5h33

Structural basis for dimerization of the death effector domains of Caspase-8

Method: X-RAY DIFFRACTION Dmax: 88.2 Å Quality: GOOD

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

Caspase-8

Homo sapiens

UniProt Q14790

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–188 Chain B; UniProt 1–188 Mutation:F122A No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:EVAPORATION;pH 8.5;293 K;50mM sodium chloride, 100mM Tris pH 8.5, 22.5% PEG3350 Resolution 3.60 Å R-free 0.313

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 45 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CASP8_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–188; UniProt 1–188 Author chain B; PDBConstruct 1–188; UniProt 1–188

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 5h33

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5h33
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5h33
Deposition date deposition_date2016-10-20
Structure title titleStructural basis for dimerization of the death effector domains of Caspase-8
Keywords keywordsDEATH EFFECTOR DOMAIN, CASPASE, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier27.74
Radius of gyration Rg (electron density) rg_electron26.68
Forward intensity I(0) i029574100.00
Molecular weight molecular_weight42968.0 kDa
Excluded volume excluded_volume54291 ų
Envelope volume envelope_volume71084 ų
Hydration-shell volume shell_volume22739 ų
Envelope diameter envelope_diameter90.4
Shell Rg shell_rg33.14
Envelope Rg envelope_rg26.38
Shape Rg shape_rg26.71
Total Rg total_rg27.34
Total atoms total_atoms3014
Residues n_residues362
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 dmax88.2
Rg (real space) rg_real27.82
Rg uncertainty (real space) rg_real_error0.59
I(0) (real space) i0_real2.9570e+07
I(0) uncertainty (real space) i0_real_error4.4620e+05
Rg (reciprocal space) rg_reciprocal27.80
I(0) (reciprocal space) i0_reciprocal29570000.0000
Solution quality estimate total_estimate0.8905
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.8
Skewness Skewness skewness0.316
Kurtosis Kurtosis kurtosis-0.653
Angular range angular_range— – 0.2850 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha10260000.0000
Real-space data points n_real_points58
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.913; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.918; Smooth: 0.916

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id5h33A01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology533 — Death Domain, Fas
Homologous superfamily homologous superfamily10 — Death Domain, Fas
Domain ID domain_id5h33B01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology533 — Death Domain, Fas
Homologous superfamily homologous superfamily10 — Death Domain, Fas

8. Citations (4)

9. Files and Curves (10)