BMRB Entry 18499
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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/BMR18499
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Title: YAP WW1 in complex with a Smad7 derived peptide. PubMed: 22921829
Deposition date: 2012-06-04 Original release date: 2012-11-19
Authors: Macias, Maria; Aragon, Eric; Goerner, Nina; Xi, Qiaoran; Lopes, Tiago; Gao, Sheng; Massague, Joan
Citation: Aragon, Eric; Goerner, Nina; Xi, Qiaoran; Gomes, Tiago; Gao, Sheng; Massague, Joan; Macias, Maria. "Structural Basis for the Versatile Interactions of Smad7 with Regulator WW Domains in TGF-beta Pathways" Structure 20, 1726-1736 (2012).
Assembly members:
YAPWW1, polymer, 36 residues, 4151.635 Da.
SMAD7, polymer, 14 residues, 1593.747 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):
YAPWW1: DVPLPAGWEMAKTSSGQRYF
LNHIDQTTTWQDPRKA
SMAD7: GESPPPPYSRYPMD
- assigned_chemical_shifts
Data type | Count |
1H chemical shifts | 269 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | YAP WW1 | 1 |
2 | Smad7 derived peptide | 2 |
Entities:
Entity 1, YAP WW1 36 residues - 4151.635 Da.
1 | ASP | VAL | PRO | LEU | PRO | ALA | GLY | TRP | GLU | MET | ||||
2 | ALA | LYS | THR | SER | SER | GLY | GLN | ARG | TYR | PHE | ||||
3 | LEU | ASN | HIS | ILE | ASP | GLN | THR | THR | THR | TRP | ||||
4 | GLN | ASP | PRO | ARG | LYS | ALA |
Entity 2, Smad7 derived peptide 14 residues - 1593.747 Da.
1 | GLY | GLU | SER | PRO | PRO | PRO | PRO | TYR | SER | ARG | ||||
2 | TYR | PRO | MET | ASP |
Samples:
Homonuclear: YAPWW1 1 mM; SMAD7 2 mM; TRIS, [U-100% 2H], 20 mM; sodium chloride 100 mM; H2O 90%; D2O 10%
15N13C: YAPWW1, [U-100% 13C; U-100% 15N], 1 mM; SMAD7 3 mM; TRIS, [U-100% 2H], 20 mM; sodium chloride 100 mM; H2O 90%; D2O 10%
sample_conditions_1: pH: 7.2; pressure: 1 atm; temperature: 285 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | 15N13C | isotropic | sample_conditions_1 |
2D 1H-1H TOCSY | Homonuclear | isotropic | sample_conditions_1 |
2D 1H-1H NOESY | Homonuclear | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | 15N13C | isotropic | sample_conditions_1 |
3D HNCACB | 15N13C | isotropic | sample_conditions_1 |
Software:
TOPSPIN, Bruker Biospin - collection
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
CARA, Keller and Wuthrich - chemical shift assignment, peak picking
CNSSOLVE, Brunger, Adams, Clore, Gros, Nilges and Read - structure solution
NMR spectrometers:
- Bruker Avance 600 MHz
Related Database Links:
BMRB | 17539 17540 |
PDB | |
DBJ | BAE34009 BAJ41471 |
EMBL | CAA56672 |
GB | EAW67012 EAW67014 EPY79954 |
REF | NP_001269026 NP_001269027 NP_001269028 NP_006097 XP_002799821 |