3bwe

Crystal structure of aggregated form of DJ1

Method: X-RAY DIFFRACTION Dmax: 156.2 Å Quality: GOOD

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

Protein DJ-1

Homo sapiens

UniProt Q99497

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 1–189 Chain B; UniProt 1–189 Non-standard monomer:Yes (specific site not provided by mmCIF) PO4 PHOSPHATE ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:EVAPORATION;EVAPORATION Resolution 2.40 Å R-free 0.282
2 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 1–189 Chain D; UniProt 1–189 Non-standard monomer:Yes (specific site not provided by mmCIF) PO4 PHOSPHATE ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:EVAPORATION;EVAPORATION Resolution 2.40 Å R-free 0.282
3 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain E; UniProt 1–189 Chain F; UniProt 1–189 Non-standard monomer:Yes (specific site not provided by mmCIF) PO4 PHOSPHATE ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:EVAPORATION;EVAPORATION Resolution 2.40 Å R-free 0.282
4 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain G; UniProt 1–189 Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:EVAPORATION;EVAPORATION Resolution 2.40 Å R-free 0.282

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.

87 other PDB entries and 94 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PARK7_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–189; UniProt 1–189 Author chain B; PDBConstruct 1–189; UniProt 1–189 Author chain C; PDBConstruct 1–189; UniProt 1–189 Author chain D; PDBConstruct 1–189; UniProt 1–189 Author chain E; PDBConstruct 1–189; UniProt 1–189 Author chain F; PDBConstruct 1–189; UniProt 1–189 Author chain G; PDBConstruct 1–189; UniProt 1–189

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 3bwe

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3bwe
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3bwe
Deposition date deposition_date2008-01-09
Structure title titleCrystal structure of aggregated form of DJ1
Keywords keywords;DJ-1, filamentous aggregates, Chaperone, Cytoplasm, Disease mutation, Nucleus, Oncogene, Oxidation, Parkinson disease, Phosphoprotein, Polymorphism, Ubl conjugation ;; CHAPERONE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier41.50
Radius of gyration Rg (electron density) rg_electron41.85
Forward intensity I(0) i0293969000.00
Molecular weight molecular_weight137420.0 kDa
Excluded volume excluded_volume171080 ų
Envelope volume envelope_volume219950 ų
Hydration-shell volume shell_volume47739 ų
Envelope diameter envelope_diameter156.8
Shell Rg shell_rg42.21
Envelope Rg envelope_rg42.16
Shape Rg shape_rg41.87
Total Rg total_rg41.80
Total atoms total_atoms9525
Residues n_residues1279
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 dmax156.2
Rg (real space) rg_real42.04
Rg uncertainty (real space) rg_real_error2.03
I(0) (real space) i0_real2.9400e+08
I(0) uncertainty (real space) i0_real_error6.0360e+06
Rg (reciprocal space) rg_reciprocal41.50
I(0) (reciprocal space) i0_reciprocal293800000.0000
Solution quality estimate total_estimate0.7546
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary41.1
Skewness Skewness skewness0.721
Kurtosis Kurtosis kurtosis0.051
Angular range angular_range— – 0.1900 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha24390000.0000
Real-space data points n_real_points39
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.441; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.703; Smooth: 0.781

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 14 domains

SCOP 2.08 (7 domains)

Domain ID domain_idd3bwea_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.23 — Flavodoxin-like
Superfamily Superfamily superfamilyc.23.16 — Class I glutamine amidotransferase-like
Family Family familyc.23.16.2 — DJ-1/PfpI
Domain ID domain_idd3bweb_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.23 — Flavodoxin-like
Superfamily Superfamily superfamilyc.23.16 — Class I glutamine amidotransferase-like
Family Family familyc.23.16.2 — DJ-1/PfpI
Domain ID domain_idd3bwec_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.23 — Flavodoxin-like
Superfamily Superfamily superfamilyc.23.16 — Class I glutamine amidotransferase-like
Family Family familyc.23.16.2 — DJ-1/PfpI
Domain ID domain_idd3bwed_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.23 — Flavodoxin-like
Superfamily Superfamily superfamilyc.23.16 — Class I glutamine amidotransferase-like
Family Family familyc.23.16.2 — DJ-1/PfpI
Domain ID domain_idd3bwee_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.23 — Flavodoxin-like
Superfamily Superfamily superfamilyc.23.16 — Class I glutamine amidotransferase-like
Family Family familyc.23.16.2 — DJ-1/PfpI
Domain ID domain_idd3bwef_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.23 — Flavodoxin-like
Superfamily Superfamily superfamilyc.23.16 — Class I glutamine amidotransferase-like
Family Family familyc.23.16.2 — DJ-1/PfpI
Domain ID domain_idd3bweg_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.23 — Flavodoxin-like
Superfamily Superfamily superfamilyc.23.16 — Class I glutamine amidotransferase-like
Family Family familyc.23.16.2 — DJ-1/PfpI

CATH v4.4 (7 domains)

Domain ID domain_id3bweA00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily880 — Class I glutamine amidotransferase (GATase) domain
Domain ID domain_id3bweB00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily880 — Class I glutamine amidotransferase (GATase) domain
Domain ID domain_id3bweC00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily880 — Class I glutamine amidotransferase (GATase) domain
Domain ID domain_id3bweD00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily880 — Class I glutamine amidotransferase (GATase) domain
Domain ID domain_id3bweE00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily880 — Class I glutamine amidotransferase (GATase) domain
Domain ID domain_id3bweF00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily880 — Class I glutamine amidotransferase (GATase) domain
Domain ID domain_id3bweG00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily880 — Class I glutamine amidotransferase (GATase) domain

8. Citations (1)

9. Files and Curves (10)