4rhw

Crystal structure of Apaf-1 CARD and caspase-9 CARD complex

Method: X-RAY DIFFRACTION Dmax: 82.7 Å Quality: REASONABLE

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

Apoptotic protease-activating factor 1

Homo sapiens

UniProt O14727

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 1–97 Chain B; UniProt 1–97 Chain C; UniProt 1–97 Chain D; UniProt 1–97 Fragment:card domain Caspase-9 × 2 (P55211) SO4 SULFATE ION × 7 CL CHLORIDE ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.5;291 K;13% PEG 3000, 0.2M ammonium sulfate, 0.1M MES (pH5.5), VAPOR DIFFUSION, HANGING DROP, temperature 291K Resolution 2.10 Å R-free 0.226

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.

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

View Construct and Data Evidence
UniProt name APAF_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–97; UniProt 1–97 Author chain B; PDBConstruct 1–97; UniProt 1–97 Author chain C; PDBConstruct 1–97; UniProt 1–97 Author chain D; PDBConstruct 1–97; UniProt 1–97

Caspase-9

Homo sapiens

UniProt P55211

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 E; UniProt 1–100 Chain F; UniProt 1–100 Fragment:card domain Apoptotic protease-activating factor 1 × 4 (O14727) SO4 SULFATE ION × 7 CL CHLORIDE ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.5;291 K;13% PEG 3000, 0.2M ammonium sulfate, 0.1M MES (pH5.5), VAPOR DIFFUSION, HANGING DROP, temperature 291K Resolution 2.10 Å R-free 0.226

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.

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

View Construct and Data Evidence
UniProt name CASP9_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain E; PDBConstruct 1–100; UniProt 1–100 Author chain F; PDBConstruct 1–100; UniProt 1–100

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 4rhw

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4rhw
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4rhw
Deposition date deposition_date2014-10-03
Structure title titleCrystal structure of Apaf-1 CARD and caspase-9 CARD complex
Keywords keywordsdeath domain superfamily, apoptosis; APOPTOSIS
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.22
Radius of gyration Rg (electron density) rg_electron25.46
Forward intensity I(0) i077576100.00
Molecular weight molecular_weight65944.0 kDa
Excluded volume excluded_volume81465 ų
Envelope volume envelope_volume97855 ų
Hydration-shell volume shell_volume31772 ų
Envelope diameter envelope_diameter84.2
Shell Rg shell_rg33.10
Envelope Rg envelope_rg25.51
Shape Rg shape_rg25.48
Total Rg total_rg26.18
Total atoms total_atoms4599
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 dmax82.7
Rg (real space) rg_real26.10
Rg uncertainty (real space) rg_real_error0.40
I(0) (real space) i0_real7.7580e+07
I(0) uncertainty (real space) i0_real_error1.1170e+06
Rg (reciprocal space) rg_reciprocal26.14
I(0) (reciprocal space) i0_reciprocal77580000.0000
Solution quality estimate total_estimate0.7215
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary35.2
Skewness Skewness skewness0.184
Kurtosis Kurtosis kurtosis-0.445
Angular range angular_range— – 0.3050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha26710000.0000
Real-space data points n_real_points62
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.913; Stabil: 1.000; Sysdev: 0.221; Positv: 1.000; Valcen: 0.997; Smooth: 0.977

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 12 domains

SCOP 2.08 (6 domains)

Domain ID domain_idd4rhwa_
Class classa — All alpha proteins
Fold Fold folda.77 — DEATH domain
Superfamily Superfamily superfamilya.77.1 — DEATH domain
Family Family familya.77.1.3 — Caspase recruitment domain, CARD
Domain ID domain_idd4rhwb_
Class classa — All alpha proteins
Fold Fold folda.77 — DEATH domain
Superfamily Superfamily superfamilya.77.1 — DEATH domain
Family Family familya.77.1.3 — Caspase recruitment domain, CARD
Domain ID domain_idd4rhwc_
Class classa — All alpha proteins
Fold Fold folda.77 — DEATH domain
Superfamily Superfamily superfamilya.77.1 — DEATH domain
Family Family familya.77.1.3 — Caspase recruitment domain, CARD
Domain ID domain_idd4rhwd_
Class classa — All alpha proteins
Fold Fold folda.77 — DEATH domain
Superfamily Superfamily superfamilya.77.1 — DEATH domain
Family Family familya.77.1.3 — Caspase recruitment domain, CARD
Domain ID domain_idd4rhwe_
Class classa — All alpha proteins
Fold Fold folda.77 — DEATH domain
Superfamily Superfamily superfamilya.77.1 — DEATH domain
Family Family familya.77.1.3 — Caspase recruitment domain, CARD
Domain ID domain_idd4rhwf_
Class classa — All alpha proteins
Fold Fold folda.77 — DEATH domain
Superfamily Superfamily superfamilya.77.1 — DEATH domain
Family Family familya.77.1.3 — Caspase recruitment domain, CARD

CATH v4.4 (6 domains)

Domain ID domain_id4rhwA00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology533 — Death Domain, Fas
Homologous superfamily homologous superfamily10 — Death Domain, Fas
Domain ID domain_id4rhwB00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology533 — Death Domain, Fas
Homologous superfamily homologous superfamily10 — Death Domain, Fas
Domain ID domain_id4rhwC00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology533 — Death Domain, Fas
Homologous superfamily homologous superfamily10 — Death Domain, Fas
Domain ID domain_id4rhwD00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology533 — Death Domain, Fas
Homologous superfamily homologous superfamily10 — Death Domain, Fas
Domain ID domain_id4rhwE00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology533 — Death Domain, Fas
Homologous superfamily homologous superfamily10 — Death Domain, Fas
Domain ID domain_id4rhwF00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology533 — Death Domain, Fas
Homologous superfamily homologous superfamily10 — Death Domain, Fas

8. Citations (1)

9. Files and Curves (10)