8bwi

Crystal structure of human Twisted gastrulation protein homolog 1 (TWSG1), crystal form 2

Method: X-RAY DIFFRACTION Dmax: 80.2 Å Quality: REASONABLE

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

Twisted gastrulation protein homolog 1

Homo sapiens

UniProt Q9GZX9

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 26–223 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;294 K;1.0 M K/Na tartrate, 0.1 M MES pH 6.0 Resolution 3.40 Å R-free 0.342

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.

5 other PDB entries and 7 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TWSG1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–201; UniProt 26–223

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 8bwi

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8bwi
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id8bwi
Deposition date deposition_date2022-12-06
Structure title titleCrystal structure of human Twisted gastrulation protein homolog 1 (TWSG1), crystal form 2
Keywords keywords;Twisted gastrulation protein homolog 1 (TWSG1), Transforming Growth Factor beta (TGF-beta) signalling pathway, extracellular protein, disulfide rich domains., SIGNALING PROTEIN ;; SIGNALING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.02
Radius of gyration Rg (electron density) rg_electron22.71
Forward intensity I(0) i07258660.00
Molecular weight molecular_weight18438.0 kDa
Excluded volume excluded_volume22363 ų
Envelope volume envelope_volume31169 ų
Hydration-shell volume shell_volume12896 ų
Envelope diameter envelope_diameter77.8
Shell Rg shell_rg26.66
Envelope Rg envelope_rg22.17
Shape Rg shape_rg22.65
Total Rg total_rg23.43
Total atoms total_atoms2442
Residues n_residues166
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 dmax80.2
Rg (real space) rg_real23.24
Rg uncertainty (real space) rg_real_error0.63
I(0) (real space) i0_real7.2590e+06
I(0) uncertainty (real space) i0_real_error1.0410e+05
Rg (reciprocal space) rg_reciprocal23.19
I(0) (reciprocal space) i0_reciprocal7258000.0000
Solution quality estimate total_estimate0.5063
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary16.0
Skewness Skewness skewness0.338
Kurtosis Kurtosis kurtosis-0.935
Angular range angular_range— – 0.3450 −1
Current regularization parameter α current_alpha0.0001
Highest regularization parameter α highest_alpha932500.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.285; Stabil: 1.000; Sysdev: 0.171; Positv: 1.000; Valcen: 0.210; Smooth: 1.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

8. Citations (1)

9. Files and Curves (10)