4grg

Crystal structure of IgE complexed with E2_79, an anti-IgE inhibitor

Method: X-RAY DIFFRACTION Dmax: 96.2 Å Quality: EXCELLENT

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

Ig epsilon chain C region

Homo sapiens

UniProt P01854

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain C; UniProt 210–428 Chain D; UniProt 210–428 Fragment:IG-LIKE DOMAINS 3 AND 4, RESIDUES 210-428 Mutation:G216C ANTI-IGE INHIBITOR E2_79 × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5;298 K;0.1 M Phosphate-citrate pH 4.2, 5% (w/v) PEG-3000, 25% (v/v) 1,2-propanediol, 10% (v/v) glycerol, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 4.24 Å R-free 0.338

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.

33 other PDB entries and 51 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name IGHE_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain C; PDBConstruct 5–223; UniProt 210–428 Author chain D; PDBConstruct 5–223; UniProt 210–428

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 4grg

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4grg
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4grg
Deposition date deposition_date2012-08-24
Structure title titleCrystal structure of IgE complexed with E2_79, an anti-IgE inhibitor
Keywords keywordsIg-fold, immunity, high/low affinity receptor, IMMUNE SYSTEM-INHIBITOR complex; IMMUNE SYSTEM/INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier30.44
Radius of gyration Rg (electron density) rg_electron29.47
Forward intensity I(0) i091642200.00
Molecular weight molecular_weight73109.0 kDa
Excluded volume excluded_volume90654 ų
Envelope volume envelope_volume122790 ų
Hydration-shell volume shell_volume35294 ų
Envelope diameter envelope_diameter93.0
Shell Rg shell_rg36.55
Envelope Rg envelope_rg28.51
Shape Rg shape_rg29.49
Total Rg total_rg30.07
Total atoms total_atoms5154
Residues n_residues675
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 dmax96.2
Rg (real space) rg_real30.32
Rg uncertainty (real space) rg_real_error0.67
I(0) (real space) i0_real9.1640e+07
I(0) uncertainty (real space) i0_real_error1.4110e+06
Rg (reciprocal space) rg_reciprocal30.38
I(0) (reciprocal space) i0_reciprocal91650000.0000
Solution quality estimate total_estimate0.9089
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary37.0
Skewness Skewness skewness0.135
Kurtosis Kurtosis kurtosis-0.596
Angular range angular_range— – 0.2600 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8472000.0000
Real-space data points n_real_points53
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.950; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.963

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)