2ltz

Smurf2 WW3 domain in complex with a Smad7 derived peptide

Method: SOLUTION NMR Dmax: 37.9 Å Quality: GOOD

1. Protein Identity and Related Structures Protein Identity & Related Structures

E3 ubiquitin-protein ligase SMURF2

Homo sapiens

UniProt Q9HAU4

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 297–333 Fragment:WW3 domain (UNP residues 297-333) Smad7 derived peptide × 1 (O15105) SOLUTION NMR NMR measurement conditions:pH 7.2;285 K;Pressure ambient NMR sample composition:1 mM SMURF2WW3, 2 mM SMAD7, 20 mM [U-100% 2H] TRIS, 100 mM sodium chloride, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:1 mM [U-100% 13C; U-100% 15N] SMURF2WW3, 3 mM SMAD7, 20 mM [U-100% 2H] TRIS, 100 mM sodium chloride, 90% H2O/10% D2O | 90% H2O/10% D2O Resolution not provided

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

7 other PDB entries and 8 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SMUF2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–37; UniProt 297–333

Smad7 derived peptide

OrganismNot specified

UniProt O15105

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 203–217 Fragment:UNP residues 203-217 E3 ubiquitin-protein ligase SMURF2 × 1 (Q9HAU4) SOLUTION NMR NMR measurement conditions:pH 7.2;285 K;Pressure ambient NMR sample composition:1 mM SMURF2WW3, 2 mM SMAD7, 20 mM [U-100% 2H] TRIS, 100 mM sodium chloride, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:1 mM [U-100% 13C; U-100% 15N] SMURF2WW3, 3 mM SMAD7, 20 mM [U-100% 2H] TRIS, 100 mM sodium chloride, 90% H2O/10% D2O | 90% H2O/10% D2O Resolution not provided

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

5 other PDB entries and 5 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SMAD7_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–15; UniProt 203–217

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 2ltz

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2ltz
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2ltz
Deposition date deposition_date2012-06-04
Structure title titleSmurf2 WW3 domain in complex with a Smad7 derived peptide
Keywords keywordsWW, SMURF2, SMAD7, PROTEIN BINDING-PEPTIDE complex; PROTEIN BINDING/PEPTIDE
Experimental Method methodSOLUTION NMR

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier10.53
Radius of gyration Rg (electron density) rg_electron10.42
Forward intensity I(0) i0219095000.00
Molecular weight molecular_weight119530.0 kDa
Excluded volume excluded_volume147080 ų
Envelope volume envelope_volume12220 ų
Hydration-shell volume shell_volume9020 ų
Envelope diameter envelope_diameter39.0
Shell Rg shell_rg17.15
Envelope Rg envelope_rg12.18
Shape Rg shape_rg10.35
Total Rg total_rg10.80
Total atoms total_atoms16400
Residues n_residues1040
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax37.9
Rg (real space) rg_real10.47
Rg uncertainty (real space) rg_real_error0.51
I(0) (real space) i0_real2.1910e+08
I(0) uncertainty (real space) i0_real_error2.6940e+06
Rg (reciprocal space) rg_reciprocal10.47
I(0) (reciprocal space) i0_reciprocal219100000.0000
Solution quality estimate total_estimate0.8439
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary12.9
Skewness Skewness skewness0.056
Kurtosis Kurtosis kurtosis-0.436
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha52720.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.670; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 0.980; Smooth: 0.981

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)