1xzx

Thyroxine-Thyroid Hormone Receptor Interactions

Method: X-RAY DIFFRACTION Dmax: 64.7 Å Quality: GOOD

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

Thyroid hormone receptor beta-1

Homo sapiens

UniProt P10828

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 X; UniProt 202–461 Fragment:ligand binding domain (residues 202-461) CAC CACODYLATE ION × 6 T3 3,5,3'TRIIODOTHYRONINE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.2;279 K;sodium acetate, cacodylate, pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 279K Resolution 2.50 Å R-free 0.244
2 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain X; UniProt 202–461 Fragment:ligand binding domain (residues 202-461) CAC CACODYLATE ION × 12 T3 3,5,3'TRIIODOTHYRONINE × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.2;279 K;sodium acetate, cacodylate, pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 279K Resolution 2.50 Å R-free 0.244

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.

33 other PDB entries and 41 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name THB1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain X; PDBConstruct 22–281; UniProt 202–461

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 1xzx

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1xzx
Deposition date deposition_date2004-11-12
Structure title titleThyroxine-Thyroid Hormone Receptor Interactions
Keywords keywordsHORMONE/GROWTH FACTOR RECEPTOR, HORMONE-GROWTH FACTOR RECEPTOR complex; HORMONE/GROWTH FACTOR RECEPTOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.29
Radius of gyration Rg (electron density) rg_electron18.33
Forward intensity I(0) i014985200.00
Molecular weight molecular_weight28382.0 kDa
Excluded volume excluded_volume34979 ų
Envelope volume envelope_volume39748 ų
Hydration-shell volume shell_volume18289 ų
Envelope diameter envelope_diameter66.6
Shell Rg shell_rg24.53
Envelope Rg envelope_rg18.80
Shape Rg shape_rg18.36
Total Rg total_rg19.14
Total atoms total_atoms1945
Residues n_residues249
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 dmax64.7
Rg (real space) rg_real19.24
Rg uncertainty (real space) rg_real_error0.43
I(0) (real space) i0_real1.4990e+07
I(0) uncertainty (real space) i0_real_error1.8280e+05
Rg (reciprocal space) rg_reciprocal19.25
I(0) (reciprocal space) i0_reciprocal14990000.0000
Solution quality estimate total_estimate0.7985
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary24.6
Skewness Skewness skewness0.310
Kurtosis Kurtosis kurtosis-0.218
Angular range angular_range— – 0.4100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3455000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.798; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.985; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd1xzxx1
Class classa — All alpha proteins
Fold Fold folda.123 — Nuclear receptor ligand-binding domain
Superfamily Superfamily superfamilya.123.1 — Nuclear receptor ligand-binding domain
Family Family familya.123.1.1 — Nuclear receptor ligand-binding domain
Domain ID domain_idd1xzxx2
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_id1xzxX00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology565 — Retinoid X Receptor
Homologous superfamily homologous superfamily10 — Retinoid X Receptor

8. Citations (1)

9. Files and Curves (10)