BMRB Entry 36008
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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/BMR36008
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Title: SOLUTION STRUCTURE OF LYS39 ACETYLATED HUMAN SUMO1
Deposition date: 2016-06-19 Original release date: 2017-06-05
Authors: Naik, M.; Naik, N.; Shih, H.; Huang, T.
Citation: Naik, M.; Naik, N.; Shih, H.; Huang, T.. "Structures of Human Sumo" . ., .-..
Assembly members:
Small ubiquitin-related modifier 1, polymer, 111 residues, 12809.266 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 BL21(DE3)
Entity Sequences (FASTA):
Small ubiquitin-related modifier 1: MGSSHHHHHHSQDPMSDQEA
KPSTEDLGDKKEGEYIKLKV
IGQDSSEIHFKVXMTTHLKK
LKESYCQRQGVPMNSLRFLF
EGQRIADNHTPKELGMEEED
VIEVYQEQTGG
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 426 |
15N chemical shifts | 103 |
1H chemical shifts | 701 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | entity_1 | 1 |
Entities:
Entity 1, entity_1 111 residues - 12809.266 Da.
1 | MET | GLY | SER | SER | HIS | HIS | HIS | HIS | HIS | HIS | ||||
2 | SER | GLN | ASP | PRO | MET | SER | ASP | GLN | GLU | ALA | ||||
3 | LYS | PRO | SER | THR | GLU | ASP | LEU | GLY | ASP | LYS | ||||
4 | LYS | GLU | GLY | GLU | TYR | ILE | LYS | LEU | LYS | VAL | ||||
5 | ILE | GLY | GLN | ASP | SER | SER | GLU | ILE | HIS | PHE | ||||
6 | LYS | VAL | ALY | MET | THR | THR | HIS | LEU | LYS | LYS | ||||
7 | LEU | LYS | GLU | SER | TYR | CYS | GLN | ARG | GLN | GLY | ||||
8 | VAL | PRO | MET | ASN | SER | LEU | ARG | PHE | LEU | PHE | ||||
9 | GLU | GLY | GLN | ARG | ILE | ALA | ASP | ASN | HIS | THR | ||||
10 | PRO | LYS | GLU | LEU | GLY | MET | GLU | GLU | GLU | ASP | ||||
11 | VAL | ILE | GLU | VAL | TYR | GLN | GLU | GLN | THR | GLY | ||||
12 | GLY |
Samples:
sample_1: DTT 2 mM; EDTA 0.1 mM; SUMO1 K39Ac, [U-100% 13C; U-100% 15N], 1 mM; potassium chloride 100 mM; potassium phosphate 10 mM; sodium azide 0.001%; H2O 90%; D2O, [U-2H], 10%
sample_2: DTT 2 mM; EDTA 0.1 mM; SUMO1 K39Ac, [U-100% 15N], 1 mM; potassium chloride 100 mM; potassium phosphate 10 mM; sodium azide 0.001%; H2O 90%; D2O, [U-2H], 10%
sample_3: DTT 2 mM; EDTA 0.1 mM; Pf1 phage 10 mg/mL; SUMO1 K39Ac, [U-100% 15N], 1 mM; potassium chloride 100 mM; potassium phosphate 10 mM; sodium azide 0.001%; H2O 90%; D2O, [U-2H], 10%
sample_4: DTT 2 mM; EDTA 0.1 mM; SUMO1 K39Ac 1 mM; potassium chloride 100 mM; potassium phosphate 10 mM; sodium azide 0.001%; H2O 90%; D2O, [U-2H], 10%
sample_conditions_1: ionic strength: 100 mM; pH: 6.5; pressure: 1 atm; temperature: 290 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_2 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D HNCA | sample_1 | isotropic | sample_conditions_1 |
3D HN(CO)CA | 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 HCCH- TOCSY | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-COSY | sample_1 | isotropic | sample_conditions_1 |
3D HBHACONH | sample_1 | isotropic | sample_conditions_1 |
2D-HBCBCGCDHD | sample_1 | isotropic | sample_conditions_1 |
2D-HBCBCGCDCEHE | sample_1 | isotropic | sample_conditions_1 |
3D 1H-15N TOCSY | sample_1 | isotropic | sample_conditions_1 |
2D 1H-1H NOESY | sample_4 | anisotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_1 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC IPAP | sample_3 | anisotropic | sample_conditions_1 |
2D NOESY F1 FILTERED | sample_1 | isotropic | sample_conditions_1 |
2D NOESY F2 FILTERED | sample_1 | isotropic | sample_conditions_1 |
2D NOESY F1/F2 FILTERED | sample_1 | isotropic | sample_conditions_1 |
2D TOCSY F1/F2 FILTERED | sample_1 | isotropic | sample_conditions_1 |
Software:
CYANA, Guntert, Mumenthaler and Wuthrich - structure calculation
SPARKY v3.113, Goddard - data analysis
TOPSPIN v3.2, Bruker Biospin - processing
X-PLOR NIH v2.34, Schwieters, Kuszewski, Tjandra and Clore - refinement
NMR spectrometers:
- Bruker Avance 500 MHz
- Bruker AvanceIII 600 MHz
- Bruker Avance 800 MHz
- Bruker AvanceIII 850 MHz
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts