3bj5

Alternative conformations of the x region of human protein disulphide-isomerase modulate exposure of the substrate binding b' domain

Method: X-RAY DIFFRACTION Dmax: 46.3 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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 230–368 Fragment:;b'x domain, UNPR residues 230-368 ; Mutation:I272A SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8.5;295.15 K;2.95M Ammonium sulfate, 0.2M NaCl, 0.1M Tris-HCl pH 8.5, VAPOR DIFFUSION, HANGING DROP, temperature 295.15K Resolution 2.20 Å R-free 0.255

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 9–147; UniProt 230–368

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 3bj5

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3bj5
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3bj5
Deposition date deposition_date2007-12-03
Structure title titleAlternative conformations of the x region of human protein disulphide-isomerase modulate exposure of the substrate binding b' domain
Keywords keywordsThioredoxin fold, Chaperone, Endoplasmic reticulum, Isomerase, Membrane, Redox-active center; ISOMERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier15.71
Radius of gyration Rg (electron density) rg_electron13.87
Forward intensity I(0) i04364860.00
Molecular weight molecular_weight15155.0 kDa
Excluded volume excluded_volume19153 ų
Envelope volume envelope_volume21990 ų
Hydration-shell volume shell_volume13130 ų
Envelope diameter envelope_diameter46.6
Shell Rg shell_rg20.02
Envelope Rg envelope_rg14.24
Shape Rg shape_rg13.85
Total Rg total_rg15.28
Total atoms total_atoms1068
Residues n_residues130
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 dmax46.3
Rg (real space) rg_real15.57
Rg uncertainty (real space) rg_real_error0.18
I(0) (real space) i0_real4.3650e+06
I(0) uncertainty (real space) i0_real_error4.5800e+04
Rg (reciprocal space) rg_reciprocal15.59
I(0) (reciprocal space) i0_reciprocal4365000.0000
Solution quality estimate total_estimate0.8276
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary21.1
Skewness Skewness skewness0.018
Kurtosis Kurtosis kurtosis-0.463
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha964300.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.929; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.970; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id3bj5A00
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)