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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, SPARTA
BMRB Entry DOI: doi:10.13018/BMR18793
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: Follis, Ariele Viacava; Chipuk, Jerry; Fisher, John; Yun, Mi-Kyung; Grace, Christy; Nourse, Amanda; Baran, Katherine; Ou, Li; Min, Lie; White, Stephen; Green, Douglas; Kriwacki, Richard. "PUMA binding induces partial unfolding within BCL-xL to disrupt p53 binding and promote apoptosis." Nat. Chem. Biol. 9, 163-168 (2013).
PubMed: 23340338
Assembly members:
BCL-xL_comp, polymer, 180 residues, 19845.008 Da.
PUMA_BH3, polymer, 25 residues, 3053.351 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 Vector: pET28
Data type | Count |
13C chemical shifts | 541 |
15N chemical shifts | 173 |
1H chemical shifts | 481 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | BCL-xL_comp | 1 |
2 | PUMA_BH3 | 2 |
Entity 1, BCL-xL_comp 180 residues - 19845.008 Da.
Wild-type Human protein with truncation of 22 C terminal residues and disordered loop between alpha helices 1 and 2
1 | MET | SER | ALA | MET | SER | GLN | SER | ASN | ARG | GLU | |
2 | LEU | VAL | VAL | ASP | PHE | LEU | SER | TYR | LYS | LEU | |
3 | SER | GLN | LYS | GLY | TYR | SER | TRP | SER | GLN | PHE | |
4 | SER | ASP | VAL | GLU | GLU | ASN | ARG | THR | GLU | ALA | |
5 | PRO | GLU | GLY | THR | GLU | SER | GLU | ALA | VAL | LYS | |
6 | GLN | ALA | LEU | ARG | GLU | ALA | GLY | ASP | GLU | PHE | |
7 | GLU | LEU | ARG | TYR | ARG | ARG | ALA | PHE | SER | ASP | |
8 | LEU | THR | SER | GLN | LEU | HIS | ILE | THR | PRO | GLY | |
9 | THR | ALA | TYR | GLN | SER | PHE | GLU | GLN | VAL | VAL | |
10 | ASN | GLU | LEU | PHE | ARG | ASP | GLY | VAL | ASN | TRP | |
11 | GLY | ARG | ILE | VAL | ALA | PHE | PHE | SER | PHE | GLY | |
12 | GLY | ALA | LEU | CYS | VAL | GLU | SER | VAL | ASP | LYS | |
13 | GLU | MET | GLN | VAL | LEU | VAL | SER | ARG | ILE | ALA | |
14 | ALA | TRP | MET | ALA | THR | TYR | LEU | ASN | ASP | HIS | |
15 | LEU | GLU | PRO | TRP | ILE | GLN | GLU | ASN | GLY | GLY | |
16 | TRP | ASP | THR | PHE | VAL | GLU | LEU | TYR | GLY | ASN | |
17 | ASN | ALA | ALA | ALA | GLU | SER | ARG | LYS | GLY | GLN | |
18 | GLU | ARG | LEU | GLU | HIS | HIS | HIS | HIS | HIS | HIS |
Entity 2, PUMA_BH3 25 residues - 3053.351 Da.
1 | GLU | GLU | GLN | TRP | ALA | ARG | GLU | ILE | GLY | ALA | ||||
2 | GLN | LEU | ARG | ARG | MET | ALA | ASP | ASP | LEU | ASN | ||||
3 | ALA | GLN | TYR | GLU | ARG |
sample_1: BCL-xL_comp, [U-100% 13C; U-100% 15N; U-95% 2H; Ile,Leu,Val C1H3], 0.9 mM; sodium phosphate 10 mM; sodium chloride 40 mM; NaN3 0.1%; H2O 92%; D2O 8%; PUMA BH3 0.9 mM
sample_2: BCL-xL, [U-100% 13C; U-100% 15N], 0.9 mM; sodium phosphate 10 mM; sodium chloride 40 mM; NaN3 0.1%; H2O 92%; D2O 8%; PUMA BH3 0.9 mM
sample_conditions_1: ionic strength: 50 mM; pH: 7.0; pressure: 1 atm; temperature: 273 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | sample_2 | isotropic | sample_conditions_1 |
2D 1H-1H TOCSY 14N edited | sample_1 | isotropic | sample_conditions_1 |
2D 1H-1H NOESY 14N edited | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_1 | isotropic | sample_conditions_1 |
3D HNCA | sample_2 | isotropic | sample_conditions_1 |
3D HNCACB | sample_2 | isotropic | sample_conditions_1 |
3D HNCACB | sample_1 | isotropic | sample_conditions_1 |
3D HNCO | sample_1 | isotropic | sample_conditions_1 |
3D HN(CA)CO | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY aliphatic | sample_1 | isotropic | sample_conditions_1 |
TOPSPIN, Bruker Biospin - collection, processing
CARA, Keller and Wuthrich - chemical shift assignment, data analysis, peak picking
CYANA, Guntert, Mumenthaler and Wuthrich - chemical shift assignment, peak picking, structure solution
AMBER, Case, Darden, Cheatham, III, Simmerling, Wang, Duke, Luo, ... and Kollm - refinement
Download HSQC peak lists in one of the following formats:
CSV: Backbone
or all simulated peaks
SPARKY: Backbone
or all simulated peaks