4us6

New Crystal Form of Glucose Isomerase Grown in Short Peptide Supramolecular Hydrogels

Method: X-RAY DIFFRACTION Dmax: 90.2 Å Quality: EXCELLENT

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

XYLOSE ISOMERASE

OrganismNot specified

UniProt P24300

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 1–388 Chain B; UniProt 1–388 Not recorded CA CALCIUM ION × 4 MG MAGNESIUM ION × 6 GOL GLYCEROL × 12 NA SODIUM ION × 4 X-RAY DIFFRACTION X-ray crystallization conditions:pH 8.5;GEL COUNTERDIFFUSION: 1 M AMMONIUM SULPHATE, 10 MM TRIS PH 8.5 Resolution 1.20 Å R-free 0.132

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.

139 other PDB entries and 143 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name XYLA_STRRU
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–388; UniProt 1–388 Author chain B; PDBConstruct 1–388; UniProt 1–388

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 4us6

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4us6
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4us6
Deposition date deposition_date2014-07-03
Structure title titleNew Crystal Form of Glucose Isomerase Grown in Short Peptide Supramolecular Hydrogels
Keywords keywordsISOMERASE, NEW POLYMORPH; ISOMERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier28.88
Radius of gyration Rg (electron density) rg_electron27.63
Forward intensity I(0) i0127838000.00
Molecular weight molecular_weight86832.0 kDa
Excluded volume excluded_volume107490 ų
Envelope volume envelope_volume126050 ų
Hydration-shell volume shell_volume37133 ų
Envelope diameter envelope_diameter96.1
Shell Rg shell_rg35.93
Envelope Rg envelope_rg27.83
Shape Rg shape_rg27.63
Total Rg total_rg28.41
Total atoms total_atoms12029
Residues n_residues773
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 dmax90.2
Rg (real space) rg_real28.79
Rg uncertainty (real space) rg_real_error0.63
I(0) (real space) i0_real1.2780e+08
I(0) uncertainty (real space) i0_real_error2.0840e+06
Rg (reciprocal space) rg_reciprocal28.83
I(0) (reciprocal space) i0_reciprocal127800000.0000
Solution quality estimate total_estimate0.9049
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary34.5
Skewness Skewness skewness0.241
Kurtosis Kurtosis kurtosis-0.479
Angular range angular_range— – 0.2750 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha34100000.0000
Real-space data points n_real_points56
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.938; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.947

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd4us6a_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.1 — TIM beta/alpha-barrel
Superfamily Superfamily superfamilyc.1.15 — Xylose isomerase-like
Family Family familyc.1.15.3 — Xylose isomerase
Domain ID domain_idd4us6b_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.1 — TIM beta/alpha-barrel
Superfamily Superfamily superfamilyc.1.15 — Xylose isomerase-like
Family Family familyc.1.15.3 — Xylose isomerase

CATH v4.4 (2 domains)

Domain ID domain_id4us6A00
Class class3 — Alpha Beta
Architecture architecture20 — Alpha-Beta Barrel
Topology topology20 — TIM Barrel
Homologous superfamily homologous superfamily150 — Divalent-metal-dependent TIM barrel enzymes
Domain ID domain_id4us6B00
Class class3 — Alpha Beta
Architecture architecture20 — Alpha-Beta Barrel
Topology topology20 — TIM Barrel
Homologous superfamily homologous superfamily150 — Divalent-metal-dependent TIM barrel enzymes

8. Citations (1)

9. Files and Curves (10)