BMRB Entry 19000
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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/BMR19000
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Title: Solution NMR structure of VV2_0175 from Vibrio vulnificus, NESG target VnR1 and CSGID target IDP91333
Deposition date: 2013-02-04 Original release date: 2013-02-20
Authors: Wu, Bin; Yee, Adelinda; Houliston, Scott; Lemak, Alexander; Garcia, Maite; Savchenko, Alexei; Arrowsmith, Cheryl
Citation: Wu, Bin; Yee, Adelinda; Houliston, Scott; Lemak, Alexander; Garcia, Maite; Savchenko, Alexei; Arrowsmith, Cheryl. "Solution NMR structure of VV2_0175 from Vibrio vulnificus, NESG target VnR1 and CSGID target IDP91333" Not known ., .-..
Assembly members:
VV2_0175, polymer, 110 residues, 9530.360 Da.
Natural source: Common Name: g-proteobacteria Taxonomy ID: 672 Superkingdom: Bacteria Kingdom: not available Genus/species: Vibrio vulnificus
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
VV2_0175: MHHHHHHSSGVDLGTENLYF
QSNAMSKTAKLNNEEKLVKK
ALEIGGKMAKMQGFDLPQSP
QPVRVKAVYLFLVDAKQIAP
LPDSKLDGANIKHRLALWIH
AALPDNDPLK
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 356 |
15N chemical shifts | 71 |
1H chemical shifts | 609 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | VV2_0175 | 1 |
Entities:
Entity 1, VV2_0175 110 residues - 9530.360 Da.
residues M-23 - A0 represents histag
1 | MET | HIS | HIS | HIS | HIS | HIS | HIS | SER | SER | GLY | |
2 | VAL | ASP | LEU | GLY | THR | GLU | ASN | LEU | TYR | PHE | |
3 | GLN | SER | ASN | ALA | MET | SER | LYS | THR | ALA | LYS | |
4 | LEU | ASN | ASN | GLU | GLU | LYS | LEU | VAL | LYS | LYS | |
5 | ALA | LEU | GLU | ILE | GLY | GLY | LYS | MET | ALA | LYS | |
6 | MET | GLN | GLY | PHE | ASP | LEU | PRO | GLN | SER | PRO | |
7 | GLN | PRO | VAL | ARG | VAL | LYS | ALA | VAL | TYR | LEU | |
8 | PHE | LEU | VAL | ASP | ALA | LYS | GLN | ILE | ALA | PRO | |
9 | LEU | PRO | ASP | SER | LYS | LEU | ASP | GLY | ALA | ASN | |
10 | ILE | LYS | HIS | ARG | LEU | ALA | LEU | TRP | ILE | HIS | |
11 | ALA | ALA | LEU | PRO | ASP | ASN | ASP | PRO | LEU | LYS |
Samples:
sample_1: VV2_0175, [U-100% 13C; U-100% 15N], 0.5 mM; TRIS, [U-100% 2H], 10 mM; sodium chloride 300 mM; DTT, [U-100% 2H], 10 mM; NaN3 0.01%; benzamidine 10 mM; inhibitor cocktail 1 x; H2O 90%; D2O 10%
sample_2: VV2_0175, [U-7% 13C; U-100% 15N], 0.2 mM; TRIS, [U-100% 2H], 10 mM; sodium chloride 300 mM; DTT, [U-100% 2H], 10 mM; NaN3 0.01%; benzamidine 10 mM; inhibitor cocktail 1 x; H2O 90%; D2O 10%
sample_conditions_1: ionic strength: 300 mM; pH: 7.0; pressure: 1 atm; temperature: 298 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HBHA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HNCA | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
3D CCH-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 |
3D 1H-13C NOESY aromatic | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_2 | isotropic | sample_conditions_1 |
3D HNCACB | sample_1 | isotropic | sample_conditions_1 |
3D HNCB | sample_1 | isotropic | sample_conditions_1 |
3D C(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D H(CCO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-COSY | sample_1 | isotropic | sample_conditions_1 |
3D TOCSY-HSQC | sample_1 | isotropic | sample_conditions_1 |
Software:
NMRPipe v2.3, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
MDDGUI v1.0, Gutmanas, Arrowsmith - processing
SPARKY v3.95, Goddard - data analysis
FMCGUI v2.4, Lemak, Arrowsmith - chemical shift assignment
CYANA v2.1, Guntert, Mumenthaler and Wuthrich - structure solution
CNS, Brunger, Adams, Clore, Gros, Nilges and Read - refinement
AutoStruct, Huang, Tejero, Powers and Montelione - NMR structure quality assessment
PSVS, Bhattacharya and Montelione - NMR structure quality assessment
FAWN, Lemak, Arrowsmith - chemical shift assignment
NMR spectrometers:
- Bruker Avance 800 MHz
- Bruker Avance 600 MHz
- Bruker Avance 500 MHz
Related Database Links:
PDB | |
DBJ | BAC96709 |
GB | AAO07148 ADV88695 AIL72739 ALM73137 EWS70635 |
REF | WP_011081156 WP_046030100 WP_047110511 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts