1bga

BETA-GLUCOSIDASE A FROM BACILLUS POLYMYXA

Method: X-RAY DIFFRACTION Dmax: 135.8 Å Quality: GOOD

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

BETA-GLUCOSIDASE A

Paenibacillus polymyxa

UniProt P22073

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 × 8 PDB declaration: octameric(8) Consistent with protein copy count Chain A; UniProt 2–448 Chain B; UniProt 2–448 Chain C; UniProt 2–448 Chain D; UniProt 2–448 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 8.3;PROTEIN WAS CRYSTALLIZED FROM 1.3 M NA/K PHOSPHATE, PH 8.3, 5 MICRO-L PROTEIN, 14 MG/ML, 5 MICRO-L RESERVOIR Resolution 2.40 Å R-free 0.270

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.

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

View Construct and Data Evidence
UniProt name BGLA_PAEPO
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–447; UniProt 2–448 Author chain B; PDBConstruct 1–447; UniProt 2–448 Author chain C; PDBConstruct 1–447; UniProt 2–448 Author chain D; PDBConstruct 1–447; UniProt 2–448

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 1bga

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1bga
Deposition date deposition_date1997-04-04
Structure title titleBETA-GLUCOSIDASE A FROM BACILLUS POLYMYXA
Keywords keywordsFAMILY 1 BETA-GLUCOSIDASE, GLYCOSYL HYDROLASE, GLYCOSIDASE; GLYCOSIDASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier42.96
Radius of gyration Rg (electron density) rg_electron42.63
Forward intensity I(0) i0635092000.00
Molecular weight molecular_weight205980.0 kDa
Excluded volume excluded_volume255910 ų
Envelope volume envelope_volume319000 ų
Hydration-shell volume shell_volume60619 ų
Envelope diameter envelope_diameter140.6
Shell Rg shell_rg49.44
Envelope Rg envelope_rg41.76
Shape Rg shape_rg42.64
Total Rg total_rg42.90
Total atoms total_atoms14576
Residues n_residues1788
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 dmax135.8
Rg (real space) rg_real42.83
Rg uncertainty (real space) rg_real_error1.15
I(0) (real space) i0_real6.3510e+08
I(0) uncertainty (real space) i0_real_error1.0980e+07
Rg (reciprocal space) rg_reciprocal42.96
I(0) (reciprocal space) i0_reciprocal635200000.0000
Solution quality estimate total_estimate0.8860
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary62.4
Skewness Skewness skewness0.109
Kurtosis Kurtosis kurtosis-0.654
Angular range angular_range— – 0.1850 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha232700000.0000
Real-space data points n_real_points38
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.908; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.791

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 8 domains

SCOP 2.08 (4 domains)

Domain ID domain_idd1bgaa_
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.1.8.4 — Family 1 of glycosyl hydrolase
Domain ID domain_idd1bgab_
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.1.8.4 — Family 1 of glycosyl hydrolase
Domain ID domain_idd1bgac_
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.1.8.4 — Family 1 of glycosyl hydrolase
Domain ID domain_idd1bgad_
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.1.8.4 — Family 1 of glycosyl hydrolase

CATH v4.4 (4 domains)

Domain ID domain_id1bgaA00
Class class3 — Alpha Beta
Architecture architecture20 — Alpha-Beta Barrel
Topology topology20 — TIM Barrel
Homologous superfamily homologous superfamily80 — Glycosidases
Domain ID domain_id1bgaB00
Class class3 — Alpha Beta
Architecture architecture20 — Alpha-Beta Barrel
Topology topology20 — TIM Barrel
Homologous superfamily homologous superfamily80 — Glycosidases
Domain ID domain_id1bgaC00
Class class3 — Alpha Beta
Architecture architecture20 — Alpha-Beta Barrel
Topology topology20 — TIM Barrel
Homologous superfamily homologous superfamily80 — Glycosidases
Domain ID domain_id1bgaD00
Class class3 — Alpha Beta
Architecture architecture20 — Alpha-Beta Barrel
Topology topology20 — TIM Barrel
Homologous superfamily homologous superfamily80 — Glycosidases

8. Citations (3)

9. Files and Curves (10)