BMRB Entry 15418
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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/BMR15418
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Title: NMR structure of the S100A6 dimer in complex with a binding fragment of the Siah-1 interacting protein PubMed: 18803400
Deposition date: 2007-08-06 Original release date: 2008-10-29
Authors: Lee, Young-Tae; Chazin, Walter
Citation: Lee, Young-Tae; Dimitrova, Yoana; Schneider, Gabriela; Ridenour, Whitney; Bhattacharya, Shibani; Soss, Sarah; Caprioli, Richard; Filipek, Anna; Chazin, Walter. "Structure of the S100A6 complex with a fragment from the C-terminal domain of Siah-1 interacting protein: a novel mode for S100 protein target recognition" Biochemistry 47, 10921-10932 (2008).
Assembly members:
S100A6, polymer, 90 residues, 10168.827 Da.
SIP(189-219), polymer, 35 residues, 3648.154 Da.
Natural source: Common Name: rabbit Taxonomy ID: 9986 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Oryctolagus cuniculus
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
S100A6: MASPLDQAIGLLIGIFHKYS
GKEGDKHTLSKKELKELIQK
ELTIGSKLQDAEIVKLMDDL
DRNKDQEVNFQEYITFLGAL
AMIYNEALKG
SIP(189-219): GPGSSEGLMNVLKKIYEDGD
DDMKRTINKAWVESR
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 295 |
15N chemical shifts | 113 |
1H chemical shifts | 391 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | protein, 1 | 1 |
2 | protein, 2 | 1 |
3 | peptide, 1 | 2 |
4 | peptide, 2 | 2 |
Entities:
Entity 1, protein, 1 90 residues - 10168.827 Da.
1 | MET | ALA | SER | PRO | LEU | ASP | GLN | ALA | ILE | GLY | |
2 | LEU | LEU | ILE | GLY | ILE | PHE | HIS | LYS | TYR | SER | |
3 | GLY | LYS | GLU | GLY | ASP | LYS | HIS | THR | LEU | SER | |
4 | LYS | LYS | GLU | LEU | LYS | GLU | LEU | ILE | GLN | LYS | |
5 | GLU | LEU | THR | ILE | GLY | SER | LYS | LEU | GLN | ASP | |
6 | ALA | GLU | ILE | VAL | LYS | LEU | MET | ASP | ASP | LEU | |
7 | ASP | ARG | ASN | LYS | ASP | GLN | GLU | VAL | ASN | PHE | |
8 | GLN | GLU | TYR | ILE | THR | PHE | LEU | GLY | ALA | LEU | |
9 | ALA | MET | ILE | TYR | ASN | GLU | ALA | LEU | LYS | GLY |
Entity 2, peptide, 1 35 residues - 3648.154 Da.
First 4 residues (GPGS) represents residual tag.
1 | GLY | PRO | GLY | SER | SER | GLU | GLY | LEU | MET | ASN | ||||
2 | VAL | LEU | LYS | LYS | ILE | TYR | GLU | ASP | GLY | ASP | ||||
3 | ASP | ASP | MET | LYS | ARG | THR | ILE | ASN | LYS | ALA | ||||
4 | TRP | VAL | GLU | SER | ARG |
Samples:
D-SIP_U-A6: SIP(189-219), [U-100% 13C; U-100% 15N], 1 mM; S100A6 1 mM; TRIS, [U-2H], 0.05 mM; Ca2+ 0.01 mM; H2O 93%; D2O 5%; d-TFE 2%
15-SIP_U-A6: SIP(189-219), [U-100% 15N], 1 mM; S100A6 1 mM; TRIS, [U-2H], 0.05 mM; Ca2+ 0.01 mM; H2O 93%; D2O 5%; d-TFE 2%
13-SIP_U-A6: SIP(189-219), [U-100% 13C], 1 mM; S100A6 1 mM; TRIS, [U-2H], 0.05 mM; Ca2+ 0.01 mM; D2O 98%; d-TFE 2%
13-SIP_15-A6: SIP(189-219), [U-100% 13C], 2.3 mM; S100A6, [U-100% 15N], 2.3 mM; TRIS, [U-2H], 0.05 mM; Ca2+ 0.01 mM; H2O 93%; D2O 5%; d-TFE 2%
U-SIP_D_A6: SIP(189-219) 1 mM; S100A6, [U-100% 13C; U-100% 15N], 1 mM; TRIS, [U-2H], 0.05 mM; Ca2+ 0.01 mM; H2O 93%; D2O 5%; d-TFE 2%
All_samples: ionic strength: 0.08 M; pH: 6.5; pressure: 1 atm; temperature: 318 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | 15-SIP_U-A6 | isotropic | All_samples |
3D 1H-15N NOESY | 15-SIP_U-A6 | isotropic | All_samples |
3D HNCA | D-SIP_U-A6 | isotropic | All_samples |
3D HNCACB | D-SIP_U-A6 | isotropic | All_samples |
3D CBCA(CO)NH | D-SIP_U-A6 | isotropic | All_samples |
3D HNCO | D-SIP_U-A6 | isotropic | All_samples |
2D 1H-13C HSQC | 13-SIP_U-A6 | isotropic | All_samples |
3D HCCH-TOCSY | 13-SIP_U-A6 | isotropic | All_samples |
3D 1H-13C NOESY | 13-SIP_U-A6 | isotropic | All_samples |
3D 13C-filtered 15N-edited NOESY | 13-SIP_15-A6 | isotropic | All_samples |
2D 1H-15N HSQC | U-SIP_D_A6 | isotropic | All_samples |
3D HNCA | U-SIP_D_A6 | isotropic | All_samples |
3D CBCA(CO)NH | U-SIP_D_A6 | isotropic | All_samples |
Software:
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
CYANA v2.1, Guntert, Mumenthaler and Wuthrich - Structure calculation
AMBER v9, Case, Darden, Cheatham, III, Simmerling, Wang, Duke, Luo, ... and Koll - refinement
NMR spectrometers:
- Bruker Avance 500 MHz
- Bruker Avance 600 MHz
- Bruker Avance 600 MHz
- Bruker Avance 800 MHz
Related Database Links:
BMRB | 4430 |
PDB | |
DBJ | BAA01707 BAE01932 BAG36086 BAG52713 |
REF | NP_001182671 NP_001004208 NP_001007215 NP_001029981 NP_001127554 NP_001253590 |
SP | P30801 Q3T168 Q4R4P3 Q5R6Z8 Q6AYK6 Q9CXW3 |
EMBL | CAA22910 CAH92462 |
GB | AAC16757 AAC21458 AAG34170 AAH05975 AAH22352 |
TPG | DAA21139 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts