BMRB Entry 25790
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, SPARTA
BMRB Entry DOI: doi:10.13018/BMR25790
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Title: Solution structure of regulatory protein PubMed: 27009356
Deposition date: 2015-09-02 Original release date: 2016-07-13
Authors: Veverka, Vaclav; Hexnerova, Rozalie
Citation: Klima, Martin; Toth, Daniel; Hexnerova, Rozalie; Baumlova, Adriana; Chalupska, Dominika; Tykvart, Jan; Rezabkova, Lenka; Sengupta, Nivedita; Man, Petr; Dubankova, Anna; Humpolickova, Jana; Nencka, Radim; Veverka, Vaclav; Balla, Tamas; Boura, Evzen. "Structural insights and in vitro reconstitution of membrane targeting and activation of human PI4KB by the ACBD3 protein" Sci. Rep. 6, 23641-23641 (2016).
Assembly members:
entity, polymer, 69 residues, 8293.291 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):
entity: MQQKQQIMAALNSQTAVQFQ
QYAAQQYPGNYEQQQILIRQ
LQEQHYQQYMQQLYQVQLAQ
QQAALQKQQ
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 289 |
15N chemical shifts | 83 |
1H chemical shifts | 508 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | entity | 1 |
Entities:
Entity 1, entity 69 residues - 8293.291 Da.
1 | MET | GLN | GLN | LYS | GLN | GLN | ILE | MET | ALA | ALA | ||||
2 | LEU | ASN | SER | GLN | THR | ALA | VAL | GLN | PHE | GLN | ||||
3 | GLN | TYR | ALA | ALA | GLN | GLN | TYR | PRO | GLY | ASN | ||||
4 | TYR | GLU | GLN | GLN | GLN | ILE | LEU | ILE | ARG | GLN | ||||
5 | LEU | GLN | GLU | GLN | HIS | TYR | GLN | GLN | TYR | MET | ||||
6 | GLN | GLN | LEU | TYR | GLN | VAL | GLN | LEU | ALA | GLN | ||||
7 | GLN | GLN | ALA | ALA | LEU | GLN | LYS | GLN | GLN |
Samples:
sample_1: entity, [U-13C; U-15N], 0.28 mM; H2O 90%; D2O 10%
sample_conditions_1: ionic strength: 0.1 M; pH: 6.5; pressure: 1 atm; temperature: 298 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
3D HNCACB | 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 HN(CO)CA | sample_1 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
Software:
CYANA, Guntert, Mumenthaler and Wuthrich - structure solution
YASARA, na - refinement
NMR spectrometers:
- Bruker Avance 600 MHz
- Bruker Avance 850 MHz
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts