4ju5

Crystal structure of the dimeric form of the bb' domains of human protein disulfide isomerase

Method: X-RAY DIFFRACTION Dmax: 101.8 Å Quality: GOOD

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

Protein disulfide-isomerase

Homo sapiens

UniProt P07237

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 135–367 Chain B; UniProt 135–367 Fragment:;bb' domain ; No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4;295 K;25% (w/v) polyethylene glycol 1500, 25 mM sodium malonate, 37.5 mM imidazole, 37.5 mM boric acid, pH 4.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K Resolution 2.28 Å R-free 0.290

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.

13 other PDB entries and 17 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PDIA1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 6–238; UniProt 135–367 Author chain B; PDBConstruct 6–238; UniProt 135–367

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 4ju5

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4ju5
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4ju5
Deposition date deposition_date2013-03-24
Structure title titleCrystal structure of the dimeric form of the bb' domains of human protein disulfide isomerase
Keywords keywordsthioredoxin-like fold, disulfide isomerase, chaperone, Isomerase; ISOMERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier28.19
Radius of gyration Rg (electron density) rg_electron27.73
Forward intensity I(0) i028721200.00
Molecular weight molecular_weight42849.0 kDa
Excluded volume excluded_volume54137 ų
Envelope volume envelope_volume68116 ų
Hydration-shell volume shell_volume23278 ų
Envelope diameter envelope_diameter103.4
Shell Rg shell_rg31.34
Envelope Rg envelope_rg27.68
Shape Rg shape_rg27.72
Total Rg total_rg28.16
Total atoms total_atoms3034
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 dmax101.8
Rg (real space) rg_real28.59
Rg uncertainty (real space) rg_real_error1.33
I(0) (real space) i0_real2.8720e+07
I(0) uncertainty (real space) i0_real_error5.2670e+05
Rg (reciprocal space) rg_reciprocal28.47
I(0) (reciprocal space) i0_reciprocal28720000.0000
Solution quality estimate total_estimate0.7964
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary98.2
Skewness Skewness skewness0.658
Kurtosis Kurtosis kurtosis0.092
Angular range angular_range— – 0.2800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha9735000.0000
Real-space data points n_real_points57
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.627; Stabil: 0.997; Sysdev: 1.000; Positv: 1.000; Valcen: 0.593; Smooth: 0.883

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 4 domains

CATH v4.4 (4 domains)

Domain ID domain_id4ju5A01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology30 — Glutaredoxin
Homologous superfamily homologous superfamily10 — Glutaredoxin
Domain ID domain_id4ju5A02
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology30 — Glutaredoxin
Homologous superfamily homologous superfamily10 — Glutaredoxin
Domain ID domain_id4ju5B01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology30 — Glutaredoxin
Homologous superfamily homologous superfamily10 — Glutaredoxin
Domain ID domain_id4ju5B02
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)