BMRB Entry 15373
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_anomalous, AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR15373
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Title: The prokaryotic Cys2His2 zinc finger adopts a novel fold as revealed by the NMR structure of A. tumefaciens Ros DNA binding domain PubMed: 17956987
Deposition date: 2007-07-10 Original release date: 2008-03-13
Authors: Malgieri, Gaetano
Citation: Malgieri, Gaetano; Russo, L.; Esposito, S.; Baglivo, I.; Zaccaro, L.; Pedone, E.; Di Blasio, B.; Isernia, C.; Pedone, P.; Fattorusso, R.. "The prokaryotic Cys2His2 zinc finger adopts a novel fold as revealed by the NMR structure of A.tumefaciens Ros DNA binding domain" Proc. Natl. Acad. Sci. U.S.A. 104, 17341-17346 (2007).
Assembly members:
Ros87_polypeptide, polymer, 87 residues, 9959.560 Da.
ZN, non-polymer, 65.409 Da.
Natural source: Common Name: Agrobacterium tumefaciens Taxonomy ID: 358 Superkingdom: Bacteria Kingdom: not available Genus/species: Agrobacterium tumefaciens
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
Ros87_polypeptide: AVNVEKQKPAVSVRKSVQDD
HIVCLECGGSFKSLKRHLTT
HHSMTPEEYREKWDLPVDYP
MVAPAYAEARSRLAKEMGLG
QRRKANR
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 341 |
15N chemical shifts | 85 |
1H chemical shifts | 505 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | Ros87 polypeptide | 1 |
2 | ZINC ION | 2 |
Entities:
Entity 1, Ros87 polypeptide 87 residues - 9959.560 Da.
1 | ALA | VAL | ASN | VAL | GLU | LYS | GLN | LYS | PRO | ALA | ||||
2 | VAL | SER | VAL | ARG | LYS | SER | VAL | GLN | ASP | ASP | ||||
3 | HIS | ILE | VAL | CYS | LEU | GLU | CYS | GLY | GLY | SER | ||||
4 | PHE | LYS | SER | LEU | LYS | ARG | HIS | LEU | THR | THR | ||||
5 | HIS | HIS | SER | MET | THR | PRO | GLU | GLU | TYR | ARG | ||||
6 | GLU | LYS | TRP | ASP | LEU | PRO | VAL | ASP | TYR | PRO | ||||
7 | MET | VAL | ALA | PRO | ALA | TYR | ALA | GLU | ALA | ARG | ||||
8 | SER | ARG | LEU | ALA | LYS | GLU | MET | GLY | LEU | GLY | ||||
9 | GLN | ARG | ARG | LYS | ALA | ASN | ARG |
Entity 2, ZINC ION - Zn - 65.409 Da.
1 | ZN |
Samples:
sample_1: Ros87, [U-100% 15N], 1 mM; Zinc ion 1 mM; phosphate buffer 20 mM; NaCl 0.2 M
sample_2: Ros87, [U-100% 13C; U-100% 15N], 1 mM; Zinc ion 1 mM; phosphate buffer 20 mM; NaCl 0.2 M
sample_3: Ros87 1 mM; Zinc ion 1 mM; phosphate buffer 20 mM; NaCl 0.2 M
sample_conditions_1: ionic strength: 0.2 M; pH: 6.8; 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_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_2 | isotropic | sample_conditions_1 |
2D 1H-1H NOESY | sample_3 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D CBCANH | sample_2 | isotropic | sample_conditions_1 |
3D HNCO | sample_2 | isotropic | sample_conditions_1 |
3D HNCA | sample_2 | isotropic | sample_conditions_1 |
3D HNHA | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
3D CCH-TOCSY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-15N TOCSY | sample_1 | isotropic | sample_conditions_1 |
2D 1H-1H TOCSY | sample_3 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC IPAP | sample_2 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC IPAP | sample_2 | anisotropic | sample_conditions_1 |
Software:
XEASY, Bartels et al. - chemical shift assignment, data analysis, peak picking
CYANA, Guntert, Mumenthaler and Wuthrich - structure solution
ProcheckNMR, Laskowski and MacArthur - structure validation
VNMRJ, Varian - collection, processing
ModelFree, Palmer - Calculation dynamic parameters, data analysis
Molmol, Koradi, Billeter and Wuthrich - data analysis, figure realization, structure visualization
SPDB, Guex, N. and Peitsch, M. C. - Energy minimization
NMR spectrometers:
- Varian INOVA 500 MHz
- Varian INOVA 600 MHz
- Bruker Avance 500 MHz
- Bruker Avance 800 MHz
Related Database Links:
PDB | |
EMBL | CAA58116 CDI07817 CDN91482 |
GB | AAA22106 AAK86720 ADY63837 AHK00781 AKC06614 |
REF | NP_353935 WP_003497181 WP_003509257 WP_003512037 WP_004440665 |
SP | P55324 Q04152 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts