BMRB Entry 5165
Chem Shift validation: AVS_anomalous, AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR5165
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Title: Solution Structure of Methanobacterium Thermoautotrophicum Protein 1598 PubMed: 11854485
Deposition date: 2001-10-09 Original release date: 2002-05-06
Authors: Yee, A.; Chang, X.; Pineda-Lucena, A.; Wu, B.; Semesi, A.; Le, B.; Ramelot, T.; Lee, G.; Bhattacharyya, S.; Gutierrez, P.; Denisov, A.; Lee, C.; Cort, J.; Kozlov, G.; Liao, J.; Finak, G.; Chen, L.; Wishart, D.; Lee, W.; McIntosh, L.; Gehring, K.; Kennedy, M.; Edwards, A.; Arrowsmith, C.
Citation: Yee, A.; Chang, X.; Pineda-Lucena, A.; Wu, B.; Semesi, A.; Le, B.; Ramelot, T.; Lee, G.; Bhattacharyya, S.; Gutierrez, P.; Denisov, A.; Lee, C.; Cort, J.; Kozlov, G.; Liao, J.; Finak, G.; Chen, L.; Wishart, D.; Lee, W.; McIntosh, L.; Gehring, K.; Kennedy, M.; Edwards, A.; Arrowsmith, C.. "An NMR Approach to Structural Proteomics" Proc. Natl. Acad. Sci. U.S.A. 99, 1825-1830 (2002).
Assembly members:
single chain biopolymer, polymer, 140 residues, Formula weight is not available
Natural source: Common Name: Methanothermobacter thermoautotrophicus Taxonomy ID: 145262 Superkingdom: Archaea Kingdom: Euryarchaeota Genus/species: Methanobacterium thermoautotrophicum
Experimental source: Production method: recombinant technology
Entity Sequences (FASTA):
single chain biopolymer: MKGFEFFDVTADAGFWAYGH
DLEEVFENAALAMFEVMTDT
SLVEAAEERRVEITSEDRVS
LLYDWLDELLFIHDTEFILF
SKFKVKIDEKDDGLHLTGTA
MGEEIKEGHERRDEVKAVTF
HMMEILDEDGLIKARVILDL
- assigned_chemical_shifts
Data type | Count |
1H chemical shifts | 903 |
13C chemical shifts | 585 |
15N chemical shifts | 141 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | Conserved Hypothetical Protein MTH1598 | 1 |
Entities:
Entity 1, Conserved Hypothetical Protein MTH1598 140 residues - Formula weight is not available
1 | MET | LYS | GLY | PHE | GLU | PHE | PHE | ASP | VAL | THR | |
2 | ALA | ASP | ALA | GLY | PHE | TRP | ALA | TYR | GLY | HIS | |
3 | ASP | LEU | GLU | GLU | VAL | PHE | GLU | ASN | ALA | ALA | |
4 | LEU | ALA | MET | PHE | GLU | VAL | MET | THR | ASP | THR | |
5 | SER | LEU | VAL | GLU | ALA | ALA | GLU | GLU | ARG | ARG | |
6 | VAL | GLU | ILE | THR | SER | GLU | ASP | ARG | VAL | SER | |
7 | LEU | LEU | TYR | ASP | TRP | LEU | ASP | GLU | LEU | LEU | |
8 | PHE | ILE | HIS | ASP | THR | GLU | PHE | ILE | LEU | PHE | |
9 | SER | LYS | PHE | LYS | VAL | LYS | ILE | ASP | GLU | LYS | |
10 | ASP | ASP | GLY | LEU | HIS | LEU | THR | GLY | THR | ALA | |
11 | MET | GLY | GLU | GLU | ILE | LYS | GLU | GLY | HIS | GLU | |
12 | ARG | ARG | ASP | GLU | VAL | LYS | ALA | VAL | THR | PHE | |
13 | HIS | MET | MET | GLU | ILE | LEU | ASP | GLU | ASP | GLY | |
14 | LEU | ILE | LYS | ALA | ARG | VAL | ILE | LEU | ASP | LEU |
Samples:
sample_1: single chain biopolymer, [U-15N; U-13C], 2 mM; NaCl 300 mM; phosphate 10 mM; H2O 90%; D2O 10%
sample_cond_1: pH: 6.5 na; temperature: 298 K; ionic strength: 300 mM; pressure: 1 atm
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
4D 13C-separated NOESY | not available | not available | not available |
3D 13C-separated NOESY | not available | not available | not available |
3D 15N-separated NOESY | not available | not available | not available |
Software:
NMRPipe v2000.02.14 - processing
Sparky v3.95 - data analysis
CNS v1.0 - structure solution
NMR spectrometers:
- Varian INOVA 500 MHz
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts