BMRB Entry 7128
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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/BMR7128
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Title: Fibronecting 1F3-2F3 backbone chemical shift assignments PubMed: 17464288
Deposition date: 2006-05-23 Original release date: 2007-05-29
Authors: Vakonakis, Ioannis; Campbell, Iain
Citation: Vakonakis, Ioannis; Staunton, David; Rooney, Luke; Campbell, Iain. "Interdomain association in fibronectin: insight into cryptic sites and fibrillogenesis" EMBO J. 26, 2575-2583 (2007).
Assembly members:
1F3-2F3, polymer, 201 residues, 22097 Da.
Natural source: Common Name: Human Taxonomy ID: 9606 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Homo sapiens
Experimental source: Production method: recombinant technology
Entity Sequences (FASTA):
1F3-2F3: SGPVEVFITETPSQPNSHPI
QWNAPQPSHISKYILRWRPK
NSVGRWKEATIPGHLNSYTI
KGLKPGVVYEGQLISIQQYG
HQEVTRFDFTTTSTSTPVTS
NTVTGETTPFSPLVATSESV
TEITASSFVVSWVSASDTVS
GFRVEYELSEEGDEPQYLDL
PSTATSVNIPDLLPGRKYIV
NVYQISEDGEQSLILSTSQT
T
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 322 |
15N chemical shifts | 175 |
1H chemical shifts | 175 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | 1F3-2F3 | 1 |
Entities:
Entity 1, 1F3-2F3 201 residues - 22097 Da.
This sequence corresponds to the first two type III domain on human Fibronectin and the connecting amino acid linker
1 | SER | GLY | PRO | VAL | GLU | VAL | PHE | ILE | THR | GLU | ||||
2 | THR | PRO | SER | GLN | PRO | ASN | SER | HIS | PRO | ILE | ||||
3 | GLN | TRP | ASN | ALA | PRO | GLN | PRO | SER | HIS | ILE | ||||
4 | SER | LYS | TYR | ILE | LEU | ARG | TRP | ARG | PRO | LYS | ||||
5 | ASN | SER | VAL | GLY | ARG | TRP | LYS | GLU | ALA | THR | ||||
6 | ILE | PRO | GLY | HIS | LEU | ASN | SER | TYR | THR | ILE | ||||
7 | LYS | GLY | LEU | LYS | PRO | GLY | VAL | VAL | TYR | GLU | ||||
8 | GLY | GLN | LEU | ILE | SER | ILE | GLN | GLN | TYR | GLY | ||||
9 | HIS | GLN | GLU | VAL | THR | ARG | PHE | ASP | PHE | THR | ||||
10 | THR | THR | SER | THR | SER | THR | PRO | VAL | THR | SER | ||||
11 | ASN | THR | VAL | THR | GLY | GLU | THR | THR | PRO | PHE | ||||
12 | SER | PRO | LEU | VAL | ALA | THR | SER | GLU | SER | VAL | ||||
13 | THR | GLU | ILE | THR | ALA | SER | SER | PHE | VAL | VAL | ||||
14 | SER | TRP | VAL | SER | ALA | SER | ASP | THR | VAL | SER | ||||
15 | GLY | PHE | ARG | VAL | GLU | TYR | GLU | LEU | SER | GLU | ||||
16 | GLU | GLY | ASP | GLU | PRO | GLN | TYR | LEU | ASP | LEU | ||||
17 | PRO | SER | THR | ALA | THR | SER | VAL | ASN | ILE | PRO | ||||
18 | ASP | LEU | LEU | PRO | GLY | ARG | LYS | TYR | ILE | VAL | ||||
19 | ASN | VAL | TYR | GLN | ILE | SER | GLU | ASP | GLY | GLU | ||||
20 | GLN | SER | LEU | ILE | LEU | SER | THR | SER | GLN | THR | ||||
21 | THR |
Samples:
sample_1: 1F3-2F3, [U-15N], 1.2 ± 0.2 mM; NaCl 150 mM; NaPi 20 mM; D2O 5%; H2O 95%
sample_2: 1F3-2F3, [U-13C; U-15N], 1 ± 0.1 ; NaCl 150 mM; NaPi 20 mM; D2O 5%; H2O 95%
conditions_1: ionic strength: 420 mM; pH: 7; pressure: 1 atm; temperature: 303 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
15N HSQC | sample_1 | not available | conditions_1 |
CBCA(CO)NH | sample_2 | not available | conditions_1 |
CBCANH | sample_2 | not available | conditions_1 |
HNCA | sample_2 | not available | conditions_1 |
HN(CO)CA | sample_2 | not available | conditions_1 |
Software:
Omega Spectrometer Operating Software vBeta 6.0.3b2, GE/Bruker - Data collection
NMRPipe v2.3 Rev 2005.319.11.22, NIH/NIDDK - Data processing
PIPP v4.3.7, NIH - Data analysis
TOPSPIN v1.3, Bruker - Data collection
NMR spectrometers:
- home build . 750 MHz
- Bruker Avance II 500 MHz
Related Database Links:
PDB |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts