1bt3

CATECHOL OXIDASE FROM IPOMOEA BATATAS (SWEET POTATOES) IN THE NATIVE CU(II)-CU(II) STATE

Method: X-RAY DIFFRACTION Dmax: 61.3 Å Quality: GOOD

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

PROTEIN (CATECHOL OXIDASE)

OrganismNot specified

UniProt Q9ZP19

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1–345 Not recorded C2O CU-O-CU LINKAGE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7;CRYSTALS WERE GROWN AT 277 K FROM SOLUTIONS CONTAINING 14 MG/ML PROTEIN, 120 MG/ML PEG6000, 500 MM NACL, 50 MM HEPES, PH 7.0, EQUILIBRATED AGAINST A SOLUTION CONTAINING 200 MG/ML PEG6000., VAPOR DIFFUSION, HANGING DROP Resolution 2.50 Å R-free 0.250

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.

3 other PDB entries and 6 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PPO1_IPOBA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–345; UniProt 1–345

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 1bt3

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1bt3
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1bt3
Deposition date deposition_date1998-09-02
Structure title titleCATECHOL OXIDASE FROM IPOMOEA BATATAS (SWEET POTATOES) IN THE NATIVE CU(II)-CU(II) STATE
Keywords keywordsCATECHOL OXIDASE, DICOPPER ENZYME, IPOMOEA BATATAS, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.62
Radius of gyration Rg (electron density) rg_electron18.54
Forward intensity I(0) i024886100.00
Molecular weight molecular_weight37896.0 kDa
Excluded volume excluded_volume47093 ų
Envelope volume envelope_volume51709 ų
Hydration-shell volume shell_volume22292 ų
Envelope diameter envelope_diameter61.6
Shell Rg shell_rg25.90
Envelope Rg envelope_rg18.92
Shape Rg shape_rg18.52
Total Rg total_rg19.53
Total atoms total_atoms2669
Residues n_residues336
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 dmax61.3
Rg (real space) rg_real19.45
Rg uncertainty (real space) rg_real_error0.26
I(0) (real space) i0_real2.4890e+07
I(0) uncertainty (real space) i0_real_error2.9540e+05
Rg (reciprocal space) rg_reciprocal19.48
I(0) (reciprocal space) i0_reciprocal24890000.0000
Solution quality estimate total_estimate0.8932
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary25.0
Skewness Skewness skewness0.099
Kurtosis Kurtosis kurtosis-0.437
Angular range angular_range— – 0.4050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6285000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.875; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.987; Smooth: 0.996

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1bt3a_
Class classa — All alpha proteins
Fold Fold folda.86 — Di-copper centre-containing domain
Superfamily Superfamily superfamilya.86.1 — Di-copper centre-containing domain
Family Family familya.86.1.2 — Catechol oxidase

CATH v4.4 (1 domains)

Domain ID domain_id1bt3A00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology1280 — di-copper center containing domain from catechol oxidase
Homologous superfamily homologous superfamily10 — Di-copper center containing domain from catechol oxidase

8. Citations (1)

9. Files and Curves (10)