BMRB Entry 7122
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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/BMR7122
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Title: Structural Studies of MJ1529, an O6 Methylguanine DNA Methyltransferase PubMed: 16826543
Deposition date: 2006-05-18 Original release date: 2007-01-11
Authors: Roberts, A.
Citation: Roberts, A.; Pelton, J.; Wemmer, D.. "Structural Studies of MJ1529, an O6 Methylguanine DNA Methyltransferase" Magn. Reson. Chem. 44, S71-S82 (2006).
Assembly members:
Methylated-DNA--protein-cysteine methyltransferase (E.C.2.1.1.63), polymer, 167 residues, Formula weight is not available
Natural source: Common Name: Methanocaldococcus jannaschii Taxonomy ID: 2190 Superkingdom: Archaea Kingdom: not available Genus/species: Methanococcus jannaschii
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
Methylated-DNA--protein-cysteine methyltransferase (E.C.2.1.1.63): MIIQIEEYFIGMIFKGNQLV
RNTIPLRREEIFNFMDGEVV
SNPEDEHLKVAEIILKLYFA
EIDDKKVRELISYKLEVPEF
TKKVLDIVKDIEFGKTLTYG
DIAKKLNTSPRAVGMALKRN
PLPLIIPCHRVVAKNSLGGY
SYGLDKKKFILERERLNMVS
FKFNKVY
- assigned_chemical_shifts
- coupling_constants
Data type | Count |
13C chemical shifts | 580 |
15N chemical shifts | 147 |
1H chemical shifts | 920 |
coupling constants | 101 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | Methylated-DNA--protein-cysteine methyltransferase | 1 |
Entities:
Entity 1, Methylated-DNA--protein-cysteine methyltransferase 167 residues - Formula weight is not available
1 | MET | ILE | ILE | GLN | ILE | GLU | GLU | TYR | PHE | ILE | ||||
2 | GLY | MET | ILE | PHE | LYS | GLY | ASN | GLN | LEU | VAL | ||||
3 | ARG | ASN | THR | ILE | PRO | LEU | ARG | ARG | GLU | GLU | ||||
4 | ILE | PHE | ASN | PHE | MET | ASP | GLY | GLU | VAL | VAL | ||||
5 | SER | ASN | PRO | GLU | ASP | GLU | HIS | LEU | LYS | VAL | ||||
6 | ALA | GLU | ILE | ILE | LEU | LYS | LEU | TYR | PHE | ALA | ||||
7 | GLU | ILE | ASP | ASP | LYS | LYS | VAL | ARG | GLU | LEU | ||||
8 | ILE | SER | TYR | LYS | LEU | GLU | VAL | PRO | GLU | PHE | ||||
9 | THR | LYS | LYS | VAL | LEU | ASP | ILE | VAL | LYS | ASP | ||||
10 | ILE | GLU | PHE | GLY | LYS | THR | LEU | THR | TYR | GLY | ||||
11 | ASP | ILE | ALA | LYS | LYS | LEU | ASN | THR | SER | PRO | ||||
12 | ARG | ALA | VAL | GLY | MET | ALA | LEU | LYS | ARG | ASN | ||||
13 | PRO | LEU | PRO | LEU | ILE | ILE | PRO | CYS | HIS | ARG | ||||
14 | VAL | VAL | ALA | LYS | ASN | SER | LEU | GLY | GLY | TYR | ||||
15 | SER | TYR | GLY | LEU | ASP | LYS | LYS | LYS | PHE | ILE | ||||
16 | LEU | GLU | ARG | GLU | ARG | LEU | ASN | MET | VAL | SER | ||||
17 | PHE | LYS | PHE | ASN | LYS | VAL | TYR |
Samples:
sample_1: Methylated-DNA--protein-cysteine methyltransferase (E.C.2.1.1.63), [U-15N], 0.8 mM; sodium phosphate 50 mM; NaCl 500 mM; H2O 95%; D2O 5%
sample_2: Methylated-DNA--protein-cysteine methyltransferase (E.C.2.1.1.63), [U-13C; U-15N], 0.8 mM; sodium phosphate 50 mM; NaCl 500 mM; H2O 95%; D2O 5%
sample_3: Methylated-DNA--protein-cysteine methyltransferase (E.C.2.1.1.63), [U-15N], 0.8 mM; sodium phosphate 50 mM; NaCl 500 mM; D2O 100%
sample_4: Methylated-DNA--protein-cysteine methyltransferase (E.C.2.1.1.63), [U-13C], 0.8 mM; sodium phosphate 50 mM; NaCl 500 mM; H2O 94%; D2O 5%
sample_cond_1: ionic strength: 550 mM; pH: 6.2; pressure: 1 atm; temperature: 303 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
3D 15N-separated NOESY | not available | not available | sample_cond_1 |
HNHA | not available | not available | sample_cond_1 |
4D 13C Separated NOESY | not available | not available | sample_cond_1 |
4D 13C/15N Separated NOESY | not available | not available | sample_cond_1 |
D20 Exchange | not available | not available | sample_cond_1 |
3d 13C Separated NOESY | not available | not available | sample_cond_1 |
Software:
CNS v1.1 - refinement, structure solution
NMRPipe v1 - processing
NMRView v5.0.4 - data analysis
NMR spectrometers:
- Bruker DRX 500 MHz
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts