BMRB Entry 18793
Click here to enlarge.
PDB ID: 2m04
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.
NMR-STAR v2.1 text file (deprecated)
XML gzip file.
RDF gzip file.
All files associated with the entry
Title: Solution structure of BCL-xL in complex with PUMA BH3 peptide PubMed: 23340338
Deposition date: 2012-10-19 Original release date: 2013-01-22
Authors: Viacava Follis, Ariele; Royappa, Grace; Kriwacki, Richard
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).
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
Entity Sequences (FASTA):
BCL-xL_comp: MSAMSQSNRELVVDFLSYKL
SQKGYSWSQFSDVEENRTEA
PEGTESEAVKQALREAGDEF
ELRYRRAFSDLTSQLHITPG
TAYQSFEQVVNELFRDGVNW
GRIVAFFSFGGALCVESVDK
EMQVLVSRIAAWMATYLNDH
LEPWIQENGGWDTFVELYGN
NAAAESRKGQERLEHHHHHH
PUMA_BH3: EEQWAREIGAQLRRMADDLN
AQYER
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 541 |
15N chemical shifts | 173 |
1H chemical shifts | 481 |
Additional metadata:
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts