Chem Shift validation: AVS_full
BMRB Entry DOI: doi:10.13018/BMR25701
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NMR-STAR v3 text file.
XML gzip file.
RDF gzip file.
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Citation: Sinha, Kaustubh; Sangani, Sahil; Kehr, Andrew; Rule, Gordon; Jen-Jacobson, Linda. "Metal Ion Binding at the Catalytic Site Induces Widely Distributed Changes in a Sequence Specific Protein-DNA Complex.'" Biochemistry 55, 6115-6132 (2016).
PubMed: 27786446
Assembly members:
EcoRV, polymer, 244 residues, 28650 Da.
5'-GCAAAGATATCTTTCG-3', polymer, 16 residues, 9760 Da.
Natural source: Common Name: E. coli Taxonomy ID: 562 Superkingdom: Bacteria Kingdom: not available Genus/species: Escherichia coli
Experimental source: Production method: recombinant technology Host organism: Escherichia coli Vector: pET 22b+
Entity Sequences (FASTA):
EcoRV: SLRSDLINALYDENQKYDVC
GIISAEGKIYPLGSDTKVLS
TIFELFSRPIINKIAEKHGY
IVEEPKQQNHYPDFTLYKPS
EPNKKIAIDIKTTYTNKENE
KIKFTLGGYTSFIRNNTKNI
VYPFDQYIAHWIIGYVYTRV
ATRKSSLKTYNINELNEIPK
PYKGVKVFLQDKWVIAGDLA
GSGNTTNIGSIHAHYKDFVE
GKGIFDSEDEFLDYWRNYER
TSQLRNDKYNNISEYRNWIY
RGRK
5'-GCAAAGATATCTTTCG-3': GCAAAGATATCTTTCG
Data type | Count |
13C chemical shifts | 371 |
15N chemical shifts | 121 |
1H chemical shifts | 295 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | RV dimer, 1 | 1 |
2 | RV dimer, 2 | 1 |
3 | AAA DNA fragment, 1 | 2 |
4 | AAA DNA fragment, 2 | 2 |
Entity 1, RV dimer, 1 244 residues - 28650 Da.
1 | SER | LEU | ARG | SER | ASP | LEU | ILE | ASN | ALA | LEU | ||||
2 | TYR | ASP | GLU | ASN | GLN | LYS | TYR | ASP | VAL | CYS | ||||
3 | GLY | ILE | ILE | SER | ALA | GLU | GLY | LYS | ILE | TYR | ||||
4 | PRO | LEU | GLY | SER | ASP | THR | LYS | VAL | LEU | SER | ||||
5 | THR | ILE | PHE | GLU | LEU | PHE | SER | ARG | PRO | ILE | ||||
6 | ILE | ASN | LYS | ILE | ALA | GLU | LYS | HIS | GLY | TYR | ||||
7 | ILE | VAL | GLU | GLU | PRO | LYS | GLN | GLN | ASN | HIS | ||||
8 | TYR | PRO | ASP | PHE | THR | LEU | TYR | LYS | PRO | SER | ||||
9 | GLU | PRO | ASN | LYS | LYS | ILE | ALA | ILE | ASP | ILE | ||||
10 | LYS | THR | THR | TYR | THR | ASN | LYS | GLU | ASN | GLU | ||||
11 | LYS | ILE | LYS | PHE | THR | LEU | GLY | GLY | TYR | THR | ||||
12 | SER | PHE | ILE | ARG | ASN | ASN | THR | LYS | ASN | ILE | ||||
13 | VAL | TYR | PRO | PHE | ASP | GLN | TYR | ILE | ALA | HIS | ||||
14 | TRP | ILE | ILE | GLY | TYR | VAL | TYR | THR | ARG | VAL | ||||
15 | ALA | THR | ARG | LYS | SER | SER | LEU | LYS | THR | TYR | ||||
16 | ASN | ILE | ASN | GLU | LEU | ASN | GLU | ILE | PRO | LYS | ||||
17 | PRO | TYR | LYS | GLY | VAL | LYS | VAL | PHE | LEU | GLN | ||||
18 | ASP | LYS | TRP | VAL | ILE | ALA | GLY | ASP | LEU | ALA | ||||
19 | GLY | SER | GLY | ASN | THR | THR | ASN | ILE | GLY | SER | ||||
20 | ILE | HIS | ALA | HIS | TYR | LYS | ASP | PHE | VAL | GLU | ||||
21 | GLY | LYS | GLY | ILE | PHE | ASP | SER | GLU | ASP | GLU | ||||
22 | PHE | LEU | ASP | TYR | TRP | ARG | ASN | TYR | GLU | ARG | ||||
23 | THR | SER | GLN | LEU | ARG | ASN | ASP | LYS | TYR | ASN | ||||
24 | ASN | ILE | SER | GLU | TYR | ARG | ASN | TRP | ILE | TYR | ||||
25 | ARG | GLY | ARG | LYS |
Entity 2, AAA DNA fragment, 1 16 residues - 9760 Da.
1 | DG | DC | DA | DA | DA | DG | DA | DT | DA | DT | ||||
2 | DC | DT | DT | DT | DC | DG |
sample_1: EcoRV, [ILV-13CH3 ; U-99% 15N; U-99% 2H], 0.5 mM; 5'-GCAAAGATATCTTTCG-3', n/a, 0.5 mM; H2O 90%; D2O, [U-2H], 10%
sample_2: EcoRV, [U-99% 13C; U-99% 15N; U-99% 2H], 1 mM; 5'-GCAAAGATATCTTTCG-3', n/a, 0.5 mM; H2O 90%; D2O, [U-2H], 10%
sample_3: EcoRV, [ILV-13CH3 ; U-99% 15N; U-99% 2H], 0.5 mM; 5'-GCAAAGATATCTTTCG-3', n/a, 0.5 mM; H2O 90%; D2O, [U-2H], 10%
sample_conditions_1: ionic strength: 200 mM; pH: 7.4; pressure: 1 atm; temperature: 308 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_2 | isotropic | sample_conditions_1 |
3D HNCO | sample_2 | isotropic | sample_conditions_1 |
3D HN(CA)CO | sample_2 | isotropic | sample_conditions_1 |
3D HNCA | sample_2 | isotropic | sample_conditions_1 |
3D HN(CO)CA | sample_2 | isotropic | sample_conditions_1 |
3D HNCB | sample_2 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC aliphatic | sample_1 | isotropic | sample_conditions_1 |
4D ILV methyl NOE | sample_1 | isotropic | sample_conditions_1 |
ILV-HMCMCG | sample_3 | isotropic | sample_conditions_1 |
ILV-HMCM[CG]CB | sample_3 | isotropic | sample_conditions_1 |
xwinnmr, Bruker Biospin - collection
TOPSPIN, Bruker Biospin - collection
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
Monte v2.03, Rule - chemical shift assignment
Download HSQC peak lists in one of the following formats:
CSV: Backbone
or all simulated peaks
SPARKY: Backbone
or all simulated peaks