7ea1

Crystal Structure of Spindlin1 bound to SPINDOC Docpep2

Method: X-RAY DIFFRACTION Dmax: 82.9 Å Quality: GOOD

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

Spindlin-1

Homo sapiens

UniProt Q9Y657

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 50–262 Not recorded Peptide from Spindlin interactor and repressor of chromatin-binding protein × 1 (Q9BUA3) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 6.5;291 K;0.1M Sodium chloride, 0.1M BIS-TRIS pH 6.5, 1.5M Ammonium sulfate Resolution 2.70 Å R-free 0.286
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 50–262 Not recorded Peptide from Spindlin interactor and repressor of chromatin-binding protein × 1 (Q9BUA3) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 6.5;291 K;0.1M Sodium chloride, 0.1M BIS-TRIS pH 6.5, 1.5M Ammonium sulfate Resolution 2.70 Å R-free 0.286

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.

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

View Construct and Data Evidence
UniProt name SPIN1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–215; UniProt 50–262 Author chain C; PDBConstruct 3–215; UniProt 50–262

Peptide from Spindlin interactor and repressor of chromatin-binding protein

OrganismNot specified

UniProt Q9BUA3

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 B; UniProt 228–239 Not recorded Spindlin-1 × 1 (Q9Y657) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 6.5;291 K;0.1M Sodium chloride, 0.1M BIS-TRIS pH 6.5, 1.5M Ammonium sulfate Resolution 2.70 Å R-free 0.286
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 228–239 Not recorded Spindlin-1 × 1 (Q9Y657) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 6.5;291 K;0.1M Sodium chloride, 0.1M BIS-TRIS pH 6.5, 1.5M Ammonium sulfate Resolution 2.70 Å R-free 0.286

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.

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

View Construct and Data Evidence
UniProt name SPNDC_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–12; UniProt 228–239 Author chain D; PDBConstruct 1–12; UniProt 228–239

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 7ea1

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7ea1
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7ea1
Deposition date deposition_date2021-03-05
Structure title titleCrystal Structure of Spindlin1 bound to SPINDOC Docpep2
Keywords keywordsSpin/Ssty repeat, TRANSCRIPTION; TRANSCRIPTION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.72
Radius of gyration Rg (electron density) rg_electron24.58
Forward intensity I(0) i034100300.00
Molecular weight molecular_weight44970.0 kDa
Excluded volume excluded_volume56396 ų
Envelope volume envelope_volume75150 ų
Hydration-shell volume shell_volume25737 ų
Envelope diameter envelope_diameter86.5
Shell Rg shell_rg31.32
Envelope Rg envelope_rg24.65
Shape Rg shape_rg24.55
Total Rg total_rg25.52
Total atoms total_atoms3168
Residues n_residues391
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 dmax82.9
Rg (real space) rg_real25.69
Rg uncertainty (real space) rg_real_error0.57
I(0) (real space) i0_real3.4100e+07
I(0) uncertainty (real space) i0_real_error4.9470e+05
Rg (reciprocal space) rg_reciprocal25.70
I(0) (reciprocal space) i0_reciprocal34100000.0000
Solution quality estimate total_estimate0.8803
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary30.7
Skewness Skewness skewness0.290
Kurtosis Kurtosis kurtosis-0.421
Angular range angular_range— – 0.3100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7323000.0000
Real-space data points n_real_points63
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.910; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.715

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)