BMRB Entry 15349
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_anomalous, AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR15349
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Title: Solution structure of second SH3 domain of adaptor Nck PubMed: 18269246
Deposition date: 2007-06-29 Original release date: 2008-02-29
Authors: Hake, Michael; Choowongkomon, Kiattawee; Carlin, Cathleen; Sonnichsen, Frank
Citation: Hake, Michael; Choowongkomon, Kiattawee; Kostenko, Olga; Carlin, Cathleen; Sonnichsen, Frank. "Specificity Determinants of a Novel Nck Interaction with the Juxtamembrane Domain of the Epidermal Growth Factor Receptor" Biochemistry 47, 3096-3108 (2008).
Assembly members:
Nck1-2, polymer, 61 residues, 6992.865 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):
Nck1-2: GSLNMPAYVKFNYMAEREDE
LSLIKGTKVIVMEKCSDGWW
RGSYNGQVGWFPSNYVTEEG
D
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 263 |
15N chemical shifts | 58 |
1H chemical shifts | 398 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | Nck1-2 SH3 | 1 |
Entities:
Entity 1, Nck1-2 SH3 61 residues - 6992.865 Da.
1 | GLY | SER | LEU | ASN | MET | PRO | ALA | TYR | VAL | LYS | ||||
2 | PHE | ASN | TYR | MET | ALA | GLU | ARG | GLU | ASP | GLU | ||||
3 | LEU | SER | LEU | ILE | LYS | GLY | THR | LYS | VAL | ILE | ||||
4 | VAL | MET | GLU | LYS | CYS | SER | ASP | GLY | TRP | TRP | ||||
5 | ARG | GLY | SER | TYR | ASN | GLY | GLN | VAL | GLY | TRP | ||||
6 | PHE | PRO | SER | ASN | TYR | VAL | THR | GLU | GLU | GLY | ||||
7 | ASP |
Samples:
sample_1: Nck1-2, [U-99% 13C; U-99% 15N], 0.5 1.0 mM; sodium phosphate 20 mM; sodium chloride 100 mM; sodium azide 2 mM; EDTA 1 mM; DTT 4 mM
sample_conditions_1: ionic strength: 100 mM; pH: 6.1; pressure: 1 atm; temperature: 310 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_1 | isotropic | sample_conditions_1 |
2D 1H-1H NOESY | sample_1 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D HNCACB | sample_1 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D H(CCO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
Software:
CYANA v2.1, Guntert, Mumenthaler and Wuthrich - structure solution
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
NMRView v5.2.1, Johnson, One Moon Scientific - chemical shift assignment, data analysis, peak picking
CNS v1.1, Brunger, Adams, Clore, Gros, Nilges and Read - water refinement
NMR spectrometers:
- Varian INOVA 600 MHz
- Varian INOVA 500 MHz
- Bruker Avance 600 MHz
Related Database Links:
PDB | |
DBJ | BAH13487 |
EMBL | CAH89589 |
REF | NP_001124702 NP_001177725 XP_003265315 XP_003992119 XP_004037761 |
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