5aht

Third WW domain from the E3 ubiquitin-protein ligase NEDD4

Method: SOLUTION NMR Dmax: 36.1 Å Quality: GOOD

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

E3 UBIQUITIN-PROTEIN LIGASE NEDD4

HOMO SAPIENS

UniProt P46934

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 838–877 Fragment:WW3, UNP RESIDUES 838-877 No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 0.05;Pressure 1.0 NMR sample composition:1.5 MM [U-99% 13C NMR sample composition:U-99% 15N] NEDD4 WW3* DOMAIN, 20 MM SODIUM PHOSPHATE, 50 MM SODIUM CHLORIDE, 0.5 MM DSS, 90% 2O/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.

14 other PDB entries and 18 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NEDD4_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–43; UniProt 838–877

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 5aht

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5aht
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5aht
Deposition date deposition_date2015-02-09
Structure title titleThird WW domain from the E3 ubiquitin-protein ligase NEDD4
Keywords keywordsISOMERASE, WW3, PROTEIN-PEPTIDE COMPLEX, PROTEIN DYNAMICS, PROEIN STRUCTURE; ISOMERASE
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier10.64
Radius of gyration Rg (electron density) rg_electron10.42
Forward intensity I(0) i080640600.00
Molecular weight molecular_weight74469.0 kDa
Excluded volume excluded_volume92880 ų
Envelope volume envelope_volume12792 ų
Hydration-shell volume shell_volume9262 ų
Envelope diameter envelope_diameter38.6
Shell Rg shell_rg17.48
Envelope Rg envelope_rg12.49
Shape Rg shape_rg10.34
Total Rg total_rg10.96
Total atoms total_atoms10395
Residues n_residues645
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 dmax36.1
Rg (real space) rg_real10.59
Rg uncertainty (real space) rg_real_error0.26
I(0) (real space) i0_real8.0640e+07
I(0) uncertainty (real space) i0_real_error7.5390e+05
Rg (reciprocal space) rg_reciprocal10.60
I(0) (reciprocal space) i0_reciprocal80640000.0000
Solution quality estimate total_estimate0.8864
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary14.2
Skewness Skewness skewness0.071
Kurtosis Kurtosis kurtosis-0.429
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha22870.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.848; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.984; Smooth: 0.991

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd5ahta1
Class classb — All beta proteins
Fold Fold foldb.72 — WW domain-like
Superfamily Superfamily superfamilyb.72.1 — WW domain
Family Family familyb.72.1.0 — automated matches
Domain ID domain_idd5ahta2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (1 domains)

Domain ID domain_id5ahtA01
Class class2 — Mainly Beta
Architecture architecture20 — Single Sheet
Topology topology70 — Ubiquitin Ligase Nedd4; Chain: W;
Homologous superfamily homologous superfamily10

8. Citations (1)

9. Files and Curves (10)