1qmr

BIRCH POLLEN ALLERGEN BET V 1 MUTANT N28T, K32Q, E45S, P108G

Method: X-RAY DIFFRACTION Dmax: 57.6 Å Quality: GOOD

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

MAJOR POLLEN ALLERGEN BET V 1-A

BETULA VERRUCOSA

UniProt P15494

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 1–159 Mutation:YES No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 6;pH 6.00 Resolution 2.15 Å R-free 0.238

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.

29 other PDB entries and 37 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BV1A_BETVE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–159; UniProt 1–159

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 1qmr

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1qmr
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id1qmr
Deposition date deposition_date1999-10-06
Structure title titleBIRCH POLLEN ALLERGEN BET V 1 MUTANT N28T, K32Q, E45S, P108G
Keywords keywordsALLERGEN, PATHOGENESIS-RELATED PROTEIN; ALLERGEN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier16.90
Radius of gyration Rg (electron density) rg_electron15.56
Forward intensity I(0) i05623190.00
Molecular weight molecular_weight17305.0 kDa
Excluded volume excluded_volume21779 ų
Envelope volume envelope_volume25323 ų
Hydration-shell volume shell_volume14068 ų
Envelope diameter envelope_diameter57.2
Shell Rg shell_rg21.04
Envelope Rg envelope_rg15.66
Shape Rg shape_rg15.56
Total Rg total_rg16.62
Total atoms total_atoms1223
Residues n_residues159
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 dmax57.6
Rg (real space) rg_real16.81
Rg uncertainty (real space) rg_real_error0.31
I(0) (real space) i0_real5.6230e+06
I(0) uncertainty (real space) i0_real_error6.5100e+04
Rg (reciprocal space) rg_reciprocal16.82
I(0) (reciprocal space) i0_reciprocal5623000.0000
Solution quality estimate total_estimate0.8583
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary56.9
Skewness Skewness skewness0.201
Kurtosis Kurtosis kurtosis-0.161
Angular range angular_range— – 0.4700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha870000.0000
Real-space data points n_real_points77
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.722; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.988

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_idd1qmra_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.129 — TBP-like
Superfamily Superfamily superfamilyd.129.3 — Bet v1-like
Family Family familyd.129.3.1 — Pathogenesis-related protein 10 (PR10)-like

CATH v4.4 (1 domains)

Domain ID domain_id1qmrA00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology530 — Alpha-D-Glucose-1,6-Bisphosphate; Chain A, domain 4
Homologous superfamily homologous superfamily20 — START domain

8. Citations (2)

9. Files and Curves (10)