
20 | ALA | SER | LEU | GLU | HIS | HIS | HIS | HIS | HIS | HIS |
Entity 2, CA - Ca - 40.078 Da.
1 | CA |
KP-TerD: potassium phosphate 20 mM; H2O 90%; D2O 10%
sample_conditions_1: ionic strength: 0.02 M; pH: 7; pressure: 1 atm; temperature: 310 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | KP-TerD | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | KP-TerD | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | KP-TerD | isotropic | sample_conditions_1 |
3D HNCACB | KP-TerD | isotropic | sample_conditions_1 |
3D HNCO | KP-TerD | isotropic | sample_conditions_1 |
3D HN(CO)CA | KP-TerD | isotropic | sample_conditions_1 |
3D C(CO)NH | KP-TerD | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | KP-TerD | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | KP-TerD | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | KP-TerD | isotropic | sample_conditions_1 |
3D HBHA(CO)NH | KP-TerD | isotropic | sample_conditions_1 |
3D HNHA | KP-TerD | isotropic | sample_conditions_1 |
2D 1H-1H NOESY | KP-TerD | isotropic | sample_conditions_1 |
2D CACO (ipap) | KP-TerD | isotropic | sample_conditions_1 |
AURELIA v3.1.6, Linge, O'Donoghue and Nilges - data analysis
xwinnmr v3.5, Bruker Biospin - processing
X-PLOR NIH, Schwieters, Kuszewski, Tjandra and Clore - structure solution
VNMR v5.0, Johnson, One Moon Scientific - chemical shift assignment
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
Download HSQC peak lists in one of the following formats:
CSV: Backbone
or all simulated peaks
SPARKY: Backbone
or all simulated peaks