4yfs

Structure of the synthetic Duffy Binding Protein (DBP) antigen DEKnull relevant for malaria vaccine design

Method: X-RAY DIFFRACTION Dmax: 85.9 Å Quality: GOOD

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

Duffy receptor

Plasmodium vivax

UniProt P22290

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 198–521 Fragment:UNP RESIDUES 198-521 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;291 K;0.2 M di-sodium tartrate, 20% PEG 3350, and microseeded into 0.2 M lithium chloride, 20% PEG 3350 Resolution 2.10 Å R-free 0.259

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.

6 other PDB entries and 11 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PVDR_PLAVS
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–326; UniProt 198–521

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 4yfs

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4yfs
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4yfs
Deposition date deposition_date2015-02-25
Structure title titleStructure of the synthetic Duffy Binding Protein (DBP) antigen DEKnull relevant for malaria vaccine design
Keywords keywordsDuffy binding like domain, invasion, malaria, vaccine, Erythrocyte binding protein; Erythrocyte binding protein
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier22.30
Radius of gyration Rg (electron density) rg_electron21.84
Forward intensity I(0) i019828500.00
Molecular weight molecular_weight33749.0 kDa
Excluded volume excluded_volume42303 ų
Envelope volume envelope_volume50754 ų
Hydration-shell volume shell_volume20538 ų
Envelope diameter envelope_diameter87.7
Shell Rg shell_rg27.35
Envelope Rg envelope_rg22.50
Shape Rg shape_rg21.78
Total Rg total_rg22.77
Total atoms total_atoms4733
Residues n_residues285
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 dmax85.9
Rg (real space) rg_real22.45
Rg uncertainty (real space) rg_real_error0.90
I(0) (real space) i0_real1.9830e+07
I(0) uncertainty (real space) i0_real_error2.9400e+05
Rg (reciprocal space) rg_reciprocal22.41
I(0) (reciprocal space) i0_reciprocal19830000.0000
Solution quality estimate total_estimate0.7836
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.4
Skewness Skewness skewness0.620
Kurtosis Kurtosis kurtosis0.244
Angular range angular_range— – 0.3550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6367000.0000
Real-space data points n_real_points67
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.503; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.725; Smooth: 0.949

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd4yfsa_
Class classa — All alpha proteins
Fold Fold folda.264 — Duffy binding domain-like
Superfamily Superfamily superfamilya.264.1 — Duffy binding domain-like
Family Family familya.264.1.1 — Duffy binding domain

CATH v4.4 (2 domains)

Domain ID domain_id4yfsA01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology1310 — 5 helical Cullin repeat like
Homologous superfamily homologous superfamily20 — Duffy-antigen binding domain
Domain ID domain_id4yfsA02
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology58 — Methane Monooxygenase Hydroxylase; Chain G, domain 1
Homologous superfamily homologous superfamily830

8. Citations (1)

9. Files and Curves (10)