3lb9

Crystal structure of the B. circulans cpA123 circular permutant

Method: X-RAY DIFFRACTION Dmax: 81.4 Å Quality: EXCELLENT

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

Endo-1,4-beta-xylanase

Bacillus circulans

UniProt P09850

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 29–146 Chain A; UniProt 152–213 Fragment:residues 65-182 and 2-63 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 8;298 K;13-20 % (NH4)2SO4 40 mM Tris-HCl, pH 8, VAPOR DIFFUSION, temperature 298K Resolution 3.00 Å R-free 0.268
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 29–146 Chain B; UniProt 152–213 Fragment:residues 65-182 and 2-63 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 8;298 K;13-20 % (NH4)2SO4 40 mM Tris-HCl, pH 8, VAPOR DIFFUSION, temperature 298K Resolution 3.00 Å R-free 0.268
3 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 29–146 Chain C; UniProt 152–213 Fragment:residues 65-182 and 2-63 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 8;298 K;13-20 % (NH4)2SO4 40 mM Tris-HCl, pH 8, VAPOR DIFFUSION, temperature 298K Resolution 3.00 Å R-free 0.268

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.

32 other PDB entries and 45 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name XYNA_BACCI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 65–182; UniProt 29–146 Author chain A; PDBConstruct 2–63; UniProt 152–213 Author chain B; PDBConstruct 65–182; UniProt 29–146 Author chain B; PDBConstruct 2–63; UniProt 152–213 Author chain C; PDBConstruct 65–182; UniProt 29–146 Author chain C; PDBConstruct 2–63; UniProt 152–213

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 3lb9

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3lb9
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3lb9
Deposition date deposition_date2010-01-08
Structure title titleCrystal structure of the B. circulans cpA123 circular permutant
Keywords keywordspermutation, BcX, Glycosidase, Xylan degradation, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.26
Radius of gyration Rg (electron density) rg_electron25.63
Forward intensity I(0) i062595700.00
Molecular weight molecular_weight59897.0 kDa
Excluded volume excluded_volume73874 ų
Envelope volume envelope_volume87893 ų
Hydration-shell volume shell_volume28791 ų
Envelope diameter envelope_diameter86.6
Shell Rg shell_rg32.64
Envelope Rg envelope_rg25.67
Shape Rg shape_rg25.60
Total Rg total_rg26.43
Total atoms total_atoms4254
Residues n_residues546
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 dmax81.4
Rg (real space) rg_real26.18
Rg uncertainty (real space) rg_real_error0.65
I(0) (real space) i0_real6.2600e+07
I(0) uncertainty (real space) i0_real_error1.0090e+06
Rg (reciprocal space) rg_reciprocal26.21
I(0) (reciprocal space) i0_reciprocal62600000.0000
Solution quality estimate total_estimate0.9085
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.1
Skewness Skewness skewness0.212
Kurtosis Kurtosis kurtosis-0.588
Angular range angular_range— – 0.3000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha19110000.0000
Real-space data points n_real_points61
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.942; Stabil: 0.996; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.992

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 3 domains

CATH v4.4 (3 domains)

Domain ID domain_id3lb9A00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily180 — Glycoside hydrolase family 11/12, catalytic domain
Domain ID domain_id3lb9B00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily180 — Glycoside hydrolase family 11/12, catalytic domain
Domain ID domain_id3lb9C00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily180 — Glycoside hydrolase family 11/12, catalytic domain

8. Citations (1)

9. Files and Curves (10)