1oe2

Atomic Resolution Structure of D92E Mutant of Alcaligenes xylosoxidans Nitrite Reductase

Method: X-RAY DIFFRACTION Dmax: 78.2 Å Quality: GOOD

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

DISSIMILATORY COPPER-CONTAINING NITRITE REDUCTASE

ALCALIGENES XYLOSOXIDANS

UniProt O68601

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 25–360 Mutation:YES Non-standard monomer:Yes (specific site not provided by mmCIF) CU COPPER (II) ION × 6 PG4 TETRAETHYLENE GLYCOL × 3 X-RAY DIFFRACTION X-ray crystallization conditions:pH 6.5;0.1M MES PH6.5 40-50% PEG-MME 550, 10MM CUSO4,, pH 6.50 Resolution 1.12 Å R-free 0.179

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.

36 other PDB entries and 48 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name O68601
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–336; UniProt 25–360

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 1oe2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1oe2
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1oe2
Deposition date deposition_date2003-03-18
Structure title titleAtomic Resolution Structure of D92E Mutant of Alcaligenes xylosoxidans Nitrite Reductase
Keywords keywordsREDUCTASE, NITRITE REDUCTASE, COPPER PROTEIN; REDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.43
Radius of gyration Rg (electron density) rg_electron20.72
Forward intensity I(0) i022463000.00
Molecular weight molecular_weight36227.0 kDa
Excluded volume excluded_volume45311 ų
Envelope volume envelope_volume53631 ų
Hydration-shell volume shell_volume21734 ų
Envelope diameter envelope_diameter84.4
Shell Rg shell_rg27.28
Envelope Rg envelope_rg21.68
Shape Rg shape_rg20.72
Total Rg total_rg21.58
Total atoms total_atoms5010
Residues n_residues334
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 dmax78.2
Rg (real space) rg_real21.45
Rg uncertainty (real space) rg_real_error0.79
I(0) (real space) i0_real2.2460e+07
I(0) uncertainty (real space) i0_real_error3.6200e+05
Rg (reciprocal space) rg_reciprocal21.44
I(0) (reciprocal space) i0_reciprocal22460000.0000
Solution quality estimate total_estimate0.7539
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary24.1
Skewness Skewness skewness0.439
Kurtosis Kurtosis kurtosis0.013
Angular range angular_range— – 0.3700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha5735000.0000
Real-space data points n_real_points69
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.630; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.909; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd1oe2a1
Class classb — All beta proteins
Fold Fold foldb.6 — Cupredoxin-like
Superfamily Superfamily superfamilyb.6.1 — Cupredoxins
Family Family familyb.6.1.3 — Multidomain cupredoxins
Domain ID domain_idd1oe2a2
Class classb — All beta proteins
Fold Fold foldb.6 — Cupredoxin-like
Superfamily Superfamily superfamilyb.6.1 — Cupredoxins
Family Family familyb.6.1.3 — Multidomain cupredoxins

CATH v4.4 (2 domains)

Domain ID domain_id1oe2A01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily420 — Cupredoxins - blue copper proteins
Domain ID domain_id1oe2A02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily420 — Cupredoxins - blue copper proteins

8. Citations (1)

9. Files and Curves (10)