5k9y

Crystal structure of a thermophilic xylanase A from Bacillus subtilis 1A1 quadruple mutant Q7H/G13R/S22P/S179C

Method: X-RAY DIFFRACTION Dmax: 71.6 Å Quality: EXCELLENT

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

Endo-1,4-beta-xylanase A

Bacillus subtilis (strain 168)

UniProt P18429

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 B; UniProt 29–213 Fragment:residues 29-213 Mutation:Q7H, G13R, S22P, S179C Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;295 K;0.1 M HEPES and 0.6 M sodium tartrate Resolution 2.20 Å R-free 0.248
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 29–213 Fragment:residues 29-213 Mutation:Q7H, G13R, S22P, S179C Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;295 K;0.1 M HEPES and 0.6 M sodium tartrate Resolution 2.20 Å R-free 0.248

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.

13 other PDB entries and 27 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name XYNA_BACSU
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–185; UniProt 29–213 Author chain B; PDBConstruct 1–185; UniProt 29–213

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 5k9y

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5k9y
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id5k9y
Deposition date deposition_date2016-06-01
Structure title titleCrystal structure of a thermophilic xylanase A from Bacillus subtilis 1A1 quadruple mutant Q7H/G13R/S22P/S179C
Keywords keywordsGlycoside Hydrolase Family 11, Endo-1, 4-beta-xylanase A, thermostability, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier22.84
Radius of gyration Rg (electron density) rg_electron22.04
Forward intensity I(0) i030542900.00
Molecular weight molecular_weight40995.0 kDa
Excluded volume excluded_volume50443 ų
Envelope volume envelope_volume56687 ų
Hydration-shell volume shell_volume22058 ų
Envelope diameter envelope_diameter73.1
Shell Rg shell_rg28.02
Envelope Rg envelope_rg21.95
Shape Rg shape_rg21.99
Total Rg total_rg22.87
Total atoms total_atoms2909
Residues n_residues368
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 dmax71.6
Rg (real space) rg_real22.85
Rg uncertainty (real space) rg_real_error0.33
I(0) (real space) i0_real3.0540e+07
I(0) uncertainty (real space) i0_real_error3.6730e+05
Rg (reciprocal space) rg_reciprocal22.85
I(0) (reciprocal space) i0_reciprocal30540000.0000
Solution quality estimate total_estimate0.9001
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.9
Skewness Skewness skewness0.352
Kurtosis Kurtosis kurtosis-0.499
Angular range angular_range— – 0.3500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7253000.0000
Real-space data points n_real_points67
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.906; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.992; Smooth: 0.987

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd5k9ya_
Class classb — All beta proteins
Fold Fold foldb.29 — Concanavalin A-like lectins/glucanases
Superfamily Superfamily superfamilyb.29.1 — Concanavalin A-like lectins/glucanases
Family Family familyb.29.1.11 — Xylanase/endoglucanase 11/12
Domain ID domain_idd5k9yb_
Class classb — All beta proteins
Fold Fold foldb.29 — Concanavalin A-like lectins/glucanases
Superfamily Superfamily superfamilyb.29.1 — Concanavalin A-like lectins/glucanases
Family Family familyb.29.1.11 — Xylanase/endoglucanase 11/12

CATH v4.4 (2 domains)

Domain ID domain_id5k9yA00
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_id5k9yB00
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)