1a3h

ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHERANS AT 1.6A RESOLUTION

Method: X-RAY DIFFRACTION Dmax: 55.0 Å Quality: EXCELLENT

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

ENDOGLUCANASE

Bacillus agaradhaerens

UniProt O85465

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 30–329 Fragment:CATALYTIC CORE DOMAIN No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 4.5;pH 4.5 Resolution 1.57 Å R-free 0.170

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.

14 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name GUN5_BACAG
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–300; UniProt 30–329

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 1a3h

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1a3h
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1a3h
Deposition date deposition_date1998-01-21
Structure title titleENDOGLUCANASE CEL5A FROM BACILLUS AGARADHERANS AT 1.6A RESOLUTION
Keywords keywordsHYDROLASE, CELLULOSE DEGRADATION, ENDOGLUCANASE, GLYCOSIDE HYDROLASE FAMILY 5; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier18.98
Radius of gyration Rg (electron density) rg_electron17.59
Forward intensity I(0) i020388100.00
Molecular weight molecular_weight33596.0 kDa
Excluded volume excluded_volume41456 ų
Envelope volume envelope_volume45525 ų
Hydration-shell volume shell_volume20755 ų
Envelope diameter envelope_diameter56.1
Shell Rg shell_rg24.68
Envelope Rg envelope_rg17.83
Shape Rg shape_rg17.59
Total Rg total_rg18.50
Total atoms total_atoms2377
Residues n_residues300
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 dmax55.0
Rg (real space) rg_real18.79
Rg uncertainty (real space) rg_real_error0.24
I(0) (real space) i0_real2.0390e+07
I(0) uncertainty (real space) i0_real_error2.2500e+05
Rg (reciprocal space) rg_reciprocal18.82
I(0) (reciprocal space) i0_reciprocal20390000.0000
Solution quality estimate total_estimate0.9057
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary25.2
Skewness Skewness skewness-0.002
Kurtosis Kurtosis kurtosis-0.552
Angular range angular_range— – 0.4200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha5259000.0000
Real-space data points n_real_points73
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.942; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.964; Smooth: 0.982

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_idd1a3ha_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.1 — TIM beta/alpha-barrel
Superfamily Superfamily superfamilyc.1.8 — (Trans)glycosidases
Family Family familyc.1.8.3 — beta-glycanases

CATH v4.4 (1 domains)

Domain ID domain_id1a3hA00
Class class3 — Alpha Beta
Architecture architecture20 — Alpha-Beta Barrel
Topology topology20 — TIM Barrel
Homologous superfamily homologous superfamily80 — Glycosidases

8. Citations (1)

9. Files and Curves (10)