4wfv

Bovine allergen Bos d 2 in the monoclinic space group C2.

Method: X-RAY DIFFRACTION Dmax: 53.5 Å Quality: GOOD

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

Allergen Bos d 2

Bos taurus

UniProt Q28133

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 17–172 Fragment:UNP Residues 17-172 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.4;293 K;2.5 M 1,6-hexanediol, 0.1 M sodium citrate Resolution 1.40 Å R-free 0.213

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 2 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ALL2_BOVIN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–156; UniProt 17–172

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 4wfv

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4wfv
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id4wfv
Deposition date deposition_date2014-09-17
Structure title titleBovine allergen Bos d 2 in the monoclinic space group C2.
Keywords keywordsAllergen, lipocalin; ALLERGEN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier15.84
Radius of gyration Rg (electron density) rg_electron14.40
Forward intensity I(0) i05935000.00
Molecular weight molecular_weight17483.0 kDa
Excluded volume excluded_volume21807 ų
Envelope volume envelope_volume24084 ų
Hydration-shell volume shell_volume13920 ų
Envelope diameter envelope_diameter48.0
Shell Rg shell_rg20.61
Envelope Rg envelope_rg14.68
Shape Rg shape_rg14.38
Total Rg total_rg15.62
Total atoms total_atoms1229
Residues n_residues153
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 dmax53.5
Rg (real space) rg_real15.70
Rg uncertainty (real space) rg_real_error0.34
I(0) (real space) i0_real5.9350e+06
I(0) uncertainty (real space) i0_real_error7.0770e+04
Rg (reciprocal space) rg_reciprocal15.72
I(0) (reciprocal space) i0_reciprocal5935000.0000
Solution quality estimate total_estimate0.7806
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary22.3
Skewness Skewness skewness0.020
Kurtosis Kurtosis kurtosis-0.441
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1609000.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.714; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd4wfva_
Class classb — All beta proteins
Fold Fold foldb.60 — Lipocalins
Superfamily Superfamily superfamilyb.60.1 — Lipocalins
Family Family familyb.60.1.1 — Retinol binding protein-like

CATH v4.4 (1 domains)

Domain ID domain_id4wfvA00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology128 — Lipocalin
Homologous superfamily homologous superfamily20 — Calycin beta-barrel core domain

8. Citations (1)

9. Files and Curves (10)