6i13

CRYSTAL STRUCTURE OF FASCIN IN COMPLEX WITH COMPOUND 7

Method: X-RAY DIFFRACTION Dmax: 85.6 Å Quality: GOOD

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

Fascin

Homo sapiens

UniProt Q16658

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1–493 Not recorded ACT ACETATE ION × 1 EDO 1,2-ETHANEDIOL × 3 H0Q 2-[(3-chlorophenyl)methyl]-~{N}-(1-methylpyrazol-4-yl)-1-oxidanylidene-isoquinoline-4-carboxamide × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5;292 K;18-22% PEG 8000, 100-130 mM MgAc2, 100 mM citric acid pH 5.0 Resolution 1.79 Å R-free 0.227

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.

27 other PDB entries and 50 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name FSCN1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–493; UniProt 1–493

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 6i13

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6i13
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6i13
Deposition date deposition_date2018-10-27
Structure title titleCRYSTAL STRUCTURE OF FASCIN IN COMPLEX WITH COMPOUND 7
Keywords keywordsactin bundling, small molecule inhibition, 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_guinier25.55
Radius of gyration Rg (electron density) rg_electron24.34
Forward intensity I(0) i052140000.00
Molecular weight molecular_weight54321.0 kDa
Excluded volume excluded_volume67231 ų
Envelope volume envelope_volume81442 ų
Hydration-shell volume shell_volume27913 ų
Envelope diameter envelope_diameter90.7
Shell Rg shell_rg31.55
Envelope Rg envelope_rg24.47
Shape Rg shape_rg24.29
Total Rg total_rg25.26
Total atoms total_atoms3828
Residues n_residues484
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 dmax85.6
Rg (real space) rg_real25.50
Rg uncertainty (real space) rg_real_error0.56
I(0) (real space) i0_real5.2140e+07
I(0) uncertainty (real space) i0_real_error7.8000e+05
Rg (reciprocal space) rg_reciprocal25.52
I(0) (reciprocal space) i0_reciprocal52140000.0000
Solution quality estimate total_estimate0.8080
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.6
Skewness Skewness skewness0.289
Kurtosis Kurtosis kurtosis-0.361
Angular range angular_range— – 0.3100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha13860000.0000
Real-space data points n_real_points63
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.835; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.996; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 8 domains

SCOP 2.08 (4 domains)

Domain ID domain_idd6i13a1
Class classb — All beta proteins
Fold Fold foldb.42 — beta-Trefoil
Superfamily Superfamily superfamilyb.42.5 — Actin-crosslinking proteins
Family Family familyb.42.5.1 — Fascin
Domain ID domain_idd6i13a2
Class classb — All beta proteins
Fold Fold foldb.42 — beta-Trefoil
Superfamily Superfamily superfamilyb.42.5 — Actin-crosslinking proteins
Family Family familyb.42.5.1 — Fascin
Domain ID domain_idd6i13a3
Class classb — All beta proteins
Fold Fold foldb.42 — beta-Trefoil
Superfamily Superfamily superfamilyb.42.5 — Actin-crosslinking proteins
Family Family familyb.42.5.1 — Fascin
Domain ID domain_idd6i13a4
Class classb — All beta proteins
Fold Fold foldb.42 — beta-Trefoil
Superfamily Superfamily superfamilyb.42.5 — Actin-crosslinking proteins
Family Family familyb.42.5.1 — Fascin

CATH v4.4 (4 domains)

Domain ID domain_id6i13A01
Class class2 — Mainly Beta
Architecture architecture80 — Trefoil
Topology topology10 — Trefoil (Acidic Fibroblast Growth Factor, subunit A)
Homologous superfamily homologous superfamily50
Domain ID domain_id6i13A02
Class class2 — Mainly Beta
Architecture architecture80 — Trefoil
Topology topology10 — Trefoil (Acidic Fibroblast Growth Factor, subunit A)
Homologous superfamily homologous superfamily50
Domain ID domain_id6i13A03
Class class2 — Mainly Beta
Architecture architecture80 — Trefoil
Topology topology10 — Trefoil (Acidic Fibroblast Growth Factor, subunit A)
Homologous superfamily homologous superfamily50
Domain ID domain_id6i13A04
Class class2 — Mainly Beta
Architecture architecture80 — Trefoil
Topology topology10 — Trefoil (Acidic Fibroblast Growth Factor, subunit A)
Homologous superfamily homologous superfamily50

8. Citations (1)

9. Files and Curves (10)