8af3

Sterol carrier protein Artifical metalloenzyme incorporating Q111C mutation coupled to 2,2'-bipyridine

Method: X-RAY DIFFRACTION Dmax: 46.0 Å Quality: GOOD

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

Enoyl-CoA hydratase 2

Homo sapiens

UniProt P51659

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 618–736 Non-standard monomer:Yes (specific site not provided by mmCIF) TRT FRAGMENT OF TRITON X-100 × 1 SO4 SULFATE ION × 2 CU COPPER (II) ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.6;278 K;well solution 2.3M ammonium sulphate, 100 mM citric acid pH 5.6 and 200 mM NaCl Resolution 1.52 Å R-free 0.239

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.

6 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DHB4_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–120; UniProt 618–736

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 8af3

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8af3
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8af3
Deposition date deposition_date2022-07-15
Structure title titleSterol carrier protein Artifical metalloenzyme incorporating Q111C mutation coupled to 2,2'-bipyridine
Keywords keywordsde novo protein, artificial metalloenzyme, bipyridine adduct, METAL BINDING PROTEIN; METAL BINDING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier14.98
Radius of gyration Rg (electron density) rg_electron13.34
Forward intensity I(0) i03475040.00
Molecular weight molecular_weight13526.0 kDa
Excluded volume excluded_volume17187 ų
Envelope volume envelope_volume19123 ų
Hydration-shell volume shell_volume12067 ų
Envelope diameter envelope_diameter44.0
Shell Rg shell_rg19.21
Envelope Rg envelope_rg13.53
Shape Rg shape_rg13.29
Total Rg total_rg14.83
Total atoms total_atoms1766
Residues n_residues115
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 dmax46.0
Rg (real space) rg_real14.83
Rg uncertainty (real space) rg_real_error0.28
I(0) (real space) i0_real3.4750e+06
I(0) uncertainty (real space) i0_real_error4.0740e+04
Rg (reciprocal space) rg_reciprocal14.84
I(0) (reciprocal space) i0_reciprocal3475000.0000
Solution quality estimate total_estimate0.8862
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary21.0
Skewness Skewness skewness-0.042
Kurtosis Kurtosis kurtosis-0.409
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha691000.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.850; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.975; Smooth: 0.993

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)