BMRB Entry 17720
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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/BMR17720
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Title: Solution Structure of N-terminal Cytosolic Domain of Rhomboid Intramembrane Protease from Escherichia Coli PubMed: 22963263
Deposition date: 2011-06-20 Original release date: 2012-09-24
Authors: Sherratt, Allison; Ghasriani, Houman; Goto, Natalie
Citation: Sherratt, Allison; Blais, David; Ghasriani, Houman; Pezacki, John Paul; Goto, Natalie. "Activity-based protein profiling of the Escherichia coli GlpG rhomboid protein delineates the catalytic core." Biochemistry 51, 7794-7803 (2012).
Assembly members:
NGlpG, polymer, 63 residues, 7142.065 Da.
Natural source: Common Name: E. coli Taxonomy ID: 562 Superkingdom: Bacteria Kingdom: not available Genus/species: Escherichia coli
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
NGlpG: MLMITSFANPRVAQAFVDYM
ATQGVILTIQQHNQSDVWLA
DESQAERVRAELARFLENPA
DLD
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 251 |
15N chemical shifts | 68 |
1H chemical shifts | 394 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | NGlpG | 1 |
Entities:
Entity 1, NGlpG 63 residues - 7142.065 Da.
1 | MET | LEU | MET | ILE | THR | SER | PHE | ALA | ASN | PRO | ||||
2 | ARG | VAL | ALA | GLN | ALA | PHE | VAL | ASP | TYR | MET | ||||
3 | ALA | THR | GLN | GLY | VAL | ILE | LEU | THR | ILE | GLN | ||||
4 | GLN | HIS | ASN | GLN | SER | ASP | VAL | TRP | LEU | ALA | ||||
5 | ASP | GLU | SER | GLN | ALA | GLU | ARG | VAL | ARG | ALA | ||||
6 | GLU | LEU | ALA | ARG | PHE | LEU | GLU | ASN | PRO | ALA | ||||
7 | ASP | LEU | ASP |
Samples:
sample_1: Nglpg, [U-100% 13C; U-100% 15N], 1.0 ± 0.05 mM; H2O 90%; D2O 10%
sample_2: Nglpg, [U-100% 13C; U-100% 15N], 1.0 ± 0.05 mM; D2O 100%
sample_conditions_1: ionic strength: 0.15 M; pH: 6.5; pressure: 1 atm; temperature: 293.15 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 HNCACB | sample_1 | isotropic | sample_conditions_1 |
3D HBHA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
3D HN(CO)CA | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY aliphatic | sample_2 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY aromatic | sample_2 | isotropic | sample_conditions_1 |
Software:
CYANA v2.1, Guntert, Mumenthaler and Wuthrich - structure solution
X-PLOR NIH v2.22, Schwieters, Kuszewski, Tjandra and Clore - refinement
NMR spectrometers:
- Varian INOVA 500 MHz
Related Database Links:
BMRB | 19713 |
PDB | |
DBJ | BAB37690 BAE77868 BAG79214 BAI27681 BAI32850 |
EMBL | CAP77869 CAQ33744 CAR00366 CAR05025 CAR10074 |
GB | AAG58528 AAN44906 AAN82639 AAP19275 AAT48182 |
REF | NP_312294 NP_709199 WP_000541600 WP_000928708 WP_000928709 |
SP | A1AGU7 A7ZSV4 A8A5N2 A8AQX4 B1IP42 |
Download simulated HSQC data in one of the following formats:
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SPARKY: Backbone
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