BMRB Entry 18443
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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/BMR18443
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Title: Solution structure of a thioredoxin from Thermus thermophilus
Deposition date: 2012-05-04 Original release date: 2012-06-05
Authors: Harris, R.; Bandaranayake, A.; Banu, R.; Bonanno, J.; Calarese, D.; Celikgil, A.; Chamala, S.; Chan, M.; Chaparro, R.; Evans, B.; Garforth, S.; Gizzi, A.; Hillerich, B.; Kar, A.; Lafleur, J.; Lim, S.; Love, J.; Matikainen, B.; Patel, H.; Seidel, R.; Smith, B.; Stead, M.; Girvin, M.; Almo, S.
Citation: Harris, R.; Bandaranayake, A.; Banu, R.; Bonanno, J.; Calarese, D.; Celikgil, A.; Chamala, S.; Chan, M.; Chaparro, R.; Evans, B.; Garforth, S.; Gizzi, A.; Hillerich, B.; Kar, A.; Lafleur, J.; Lim, S.; Love, J.; Matikainen, B.; Patel, H.; Seidel, R.; Smith, B.; Stead, M.; Girvin, M.; Almo, S.. "Solution structure of a thioredoxin from Thermus thermophilus" To be published ., .-..
Assembly members:
thioredoxin, polymer, 130 residues, 14740.037 Da.
Natural source: Common Name: bacteria Taxonomy ID: 274 Superkingdom: Bacteria Kingdom: not available Genus/species: Thermus thermophilus
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
thioredoxin: MSLRWYPYPEALALAQAHGR
MVMVYFHSEHCPYCQQMNTF
VLSDPGVSRLLEARFVVASV
SVDTPEGQELARRYRVPGTP
TFVFLVPKAGAWEEVGRLFG
SRPRAEFLKELRQVCVKGGA
CGEGHHHHHH
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 547 |
15N chemical shifts | 121 |
1H chemical shifts | 848 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | thioredoxin | 1 |
Entities:
Entity 1, thioredoxin 130 residues - 14740.037 Da.
expressed sequence start-stop 35-153 (130 aa incl tag) N-term cloning artifact: MSL C-term cloning artifact: EGHHHHHH
1 | MET | SER | LEU | ARG | TRP | TYR | PRO | TYR | PRO | GLU | |
2 | ALA | LEU | ALA | LEU | ALA | GLN | ALA | HIS | GLY | ARG | |
3 | MET | VAL | MET | VAL | TYR | PHE | HIS | SER | GLU | HIS | |
4 | CYS | PRO | TYR | CYS | GLN | GLN | MET | ASN | THR | PHE | |
5 | VAL | LEU | SER | ASP | PRO | GLY | VAL | SER | ARG | LEU | |
6 | LEU | GLU | ALA | ARG | PHE | VAL | VAL | ALA | SER | VAL | |
7 | SER | VAL | ASP | THR | PRO | GLU | GLY | GLN | GLU | LEU | |
8 | ALA | ARG | ARG | TYR | ARG | VAL | PRO | GLY | THR | PRO | |
9 | THR | PHE | VAL | PHE | LEU | VAL | PRO | LYS | ALA | GLY | |
10 | ALA | TRP | GLU | GLU | VAL | GLY | ARG | LEU | PHE | GLY | |
11 | SER | ARG | PRO | ARG | ALA | GLU | PHE | LEU | LYS | GLU | |
12 | LEU | ARG | GLN | VAL | CYS | VAL | LYS | GLY | GLY | ALA | |
13 | CYS | GLY | GLU | GLY | HIS | HIS | HIS | HIS | HIS | HIS |
Samples:
sample_1: thioredoxin, [U-13C; U-15N], 0.5 mM; sodium phosphate 20 mM; sodium chloride 50 mM; DTT 5 mM; EDTA 1 mM
sample_2: thioredoxin, [U-13C; U-15N], 0.5 mM; sodium phosphate 20 mM; sodium chloride 50 mM; DTT 5 mM; EDTA 1 mM
sample_conditions_1: ionic strength: 70 mM; pH: 5.8; pressure: 1 ATM; temperature: 303 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
15N HSQC | sample_1 | isotropic | sample_conditions_1 |
15N NOESY-HSQC | sample_1 | isotropic | sample_conditions_1 |
13C HSQC | sample_2 | isotropic | sample_conditions_1 |
aromatic 13C HSQC | sample_2 | isotropic | sample_conditions_1 |
13C NOESY-HSQC | sample_2 | isotropic | sample_conditions_1 |
13C aromatic NOESY-HSQC | sample_2 | isotropic | sample_conditions_1 |
HNCO | sample_1 | isotropic | sample_conditions_1 |
HNCACO | sample_1 | isotropic | sample_conditions_1 |
HNCA | sample_1 | isotropic | sample_conditions_1 |
HNCOCA | sample_1 | isotropic | sample_conditions_1 |
HNCACB | sample_1 | isotropic | sample_conditions_1 |
CBCACONH | sample_1 | isotropic | sample_conditions_1 |
Software:
CNS v1.21, Brunger, Adams, Clore, Gros, Nilges and Read - refinement, structure solution
ARIA v2.3, Linge, O, . - data analysis
CCPN v2.1.5, CCPN - chemical shift assignment, data analysis, peak picking
NMRPipe v5.4, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
VNMRJ v2.2D, Varian - collection
TOPSPIN v1.3, Bruker Biospin - collection
MDDNMR v2.0, (MDDNMR) Orekhov, Jaravine, Kazimierczuk - collection, processing
MDDGUI v1.0, (MDDGUI) Lemak, Gutmanas, Chitayat, Karra, Fares, Sunnerhagen, Arrowsmith - collection, processing
SIDER, Hansen - data analysis
NMR spectrometers:
- Varian Inova 600 MHz
- Bruker Avance 600 MHz
Related Database Links:
PDB | |
DBJ | BAD71245 |
GB | AAS81399 AEG33835 AFH38530 |
REF | WP_011228670 WP_024119461 WP_041443497 WP_041445022 YP_144688 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts