5sy7

Crystal Structure of the Heterodimeric NPAS3-ARNT Complex with HRE DNA

Method: X-RAY DIFFRACTION Dmax: 118.4 Å Quality: GOOD

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

Aryl hydrocarbon receptor nuclear translocator

Mus musculus

UniProt P53762

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 82–464 Not recorded Neuronal PAS domain-containing protein 3 × 1 (Q9QZQ0) ;DNA (5'-D(*GP*GP*CP*TP*GP*CP*GP*TP*AP*CP*GP*TP*GP*CP*GP*GP*GP*TP*CP*GP*T)-3') ; × 1 ;DNA (5'-D(*CP*AP*CP*GP*AP*CP*CP*CP*GP*CP*AP*CP*GP*TP*AP*CP*GP*CP*AP*GP*C)-3') ; × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6;289 K;100 mM NH4F, 9% PEG 3350 Resolution 4.20 Å R-free 0.361

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.

20 other PDB entries and 28 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ARNT_MOUSE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–384; UniProt 82–464

Neuronal PAS domain-containing protein 3

Mus musculus

UniProt Q9QZQ0

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 56–455 Not recorded Aryl hydrocarbon receptor nuclear translocator × 1 (P53762) ;DNA (5'-D(*GP*GP*CP*TP*GP*CP*GP*TP*AP*CP*GP*TP*GP*CP*GP*GP*GP*TP*CP*GP*T)-3') ; × 1 ;DNA (5'-D(*CP*AP*CP*GP*AP*CP*CP*CP*GP*CP*AP*CP*GP*TP*AP*CP*GP*CP*AP*GP*C)-3') ; × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6;289 K;100 mM NH4F, 9% PEG 3350 Resolution 4.20 Å R-free 0.361

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.

No other PDB entry for the same UniProt protein was found.

View Construct and Data Evidence
UniProt name NPAS3_MOUSE
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 3–402; UniProt 56–455

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 5sy7

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5sy7
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5sy7
Deposition date deposition_date2016-08-10
Structure title titleCrystal Structure of the Heterodimeric NPAS3-ARNT Complex with HRE DNA
Keywords keywordsbHLH-PAS protein, transcription factor, heterodimeric complex, 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_guinier34.84
Radius of gyration Rg (electron density) rg_electron33.42
Forward intensity I(0) i0113548000.00
Molecular weight molecular_weight76295.0 kDa
Excluded volume excluded_volume91896 ų
Envelope volume envelope_volume126780 ų
Hydration-shell volume shell_volume34019 ų
Envelope diameter envelope_diameter118.2
Shell Rg shell_rg37.42
Envelope Rg envelope_rg33.38
Shape Rg shape_rg33.34
Total Rg total_rg33.95
Total atoms total_atoms5313
Residues n_residues594
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 dmax118.4
Rg (real space) rg_real35.05
Rg uncertainty (real space) rg_real_error1.35
I(0) (real space) i0_real1.1350e+08
I(0) uncertainty (real space) i0_real_error2.1020e+06
Rg (reciprocal space) rg_reciprocal34.93
I(0) (reciprocal space) i0_reciprocal113500000.0000
Solution quality estimate total_estimate0.8570
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary34.2
Skewness Skewness skewness0.411
Kurtosis Kurtosis kurtosis-0.563
Angular range angular_range— – 0.2250 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8029000.0000
Real-space data points n_real_points46
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.832; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.796; Smooth: 0.843

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)