8gtx

Crystal Structure of human Spindlin1-HBx complex

Method: X-RAY DIFFRACTION Dmax: 59.6 Å Quality: EXCELLENT

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 HBx × 1 GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8;291 K;16%(w/v) PEG 8000, 0.04M Potassium phosphate dibasic, 20% (v/v) Glycerol Resolution 1.80 Å R-free 0.197

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 34 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 6–218; UniProt 50–262

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 8gtx

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8gtx
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8gtx
Deposition date deposition_date2022-09-09
Structure title titleCrystal Structure of human Spindlin1-HBx complex
Keywords keywordsTudor domain, STRUCTURAL PROTEIN; STRUCTURAL PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.72
Radius of gyration Rg (electron density) rg_electron18.24
Forward intensity I(0) i011476400.00
Molecular weight molecular_weight25312.0 kDa
Excluded volume excluded_volume31755 ų
Envelope volume envelope_volume37968 ų
Hydration-shell volume shell_volume17550 ų
Envelope diameter envelope_diameter59.9
Shell Rg shell_rg24.37
Envelope Rg envelope_rg18.58
Shape Rg shape_rg18.20
Total Rg total_rg19.35
Total atoms total_atoms1777
Residues n_residues220
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 dmax59.6
Rg (real space) rg_real19.58
Rg uncertainty (real space) rg_real_error0.28
I(0) (real space) i0_real1.1480e+07
I(0) uncertainty (real space) i0_real_error1.2130e+05
Rg (reciprocal space) rg_reciprocal19.60
I(0) (reciprocal space) i0_reciprocal11480000.0000
Solution quality estimate total_estimate0.9112
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary58.0
Skewness Skewness skewness0.074
Kurtosis Kurtosis kurtosis-0.604
Angular range angular_range— – 0.4050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2799000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.949; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.995; Smooth: 0.998

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)