4ync

OYE1 W116A COMPLEXED WITH (Z)-METHYL-3-CYANO-3-PHENYLACRYLATE IN A NON PRODUCTIVE BINDING MODE

Method: X-RAY DIFFRACTION Dmax: 66.3 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 2–398 Mutation:W116A FMN FLAVIN MONONUCLEOTIDE × 1 4EG methyl (2Z)-3-cyano-3-phenylprop-2-enoate × 1 CL CHLORIDE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8.3;277 K;0.2M MgCl2, 0.1M NaHEPES, 35% PEG 400 Resolution 1.50 Å R-free 0.172

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 33 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 1–397; UniProt 2–398

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 4ync

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id4ync
Deposition date deposition_date2015-03-09
Structure title titleOYE1 W116A COMPLEXED WITH (Z)-METHYL-3-CYANO-3-PHENYLACRYLATE IN A NON PRODUCTIVE BINDING MODE
Keywords keywordsOXIDOREDUCTASE, CATALYTIC ACTIVITY, FMN BINDING, OLD YELLOW ENZYME; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.22
Radius of gyration Rg (electron density) rg_electron20.02
Forward intensity I(0) i034158200.00
Molecular weight molecular_weight45183.0 kDa
Excluded volume excluded_volume56449 ų
Envelope volume envelope_volume62173 ų
Hydration-shell volume shell_volume24960 ų
Envelope diameter envelope_diameter66.9
Shell Rg shell_rg27.68
Envelope Rg envelope_rg20.30
Shape Rg shape_rg20.00
Total Rg total_rg21.01
Total atoms total_atoms3206
Residues n_residues397
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 dmax66.3
Rg (real space) rg_real21.07
Rg uncertainty (real space) rg_real_error0.32
I(0) (real space) i0_real3.4160e+07
I(0) uncertainty (real space) i0_real_error4.0600e+05
Rg (reciprocal space) rg_reciprocal21.10
I(0) (reciprocal space) i0_reciprocal34160000.0000
Solution quality estimate total_estimate0.8960
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary26.3
Skewness Skewness skewness0.140
Kurtosis Kurtosis kurtosis-0.413
Angular range angular_range— – 0.3750 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7537000.0000
Real-space data points n_real_points69
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.887; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.987; Smooth: 0.995

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 1 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd4ynca_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.1 — TIM beta/alpha-barrel
Superfamily Superfamily superfamilyc.1.4 — FMN-linked oxidoreductases
Family Family familyc.1.4.1 — FMN-linked oxidoreductases

8. Citations (1)

9. Files and Curves (10)