BMRB Entry 18088
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_anomalous, AVS_full, LACS, SPARTA
BMRB Entry DOI: doi:10.13018/BMR18088
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Title: Post-translational S-nitrosylation is an endogenous factor fine-tuning human S100A1 protein properties PubMed: 22989881
Deposition date: 2011-11-17 Original release date: 2012-09-24
Authors: Lenarcic Zivkovic, Martina; Zareba-Koziol, Monika; Zhukova, Lilia; Poznanski, Jarek; Zhukov, Igor; Wyslouch-Cieszynska, Aleksandra
Citation: Lenari ivkovic, Martina; Zarba-Kozio, Monika; Zhukova, Liliya; Poznaski, Jarosaw; Zhukov, Igor; Wysouch-Cieszyska, Aleksandra. "Post-translational S-nitrosylation is an endogenous factor fine tuning the properties of human S100A1 protein." J. Biol. Chem. 287, 40457-40470 (2012).
Assembly members:
S100A1 with post-translational S-nitrosylation, strand 1, polymer, 93 residues, 10454.682 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):
S100A1 with post-translational S-nitrosylation, strand 1: GSELETAMETLINVFHAHSG
KEGDKYKLSKKELKELLQTE
LSGFLDAQKDVDAVDKVMKE
LDENGDGEVDFQEYVVLVAA
LTVAXNNFFWENS
- assigned_chemical_shifts
| Data type | Count |
| 13C chemical shifts | 321 |
| 15N chemical shifts | 100 |
| 1H chemical shifts | 652 |
Additional metadata:
Assembly:
| Entity Assembly ID | Entity Name | Entity ID |
|---|---|---|
| 1 | S100A1 with post-translational S-nitrosylation, strand 1 | 1 |
| 2 | S100A1 with post-translational S-nitrosylation, strand 2 | 1 |
Entities:
Entity 1, S100A1 with post-translational S-nitrosylation, strand 1 93 residues - 10454.682 Da.
| 1 | GLY | SER | GLU | LEU | GLU | THR | ALA | MET | GLU | THR | ||||
| 2 | LEU | ILE | ASN | VAL | PHE | HIS | ALA | HIS | SER | GLY | ||||
| 3 | LYS | GLU | GLY | ASP | LYS | TYR | LYS | LEU | SER | LYS | ||||
| 4 | LYS | GLU | LEU | LYS | GLU | LEU | LEU | GLN | THR | GLU | ||||
| 5 | LEU | SER | GLY | PHE | LEU | ASP | ALA | GLN | LYS | ASP | ||||
| 6 | VAL | ASP | ALA | VAL | ASP | LYS | VAL | MET | LYS | GLU | ||||
| 7 | LEU | ASP | GLU | ASN | GLY | ASP | GLY | GLU | VAL | ASP | ||||
| 8 | PHE | GLN | GLU | TYR | VAL | VAL | LEU | VAL | ALA | ALA | ||||
| 9 | LEU | THR | VAL | ALA | SNC | ASN | ASN | PHE | PHE | TRP | ||||
| 10 | GLU | ASN | SER |
Samples:
sample_1: S100A1_pt, [U-98% 13C; U-98% 15N], 0.8 mM; H2O 90%; D2O 10%; sodium chloride 150 mM
sample_conditions_1: ionic strength: 150 mM; pH: 7.2; pressure: 1 atm; temperature: 298 K
Experiments:
| Name | Sample | Sample state | Sample conditions |
|---|---|---|---|
| 2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
| 3D HNCO | sample_1 | isotropic | sample_conditions_1 |
| 3D HNCA | sample_1 | isotropic | sample_conditions_1 |
| 3D HN(CO)CA | 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 HBHA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
| 3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
| 2D 1H-13C HSQC aliphatic | sample_1 | isotropic | sample_conditions_1 |
| 3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
| 3D 1H-13C NOESY aliphatic | sample_1 | isotropic | sample_conditions_1 |
| 3D 1H-13C NOESY aromatic | sample_1 | isotropic | sample_conditions_1 |
Software:
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
SPARKY, Goddard - chemical shift assignment, peak picking
CYANA v3.0, Guntert, Mumenthaler and Wuthrich - structure solution
X-PLOR NIH, Schwieters, Kuszewski, Tjandra and Clore - refinement, structure solution
NMR spectrometers:
- Varian Uniform NMR System 800 MHz
Related Database Links:
| BMRB | 16360 17857 18087 18089 18101 18230 18231 18545 |
| PDB | |
| DBJ | BAE90380 BAG35086 BAG70130 BAG70260 |
| EMBL | CAA41107 CAH90674 |
| GB | AAH14392 AAI41992 AAI48020 AAP35584 AAP36328 |
| PRF | 2003367A |
| REF | NP_001092512 NP_001127319 NP_001270255 NP_006262 XP_001111015 |
| SP | P02639 P23297 Q5RC36 |
| TPG | DAA31796 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts