7yxn

Crystal structure of WT AncGR2-LBD bound to dexamethasone and SHP coregulator fragment

Method: X-RAY DIFFRACTION Dmax: 87.5 Å Quality: EXCELLENT

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

Ancestral Glucocorticoid Receptor2

unidentified

UniProt A0A1X8XLE9

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 2–248 Not recorded SHP NR Box 1 Peptide × 1 (Q15466) DEX DEXAMETHASONE × 1 FMT FORMIC ACID × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293.15 K;0.1 M PIPES, pH 7.0, 0.1 M ammonium acetate, 2.5 M sodium formate Resolution 2.46 Å R-free 0.247
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 2–248 Not recorded SHP NR Box 1 Peptide × 1 (Q15466) DEX DEXAMETHASONE × 1 FMT FORMIC ACID × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293.15 K;0.1 M PIPES, pH 7.0, 0.1 M ammonium acetate, 2.5 M sodium formate Resolution 2.46 Å R-free 0.247

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.

8 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A0A1X8XLE9_9ZZZZ
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–250; UniProt 2–248 Author chain C; PDBConstruct 4–250; UniProt 2–248

SHP NR Box 1 Peptide

OrganismNot specified

UniProt Q15466

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain R; UniProt 17–27 Not recorded Ancestral Glucocorticoid Receptor2 × 1 (A0A1X8XLE9) DEX DEXAMETHASONE × 1 FMT FORMIC ACID × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293.15 K;0.1 M PIPES, pH 7.0, 0.1 M ammonium acetate, 2.5 M sodium formate Resolution 2.46 Å R-free 0.247
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain S; UniProt 17–27 Not recorded Ancestral Glucocorticoid Receptor2 × 1 (A0A1X8XLE9) DEX DEXAMETHASONE × 1 FMT FORMIC ACID × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293.15 K;0.1 M PIPES, pH 7.0, 0.1 M ammonium acetate, 2.5 M sodium formate Resolution 2.46 Å R-free 0.247

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.

11 other PDB entries and 38 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NR0B2_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain R; PDBConstruct 1–11; UniProt 17–27 Author chain S; PDBConstruct 1–11; UniProt 17–27

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 7yxn

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7yxn
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7yxn
Deposition date deposition_date2022-02-16
Structure title titleCrystal structure of WT AncGR2-LBD bound to dexamethasone and SHP coregulator fragment
Keywords keywordsNuclear Receptor, Transcription Factor, Dexamethasone, NUCLEAR PROTEIN; NUCLEAR PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier28.26
Radius of gyration Rg (electron density) rg_electron27.13
Forward intensity I(0) i052222700.00
Molecular weight molecular_weight59594.0 kDa
Excluded volume excluded_volume75993 ų
Envelope volume envelope_volume93843 ų
Hydration-shell volume shell_volume28763 ų
Envelope diameter envelope_diameter94.4
Shell Rg shell_rg34.57
Envelope Rg envelope_rg26.87
Shape Rg shape_rg27.14
Total Rg total_rg27.93
Total atoms total_atoms4183
Residues n_residues509
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 dmax87.5
Rg (real space) rg_real28.23
Rg uncertainty (real space) rg_real_error0.47
I(0) (real space) i0_real5.2220e+07
I(0) uncertainty (real space) i0_real_error7.3300e+05
Rg (reciprocal space) rg_reciprocal28.24
I(0) (reciprocal space) i0_reciprocal52220000.0000
Solution quality estimate total_estimate0.9105
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary28.1
Skewness Skewness skewness0.220
Kurtosis Kurtosis kurtosis-0.720
Angular range angular_range— – 0.2800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha14010000.0000
Real-space data points n_real_points57
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.956; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.980; Smooth: 0.984

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id7yxnA01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology565 — Retinoid X Receptor
Homologous superfamily homologous superfamily10 — Retinoid X Receptor
Domain ID domain_id7yxnC01
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)