4x43

Structure of proline-free E. coli Thioredoxin

Method: X-RAY DIFFRACTION Dmax: 77.7 Å Quality: GOOD

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

Thioredoxin-1

Escherichia coli K-12

UniProt P0AA25

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 2–109 Mutation:P34A, P40A, P64A, P68A, P76A No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;277 K;10% (w/v) PEG 1000, 10% (w/v) PEG 8000 Resolution 1.65 Å R-free 0.218
2 Protein monomer Monomer Protein × 1 PDB declaration: Monomeric(1) Consistent with protein copy count Chain B; UniProt 2–109 Mutation:P34A, P40A, P64A, P68A, P76A No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;277 K;10% (w/v) PEG 1000, 10% (w/v) PEG 8000 Resolution 1.65 Å R-free 0.218
3 Protein monomer Monomer Protein × 1 PDB declaration: Monomeric(1) Consistent with protein copy count Chain C; UniProt 2–109 Mutation:P34A, P40A, P64A, P68A, P76A No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;277 K;10% (w/v) PEG 1000, 10% (w/v) PEG 8000 Resolution 1.65 Å R-free 0.218

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.

52 other PDB entries and 98 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name THIO_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–108; UniProt 2–109 Author chain B; PDBConstruct 1–108; UniProt 2–109 Author chain C; PDBConstruct 1–108; UniProt 2–109

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 4x43

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4x43
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4x43
Deposition date deposition_date2014-12-02
Structure title titleStructure of proline-free E. coli Thioredoxin
Keywords keywordsProtein folding, THIOREDOXIN FOLD, PROTEIN DISULFIDE OXIDOREDUCTASE ACTIVITY, REDOX PROTEIN, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.74
Radius of gyration Rg (electron density) rg_electron22.70
Forward intensity I(0) i019147900.00
Molecular weight molecular_weight34332.0 kDa
Excluded volume excluded_volume43524 ų
Envelope volume envelope_volume52860 ų
Hydration-shell volume shell_volume20330 ų
Envelope diameter envelope_diameter81.0
Shell Rg shell_rg28.65
Envelope Rg envelope_rg22.73
Shape Rg shape_rg22.68
Total Rg total_rg23.58
Total atoms total_atoms2416
Residues n_residues321
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 dmax77.7
Rg (real space) rg_real23.80
Rg uncertainty (real space) rg_real_error0.57
I(0) (real space) i0_real1.9150e+07
I(0) uncertainty (real space) i0_real_error2.6830e+05
Rg (reciprocal space) rg_reciprocal23.79
I(0) (reciprocal space) i0_reciprocal19150000.0000
Solution quality estimate total_estimate0.8069
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.3
Skewness Skewness skewness0.386
Kurtosis Kurtosis kurtosis-0.431
Angular range angular_range— – 0.3350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha5094000.0000
Real-space data points n_real_points65
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.850; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.941; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd4x43a_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.47 — Thioredoxin fold
Superfamily Superfamily superfamilyc.47.1 — Thioredoxin-like
Family Family familyc.47.1.1 — Thioltransferase
Domain ID domain_idd4x43b_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.47 — Thioredoxin fold
Superfamily Superfamily superfamilyc.47.1 — Thioredoxin-like
Family Family familyc.47.1.1 — Thioltransferase
Domain ID domain_idd4x43c_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.47 — Thioredoxin fold
Superfamily Superfamily superfamilyc.47.1 — Thioredoxin-like
Family Family familyc.47.1.1 — Thioltransferase

CATH v4.4 (3 domains)

Domain ID domain_id4x43A00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology30 — Glutaredoxin
Homologous superfamily homologous superfamily10 — Glutaredoxin
Domain ID domain_id4x43B00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology30 — Glutaredoxin
Homologous superfamily homologous superfamily10 — Glutaredoxin
Domain ID domain_id4x43C00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology30 — Glutaredoxin
Homologous superfamily homologous superfamily10 — Glutaredoxin

8. Citations (1)

9. Files and Curves (10)