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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/BMR16219
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: Ko, Sunggeon; Ahn, Kyo-Eun; Lee, Young-Min; Ahn, Hee-Chul; Lee, Weontae. "Structural basis of the auto-inhibition mechanism of nonreceptor tyrosine kinase PTK6." Biochem. Biophys. Res. Commun. 384, 236-242 (2009).
PubMed: 19401189
Assembly members:
SH_domain, polymer, 72 residues, 8334.291 Da.
Natural source: Common Name: E. coli Taxonomy ID: 562 Superkingdom: Eubacteria Kingdom: not available Genus/species: Escherichia coli
Experimental source: Production method: recombinant technology Host organism: Escherichia coli Vector: pGEX4T-1
Entity Sequences (FASTA):
SH_domain: MVSRDQAHLGPKYVGLWDFK
SRTDEELSFRAGDVFHVARK
EEQWWWATLLDEAGGAVAQG
YVPHNYLAERET
Data type | Count |
13C chemical shifts | 256 |
15N chemical shifts | 72 |
1H chemical shifts | 440 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | SH_domain | 1 |
Entity 1, SH_domain 72 residues - 8334.291 Da.
1 | MET | VAL | SER | ARG | ASP | GLN | ALA | HIS | LEU | GLY | ||||
2 | PRO | LYS | TYR | VAL | GLY | LEU | TRP | ASP | PHE | LYS | ||||
3 | SER | ARG | THR | ASP | GLU | GLU | LEU | SER | PHE | ARG | ||||
4 | ALA | GLY | ASP | VAL | PHE | HIS | VAL | ALA | ARG | LYS | ||||
5 | GLU | GLU | GLN | TRP | TRP | TRP | ALA | THR | LEU | LEU | ||||
6 | ASP | GLU | ALA | GLY | GLY | ALA | VAL | ALA | GLN | GLY | ||||
7 | TYR | VAL | PRO | HIS | ASN | TYR | LEU | ALA | GLU | ARG | ||||
8 | GLU | THR |
sample_1: SH domain, [U-99% 15N], 0.2 mM; H2O 90%; D2O 10%
sample_2: SH domain, [U-99% 13C; U-99% 15N], 0.2 mM; H2O 90%; D2O 10%
sample_conditions_1: ionic strength: 100 mM; pH: 7; pressure: 1 atm; temperature: 298 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
3D HNCACB | sample_2 | isotropic | sample_conditions_1 |
3D HNCA | sample_2 | isotropic | sample_conditions_1 |
3D HNCO | sample_2 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D HBHA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_2 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
CYANA v2.2.5, P.GUNTERT ET AL. - refinement, structure solution
NMRDraw, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - data analysis
AutoAssign, Zimmerman, Moseley, Kulikowski and Montelione - chemical shift assignment
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
SPARKY, Goddard - chemical shift assignment, peak picking
Molmol, Koradi, Billeter and Wuthrich - structure analysis
PyMol, DeLano Scientific LLC. - peak picking, structure analysis
PDB | |
DBJ | BAG37660 BAG63163 BAI45737 |
EMBL | CAA55295 |
GB | AAC34935 AAH35843 EAW75262 EAW75263 EHH19516 |
REF | NP_001243287 NP_005966 XP_003280201 XP_003809959 XP_003904548 |
SP | Q13882 |
AlphaFold | Q13882 |
Download HSQC peak lists in one of the following formats:
CSV: Backbone
or all simulated peaks
SPARKY: Backbone
or all simulated peaks