BMRB Entry 15851
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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/BMR15851
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Title: NMR structure of calcium-loaded STIM1 EF-SAM PubMed: 18854159
Deposition date: 2008-07-02 Original release date: 2008-10-14
Authors: Stathopulos, Peter; Ikura, Mitsuhiko
Citation: Stathopulos, Peter; Zheng, Le; Li, Guang-Yao; Plevin, Michael; Ikura, Mitsuhiko. "Structural and Mechanistic Insights into STIM1-Mediated Initiation of Store-Operated Calcium Entry" Cell 135, 110-122 (2008).
Assembly members:
stromal_interaction_molecule_1, polymer, 150 residues, 17380.514 Da.
CA, non-polymer, 40.078 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):
stromal_interaction_molecule_1: GSHMASSEDEKLSFEAVRNI
HKLMDDDANGDVDVEESDEF
LREDLNYHDPTVKHSTFHGE
DKLISVEDLWKAWKSSEVYN
WTVDEVVQWLITYVELPQYE
ETFRKLQLSGHAMPRLAVTN
TTMTGTVLKMTDRSHRQKLQ
LKALDTVLFG
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 569 |
15N chemical shifts | 125 |
1H chemical shifts | 978 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | Stromal interaction molecule 1 | 1 |
2 | CALCIUM ION | 2 |
Entities:
Entity 1, Stromal interaction molecule 1 150 residues - 17380.514 Da.
The first 6 residues (numbered -5, -4, -3, -2, -1, 0) are remnants of the non-native affinity tag. The remaining residues are situated in the endoplasmic reticulum luminal portion of STIM1 (58 to 201).
1 | GLY | SER | HIS | MET | ALA | SER | SER | GLU | ASP | GLU | |
2 | LYS | LEU | SER | PHE | GLU | ALA | VAL | ARG | ASN | ILE | |
3 | HIS | LYS | LEU | MET | ASP | ASP | ASP | ALA | ASN | GLY | |
4 | ASP | VAL | ASP | VAL | GLU | GLU | SER | ASP | GLU | PHE | |
5 | LEU | ARG | GLU | ASP | LEU | ASN | TYR | HIS | ASP | PRO | |
6 | THR | VAL | LYS | HIS | SER | THR | PHE | HIS | GLY | GLU | |
7 | ASP | LYS | LEU | ILE | SER | VAL | GLU | ASP | LEU | TRP | |
8 | LYS | ALA | TRP | LYS | SER | SER | GLU | VAL | TYR | ASN | |
9 | TRP | THR | VAL | ASP | GLU | VAL | VAL | GLN | TRP | LEU | |
10 | ILE | THR | TYR | VAL | GLU | LEU | PRO | GLN | TYR | GLU | |
11 | GLU | THR | PHE | ARG | LYS | LEU | GLN | LEU | SER | GLY | |
12 | HIS | ALA | MET | PRO | ARG | LEU | ALA | VAL | THR | ASN | |
13 | THR | THR | MET | THR | GLY | THR | VAL | LEU | LYS | MET | |
14 | THR | ASP | ARG | SER | HIS | ARG | GLN | LYS | LEU | GLN | |
15 | LEU | LYS | ALA | LEU | ASP | THR | VAL | LEU | PHE | GLY |
Entity 2, CALCIUM ION - Ca - 40.078 Da.
1 | CA |
Samples:
sample_1: stromal interaction molecule 1, [U-100% 13C; U-100% 15N], 0.5-1.0 mM; TRIS 20 mM; sodium chloride 100 mM; CALCIUM ION 5 mM
sample_2: stromal interaction molecule 1, [U-100% 13C; U-100% 15N], 0.5-1.0 mM; TRIS, [U-99% 2H], 20 mM; sodium chloride 100 mM; CALCIUM ION 5 mM
sample_condition_1: ionic strength: 105 mM; pH: 8.0; pressure: 1 atm; temperature: 293 K
sample_condition_2: ionic strength: 105 mM; pD: 8.0; pressure: 1 atm; temperature: 293 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_condition_1 |
3D CBCA(CO)NH | sample_1 | isotropic | sample_condition_1 |
3D HNCACB | sample_1 | isotropic | sample_condition_1 |
3D HNCO | sample_1 | isotropic | sample_condition_1 |
3D H(CCO)NH | sample_1 | isotropic | sample_condition_1 |
3D C(CO)NH | sample_1 | isotropic | sample_condition_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_condition_1 |
3D HCCH-TOCSY | sample_2 | isotropic | sample_condition_2 |
2D 1H-13C HSQC | sample_2 | isotropic | sample_condition_2 |
3D 1H-13C NOESY | sample_2 | isotropic | sample_condition_2 |
Software:
CNS vv1.1, Brunger A. T. et.al. - refinement
CYANA vv2.1, Guntert, Mumenthaler and Wuthrich - structure solution
XEASY, Bartels et al. - chemical shift assignment
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
NMR spectrometers:
- Varian INOVA 500 MHz
- Varian INOVA 600 MHz
- Bruker Avance 800 MHz
- Bruker Avance 900 MHz
Related Database Links:
PDB | |
DBJ | BAG54839 |
GB | AAC51627 AAH21300 ABM86435 ABW03792 ADO20317 |
REF | NP_001248464 NP_001264890 NP_001264891 NP_003147 XP_001160553 |
SP | Q13586 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts