BMRB Entry 15000
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_anomalous, AVS_full
BMRB Entry DOI: doi:10.13018/BMR15000
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Title: Solution structure of chicken villin headpiece subdomain containing a fluorinated side chain in the core PubMed: 17123960
Deposition date: 2006-09-07 Original release date: 2006-10-20
Authors: Cornilescu, Claudia; Cornilescu, Gabriel; Hadley, Erik; Gellman, Samuel; Markley, John
Citation: Cornilescu, Gabriel; Hadley, Erik; Woll, Matthew; Markley, John; Gellman, Samuel; Cornilescu, Claudia. "Solution structure of a small protein containing a fluorinated side chain in the core." Protein Sci. 16, 14-19 (2007).
Assembly members:
F5-Phe-cVHP, polymer, 35 residues, Formula weight is not available
Natural source: Common Name: chicken Taxonomy ID: 9031 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Gallus gallus
Experimental source: Production method: chemical synthesis
Entity Sequences (FASTA):
F5-Phe-cVHP: LSDEDFRAVXGMTRSAFANL
PLWRQQNLRRERGLF
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 77 |
15N chemical shifts | 40 |
1H chemical shifts | 223 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | F5-Phe-cVHP | 1 |
Entities:
Entity 1, F5-Phe-cVHP 35 residues - Formula weight is not available
1 | LEU | SER | ASP | GLU | ASP | PHE | ARG | ALA | VAL | PHF | ||||
2 | GLY | MET | THR | ARG | SER | ALA | PHE | ALA | ASN | LEU | ||||
3 | PRO | LEU | TRP | ARG | GLN | GLN | ASN | LEU | ARG | ARG | ||||
4 | GLU | ARG | GLY | LEU | PHE |
Samples:
unlabeled_sample: F5-Phe-cVHP 4 mM
selectively_labeled_sample: F5-Phe-cVHP, [15N]-Ala, Phe, Leu, 2 mM
sample_conditions: ionic strength: 10 mM; pH: 5.0; pressure: 1 atm; temperature: 298 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | unlabeled_sample | isotropic | sample_conditions |
2D 1H-13C HSQC | unlabeled_sample | isotropic | sample_conditions |
2D COSY | unlabeled_sample | isotropic | sample_conditions |
2D TOCSY | unlabeled_sample | isotropic | sample_conditions |
2D NOESY | unlabeled_sample | isotropic | sample_conditions |
2D 1H-15N HSQC | selectively_labeled_sample | isotropic | sample_conditions |
2D HNCO | selectively_labeled_sample | isotropic | sample_conditions |
2D HNCACB | selectively_labeled_sample | isotropic | sample_conditions |
2D HNHA | selectively_labeled_sample | isotropic | sample_conditions |
2D HNHB | selectively_labeled_sample | isotropic | sample_conditions |
19F-HOESY | unlabeled_sample | isotropic | sample_conditions |
Software:
NMRPipe, F Delaglio, S Grzesiek, GW Vuister, G Zhu, J Pfeifer and A Bax - processing
PIPP, D Garrett - chemical shift assignment, data analysis, peak picking
SPARKY, T Goddard - chemical shift assignment
CYANA, P Guntert, C Mumenthaler and K Wuthrich - structure solution
X-PLOR NIH, CD Schwieters, JJ Kuszewski, N Tjandra and GM Clore - refinement, structure solution
NMR spectrometers:
- Bruker Avance 500 MHz
- Bruker Avance 500 MHz
- Bruker Avance 750 MHz
- Varian INOVA 600 MHz
- Varian INOVA 800 MHz
- Varian INOVA 900 MHz
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts