2vik

REFINED STRUCTURE OF THE ACTIN-SEVERING DOMAIN VILLIN 14T, DETERMINED BY SOLUTION NMR, MINIMIZED AVERAGE STRUCTURE

Method: SOLUTION NMR Dmax: 57.1 Å Quality: REASONABLE

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

VILLIN 14T

Gallus gallus

UniProt P02640

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 2–127 Fragment:RESIDUES 1 - 126 No other associated polymer SOLUTION NMR NMR measurement conditions:pH 4.15;298 K Resolution not provided

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.

45 other PDB entries and 51 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name VILI_CHICK
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–126; UniProt 2–127

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 2vik

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2vik
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2vik
Deposition date deposition_date1997-01-16
Structure title titleREFINED STRUCTURE OF THE ACTIN-SEVERING DOMAIN VILLIN 14T, DETERMINED BY SOLUTION NMR, MINIMIZED AVERAGE STRUCTURE
Keywords keywordsACTIN-BINDING PROTEIN, CAPPING PROTEIN, CALCIUM-BINDING PROTEIN, CYTOSKELETAL PROTEIN; ACTIN-BINDING PROTEIN
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier15.30
Radius of gyration Rg (electron density) rg_electron13.95
Forward intensity I(0) i04090480.00
Molecular weight molecular_weight14159.0 kDa
Excluded volume excluded_volume17664 ų
Envelope volume envelope_volume19956 ų
Hydration-shell volume shell_volume12102 ų
Envelope diameter envelope_diameter55.8
Shell Rg shell_rg19.85
Envelope Rg envelope_rg14.70
Shape Rg shape_rg13.87
Total Rg total_rg15.41
Total atoms total_atoms1968
Residues n_residues126
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 dmax57.1
Rg (real space) rg_real15.25
Rg uncertainty (real space) rg_real_error0.41
I(0) (real space) i0_real4.0900e+06
I(0) uncertainty (real space) i0_real_error5.1540e+04
Rg (reciprocal space) rg_reciprocal15.26
I(0) (reciprocal space) i0_reciprocal4090000.0000
Solution quality estimate total_estimate0.7376
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary18.8
Skewness Skewness skewness0.325
Kurtosis Kurtosis kurtosis-0.028
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1185000.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.559; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.906; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2vika_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.109 — Gelsolin-like
Superfamily Superfamily superfamilyd.109.1 — Actin depolymerizing proteins
Family Family familyd.109.1.1 — Gelsolin-like

CATH v4.4 (1 domains)

Domain ID domain_id2vikA00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology20 — Severin
Homologous superfamily homologous superfamily10 — Severin

8. Citations (4)

9. Files and Curves (10)