BMRB Entry 17524
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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/BMR17524
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Title: Solution NMR Structure of Mitotic checkpoint serine/threonine-protein kinase BUB1 N-terminal domain from Homo sapiens, Northeast Structural Genomics Consortium Target HR5460A
Deposition date: 2011-03-14 Original release date: 2011-05-09
Authors: Liu, G.; Xiao, R.; Lee, H.; Hamilton, K.; Acton, T.; Ciccosanti, C.; Everett, J.; Shastry, R.; Huang, Y.; Montelione, G.
Citation: Liu, G.; Shastry, R.; Ciccosanti, C.; Hamilton, K.; Acton, T.; Xiao, R.; Everett, J.; Montelione, G.. "Northeast Structural Genomics Consortium Target HR5460A" To be published ., .-..
Assembly members:
HR5460A, polymer, 160 residues, 19209.656 Da.
Natural source: Common Name: Human Taxonomy ID: 9606 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Homo sapiens
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
HR5460A: MGHHHHHHSHMDTPENVLQM
LEAHMQSYKGNDPLGEWERY
IQWVEENFPENKEYLITLLE
HLMKEFLDKKKYHNDPRFIS
YCLKFAEYNSDLHQFFEFLY
NHGIGTLSSPLYIAWAGHLE
AQGELQHASAVLQRGIQNQA
EPREFLQQQYRLFQTRLTET
- assigned_chemical_shifts
- RDCs
Data type | Count |
13C chemical shifts | 695 |
15N chemical shifts | 156 |
1H chemical shifts | 1101 |
residual dipolar couplings | 84 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | HR5460A | 1 |
Entities:
Entity 1, HR5460A 160 residues - 19209.656 Da.
1 | MET | GLY | HIS | HIS | HIS | HIS | HIS | HIS | SER | HIS | |
2 | MET | ASP | THR | PRO | GLU | ASN | VAL | LEU | GLN | MET | |
3 | LEU | GLU | ALA | HIS | MET | GLN | SER | TYR | LYS | GLY | |
4 | ASN | ASP | PRO | LEU | GLY | GLU | TRP | GLU | ARG | TYR | |
5 | ILE | GLN | TRP | VAL | GLU | GLU | ASN | PHE | PRO | GLU | |
6 | ASN | LYS | GLU | TYR | LEU | ILE | THR | LEU | LEU | GLU | |
7 | HIS | LEU | MET | LYS | GLU | PHE | LEU | ASP | LYS | LYS | |
8 | LYS | TYR | HIS | ASN | ASP | PRO | ARG | PHE | ILE | SER | |
9 | TYR | CYS | LEU | LYS | PHE | ALA | GLU | TYR | ASN | SER | |
10 | ASP | LEU | HIS | GLN | PHE | PHE | GLU | PHE | LEU | TYR | |
11 | ASN | HIS | GLY | ILE | GLY | THR | LEU | SER | SER | PRO | |
12 | LEU | TYR | ILE | ALA | TRP | ALA | GLY | HIS | LEU | GLU | |
13 | ALA | GLN | GLY | GLU | LEU | GLN | HIS | ALA | SER | ALA | |
14 | VAL | LEU | GLN | ARG | GLY | ILE | GLN | ASN | GLN | ALA | |
15 | GLU | PRO | ARG | GLU | PHE | LEU | GLN | GLN | GLN | TYR | |
16 | ARG | LEU | PHE | GLN | THR | ARG | LEU | THR | GLU | THR |
Samples:
sample_NC: HR5460A, [U-100% 13C; U-100% 15N], 1.164 mM; H2O 95%; D2O 5%
sample_NC5: HR5460A, [U-10% 13C; U-100% 15N], 1.033 mM; H2O 95%; D2O 95%; NaCl 100 mM; NaN3 0.02%; DTT 4 mM; Tris-HCl 10 mM
sample_conditions_1: pH: 7.5; pressure: 1 atm; temperature: 298 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_NC | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_NC5 | isotropic | sample_conditions_1 |
3D HNCO | sample_NC | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_NC | isotropic | sample_conditions_1 |
3D HNCACB | sample_NC | isotropic | sample_conditions_1 |
3D 1H-13C arom NOESY | sample_NC | isotropic | sample_conditions_1 |
3D simutaneous 13C-aromatic,13C-aliphatic,15N edited 1H-1H NOESY | sample_NC | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | sample_NC5 | isotropic | sample_conditions_1 |
Software:
CNS, Brunger, Adams, Clore, Gros, Nilges and Read - refinemen,structure solution,geometry optimization
CYANA v3.0, Guntert, Mumenthaler and Wuthrich - refinement,geometry optimization,structure solution
AutoStruct v2.1, Huang, Tejero, Powers and Montelione - data analysis,refinement
AutoAssign v2.1, Zimmerman, Moseley, Kulikowski and Montelione - data analysis,chemical shift assignment
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
XEASY, Bartels et al. - data analysis,peak picking,chemical shift assignment
TOPSPIN, Bruker Biospin - collection
VNMRJ, Varian - collection
SPARKY, Goddard - data analysis
TALOS+, Shen, Cornilescu, Delaglio and Bax - geometry optimization
NMR spectrometers:
- Bruker Avance 800 MHz
- Varian INOVA 600 MHz
- Varian INOVA 600 MHz
Related Database Links:
PDB | |
DBJ | BAF83910 |
GB | AAB97855 AAC03122 AAC06259 AAC12729 AAD43675 |
REF | NP_001265546 NP_004327 XP_001142040 XP_002811811 XP_003804751 |
SP | O43683 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts