1yai

X-RAY STRUCTURE OF A BACTERIAL COPPER,ZINC SUPEROXIDE DISMUTASE

Method: X-RAY DIFFRACTION Dmax: 81.1 Å Quality: EXCELLENT

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

COPPER, ZINC SUPEROXIDE DISMUTASE

Photobacterium leiognathi

UniProt P00446

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 23–173 Not recorded CU COPPER (II) ION × 2 ZN ZINC ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:pH 6.5;42% MPD, 60 MM POTASSIUM PHOSPHATE, PH 6.5 Resolution 1.90 Å R-free 0.210
2 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 23–173 Chain C; UniProt 23–173 Not recorded CU COPPER (II) ION × 2 ZN ZINC ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:pH 6.5;42% MPD, 60 MM POTASSIUM PHOSPHATE, PH 6.5 Resolution 1.90 Å R-free 0.210

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.

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

View Construct and Data Evidence
UniProt name SODC_PHOLE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–151; UniProt 23–173 Author chain B; PDBConstruct 1–151; UniProt 23–173 Author chain C; PDBConstruct 1–151; UniProt 23–173

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 1yai

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1yai
Deposition date deposition_date1996-02-03
Structure title titleX-RAY STRUCTURE OF A BACTERIAL COPPER,ZINC SUPEROXIDE DISMUTASE
Keywords keywordsOXIDOREDUCTASE, BETA-BARREL, METALLOENZYME, MACROMOLECULAR ASSEMBLY; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier27.02
Radius of gyration Rg (electron density) rg_electron26.58
Forward intensity I(0) i041012600.00
Molecular weight molecular_weight47531.0 kDa
Excluded volume excluded_volume58496 ų
Envelope volume envelope_volume75806 ų
Hydration-shell volume shell_volume24047 ų
Envelope diameter envelope_diameter87.1
Shell Rg shell_rg33.60
Envelope Rg envelope_rg26.02
Shape Rg shape_rg26.60
Total Rg total_rg27.26
Total atoms total_atoms3320
Residues n_residues452
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 dmax81.1
Rg (real space) rg_real26.98
Rg uncertainty (real space) rg_real_error0.54
I(0) (real space) i0_real4.1010e+07
I(0) uncertainty (real space) i0_real_error6.0870e+05
Rg (reciprocal space) rg_reciprocal27.00
I(0) (reciprocal space) i0_reciprocal41010000.0000
Solution quality estimate total_estimate0.9093
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary23.4
Skewness Skewness skewness0.143
Kurtosis Kurtosis kurtosis-0.789
Angular range angular_range— – 0.2950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4917000.0000
Real-space data points n_real_points60
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.968; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.960; Smooth: 0.952

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd1yaia_
Class classb — All beta proteins
Fold Fold foldb.1 — Immunoglobulin-like beta-sandwich
Superfamily Superfamily superfamilyb.1.8 — Cu,Zn superoxide dismutase-like
Family Family familyb.1.8.1 — Cu,Zn superoxide dismutase-like
Domain ID domain_idd1yaib_
Class classb — All beta proteins
Fold Fold foldb.1 — Immunoglobulin-like beta-sandwich
Superfamily Superfamily superfamilyb.1.8 — Cu,Zn superoxide dismutase-like
Family Family familyb.1.8.1 — Cu,Zn superoxide dismutase-like
Domain ID domain_idd1yaic_
Class classb — All beta proteins
Fold Fold foldb.1 — Immunoglobulin-like beta-sandwich
Superfamily Superfamily superfamilyb.1.8 — Cu,Zn superoxide dismutase-like
Family Family familyb.1.8.1 — Cu,Zn superoxide dismutase-like

CATH v4.4 (3 domains)

Domain ID domain_id1yaiA00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily200 — Superoxide dismutase, copper/zinc binding domain
Domain ID domain_id1yaiB00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily200 — Superoxide dismutase, copper/zinc binding domain
Domain ID domain_id1yaiC00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily200 — Superoxide dismutase, copper/zinc binding domain

8. Citations (2)

9. Files and Curves (10)