BMRB Entry 18753
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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/BMR18753
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Title: Structure of the biofilm matrix promoter AbbA from B. subtilis
Deposition date: 2012-10-02 Original release date: 2013-09-10
Authors: Bobay, Benjamin; Tucker, Ashley; Losick, Richard; Cavanagh, John
Citation: Tucker, Ashley; Bobay, Benjamin; Banse, Allison; Olson, Andrew; Thompson, Richele; Varney, Kristen; Losick, Richard; Cavanagh, John. "Structure of the biofilm matrix promoter AbbA from B. subtilis" Not known ., .-..
Assembly members:
entity, polymer, 68 residues,   7989.087 Da.
Natural source: Common Name: Bacillus subtilis Taxonomy ID: 1423 Superkingdom: Bacteria Kingdom: not available Genus/species: Bacillus subtilis
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
entity: GSHMRMSLIGERFTEEEQKL
LLNILINHEYAIELLSSEIN
DIETGTKNVDGTTYKKLVTL
YDRFRFEN
- assigned_chemical_shifts
 
| Data type | Count | 
| 13C chemical shifts | 274 | 
| 15N chemical shifts | 68 | 
| 1H chemical shifts | 443 | 
Additional metadata:
Assembly:
| Entity Assembly ID | Entity Name | Entity ID | 
|---|---|---|
| 1 | biofilm matrix promoter AbbA from B. subtilis, 1 | 1 | 
| 2 | biofilm matrix promoter AbbA from B. subtilis, 2 | 1 | 
Entities:
Entity 1, biofilm matrix promoter AbbA from B. subtilis, 1 68 residues - 7989.087 Da.
Residues 1-3 represent a non-native sequence left after cleavage of affinity tag
| 1 | GLY | SER | HIS | MET | ARG | MET | SER | LEU | ILE | GLY | ||||
| 2 | GLU | ARG | PHE | THR | GLU | GLU | GLU | GLN | LYS | LEU | ||||
| 3 | LEU | LEU | ASN | ILE | LEU | ILE | ASN | HIS | GLU | TYR | ||||
| 4 | ALA | ILE | GLU | LEU | LEU | SER | SER | GLU | ILE | ASN | ||||
| 5 | ASP | ILE | GLU | THR | GLY | THR | LYS | ASN | VAL | ASP | ||||
| 6 | GLY | THR | THR | TYR | LYS | LYS | LEU | VAL | THR | LEU | ||||
| 7 | TYR | ASP | ARG | PHE | ARG | PHE | GLU | ASN | 
Samples:
sample_1: entity, [U-100% 13C; U-100% 15N], 0.5  1.0 mM; DTT 1 mM; TRIS 20 mM; sodium chloride 200 mM; EDTA 1 mM; sodium azide 0.02%; H2O 90%; D2O 10%
sample_2: entity, [U-100% 13C; U-100% 15N], 0.5  1.0 mM; DTT 1 mM; TRIS 20 mM; sodium chloride 200 mM; EDTA 1 mM; sodium azide 0.02%; D2O 100%
sample_conditions_1: ionic strength: 200 mM; pH: 6.5; pressure: 1 atm; temperature: 273 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 C(CO)NH | sample_1 | isotropic | sample_conditions_1 | 
| 3D HNCO | sample_1 | isotropic | sample_conditions_1 | 
| 3D HNCA | sample_1 | isotropic | sample_conditions_1 | 
| 3D HNCACB | sample_1 | isotropic | sample_conditions_1 | 
| 3D HBHA(CO)NH | sample_1 | isotropic | sample_conditions_1 | 
| 3D HN(CO)CA | sample_1 | isotropic | sample_conditions_1 | 
| 3D H(CCO)NH | sample_1 | isotropic | sample_conditions_1 | 
| 3D HCCH-TOCSY | sample_2 | isotropic | sample_conditions_1 | 
| 3D HNHA | sample_1 | isotropic | sample_conditions_1 | 
| 3D 1H-15N TOCSY | sample_1 | isotropic | sample_conditions_1 | 
| 3D HN(CA)CO | sample_1 | isotropic | sample_conditions_1 | 
| 3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 | 
| 3D 1H-13C NOESY | sample_2 | isotropic | sample_conditions_1 | 
| 3D 13C-12C isotope filtered NOESY | sample_2 | isotropic | sample_conditions_1 | 
| 2D 1H-15N HSQC RDC | sample_1 | isotropic | sample_conditions_1 | 
| 2D 1H-15N HSQC RDC | sample_1 | anisotropic | sample_conditions_1 | 
Software:
NMRPipe vVersion 7.5 Rev 2012.204.11.07, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
NMRDraw vVersion 7.5 Rev 2012.204.11.07, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
NMRView v8a, Johnson, One Moon Scientific - chemical shift assignment, data analysis, peak picking
CYANA v3.0, Guntert, Mumenthaler and Wuthrich - structure solution
AMBER v11, Case, Darden, Cheatham, III, Simmerling, Wang, Duke, Luo, ... and Kollman - refinement
NMR spectrometers:
- Bruker Avance 700 MHz
 - Bruker Avance 950 MHz
 
Related Database Links:
| PDB | |
| DBJ | BAI85022 BAM52057 BAM57634 GAK78528 | 
| EMBL | CAB13285 CCU57976 CEI56592 CEJ76998 CJS26336 | 
| GB | ADM37499 ADP31919 ADV96430 AEP86387 AEP90557 | 
| REF | NP_389295 WP_003218673 WP_003327264 WP_010886502 WP_046160339 | 
| SP | O31697 | 
Download simulated HSQC data in one of the following formats:
            
CSV: Backbone
            or all simulated shifts
            
SPARKY: Backbone
            or all simulated shifts