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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR30290
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
XML gzip file.
RDF gzip file.
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Citation: Barnwal, R.; Varani, G.. "Assignment and Structure of Thioredoxin (Rv1471 ortholog) type protein from Mycobacterium smegmatis ATCC 700084 / mc(2)155" .
Assembly members:
entity_1, polymer, 110 residues, 11634.341 Da.
Natural source: Common Name: Mycobacterium smegmatis Taxonomy ID: 1772 Superkingdom: Bacteria Kingdom: not available Genus/species: Mycobacterium smegmatis
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
entity_1: MSEDSATVAVTDDSFSTDVL
GSSKPVLVDFWATWCGPCKM
VAPVLEEIAAEKGDQLTVAK
IDVDANPATARDFQVVSIPT
MILFKDGAPVKRIVGAKGKA
ALLRELSDAL
| Data type | Count |
| 13C chemical shifts | 448 |
| 15N chemical shifts | 105 |
| 1H chemical shifts | 661 |
| Entity Assembly ID | Entity Name | Entity ID |
|---|---|---|
| 1 | entity_1 | 1 |
Entity 1, entity_1 110 residues - 11634.341 Da.
| 1 | MET | SER | GLU | ASP | SER | ALA | THR | VAL | ALA | VAL | |
| 2 | THR | ASP | ASP | SER | PHE | SER | THR | ASP | VAL | LEU | |
| 3 | GLY | SER | SER | LYS | PRO | VAL | LEU | VAL | ASP | PHE | |
| 4 | TRP | ALA | THR | TRP | CYS | GLY | PRO | CYS | LYS | MET | |
| 5 | VAL | ALA | PRO | VAL | LEU | GLU | GLU | ILE | ALA | ALA | |
| 6 | GLU | LYS | GLY | ASP | GLN | LEU | THR | VAL | ALA | LYS | |
| 7 | ILE | ASP | VAL | ASP | ALA | ASN | PRO | ALA | THR | ALA | |
| 8 | ARG | ASP | PHE | GLN | VAL | VAL | SER | ILE | PRO | THR | |
| 9 | MET | ILE | LEU | PHE | LYS | ASP | GLY | ALA | PRO | VAL | |
| 10 | LYS | ARG | ILE | VAL | GLY | ALA | LYS | GLY | LYS | ALA | |
| 11 | ALA | LEU | LEU | ARG | GLU | LEU | SER | ASP | ALA | LEU |
sample_1: Thioredoxin (Rv1471 ortholog) from Mycobacterium smegmatis ATCC 700084 / mc(2)15513C, [U-99% 13C; U-99% 15N], 1.1 ± 0.1 mM; NaCl 100 mM
sample_conditions_1: ionic strength: 100 mM; pH: 6.0; pressure: 1 atm; temperature: 298 K
| Name | Sample | Sample state | Sample conditions |
|---|---|---|---|
| 2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
| 2D 1H-13C HSQC | sample_1 | isotropic | sample_conditions_1 |
| 3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
| 3D HNCACB | sample_1 | isotropic | sample_conditions_1 |
| 3D HNCO | sample_1 | isotropic | sample_conditions_1 |
| 3D 1H-13C NOESY | sample_1 | isotropic | sample_conditions_1 |
| 3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
| 3D HBHA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
| 3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
Analysis, CCPN - chemical shift assignment
CYANA v3.97, Guntert, Mumenthaler and Wuthrich - refinement, structure calculation
CcpNMR, CCPN - data analysis, peak picking
TOPSPIN, Bruker Biospin - collection
Download HSQC peak lists in one of the following formats:
CSV: Backbone
or all simulated peaks
SPARKY: Backbone
or all simulated peaks