4rnv

G303 Circular Permutation of Old Yellow Enzyme with the Inhibitor p-Hydroxybenzaldehyde

Method: X-RAY DIFFRACTION Dmax: 133.2 Å Quality: GOOD

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

NADPH dehydrogenase 1

Saccharomyces pastorianus

UniProt Q02899

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 303–397 Chain A; UniProt 2–302 Fragment:UNP residues 303-397, 2-302 FMN FLAVIN MONONUCLEOTIDE × 1 HBA P-HYDROXYBENZALDEHYDE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;289 K;18% PEG 3350, 0.2 M MgCl2, 0.25% glucoside, 0.1 M HEPES, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 289K Resolution 2.47 Å R-free 0.249
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 303–397 Chain B; UniProt 2–302 Fragment:UNP residues 303-397, 2-302 FMN FLAVIN MONONUCLEOTIDE × 1 HBA P-HYDROXYBENZALDEHYDE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;289 K;18% PEG 3350, 0.2 M MgCl2, 0.25% glucoside, 0.1 M HEPES, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 289K Resolution 2.47 Å R-free 0.249
3 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain C; UniProt 303–397 Chain C; UniProt 2–302 Fragment:UNP residues 303-397, 2-302 FMN FLAVIN MONONUCLEOTIDE × 1 HBA P-HYDROXYBENZALDEHYDE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;289 K;18% PEG 3350, 0.2 M MgCl2, 0.25% glucoside, 0.1 M HEPES, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 289K Resolution 2.47 Å R-free 0.249
4 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain D; UniProt 303–397 Chain D; UniProt 2–302 Fragment:UNP residues 303-397, 2-302 FMN FLAVIN MONONUCLEOTIDE × 1 HBA P-HYDROXYBENZALDEHYDE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;289 K;18% PEG 3350, 0.2 M MgCl2, 0.25% glucoside, 0.1 M HEPES, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 289K Resolution 2.47 Å R-free 0.249

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.

25 other PDB entries and 30 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name OYE1_SACPS
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–96; UniProt 303–397 Author chain A; PDBConstruct 100–400; UniProt 2–302 Author chain B; PDBConstruct 2–96; UniProt 303–397 Author chain B; PDBConstruct 100–400; UniProt 2–302 Author chain C; PDBConstruct 2–96; UniProt 303–397 Author chain C; PDBConstruct 100–400; UniProt 2–302 Author chain D; PDBConstruct 2–96; UniProt 303–397 Author chain D; PDBConstruct 100–400; UniProt 2–302

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 4rnv

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id4rnv
Deposition date deposition_date2014-10-26
Structure title titleG303 Circular Permutation of Old Yellow Enzyme with the Inhibitor p-Hydroxybenzaldehyde
Keywords keywordsCIRCULAR PERMUTATION, CATALYSIS, OLD YELLOW ENZYME, FLAVIN COFACTOR, OXIDOREDUCTASE-Inhibitor complex; OXIDOREDUCTASE/Inhibitor
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier40.99
Radius of gyration Rg (electron density) rg_electron40.78
Forward intensity I(0) i0447615000.00
Molecular weight molecular_weight173830.0 kDa
Excluded volume excluded_volume217480 ų
Envelope volume envelope_volume278890 ų
Hydration-shell volume shell_volume57040 ų
Envelope diameter envelope_diameter143.1
Shell Rg shell_rg45.96
Envelope Rg envelope_rg40.33
Shape Rg shape_rg40.76
Total Rg total_rg41.08
Total atoms total_atoms12304
Residues n_residues1532
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 dmax133.2
Rg (real space) rg_real40.92
Rg uncertainty (real space) rg_real_error0.91
I(0) (real space) i0_real4.4760e+08
I(0) uncertainty (real space) i0_real_error7.0020e+06
Rg (reciprocal space) rg_reciprocal40.99
I(0) (reciprocal space) i0_reciprocal447600000.0000
Solution quality estimate total_estimate0.8876
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary58.1
Skewness Skewness skewness0.194
Kurtosis Kurtosis kurtosis-0.506
Angular range angular_range— – 0.1950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha118600000.0000
Real-space data points n_real_points40
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.901; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.987; Smooth: 0.844

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)