BMRB Entry 11017
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_anomalous, AVS_full, LACS, SPARTA
BMRB Entry DOI: doi:10.13018/BMR11017
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Title: NMR solution structure of TnpE protein from Shigella flexneri. Northeast Structural Genomics Target SfR125.
Deposition date: 2007-12-07 Original release date: 2008-03-24
Authors: Ramelot, Theresa; Cort, John; Semesi, Anthony; Garcia, M; Yee, Adelinda; Arrowsmith, Cheryl; Kennedy, Michael
Citation: Ramelot, Theresa; Cort, John; Semesi, Anthony; Garcia, M; Yee, Adelinda; Arrowsmith, Cheryl; Kennedy, Michael. "NMR solution structure of TnpE protein from Shigella flexneri. Northeast Structural Genomics Target SfR125." . ., .-..
Assembly members:
TnpE, polymer, 108 residues, 12666.427 Da.
Natural source: Common Name: Shigella flexneri Taxonomy ID: 623 Superkingdom: Bacteria Kingdom: not available Genus/species: Shigella flexneri
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
TnpE: MTKNTRFSPEVRQRAVRMVL
ESQGEYDSQWATICSIAPKI
GCTPETLRVWVRQHERDTGG
DDGGLTTAERQRLKEPEREN
RELRRSNDILRLASAYFAKA
EFDRLWKK
- assigned_chemical_shifts
- spectral_peak_list
Data type | Count |
13C chemical shifts | 386 |
15N chemical shifts | 94 |
1H chemical shifts | 606 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | TnpE | 1 |
Entities:
Entity 1, TnpE 108 residues - 12666.427 Da.
1 | MET | THR | LYS | ASN | THR | ARG | PHE | SER | PRO | GLU | ||||
2 | VAL | ARG | GLN | ARG | ALA | VAL | ARG | MET | VAL | LEU | ||||
3 | GLU | SER | GLN | GLY | GLU | TYR | ASP | SER | GLN | TRP | ||||
4 | ALA | THR | ILE | CYS | SER | ILE | ALA | PRO | LYS | ILE | ||||
5 | GLY | CYS | THR | PRO | GLU | THR | LEU | ARG | VAL | TRP | ||||
6 | VAL | ARG | GLN | HIS | GLU | ARG | ASP | THR | GLY | GLY | ||||
7 | ASP | ASP | GLY | GLY | LEU | THR | THR | ALA | GLU | ARG | ||||
8 | GLN | ARG | LEU | LYS | GLU | PRO | GLU | ARG | GLU | ASN | ||||
9 | ARG | GLU | LEU | ARG | ARG | SER | ASN | ASP | ILE | LEU | ||||
10 | ARG | LEU | ALA | SER | ALA | TYR | PHE | ALA | LYS | ALA | ||||
11 | GLU | PHE | ASP | ARG | LEU | TRP | LYS | LYS |
Samples:
CN_sample: TnpE, [U-100% 13C; U-100% 15N], 1 ± 0.1 mM; TRIS 10 ± 1 mM; sodium chloride 500 ± 50 mM; DTT 10 ± 1 mM; Zn+2 10 ± 1 uM; sodium azide 0.01 ± 0.01 %; benzamidine 1 ± 0.1 mM; H2O 90%; D2O 10%
NC7_sample: TnpE, [U-7% 13C; U-100% 15N], 1 ± 0.1 mM; TRIS 10 ± 1 mM; sodium chloride 500 ± 50 mM; DTT 10 ± 1 mM; Zn+2 10 ± 1 uM; sodium azide 0.01 ± 0.01 %; benzamidine 1 ± 0.1 mM; H2O 90%; D2O 10%
sample_conditions_1: ionic strength: 0.5 M; pH: 7.7; pressure: 1 atm; temperature: 293 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | CN_sample | isotropic | sample_conditions_1 |
2D 1H-13C HSQC (aliph) | CN_sample | isotropic | sample_conditions_1 |
3D HNCACB | CN_sample | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | CN_sample | isotropic | sample_conditions_1 |
3D HNCO | CN_sample | isotropic | sample_conditions_1 |
3D HBHA(CO)NH | CN_sample | isotropic | sample_conditions_1 |
3D C(CO)NH | CN_sample | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | CN_sample | isotropic | sample_conditions_1 |
3D (H)CCH-TOCSY | CN_sample | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | CN_sample | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | CN_sample | isotropic | sample_conditions_1 |
3D 1H-13C NOESY aliph | CN_sample | isotropic | sample_conditions_1 |
3D 1H-13C NOESY arom | CN_sample | isotropic | sample_conditions_1 |
3D HCCH-COSY | CN_sample | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | CN_sample | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | NC7_sample | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | NC7_sample | isotropic | sample_conditions_1 |
2D 1H-13C HSQC (arom ct) | CN_sample | isotropic | sample_conditions_1 |
Software:
NMRPipe vnmrpipe linux, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
VNMR v6.1C, Varian - collection
AutoStruct v2.1.1, Huang, Tejero, Powers and Montelione - data analysis
X-PLOR NIH v2.15.0, Schwieters, Kuszewski, Tjandra and Clore - structure solution
CNS v1.1, Brunger, Adams, Clore, Gros, Nilges and Read - refinement
SPARKY v3.1, Goddard - data analysis
NMR spectrometers:
- Varian INOVA 600 MHz
- Varian INOVA 750 MHz
Related Database Links:
SWS | Q99Q67 |
UNP | Q99Q67_SHIFL |
PDB | |
DBJ | BAI57971 BAN82908 BAN82936 |
EMBL | CAR16451 CAR16627 CAR18772 CAR19494 CAR19546 |
GB | AAC44574 AAD44738 AAF09023 AAK18356 AAK18368 |
REF | NP_085200 NP_085212 NP_085224 NP_085240 NP_085247 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts