4rnw

Truncated version of the G303 Circular Permutation of Old Yellow Enzyme

Method: X-RAY DIFFRACTION Dmax: 99.0 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 307–397 Chain A; UniProt 2–292 Fragment:UNP residues 307-397, 2-292 FMN FLAVIN MONONUCLEOTIDE × 1 EPE 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID × 1 EDO 1,2-ETHANEDIOL × 9 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;289 K;20% PEG 10000, 0.1 M HEPES, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 289K Resolution 1.55 Å R-free 0.231
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 307–397 Chain B; UniProt 2–292 Fragment:UNP residues 307-397, 2-292 FMN FLAVIN MONONUCLEOTIDE × 1 EPE 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID × 1 EDO 1,2-ETHANEDIOL × 11 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;289 K;20% PEG 10000, 0.1 M HEPES, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 289K Resolution 1.55 Å R-free 0.231

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 32 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 2–92; UniProt 307–397 Author chain A; PDBConstruct 96–386; UniProt 2–292 Author chain B; PDBConstruct 2–92; UniProt 307–397 Author chain B; PDBConstruct 96–386; UniProt 2–292

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 4rnw

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4rnw
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id4rnw
Deposition date deposition_date2014-10-26
Structure title titleTruncated version of the G303 Circular Permutation of Old Yellow Enzyme
Keywords keywordsCIRCULAR PERMUTATION, CATALYSIS, OLD YELLOW ENZYME, FLAVIN COFACTOR, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier30.98
Radius of gyration Rg (electron density) rg_electron30.34
Forward intensity I(0) i0122809000.00
Molecular weight molecular_weight88175.0 kDa
Excluded volume excluded_volume110290 ų
Envelope volume envelope_volume130330 ų
Hydration-shell volume shell_volume35882 ų
Envelope diameter envelope_diameter101.6
Shell Rg shell_rg37.33
Envelope Rg envelope_rg30.42
Shape Rg shape_rg30.34
Total Rg total_rg30.95
Total atoms total_atoms6230
Residues n_residues764
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 dmax99.0
Rg (real space) rg_real31.03
Rg uncertainty (real space) rg_real_error0.56
I(0) (real space) i0_real1.2280e+08
I(0) uncertainty (real space) i0_real_error1.6110e+06
Rg (reciprocal space) rg_reciprocal31.01
I(0) (reciprocal space) i0_reciprocal122800000.0000
Solution quality estimate total_estimate0.8916
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary31.1
Skewness Skewness skewness0.342
Kurtosis Kurtosis kurtosis-0.602
Angular range angular_range— – 0.2550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha34200000.0000
Real-space data points n_real_points52
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: 0.941; Smooth: 0.926

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)