BMRB Entry 25307
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, SPARTA
BMRB Entry DOI: doi:10.13018/BMR25307
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Title: solution structure of SATB1 homeodomain PubMed: 27462121
Deposition date: 2014-10-31 Original release date: 2015-11-02
Authors: Yamasaki, Kazuhiko; Yamasaki, Tomoko
Citation: Yamasaki, Kazuhiko; Yamasaki, Tomoko. "The combination of sequence-specific and nonspecific DNA-binding modes of transcription factor SATB1" Biochem. J. 473, 3321-3339 (2016).
Assembly members:
SATB1, polymer, 71 residues, 7903.208 Da.
Natural source: Common Name: human Taxonomy ID: 9606 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Homo sapiens
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
SATB1: GSHMNRQKTRPRTKISVEAL
GILQSFIQDVGLYPDEEAIQ
TLSAQLDLPKYTIIKFFQNQ
RYYLKHHGKLK
- assigned_chemical_shifts
Data type | Count |
15N chemical shifts | 73 |
1H chemical shifts | 82 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | SATB1 homeodomain | 1 |
Entities:
Entity 1, SATB1 homeodomain 71 residues - 7903.208 Da.
1 | GLY | SER | HIS | MET | ASN | ARG | GLN | LYS | THR | ARG | ||||
2 | PRO | ARG | THR | LYS | ILE | SER | VAL | GLU | ALA | LEU | ||||
3 | GLY | ILE | LEU | GLN | SER | PHE | ILE | GLN | ASP | VAL | ||||
4 | GLY | LEU | TYR | PRO | ASP | GLU | GLU | ALA | ILE | GLN | ||||
5 | THR | LEU | SER | ALA | GLN | LEU | ASP | LEU | PRO | LYS | ||||
6 | TYR | THR | ILE | ILE | LYS | PHE | PHE | GLN | ASN | GLN | ||||
7 | ARG | TYR | TYR | LEU | LYS | HIS | HIS | GLY | LYS | LEU | ||||
8 | LYS |
Samples:
sample_1: SATB1 homeodomain, [U-15N], 0.3 mM; sodium phosphate 50 mM; sodium chloride 50 mM; DSS 0.5 mM; H2O 95%; D2O 5%
sample_2: SATB1 homeodomain, [U-15N], 0.7 1.2 mM; sodium phosphate 50 mM; sodium chloride 200 mM; DSS 0.5 mM; H2O 90%; D2O 5%
sample_3: SATB1 homeodomain, [U-15N], 0.7 1.2 mM; sodium phosphate 50 mM; sodium chloride 200 mM; DSS 0.5 mM; H2O 95%; D2O 5%
sample_conditions_1: ionic strength: 0.1 M; pH: 5.5; pressure: 1 atm; temperature: 298 K
sample_conditions_2: ionic strength: 0.25 M; pH: 5.5; pressure: 1 atm; temperature: 298 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | sample_2 | isotropic | sample_conditions_2 |
3D 1H-15N NOESY | sample_2 | isotropic | sample_conditions_2 |
3D 1H-15N TOCSY | sample_2 | isotropic | sample_conditions_2 |
2D 1H-1H NOESY | sample_3 | isotropic | sample_conditions_2 |
2D DQF-COSY | sample_3 | isotropic | sample_conditions_2 |
2D 1H-1H TOCSY | sample_3 | isotropic | sample_conditions_2 |
Software:
CNS, Brunger, Adams, Clore, Gros, Nilges and Read - structure solution
Felix, Accelrys Software Inc. - data analysis
NMR spectrometers:
- Bruker Avance 500 MHz
- Bruker DMX 750 MHz
- Bruker DMX 500 MHz
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts