Click here to enlarge.
PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full
BMRB Entry DOI: doi:10.13018/BMR36102
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
All files associated with the entry
Citation: Lee, Yeongjoon; Kwak, Chulhee; Jeong, Ki-Woong; Durai, Prasannavenkatesh; Ryu, Kyoung-Seok; Kim, Eun-Hee; Cheong, Chaejoon; Ahn, Hee-Chul; Kim, Hak; Kim, Yangmee. "Tyr51: Key Determinant of the Low Thermostability of the Colwellia psychrerythraea Cold-Shock Protein." Biochemistry 57, 3625-3640 (2018).
PubMed: 29737840
Assembly members:
Cold-shock DNA-binding domain family protein, polymer, 68 residues, 7299.082 Da.
Natural source: Common Name: not available Taxonomy ID: 167879 Superkingdom: Bacteria Kingdom: Pseudomonadati Genus/species: Colwellia psychrerythraea
Experimental source: Production method: recombinant technology Host organism: Escherichia coli BL21(DE3)
Entity Sequences (FASTA):
Cold-shock DNA-binding domain family protein: MSKGIVKWFNSDKGFGFITP
EDGSKDLFVHHSEIQSGGEY
ATLADGQTVEYEVGQGQKGP
CANKVVAV
| Data type | Count |
| 13C chemical shifts | 249 |
| 15N chemical shifts | 71 |
| 1H chemical shifts | 415 |
| Entity Assembly ID | Entity Name | Entity ID |
|---|---|---|
| 1 | entity_1 | 1 |
Entity 1, entity_1 68 residues - 7299.082 Da.
| 1 | MET | SER | LYS | GLY | ILE | VAL | LYS | TRP | PHE | ASN | ||||
| 2 | SER | ASP | LYS | GLY | PHE | GLY | PHE | ILE | THR | PRO | ||||
| 3 | GLU | ASP | GLY | SER | LYS | ASP | LEU | PHE | VAL | HIS | ||||
| 4 | HIS | SER | GLU | ILE | GLN | SER | GLY | GLY | GLU | TYR | ||||
| 5 | ALA | THR | LEU | ALA | ASP | GLY | GLN | THR | VAL | GLU | ||||
| 6 | TYR | GLU | VAL | GLY | GLN | GLY | GLN | LYS | GLY | PRO | ||||
| 7 | CYS | ALA | ASN | LYS | VAL | VAL | ALA | VAL |
sample_1: Colwellia psychrerythraea Cold Shock Protein, [U-99% 15N], 0.5 ± 0.2 mM; sodium azide 0.5 mg/mL; DTT 2 mM; EDTA 0.1 mM; potassium chloride 100 mM; potassium phosphate 50 mM; DSS 50 nM; H2O 90%; D2O, [U-2H], 10%
sample_2: Colwellia psychrerythraea Cold Shock Protein, [U-99% 13C; U-99% 15N], 0.5 ± 0.2 mM; sodium azide 0.5 mg/mL; DTT 2 mM; EDTA 0.1 mM; potassium chloride 100 mM; potassium phosphate 50 mM; DSS 50 nM; H2O 90%; D2O, [U-2H], 10%
sample_3: Colwellia psychrerythraea Cold Shock Protein, [U-99% 15N], 0.5 ± 0.2 mM; sodium azide 0.5 mg/mL; DTT 2 mM; EDTA 0.1 mM; potassium chloride 100 mM; potassium phosphate 50 mM; DSS 50 nM; H2O 90%; D2O, [U-2H], 10%
sample_4: Colwellia psychrerythraea Cold Shock Protein 0.5 ± 0.2 mM; sodium azide 0.5 mg/mL; DTT 2 mM; EDTA 0.1 mM; potassium chloride 100 mM; potassium phosphate 50 mM; DSS 50 nM; H2O 90%; D2O, [U-2H], 10%
sample_conditions_1: ionic strength: 100 mM; pH: 6.0; pressure: 1 atm; temperature: 298 K
| Name | Sample | Sample state | Sample conditions |
|---|---|---|---|
| 2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
| 2D 1H-13C HSQC | sample_2 | isotropic | sample_conditions_1 |
| 3D HNCACB | sample_2 | isotropic | sample_conditions_1 |
| 3D CBCA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
| 3D HNCO | sample_2 | isotropic | sample_conditions_1 |
| 3D C(CO)NH | sample_2 | isotropic | sample_conditions_1 |
| 3D HBHA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
| 3D H(CCO)NH | sample_2 | isotropic | sample_conditions_1 |
| 3D HCCH-TOCSY | sample_2 | isotropic | sample_conditions_1 |
| 2D 1H-1H TOCSY | sample_4 | isotropic | sample_conditions_1 |
| 2D 1H-1H NOESY | sample_4 | 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 |
| 2D 1H-15N HSQC-DSSE(IPAP) | sample_1 | isotropic | sample_conditions_1 |
| 2D 1H-15N HSQC-DSSE(IPAP) | sample_3 | anisotropic | sample_conditions_1 |
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
NMRFAM-SPARKY, Lee, W., M. Tonelli and J.L. Markley - chemical shift assignment
CYANA, Guntert, Mumenthaler and Wuthrich - structure calculation
PONDEROSA-C/S, Lee W, Cornilescu G, Dashti H, Eghbalnia HR, Tonelli M, Westler WM, Butcher SE, Wildman-Henzler K, Markley JL. - refinement
Download HSQC peak lists in one of the following formats:
CSV: Backbone
or all simulated peaks
SPARKY: Backbone
or all simulated peaks