3d57

TR Variant D355R

Method: X-RAY DIFFRACTION Dmax: 84.4 Å Quality: GOOD

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

Thyroid hormone receptor beta

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 209–460 Chain B; UniProt 209–460 Fragment:C-terminal domain Mutation:D355R 4HY [4-(4-HYDROXY-3-IODO-PHENOXY)-3,5-DIIODO-PHENYL]-ACETIC ACID × 2 SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7;298 K;25% ethylene glycol, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 2.20 Å R-free 0.240

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 42 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name THB_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 15–266; UniProt 209–460 Author chain B; PDBConstruct 15–266; UniProt 209–460

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 3d57

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3d57
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3d57
Deposition date deposition_date2008-05-15
Structure title titleTR Variant D355R
Keywords keywords;thyroid hormone receptor, ligand binding domain, D355R mutant, homodimer, Alternative splicing, Deafness, Disease mutation, DNA-binding, Metal-binding, Nucleus, Polymorphism, Receptor, Transcription, Transcription regulation, Zinc, Zinc-finger, HORMONE, TRANSCRIPTION RECEPTOR ;; HORMONE, TRANSCRIPTION RECEPTOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.16
Radius of gyration Rg (electron density) rg_electron25.64
Forward intensity I(0) i054150400.00
Molecular weight molecular_weight57149.0 kDa
Excluded volume excluded_volume71324 ų
Envelope volume envelope_volume86137 ų
Hydration-shell volume shell_volume28331 ų
Envelope diameter envelope_diameter87.3
Shell Rg shell_rg32.62
Envelope Rg envelope_rg25.66
Shape Rg shape_rg25.63
Total Rg total_rg26.43
Total atoms total_atoms3964
Residues n_residues493
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 dmax84.4
Rg (real space) rg_real26.16
Rg uncertainty (real space) rg_real_error0.54
I(0) (real space) i0_real5.4150e+07
I(0) uncertainty (real space) i0_real_error6.7670e+05
Rg (reciprocal space) rg_reciprocal26.16
I(0) (reciprocal space) i0_reciprocal54150000.0000
Solution quality estimate total_estimate0.8990
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary83.0
Skewness Skewness skewness0.324
Kurtosis Kurtosis kurtosis-0.436
Angular range angular_range— – 0.3050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha10950000.0000
Real-space data points n_real_points62
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.920; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.986; Smooth: 0.937

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd3d57a_
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_idd3d57b_
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

CATH v4.4 (2 domains)

Domain ID domain_id3d57A00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology565 — Retinoid X Receptor
Homologous superfamily homologous superfamily10 — Retinoid X Receptor
Domain ID domain_id3d57B00
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)