8h8o

Crystal structure of apo-R52W/E56W/R59W/E63W-rHLFr

Method: X-RAY DIFFRACTION Dmax: 70.0 Å Quality: GOOD

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

Ferritin light chain

Equus caballus

UniProt P02791

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 homooligomer Homooligomer Protein × 24 PDB declaration: 24-meric(24) Consistent with protein copy count Chain A; UniProt 2–175 Mutation:R52W,E56W,R59W,E63W EDO 1,2-ETHANEDIOL × 48 CD CADMIUM ION × 168 SO4 SULFATE ION × 24 CL CHLORIDE ION × 24 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;Ammonium sulphate, Cadmium sulphate Resolution 1.50 Å R-free 0.179

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.

138 other PDB entries and 138 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name FRIL_HORSE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–174; UniProt 2–175

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 8h8o

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8h8o
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8h8o
Deposition date deposition_date2022-10-23
Structure title titleCrystal structure of apo-R52W/E56W/R59W/E63W-rHLFr
Keywords keywordsFerritin, METAL BINDING PROTEIN; METAL BINDING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.70
Radius of gyration Rg (electron density) rg_electron18.48
Forward intensity I(0) i08859170.00
Molecular weight molecular_weight20740.0 kDa
Excluded volume excluded_volume25220 ų
Envelope volume envelope_volume29476 ų
Hydration-shell volume shell_volume14434 ų
Envelope diameter envelope_diameter69.1
Shell Rg shell_rg23.24
Envelope Rg envelope_rg18.74
Shape Rg shape_rg18.33
Total Rg total_rg19.64
Total atoms total_atoms1414
Residues n_residues174
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 dmax70.0
Rg (real space) rg_real19.80
Rg uncertainty (real space) rg_real_error0.70
I(0) (real space) i0_real8.8590e+06
I(0) uncertainty (real space) i0_real_error1.3060e+05
Rg (reciprocal space) rg_reciprocal19.78
I(0) (reciprocal space) i0_reciprocal8859000.0000
Solution quality estimate total_estimate0.8309
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary19.7
Skewness Skewness skewness0.444
Kurtosis Kurtosis kurtosis-0.319
Angular range angular_range— – 0.4050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1205000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.682; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.758; Smooth: 0.994

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

8. Citations (1)

9. Files and Curves (10)