8sv1

Caspase-1 complex with interleukin-18

Method: ELECTRON MICROSCOPY Dmax: 121.3 Å Quality: GOOD

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

Caspase-1

Homo sapiens

UniProt P29466

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 150–297 Chain B; UniProt 317–404 Chain a; UniProt 150–297 Chain b; UniProt 317–404 Fragment:subunit P20 (UNP residues 120-297) Fragment:subunit P10 (UNP residues 317-404) Interleukin-18 × 2 (Q14116) ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.50 Å

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.

41 other PDB entries and 46 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CASP1_HUMAN
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 1–148; UniProt 150–297 Author chain a; PDBConstruct 1–148; UniProt 150–297 Author chain B; PDBConstruct 1–88; UniProt 317–404 Author chain b; PDBConstruct 1–88; UniProt 317–404

Interleukin-18

Homo sapiens

UniProt Q14116

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 C; UniProt 6–193 Chain c; UniProt 6–193 Not recorded Caspase-1 × 2 (P29466) Caspase-1 × 2 (P29466) ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.50 Å

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.

19 other PDB entries and 36 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name IL18_HUMAN
Isoform
PDB entities 3
Chains and sequence ranges Author chain C; PDBConstruct 1–188; UniProt 6–193 Author chain c; PDBConstruct 1–188; UniProt 6–193

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 8sv1

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8sv1
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8sv1
Deposition date deposition_date2023-05-15
Structure title titleCaspase-1 complex with interleukin-18
Keywords keywordsInnate immune, Complex, HYDROLASE, IMMUNE SYSTEM; HYDROLASE, IMMUNE SYSTEM
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier33.57
Radius of gyration Rg (electron density) rg_electron33.61
Forward intensity I(0) i0128933000.00
Molecular weight molecular_weight90364.0 kDa
Excluded volume excluded_volume112870 ų
Envelope volume envelope_volume149880 ų
Hydration-shell volume shell_volume39212 ų
Envelope diameter envelope_diameter129.8
Shell Rg shell_rg37.63
Envelope Rg envelope_rg34.54
Shape Rg shape_rg33.59
Total Rg total_rg33.98
Total atoms total_atoms6330
Residues n_residues792
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 dmax121.3
Rg (real space) rg_real33.87
Rg uncertainty (real space) rg_real_error1.26
I(0) (real space) i0_real1.2890e+08
I(0) uncertainty (real space) i0_real_error2.0760e+06
Rg (reciprocal space) rg_reciprocal33.68
I(0) (reciprocal space) i0_reciprocal128900000.0000
Solution quality estimate total_estimate0.7839
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary33.5
Skewness Skewness skewness0.695
Kurtosis Kurtosis kurtosis0.366
Angular range angular_range— – 0.2350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha45260000.0000
Real-space data points n_real_points48
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.648; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.706; Smooth: 0.536

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)