BMRB Entry 15388
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR15388
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Title: Solution Structure of F153W cardiac troponin C PubMed: 16131667
Deposition date: 2007-07-18 Original release date: 2008-03-13
Authors: Wang, Xu; Mercier, Pascal; Letourneau, Paul-Jean; Sykes, Brian
Citation: Wang, Xu; Mercier, Pascal; Letourneau, Paul-Jean; Sykes, Brian. "Effects of Phe-to-Trp mutation and fluorotryptophan incorporation on the solution structure of cardiac troponin C, and analysis of its suitability as a potential probe for in situ NMR studies" Protein Sci. 14, 2447-2460 (2005).
Assembly members:
F153W, polymer, 161 residues, 18428.521 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):
F153W: MDDIYKAAVEQLTEEQKNEF
KAAFDIFVLGAEDGSISTKE
LGKVMRMLGQNPTPEELQEM
IDEVDEDGSGTVDFDEFLVM
MVRSMKDDSKGKSEEELSDL
FRMFDKNADGYIDLDELKIM
LQATGETITEDDIEELMKDG
DKNNDGRIDYDEWLEFMKGV
E
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 509 |
15N chemical shifts | 154 |
1H chemical shifts | 956 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | F153W cTnC | 1 |
2 | Calcium | 2 |
Entities:
Entity 1, F153W cTnC 161 residues - 18428.521 Da.
This protein is a version of cardiac troponin C with F153 mutated to W
1 | MET | ASP | ASP | ILE | TYR | LYS | ALA | ALA | VAL | GLU | ||||
2 | GLN | LEU | THR | GLU | GLU | GLN | LYS | ASN | GLU | PHE | ||||
3 | LYS | ALA | ALA | PHE | ASP | ILE | PHE | VAL | LEU | GLY | ||||
4 | ALA | GLU | ASP | GLY | SER | ILE | SER | THR | LYS | GLU | ||||
5 | LEU | GLY | LYS | VAL | MET | ARG | MET | LEU | GLY | GLN | ||||
6 | ASN | PRO | THR | PRO | GLU | GLU | LEU | GLN | GLU | MET | ||||
7 | ILE | ASP | GLU | VAL | ASP | GLU | ASP | GLY | SER | GLY | ||||
8 | THR | VAL | ASP | PHE | ASP | GLU | PHE | LEU | VAL | MET | ||||
9 | MET | VAL | ARG | SER | MET | LYS | ASP | ASP | SER | LYS | ||||
10 | GLY | LYS | SER | GLU | GLU | GLU | LEU | SER | ASP | LEU | ||||
11 | PHE | ARG | MET | PHE | ASP | LYS | ASN | ALA | ASP | GLY | ||||
12 | TYR | ILE | ASP | LEU | ASP | GLU | LEU | LYS | ILE | MET | ||||
13 | LEU | GLN | ALA | THR | GLY | GLU | THR | ILE | THR | GLU | ||||
14 | ASP | ASP | ILE | GLU | GLU | LEU | MET | LYS | ASP | GLY | ||||
15 | ASP | LYS | ASN | ASN | ASP | GLY | ARG | ILE | ASP | TYR | ||||
16 | ASP | GLU | TRP | LEU | GLU | PHE | MET | LYS | GLY | VAL | ||||
17 | GLU |
Entity 2, Calcium - Ca - 40.078 Da.
1 | CA |
Samples:
sample_1: F153W 1.0 ± 0.2 mM; Calcium 10 ± 1 mM; potassium chloride 100 ± 10 mM
sample_conditions_1: ionic strength: 0.1 M; pH: 6.7; pressure: 1 atm; temperature: 303 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | 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 HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
Software:
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
NMRView, Johnson, One Moon Scientific - data analysis
CYANA, Guntert, Mumenthaler and Wuthrich - structure solution
NMR spectrometers:
- Varian INOVA 600 MHz
Related Database Links:
BMRB | 15385 15400 15427 16190 17103 19789 25034 25035 25120 25495 25797 |
PDB | |
DBJ | BAG36483 |
EMBL | CAA30736 CAG46663 CAG46683 |
GB | AAA36772 AAA37492 AAA37493 AAB91994 AAH30244 |
PIR | TPHUCC |
PRF | 1510257A 750650A |
REF | NP_001029277 NP_001029523 NP_001123715 NP_001272501 NP_003271 |
SP | P02591 P19123 P63315 P63316 P63317 |
TPG | DAA16908 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts