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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/BMR19196
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
XML gzip file.
RDF gzip file.
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Citation: Rout, Ashok; Patel, Sunita; Somlata, .; Shukla, Manish; Saraswathi, Deepa; Bhattacharya, Alok; Chary, Kandala. "Functional manipulation of a calcium-binding protein from Entamoeba histolytica guided by paramagnetic NMR." J. Biol. Chem. 288, 23473-23487 (2013).
PubMed: 23782698
Assembly members:
(Y81F)-EhCaBP1, polymer, 66 residues, 7380.329 Da.
EhCaBP1, polymer, 134 residues, 851.608 Da.
Natural source: Common Name: Eukaryotes Taxonomy ID: 5759 Superkingdom: Eukaryota Kingdom: not available Genus/species: Entamoeba histolytica
Experimental source: Production method: recombinant technology Host organism: Escherichia coli Vector: pET30a
Data type | Count |
13C chemical shifts | 248 |
15N chemical shifts | 60 |
1H chemical shifts | 321 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | (Y81F)-EhCaBP1 | 1 |
2 | EhCaBP1 | 2 |
Entity 1, (Y81F)-EhCaBP1 66 residues - 7380.329 Da.
1 | MET | ALA | GLU | ALA | LEU | PHE | LYS | GLU | ILE | ASP | ||||
2 | VAL | ASN | GLY | ASP | GLY | ALA | VAL | SER | TYR | GLU | ||||
3 | GLU | VAL | LYS | ALA | PHE | VAL | SER | LYS | LYS | ARG | ||||
4 | ALA | ILE | LYS | ASN | GLU | GLN | LEU | LEU | GLN | LEU | ||||
5 | ILE | PHE | LYS | SER | ILE | ASP | ALA | ASP | GLY | ASN | ||||
6 | GLY | GLU | ILE | ASP | GLN | ASN | GLU | PHE | ALA | LYS | ||||
7 | PHE | TYR | GLY | SER | ILE | GLN |
Entity 2, EhCaBP1 134 residues - 851.608 Da.
1 | MET | ALA | GLU | ALA | LEU | PHE | LYS | GLU | ILE | ASP | ||||
2 | VAL | ASN | GLY | ASP | GLY | ALA | VAL | SER | TYR | GLU | ||||
3 | GLU | VAL | LYS | ALA | PHE | VAL | SER | LYS | LYS | ARG | ||||
4 | ALA | ILE | LYS | ASN | GLU | GLN | LEU | LEU | GLN | LEU | ||||
5 | ILE | PHE | LYS | SER | ILE | ASP | ALA | ASP | GLY | ASN | ||||
6 | GLY | GLU | ILE | ASP | GLN | ASN | GLU | PHE | ALA | LYS | ||||
7 | PHE | TYR | GLY | SER | ILE | GLN | GLY | GLN | ASP | LEU | ||||
8 | SER | ASP | ASP | LYS | ILE | GLY | LEU | LYS | VAL | LEU | ||||
9 | PHE | LYS | LEU | MET | ASP | VAL | ASP | GLY | ASP | GLY | ||||
10 | LYS | LEU | THR | LYS | GLU | GLU | VAL | THR | SER | PHE | ||||
11 | PHE | LYS | LYS | HIS | GLY | ILE | GLU | LYS | VAL | ALA | ||||
12 | GLU | GLN | VAL | MET | LYS | ALA | ASP | ALA | ASN | GLY | ||||
13 | ASP | GLY | TYR | ILE | THR | LEU | GLU | GLU | PHE | LEU | ||||
14 | GLU | PHE | SER | LEU |
sample_1: (Y81F)-EhCaBP1, [U-99% 15N], 0.8 ± 0.1 mM; H2O 90%; D2O 10%
sample_2: (Y81F)-EhCaBP1, [U-99% 13C; U-99% 15N], 0.8 ± 0.1 mM; H2O 90%; D2O 10%
sample_3: (Y81F)-EhCaBP1, [U-99% 13C; U-99% 15N], 0.8 ± 0.1 mM; D2O 100%
sample_conditions_1: ionic strength: 0.05 M; pH: 7.4; pressure: 1 atm; temperature: 298 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_3 | isotropic | sample_conditions_1 |
3D HNCO | sample_2 | isotropic | sample_conditions_1 |
3D HNCACB | sample_2 | isotropic | sample_conditions_1 |
3D 1H-15N TOCSY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_2 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_3 | isotropic | sample_conditions_1 |
TOPSPIN, Bruker Biospin - collection, data analysis, processing
FELIX, Accelrys Software Inc. - data analysis, processing
CARA, Keller and Wuthrich - chemical shift assignment, data analysis
CYANA, Guntert, Mumenthaler and Wuthrich - refinement, structure solution
BMRB | 19193 19197 4271 |
PDB | |
DBJ | BAN39246 |
GB | AAA29089 EAL48959 EKE39141 EMD43507 EMH75928 |
REF | XP_008858522 XP_654345 |
SP | P38505 |
AlphaFold | P38505 |
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