1x5c

The solution structure of the second thioredoxin-like domain of human Protein disulfide-isomerase

Method: SOLUTION NMR Dmax: 56.5 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 368–475 Fragment:Thioredoxin like domain No other associated polymer SOLUTION NMR NMR measurement conditions:pH 7;296 K;Ionic strength (raw mmCIF value) 120mM;Pressure ambient NMR sample composition:1.2mM thioredoxin like domain U-15N,13C; 20mM d-Tris HCl; 100mM NaCl; 1mM d-DTT; 0.02% NaN3; 10% D2O | 90% H2O/10% D2O Resolution not provided

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 8–115; UniProt 368–475

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 1x5c

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1x5c
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1x5c
Deposition date deposition_date2005-05-15
Structure title titleThe solution structure of the second thioredoxin-like domain of human Protein disulfide-isomerase
Keywords keywords;DSI, ERBA2L, GIT, PDI, PDIA1, PO4DB, PO4HB, PROHB, thioredoxin like domain, redox, structural genomics, NPPSFA, National Project on Protein Structural and Functional Analyses, RIKEN Structural Genomics/Proteomics Initiative, RSGI, ISOMERASE ;; ISOMERASE
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier14.22
Radius of gyration Rg (electron density) rg_electron13.51
Forward intensity I(0) i0956521000.00
Molecular weight molecular_weight264300.0 kDa
Excluded volume excluded_volume330770 ų
Envelope volume envelope_volume32098 ų
Hydration-shell volume shell_volume16111 ų
Envelope diameter envelope_diameter63.0
Shell Rg shell_rg23.00
Envelope Rg envelope_rg17.48
Shape Rg shape_rg13.47
Total Rg total_rg13.84
Total atoms total_atoms36720
Residues n_residues2420
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 dmax56.5
Rg (real space) rg_real14.11
Rg uncertainty (real space) rg_real_error0.48
I(0) (real space) i0_real9.5650e+08
I(0) uncertainty (real space) i0_real_error1.0700e+07
Rg (reciprocal space) rg_reciprocal14.12
I(0) (reciprocal space) i0_reciprocal956500000.0000
Solution quality estimate total_estimate0.7628
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary17.9
Skewness Skewness skewness0.109
Kurtosis Kurtosis kurtosis-0.164
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha488600.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.343; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.885; Smooth: 1.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd1x5ca1
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.47 — Thioredoxin fold
Superfamily Superfamily superfamilyc.47.1 — Thioredoxin-like
Family Family familyc.47.1.0 — automated matches
Domain ID domain_idd1x5ca2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags
Domain ID domain_idd1x5ca3
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (1 domains)

Domain ID domain_id1x5cA01
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)