2xbf

Nedd4 HECT structure

Method: X-RAY DIFFRACTION Dmax: 78.2 Å Quality: EXCELLENT

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 519–900 Fragment:HECT DOMAIN, RESIDUES 519-900 EDO 1,2-ETHANEDIOL × 4 CA CALCIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 6;100 MM NA-MES, PH 6.0, 4% PEG 400, 35 MM CACL2, 5 MM TCEP Resolution 2.50 Å R-free 0.256

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 5–386; UniProt 519–900

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 2xbf

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2xbf
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id2xbf
Deposition date deposition_date2010-04-09
Structure title titleNedd4 HECT structure
Keywords keywordsLIGASE; LIGASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.23
Radius of gyration Rg (electron density) rg_electron24.13
Forward intensity I(0) i032478600.00
Molecular weight molecular_weight44828.0 kDa
Excluded volume excluded_volume56472 ų
Envelope volume envelope_volume68986 ų
Hydration-shell volume shell_volume24559 ų
Envelope diameter envelope_diameter79.5
Shell Rg shell_rg30.43
Envelope Rg envelope_rg24.10
Shape Rg shape_rg24.12
Total Rg total_rg24.94
Total atoms total_atoms3165
Residues n_residues375
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 dmax78.2
Rg (real space) rg_real25.16
Rg uncertainty (real space) rg_real_error0.54
I(0) (real space) i0_real3.2480e+07
I(0) uncertainty (real space) i0_real_error4.3220e+05
Rg (reciprocal space) rg_reciprocal25.19
I(0) (reciprocal space) i0_reciprocal32480000.0000
Solution quality estimate total_estimate0.9120
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary32.3
Skewness Skewness skewness0.185
Kurtosis Kurtosis kurtosis-0.588
Angular range angular_range— – 0.3150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7610000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.954; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.996; Smooth: 0.995

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2xbfa_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.148 — Hect, E3 ligase catalytic domain
Superfamily Superfamily superfamilyd.148.1 — Hect, E3 ligase catalytic domain
Family Family familyd.148.1.0 — automated matches

CATH v4.4 (3 domains)

Domain ID domain_id2xbfA01
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology1750 — Hect, E3 ligase catalytic domain fold
Homologous superfamily homologous superfamily10 — Hect, E3 ligase catalytic domains
Domain ID domain_id2xbfA02
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology2160 — Hect, E3 ligase catalytic domain
Homologous superfamily homologous superfamily10 — Hect, E3 ligase catalytic domain
Domain ID domain_id2xbfA03
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology2410 — Hect, E3 ligase catalytic fold
Homologous superfamily homologous superfamily10 — Hect, E3 ligase catalytic domain

8. Citations (1)

9. Files and Curves (10)