1bhe

POLYGALACTURONASE FROM ERWINIA CAROTOVORA SSP. CAROTOVORA

Method: X-RAY DIFFRACTION Dmax: 70.1 Å Quality: GOOD

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

POLYGALACTURONASE

Pectobacterium carotovorum subsp. carotovorum

UniProt P26509

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 27–402 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 6.5;PROTEIN WAS CRYSTALLIZED FROM 18% PEG 8000, 0.1M SODIUM CACODYLATE, PH 6.5, 0.2M MAGNESIUM ACETATE. Resolution 1.90 Å R-free 0.239

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.

No other PDB entry for the same UniProt protein was found.

View Construct and Data Evidence
UniProt name PGLR2_ERWCA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–376; UniProt 27–402

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 1bhe

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1bhe
Deposition date deposition_date1998-06-05
Structure title titlePOLYGALACTURONASE FROM ERWINIA CAROTOVORA SSP. CAROTOVORA
Keywords keywordsFAMILY 28 GLYCOSYL HYDROLASE, HYDROLYSES POLYGALACTURONIC ACID, GLYCOSIDASE; GLYCOSIDASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.58
Radius of gyration Rg (electron density) rg_electron20.76
Forward intensity I(0) i028191600.00
Molecular weight molecular_weight40099.0 kDa
Excluded volume excluded_volume50029 ų
Envelope volume envelope_volume58199 ų
Hydration-shell volume shell_volume23182 ų
Envelope diameter envelope_diameter70.1
Shell Rg shell_rg27.53
Envelope Rg envelope_rg21.12
Shape Rg shape_rg20.71
Total Rg total_rg21.74
Total atoms total_atoms2813
Residues n_residues376
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 dmax70.1
Rg (real space) rg_real21.51
Rg uncertainty (real space) rg_real_error0.37
I(0) (real space) i0_real2.8190e+07
I(0) uncertainty (real space) i0_real_error3.7740e+05
Rg (reciprocal space) rg_reciprocal21.52
I(0) (reciprocal space) i0_reciprocal28190000.0000
Solution quality estimate total_estimate0.8890
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary25.8
Skewness Skewness skewness0.284
Kurtosis Kurtosis kurtosis-0.287
Angular range angular_range— – 0.3700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3481000.0000
Real-space data points n_real_points69
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.854; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.992

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1bhea_
Class classb — All beta proteins
Fold Fold foldb.80 — Single-stranded right-handed beta-helix
Superfamily Superfamily superfamilyb.80.1 — Pectin lyase-like
Family Family familyb.80.1.3 — Galacturonase

CATH v4.4 (1 domains)

Domain ID domain_id1bheA00
Class class2 — Mainly Beta
Architecture architecture160 — 3 Solenoid
Topology topology20 — Pectate Lyase C-like
Homologous superfamily homologous superfamily10 — Single-stranded right-handed beta-helix, Pectin lyase-like

8. Citations (1)

9. Files and Curves (10)