BMRB Entry 17629
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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/BMR17629
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Title: Yeast Nbp2p SH3 domain in complex with a peptide from Ste20p
Deposition date: 2011-05-07 Original release date: 2011-06-03
Authors: Gorelik, Maryna; Davidson, Alan
Citation: Gorelik, Maryna; Davidson, Alan. "Not known" Not known ., .-..
Assembly members:
Nbp2_SH3, polymer, 73 residues, 7562.403 Da.
Ste20_peptide, polymer, 16 residues, 1639.933 Da.
Natural source: Common Name: baker Taxonomy ID: 4932 Superkingdom: not available Kingdom: not available Genus/species: Eukaryota Fungi
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
Nbp2_SH3: MAIVNQRAVALYDFEPENDN
ELRLAEGDIVFISYKHGQGW
LVAENESGSKTGLVPEEFVS
YIQPELEHHHHHH
Ste20_peptide: GKFIPSRPAPKPPSSA
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 280 |
15N chemical shifts | 71 |
1H chemical shifts | 564 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | Nbp2_SH3 | 1 |
2 | Ste20_peptide | 2 |
Entities:
Entity 1, Nbp2_SH3 73 residues - 7562.403 Da.
Residues 1-2 and 66-67 represent non-native residues obtained from cloning. Residues 68-73 represent His tag.
1 | MET | ALA | ILE | VAL | ASN | GLN | ARG | ALA | VAL | ALA | ||||
2 | LEU | TYR | ASP | PHE | GLU | PRO | GLU | ASN | ASP | ASN | ||||
3 | GLU | LEU | ARG | LEU | ALA | GLU | GLY | ASP | ILE | VAL | ||||
4 | PHE | ILE | SER | TYR | LYS | HIS | GLY | GLN | GLY | TRP | ||||
5 | LEU | VAL | ALA | GLU | ASN | GLU | SER | GLY | SER | LYS | ||||
6 | THR | GLY | LEU | VAL | PRO | GLU | GLU | PHE | VAL | SER | ||||
7 | TYR | ILE | GLN | PRO | GLU | LEU | GLU | HIS | HIS | HIS | ||||
8 | HIS | HIS | HIS |
Entity 2, Ste20_peptide 16 residues - 1639.933 Da.
1 | GLY | LYS | PHE | ILE | PRO | SER | ARG | PRO | ALA | PRO | ||||
2 | LYS | PRO | PRO | SER | SER | ALA |
Samples:
sample_1: Nbp2 SH3, [U-99% 13C; U-99% 15N], 0.7 ± 0.1 mM; Ste20 peptide 1.4 ± 0.1 mM; sodium chloride 100 mM; sodium phosphate 50 mM; sodium azide 0.05%%; D2O 5%%; H2O 95%%
sample_2: Nbp2 SH3, [U-99% 13C; U-99% 15N], 0.7 ± 0.1 mM; Ste20 peptide 1.4 ± 0.1 mM; sodium chloride 100 mM; sodium phosphate 50 mM; sodium azide 0.05%; D2O 100%
sample_3: Nbp2 SH3, [U-99% 13C; U-99% 15N], 0.7 ± 0.1 mM; Ste20 peptide 0.7 ± 0.1 mM; sodium chloride 100 mM; sodium phosphate 50 mM; sodium azide 0.05%; D2O 5%; H2O 95%
sample_4: Nbp2 SH3, [U-99% 13C; U-99% 15N], 0.7 ± 0.1 mM; Ste20 peptide 0.7 ± 0.1 mM; sodium chloride 100 mM; sodium phosphate 50 mM; sodium azide 0.05%; D2O 100%
sample_conditions_1: ionic strength: 100 mM; pH: 6.8; pressure: 1 atm; temperature: 273 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 HNCACB | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D HN(CO)CA | sample_1 | isotropic | sample_conditions_1 |
3D C(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D H(CCO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-COSY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_2 | isotropic | sample_conditions_1 |
N15 C13 filtered 2D 1H-1H TOCSY | sample_3 | isotropic | sample_conditions_1 |
15N C13 filtered 2D 1H-1H NOESY | sample_3 | isotropic | sample_conditions_1 |
13C half-filtered 3D 1H-13C NOESY | sample_4 | isotropic | sample_conditions_1 |
13C filtered 2D 1H-1H COSY | sample_4 | isotropic | sample_conditions_1 |
Software:
SPARKY, Goddard - chemical shift assignment, peak picking
CYANA, Guntert, Mumenthaler and Wuthrich - chemical shift assignment, data analysis, structure solution
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
TALOS, Cornilescu, Delaglio and Bax - geometry optimization
NMR spectrometers:
- Bruker INOVA 500 MHz
- Bruker INOVA 800 MHz
Related Database Links:
PDB | |
DBJ | BAA07790 GAA22392 GAA23703 |
EMBL | CAA90382 CAY78665 |
GB | AAS56004 AHY75148 AJP37876 AJU57998 AJU58693 AAA35038 AAA35111 AAB69747 AHY77690 EDN62227 |
REF | NP_010446 NP_011856 |
SP | Q12163 Q03497 |
TPG | DAA12002 DAA06681 |
BMRB | 16970 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts