BMRB Entry 17532
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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/BMR17532
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Title: NMR structure of Ca2+-bound CaBP1 C-domain with RDC PubMed: 21608059
Deposition date: 2011-03-16 Original release date: 2011-06-07
Authors: Ames, James
Citation: Park, Saebomi; Li, Congmin; Ames, James. "Nuclear magnetic resonance structure of calcium-binding protein 1 in a Ca(2+) -bound closed state: implications for target recognition." Protein Sci. 20, 1356-1366 (2011).
Assembly members:
CaBP1, polymer, 167 residues, Formula weight is not available
CA, non-polymer, 40.078 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):
CaBP1: MGNCVKYPLRNLSRKDRSLR
PEEIEELREAFREFDKDKDG
YINCRDLGNCMRTMGYMPTE
MELIELSQQINMNLGGHVDF
DDFVELMGPKLLAETADMIG
VKELRDAFREFDTNGDGEIS
TSELREAMRKLLGHQVGHRD
IEEIIRDVDLNGDGRVDFEE
FVRMMSR
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 484 |
15N chemical shifts | 139 |
1H chemical shifts | 731 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | CaBP1 | 1 |
2 | CA | 2 |
Entities:
Entity 1, CaBP1 167 residues - Formula weight is not available
1 | MET | GLY | ASN | CYS | VAL | LYS | TYR | PRO | LEU | ARG | ||||
2 | ASN | LEU | SER | ARG | LYS | ASP | ARG | SER | LEU | ARG | ||||
3 | PRO | GLU | GLU | ILE | GLU | GLU | LEU | ARG | GLU | ALA | ||||
4 | PHE | ARG | GLU | PHE | ASP | LYS | ASP | LYS | ASP | GLY | ||||
5 | TYR | ILE | ASN | CYS | ARG | ASP | LEU | GLY | ASN | CYS | ||||
6 | MET | ARG | THR | MET | GLY | TYR | MET | PRO | THR | GLU | ||||
7 | MET | GLU | LEU | ILE | GLU | LEU | SER | GLN | GLN | ILE | ||||
8 | ASN | MET | ASN | LEU | GLY | GLY | HIS | VAL | ASP | PHE | ||||
9 | ASP | ASP | PHE | VAL | GLU | LEU | MET | GLY | PRO | LYS | ||||
10 | LEU | LEU | ALA | GLU | THR | ALA | ASP | MET | ILE | GLY | ||||
11 | VAL | LYS | GLU | LEU | ARG | ASP | ALA | PHE | ARG | GLU | ||||
12 | PHE | ASP | THR | ASN | GLY | ASP | GLY | GLU | ILE | SER | ||||
13 | THR | SER | GLU | LEU | ARG | GLU | ALA | MET | ARG | LYS | ||||
14 | LEU | LEU | GLY | HIS | GLN | VAL | GLY | HIS | ARG | ASP | ||||
15 | ILE | GLU | GLU | ILE | ILE | ARG | ASP | VAL | ASP | LEU | ||||
16 | ASN | GLY | ASP | GLY | ARG | VAL | ASP | PHE | GLU | GLU | ||||
17 | PHE | VAL | ARG | MET | MET | SER | ARG |
Entity 2, CA - Ca - 40.078 Da.
1 | CA |
Samples:
sample_1: CaBP1, [U-98% 13C; U-98% 15N], 1.0 mM; CA 5.0 mM; TRIS 10.0 mM; H2O 95%; D2O 5%
sample_conditions_1: ionic strength: 0.01 M; pH: 7.4; pressure: 1 atm; temperature: 310 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | 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 HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
Software:
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
X-PLOR NIH v2.23, Schwieters, Kuszewski, Tjandra and Clore - refinement, structure solution
SPARKY, Goddard - data analysis
NMR spectrometers:
- Bruker Avance 800 MHz
Related Database Links:
BMRB | 15197 15623 16862 |
PDB | |
DBJ | BAE24603 |
EMBL | CAC43037 CAD20347 |
GB | AAF25782 AAF25784 AAF25787 AAH30201 ABM86439 |
REF | NP_001028847 NP_001028848 NP_001028849 NP_001297641 NP_001297644 |
SP | O88751 Q9NZU7 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts