BMRB Entry 15841
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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/BMR15841
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Title: Solution NMR Structure of Protein FeoA from Clostridium thermocellum, Northeast Structural Genomics Consortium Target CmR17
Deposition date: 2008-06-29 Original release date: 2008-08-19
Authors: Zeri, Ana; Singarapu, Kiran; Mills, Jeffrey; Wu, Yibing; Garcia, Erwin; Wang, Huang; Jiang, Mei; Foote, Erica; Xiao, Rong; Nair, Rajesh; Everett, John; Swapna, G; Acton, Thomas; Rost, Burkhard; Montelione, Gaetano; Szyperski, Thomas
Citation: Zeri, Ana; Singarapu, Kiran; Mills, Jeffrey; Wu, Yibing; Garcia, Erwin; Wang, Huang; Jiang, Mei; Foote, Erica; Xiao, Rong; Nair, Rajesh; Everett, John; Swapna, G; Acton, Thomas; Rost, Burkhard; Montelione, Gaetano; Szyperski, Thomas. "Solution NMR Structure of Protein FeoA from Clostridium thermocellum, Northeast Structural Genomics Consortium Target CmR17" Not known ., .-..
Assembly members:
CmR17, polymer, 81 residues, 9247.962 Da.
Natural source: Common Name: Clostridium thermocellum Taxonomy ID: 1515 Superkingdom: Bacteria Kingdom: not available Genus/species: Clostridium thermocellum
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
CmR17: MFSLRDAKCGQTVKVVKLHG
TGALKRRIMDMGITRGCEIY
IRKVAPLGDPIQINVRGYEL
SLRKSAAEMIEVELEHHHHH
H
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 363 |
15N chemical shifts | 82 |
1H chemical shifts | 595 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | CmR17 | 1 |
Entities:
Entity 1, CmR17 81 residues - 9247.962 Da.
1 | MET | PHE | SER | LEU | ARG | ASP | ALA | LYS | CYS | GLY | ||||
2 | GLN | THR | VAL | LYS | VAL | VAL | LYS | LEU | HIS | GLY | ||||
3 | THR | GLY | ALA | LEU | LYS | ARG | ARG | ILE | MET | ASP | ||||
4 | MET | GLY | ILE | THR | ARG | GLY | CYS | GLU | ILE | TYR | ||||
5 | ILE | ARG | LYS | VAL | ALA | PRO | LEU | GLY | ASP | PRO | ||||
6 | ILE | GLN | ILE | ASN | VAL | ARG | GLY | TYR | GLU | LEU | ||||
7 | SER | LEU | ARG | LYS | SER | ALA | ALA | GLU | MET | ILE | ||||
8 | GLU | VAL | GLU | LEU | GLU | HIS | HIS | HIS | HIS | HIS | ||||
9 | HIS |
Samples:
sample_1: entity, [U-100% 13C; U-100% 15N], 1.1 mM; H2O 90%; D2O, [U-100% 2H], 10%
sample_2: entity, [U-10% 13C; U-100% 15N], 1.2 mM; H2O 90%; D2O, [U-100% 2H], 10%
sample_conditions_1: ionic strength: 0.5 M; pH: 6.5; pressure: 1 atm; temperature: 298 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-13C HSQC | sample_2 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
GFT (4,3)D HCCH COSY | sample_1 | isotropic | sample_conditions_1 |
GFT (4,3)D simNOESY | sample_1 | isotropic | sample_conditions_1 |
GFT (4,3)D HNCABCA | sample_1 | isotropic | sample_conditions_1 |
GFT (4,3)D CABCACONH | sample_1 | isotropic | sample_conditions_1 |
GFT (4,3)D HABCABCONHN | sample_1 | isotropic | sample_conditions_1 |
Software:
CNS, Brunger, Adams, Clore, Gros, Nilges and Read - refinement
AutoAssign, Zimmerman, Moseley, Kulikowski and Montelione - chemical shift assignment
AutoStruct, Huang, Tejero, Powers and Montelione - structure solution
CYANA, Guntert, Mumenthaler and Wuthrich - structure solution
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
VNMRJ, Varian - collection
XEASY, Bartels et al. - data analysis, peak picking
Molmol, Koradi, Billeter and Wuthrich - data analysis, refinement
SPSCAN, Glaser - processing
NMR spectrometers:
- Varian INOVA 750 MHz
- Varian INOVA 600 MHz
Related Database Links:
PDB | |
DBJ | GAE86915 |
EMBL | CDG35310 |
GB | ABN51854 ADU74670 EEU02157 EFB38990 EIC05553 |
REF | WP_003516537 WP_003520966 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts