Chem Shift validation: AVS_full
BMRB Entry DOI: doi:10.13018/BMR50681
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NMR-STAR v3 text file.
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Citation: Camponeschi, Francesca; Gallo, Angelo; Piccioli, Mario; Banci, Lucia. "The long-standing relationship between paramagnetic NMR and iron-sulfur proteins: the mitoNEET example. An old method for new stories or the other way around?" Magn. Reson. 2, 203-221 (2021).
Assembly members:
entity_1, polymer, 83 residues, Formula weight is not available
entity_FES, non-polymer, 175.820 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 Vector: pET151-D/TOPO
Entity Sequences (FASTA):
entity_1: GIDPFMKRFYVKDHRNKAMI
NLHIQKDNPKIVHAFDMEDL
GDKAVYCRCWRSKKFPFCDG
AHTKHNEETGDNVGPLIIKK
KET
Data type | Count |
13C chemical shifts | 179 |
15N chemical shifts | 44 |
1H chemical shifts | 286 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | mitoNEET | 1 |
2 | FES | 2 |
Entity 1, mitoNEET 83 residues - Formula weight is not available
The real sequence start from residue 7 and it should be translated to number 32
1 | GLY | ILE | ASP | PRO | PHE | MET | LYS | ARG | PHE | TYR | ||||
2 | VAL | LYS | ASP | HIS | ARG | ASN | LYS | ALA | MET | ILE | ||||
3 | ASN | LEU | HIS | ILE | GLN | LYS | ASP | ASN | PRO | LYS | ||||
4 | ILE | VAL | HIS | ALA | PHE | ASP | MET | GLU | ASP | LEU | ||||
5 | GLY | ASP | LYS | ALA | VAL | TYR | CYS | ARG | CYS | TRP | ||||
6 | ARG | SER | LYS | LYS | PHE | PRO | PHE | CYS | ASP | GLY | ||||
7 | ALA | HIS | THR | LYS | HIS | ASN | GLU | GLU | THR | GLY | ||||
8 | ASP | ASN | VAL | GLY | PRO | LEU | ILE | ILE | LYS | LYS | ||||
9 | LYS | GLU | THR |
Entity 2, FES - Fe2 S2 - 175.820 Da.
1 | FES |
sample_1: mitoNEET protein cytosolic region, [U-13C; U-15N], 0.5 mM; D2O, [U-2H], 10%; H2O 90%; potassium phosphate 50 mM; sodium dithionite 10 mM
sample_conditions_1: ionic strength: 60 mM; pH: 7.0; pressure: 1 atm; temperature: 298 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D HN(CA)CO | sample_1 | isotropic | sample_conditions_1 |
3D HNCA | sample_1 | isotropic | sample_conditions_1 |
3D HN(CO)CA | sample_1 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D CBCANH | sample_1 | isotropic | sample_conditions_1 |
3D (H)CCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
3D HBHA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
TOPSPIN v3.2 - collection
TOPSPIN v3.2 - processing
CARA v1.9.2a4 - 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