BMRB Entry 30708
Chem Shift validation: AVS_full
BMRB Entry DOI: doi:10.13018/BMR30708
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Title: De novo designed Rossmann fold protein ROS2_36830
Deposition date: 2020-01-07 Original release date: 2020-08-14
Authors: Pan, X.; Zhang, Y.; Kelly, M.; Kortemme, T.
Citation: Pan, X.. "De novo designed Rossmann fold protein ROS2_36830" . ., .-..
Assembly members:
entity_1, polymer, 121 residues, 13953.312 Da.
Natural source: Common Name: not available Taxonomy ID: 32630 Superkingdom: not available Kingdom: not available Genus/species: not available not available
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
entity_1: MGSSHHHHHHSSGLVPRGSH
MGLLVLIWSNDKKLIEEARK
MAEKANLYLLTLETDDKKIE
DILKSLGPPVKILVLLEDTK
DADKVKKEIEKKARKKNLPV
RIRKVTSPDEAKRWIKEFSE
E
- assigned_chemical_shifts
| Data type | Count |
| 13C chemical shifts | 370 |
| 15N chemical shifts | 101 |
| 1H chemical shifts | 746 |
Additional metadata:
Assembly:
| Entity Assembly ID | Entity Name | Entity ID |
|---|---|---|
| 1 | unit_1 | 1 |
Entities:
Entity 1, unit_1 121 residues - 13953.312 Da.
| 1 | MET | GLY | SER | SER | HIS | HIS | HIS | HIS | HIS | HIS | ||||
| 2 | SER | SER | GLY | LEU | VAL | PRO | ARG | GLY | SER | HIS | ||||
| 3 | MET | GLY | LEU | LEU | VAL | LEU | ILE | TRP | SER | ASN | ||||
| 4 | ASP | LYS | LYS | LEU | ILE | GLU | GLU | ALA | ARG | LYS | ||||
| 5 | MET | ALA | GLU | LYS | ALA | ASN | LEU | TYR | LEU | LEU | ||||
| 6 | THR | LEU | GLU | THR | ASP | ASP | LYS | LYS | ILE | GLU | ||||
| 7 | ASP | ILE | LEU | LYS | SER | LEU | GLY | PRO | PRO | VAL | ||||
| 8 | LYS | ILE | LEU | VAL | LEU | LEU | GLU | ASP | THR | LYS | ||||
| 9 | ASP | ALA | ASP | LYS | VAL | LYS | LYS | GLU | ILE | GLU | ||||
| 10 | LYS | LYS | ALA | ARG | LYS | LYS | ASN | LEU | PRO | VAL | ||||
| 11 | ARG | ILE | ARG | LYS | VAL | THR | SER | PRO | ASP | GLU | ||||
| 12 | ALA | LYS | ARG | TRP | ILE | LYS | GLU | PHE | SER | GLU | ||||
| 13 | GLU |
Samples:
sample_1: de novo protein RO2_20, [U-99% 13C; U-99% 15N], 0.8 mM; potassium phosphate monobasic 21.1 mM; sodium phosphate dibasic 28.9 mM
sample_conditions_1: ionic strength: 0 M; pH: 7.0; pressure: 1 atm; temperature: 300 K
Experiments:
| 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 HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
| 3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
| 3D 1H-13C NOESY | sample_1 | isotropic | sample_conditions_1 |
Software:
TopSpin v4.0.6, Bruker Biospin - collection
NMRPipe v9.8, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
CcpNmr Analysis v2.4.2, CCPN - chemical shift assignment
ARIA v2.3.2, Linge, O'Donoghue and Nilges - structure calculation
CNS v1.21, Brunger, Adams, Clore, Gros, Nilges and Read - refinement
CcpNmr Analysis, CCPN - peak picking
NMR spectrometers:
- Bruker AVANCE 800 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