4lnc

Neutron structure of the cyclic glucose bound Xylose Isomerase E186Q mutant

Dmax: 85.5 Å Quality: GOOD

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

Xylose isomerase

Streptomyces rubiginosus

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 Not recorded GLC alpha-D-glucopyranose × 4 MN MANGANESE (II) ION × 8 MG MAGNESIUM ION × 4 Experimental method not declared X-ray crystallization conditions:pH 7.7;295 K;Large crystals were grown in 1.5 ml Eppendorf tubes with 15% ammonium sulfate, 72 mg/ml D-xylose isomerase at ph 7.7, Batch method, temperature 295K Resolution not provided

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

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 4lnc

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id4lnc
Deposition date deposition_date2013-07-11
Structure title titleNeutron structure of the cyclic glucose bound Xylose Isomerase E186Q mutant
Keywords keywordsISOMERASE, MUTANT ENZYME, METALLOENZYME, TWO METAL BINDING SITES; ISOMERASE

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

Radius of gyration Rg (Guinier) rg_guinier24.95
Radius of gyration Rg (electron density) rg_electron23.72
Forward intensity I(0) i046033400.00
Molecular weight molecular_weight48853.0 kDa
Excluded volume excluded_volume59091 ų
Envelope volume envelope_volume80783 ų
Hydration-shell volume shell_volume27924 ų
Envelope diameter envelope_diameter88.0
Shell Rg shell_rg31.15
Envelope Rg envelope_rg25.19
Shape Rg shape_rg23.99
Total Rg total_rg23.78
Total atoms total_atoms6642
Residues n_residues385
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 dmax85.5
Rg (real space) rg_real25.03
Rg uncertainty (real space) rg_real_error0.62
I(0) (real space) i0_real4.6030e+07
I(0) uncertainty (real space) i0_real_error6.3190e+05
Rg (reciprocal space) rg_reciprocal25.02
I(0) (reciprocal space) i0_reciprocal46030000.0000
Solution quality estimate total_estimate0.8623
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.2
Skewness Skewness skewness0.465
Kurtosis Kurtosis kurtosis-0.171
Angular range angular_range— – 0.3200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7699000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.770; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.918; Smooth: 0.976

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd4lnca_
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 (1 domains)

Domain ID domain_id4lncA00
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)