1i4e

CRYSTAL STRUCTURE OF THE CASPASE-8/P35 COMPLEX

Method: X-RAY DIFFRACTION Dmax: 110.0 Å Quality: GOOD

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

Early 35 kDa protein

Autographa californica nucleopolyhedrovirus

UniProt P08160

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 2–299 Non-standard monomer:Yes (specific site not provided by mmCIF) Caspase-8 × 1 (Q14790) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;VAPOR DIFFUSION, HANGING DROP Resolution 3.00 Å R-free 0.296
2 Protein heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 2–299 Non-standard monomer:Yes (specific site not provided by mmCIF) Caspase-8 × 2 (Q14790) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;VAPOR DIFFUSION, HANGING DROP Resolution 3.00 Å R-free 0.296

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.

4 other PDB entries and 8 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name VP35_NPVAC
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–299; UniProt 2–299

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 222–479 Not recorded Early 35 kDa protein × 1 (P08160) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;VAPOR DIFFUSION, HANGING DROP Resolution 3.00 Å R-free 0.296
2 Protein heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain B; UniProt 222–479 Not recorded Early 35 kDa protein × 2 (P08160) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;VAPOR DIFFUSION, HANGING DROP Resolution 3.00 Å R-free 0.296

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 44 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CASP8_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–258; UniProt 222–479

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 1i4e

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1i4e
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1i4e
Deposition date deposition_date2001-02-20
Structure title titleCRYSTAL STRUCTURE OF THE CASPASE-8/P35 COMPLEX
Keywords keywordscovalent complex protease-inhibitor, APOPTOSIS-HYDROLASE COMPLEX; APOPTOSIS/HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier30.43
Radius of gyration Rg (electron density) rg_electron30.55
Forward intensity I(0) i060894400.00
Molecular weight molecular_weight61947.0 kDa
Excluded volume excluded_volume77746 ų
Envelope volume envelope_volume99662 ų
Hydration-shell volume shell_volume28681 ų
Envelope diameter envelope_diameter112.0
Shell Rg shell_rg35.42
Envelope Rg envelope_rg30.49
Shape Rg shape_rg30.51
Total Rg total_rg31.11
Total atoms total_atoms4354
Residues n_residues536
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 dmax110.0
Rg (real space) rg_real30.69
Rg uncertainty (real space) rg_real_error1.06
I(0) (real space) i0_real6.0890e+07
I(0) uncertainty (real space) i0_real_error9.2310e+05
Rg (reciprocal space) rg_reciprocal30.58
I(0) (reciprocal space) i0_reciprocal60890000.0000
Solution quality estimate total_estimate0.8030
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary27.5
Skewness Skewness skewness0.520
Kurtosis Kurtosis kurtosis-0.379
Angular range angular_range— – 0.2600 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha12390000.0000
Real-space data points n_real_points53
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.614; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.599; Smooth: 0.994

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd1i4ea_
Class classb — All beta proteins
Fold Fold foldb.28 — Baculovirus p35 protein
Superfamily Superfamily superfamilyb.28.1 — Baculovirus p35 protein
Family Family familyb.28.1.1 — Baculovirus p35 protein
Domain ID domain_idd1i4eb_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.17 — Caspase-like
Superfamily Superfamily superfamilyc.17.1 — Caspase-like
Family Family familyc.17.1.1 — Caspase catalytic domain

CATH v4.4 (2 domains)

Domain ID domain_id1i4eA00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology250 — Baculovirus p35
Homologous superfamily homologous superfamily10 — Baculovirus p35
Domain ID domain_id1i4eB00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1460

8. Citations (1)

9. Files and Curves (10)