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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/BMR15688
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
XML gzip file.
RDF gzip file.
All files associated with the entry
Citation: Lee, Woonghee; Jung, Jin-Won; Lee, Weontae. "The Automated Suite for Protein Structure by NMR Spectroscopy" .
Assembly members:
TA0956, polymer, 110 residues, 12572.573 Da.
Natural source: Common Name: THERMOPLASMA ACIDOPHILUM Taxonomy ID: 2303 Superkingdom: Archaea Kingdom: not available Genus/species: THERMOPLASMA ACIDOPHILUM
Experimental source: Production method: recombinant technology Host organism: ESCHERICHIA COLI Vector: PET
Entity Sequences (FASTA):
TA0956: MTLCAMYNISMAGSHPTTIC
VVMDRFLESFSELYDIIDEN
DTDVMMDFISRFARTDEIMP
EDKTVGFVVVNADKKLMSVS
FSDIDENMKKVIKATAEKFK
NKGFKVETDM
| Data type | Count |
| 13C chemical shifts | 303 |
| 15N chemical shifts | 110 |
| 1H chemical shifts | 697 |
| Entity Assembly ID | Entity Name | Entity ID |
|---|---|---|
| 1 | TA0956 | 1 |
Entity 1, TA0956 110 residues - 12572.573 Da.
| 1 | MET | THR | LEU | CYS | ALA | MET | TYR | ASN | ILE | SER | |
| 2 | MET | ALA | GLY | SER | HIS | PRO | THR | THR | ILE | CYS | |
| 3 | VAL | VAL | MET | ASP | ARG | PHE | LEU | GLU | SER | PHE | |
| 4 | SER | GLU | LEU | TYR | ASP | ILE | ILE | ASP | GLU | ASN | |
| 5 | ASP | THR | ASP | VAL | MET | MET | ASP | PHE | ILE | SER | |
| 6 | ARG | PHE | ALA | ARG | THR | ASP | GLU | ILE | MET | PRO | |
| 7 | GLU | ASP | LYS | THR | VAL | GLY | PHE | VAL | VAL | VAL | |
| 8 | ASN | ALA | ASP | LYS | LYS | LEU | MET | SER | VAL | SER | |
| 9 | PHE | SER | ASP | ILE | ASP | GLU | ASN | MET | LYS | LYS | |
| 10 | VAL | ILE | LYS | ALA | THR | ALA | GLU | LYS | PHE | LYS | |
| 11 | ASN | LYS | GLY | PHE | LYS | VAL | GLU | THR | ASP | MET |
sample_1: TA0956, [U-98% 13C; U-98% 15N], 1.5 mM
sample_conditions_1: ionic strength: 373.15 mM; pH: 6.5; pressure: 1 atm; temperature: 298 K
| Name | Sample | Sample state | Sample conditions |
|---|---|---|---|
| 2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
| 3D HNCA | sample_1 | isotropic | sample_conditions_1 |
| 3D HNCACB | sample_1 | isotropic | sample_conditions_1 |
| 3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
| 3D HNHA | sample_1 | isotropic | sample_conditions_1 |
| 3D C(CO)NH | sample_1 | isotropic | sample_conditions_1 |
| 3D 1H-13C NOESY | sample_1 | isotropic | sample_conditions_1 |
| 3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
| 3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
CYANA, Guntert P. - refinement
Download HSQC peak lists in one of the following formats:
CSV: Backbone
or all simulated peaks
SPARKY: Backbone
or all simulated peaks