1kdk

THE STRUCTURE OF THE N-TERMINAL LG DOMAIN OF SHBG IN CRYSTALS SOAKED WITH EDTA

Method: X-RAY DIFFRACTION Dmax: 49.6 Å Quality: REASONABLE

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

Sex Hormone-Binding Globulin

Homo sapiens

UniProt P04278

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 1–170 Fragment:N-terminal LG-domain DHT 5-ALPHA-DIHYDROTESTOSTERONE × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;293 K;PEG400, Isopropanol, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K Resolution 1.70 Å R-free 0.245

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.

12 other PDB entries and 12 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SHBG_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–177; UniProt 1–170

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 1kdk

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1kdk
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id1kdk
Deposition date deposition_date2001-11-13
Structure title titleTHE STRUCTURE OF THE N-TERMINAL LG DOMAIN OF SHBG IN CRYSTALS SOAKED WITH EDTA
Keywords keywordsSHBG, DHT, TRANSPORT PROTEIN; TRANSPORT PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier16.66
Radius of gyration Rg (electron density) rg_electron15.11
Forward intensity I(0) i07310660.00
Molecular weight molecular_weight19856.0 kDa
Excluded volume excluded_volume24908 ų
Envelope volume envelope_volume27451 ų
Hydration-shell volume shell_volume15070 ų
Envelope diameter envelope_diameter48.6
Shell Rg shell_rg21.29
Envelope Rg envelope_rg15.29
Shape Rg shape_rg15.10
Total Rg total_rg16.21
Total atoms total_atoms1399
Residues n_residues177
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 dmax49.6
Rg (real space) rg_real16.52
Rg uncertainty (real space) rg_real_error0.24
I(0) (real space) i0_real7.3110e+06
I(0) uncertainty (real space) i0_real_error9.1340e+04
Rg (reciprocal space) rg_reciprocal16.54
I(0) (reciprocal space) i0_reciprocal7311000.0000
Solution quality estimate total_estimate0.7495
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary22.5
Skewness Skewness skewness0.004
Kurtosis Kurtosis kurtosis-0.489
Angular range angular_range— – 0.4800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1345000.0000
Real-space data points n_real_points78
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.929; Stabil: 1.000; Sysdev: 0.338; Positv: 1.000; Valcen: 0.971; Smooth: 0.967

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1kdka_
Class classb — All beta proteins
Fold Fold foldb.29 — Concanavalin A-like lectins/glucanases
Superfamily Superfamily superfamilyb.29.1 — Concanavalin A-like lectins/glucanases
Family Family familyb.29.1.4 — Laminin G-like module

CATH v4.4 (1 domains)

Domain ID domain_id1kdkA00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily200

8. Citations (1)

9. Files and Curves (10)