5v0l

Crystal structure of the AHR-ARNT heterodimer in complex with the DRE

Method: X-RAY DIFFRACTION Dmax: 93.4 Å Quality: GOOD

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

Aryl hydrocarbon receptor nuclear translocator

Homo sapiens

UniProt P27540

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–DNA Heteromer Protein × 2 DNA 2 PDB declaration: tetrameric(4) Consistent with all polymer counts Chain A; UniProt 70–346 Not recorded Aryl hydrocarbon receptor × 1 (P30561) ;DNA (5'-D(P*GP*GP*AP*TP*TP*GP*CP*GP*TP*GP*AP*GP*AP*AP*CP*TP*G)-3') ; × 1 ;DNA (5'-D(P*AP*GP*TP*TP*CP*TP*CP*AP*CP*GP*CP*AP*AP*T)-3') ; × 1 PEG DI(HYDROXYETHYL)ETHER × 2 CIT CITRIC ACID × 2 X-RAY DIFFRACTION X-ray crystallization conditions:EVAPORATION;277 K;10%-12% PEG 20000, 4-6% Tacsimate pH 7.0 or 0.1 M Bis-Tris pH 6.5 Resolution 4.00 Å R-free 0.323

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.

42 other PDB entries and 48 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ARNT_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–279; UniProt 70–346

Aryl hydrocarbon receptor

Mus musculus

UniProt P30561

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–DNA Heteromer Protein × 2 DNA 2 PDB declaration: tetrameric(4) Consistent with all polymer counts Chain B; UniProt 29–267 Not recorded Aryl hydrocarbon receptor nuclear translocator × 1 (P27540) ;DNA (5'-D(P*GP*GP*AP*TP*TP*GP*CP*GP*TP*GP*AP*GP*AP*AP*CP*TP*G)-3') ; × 1 ;DNA (5'-D(P*AP*GP*TP*TP*CP*TP*CP*AP*CP*GP*CP*AP*AP*T)-3') ; × 1 PEG DI(HYDROXYETHYL)ETHER × 2 CIT CITRIC ACID × 2 X-RAY DIFFRACTION X-ray crystallization conditions:EVAPORATION;277 K;10%-12% PEG 20000, 4-6% Tacsimate pH 7.0 or 0.1 M Bis-Tris pH 6.5 Resolution 4.00 Å R-free 0.323

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.

3 other PDB entries and 3 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name AHR_MOUSE
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 3–241; UniProt 29–267

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 5v0l

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5v0l
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5v0l
Deposition date deposition_date2017-02-28
Structure title titleCrystal structure of the AHR-ARNT heterodimer in complex with the DRE
Keywords keywordsAHR, ARNT, transcription factor, heterodimer, TRANSCRIPTION-DNA complex; TRANSCRIPTION/DNA
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier27.87
Radius of gyration Rg (electron density) rg_electron26.54
Forward intensity I(0) i052473000.00
Molecular weight molecular_weight49191.0 kDa
Excluded volume excluded_volume58656 ų
Envelope volume envelope_volume83733 ų
Hydration-shell volume shell_volume27641 ų
Envelope diameter envelope_diameter96.5
Shell Rg shell_rg32.37
Envelope Rg envelope_rg26.55
Shape Rg shape_rg26.48
Total Rg total_rg27.30
Total atoms total_atoms3418
Residues n_residues373
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 dmax93.4
Rg (real space) rg_real27.98
Rg uncertainty (real space) rg_real_error0.58
I(0) (real space) i0_real5.2470e+07
I(0) uncertainty (real space) i0_real_error6.7920e+05
Rg (reciprocal space) rg_reciprocal27.95
I(0) (reciprocal space) i0_reciprocal52470000.0000
Solution quality estimate total_estimate0.8802
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary29.5
Skewness Skewness skewness0.444
Kurtosis Kurtosis kurtosis-0.287
Angular range angular_range— – 0.2850 −1
Current regularization parameter α current_alpha0.0001
Highest regularization parameter α highest_alpha8638000.0000
Real-space data points n_real_points58
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.850; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.945; Smooth: 0.944

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

8. Citations (1)

9. Files and Curves (10)