8ywr

Crystal structure of the Fab fragment of the anti-IL-6 antibody 68F2 in complex with a domain-swapped IL-6 dimer

Method: X-RAY DIFFRACTION Dmax: 101.5 Å Quality: GOOD

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

Interleukin-6

Homo sapiens

UniProt P05231

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 × 6 PDB declaration: hexameric(6) Consistent with protein copy count Chain A; UniProt 42–212 Not recorded Heavy chain of the Fab fragment of anti-IL-6 antibody 68F2 × 2 Light chain of the Fab fragment of anti-IL-6 antibody 68F2 × 2 SO4 SULFATE ION × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.5;277 K;25% PEG 4K, 0.15 M (NH4)2SO4, 0.1 M MES Resolution 2.93 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.

16 other PDB entries and 20 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name IL6_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–171; UniProt 42–212

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 8ywr

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8ywr
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8ywr
Deposition date deposition_date2024-03-31
Structure title titleCrystal structure of the Fab fragment of the anti-IL-6 antibody 68F2 in complex with a domain-swapped IL-6 dimer
Keywords keywordsinterleukin, dimer, swap, IMMUNE SYSTEM; IMMUNE SYSTEM
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier30.85
Radius of gyration Rg (electron density) rg_electron30.64
Forward intensity I(0) i060656100.00
Molecular weight molecular_weight60774.0 kDa
Excluded volume excluded_volume75874 ų
Envelope volume envelope_volume106820 ų
Hydration-shell volume shell_volume30836 ų
Envelope diameter envelope_diameter107.3
Shell Rg shell_rg35.72
Envelope Rg envelope_rg31.12
Shape Rg shape_rg30.59
Total Rg total_rg31.27
Total atoms total_atoms4278
Residues n_residues564
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 dmax101.5
Rg (real space) rg_real31.06
Rg uncertainty (real space) rg_real_error0.72
I(0) (real space) i0_real6.0660e+07
I(0) uncertainty (real space) i0_real_error9.9720e+05
Rg (reciprocal space) rg_reciprocal30.98
I(0) (reciprocal space) i0_reciprocal60650000.0000
Solution quality estimate total_estimate0.8680
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary99.5
Skewness Skewness skewness0.493
Kurtosis Kurtosis kurtosis-0.347
Angular range angular_range— – 0.2550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha5632000.0000
Real-space data points n_real_points52
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.847; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.882; Smooth: 0.856

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)