5efm

Beclin 1 Flexible-helical Domian (FHD) (141-171)

Method: X-RAY DIFFRACTION Dmax: 31.9 Å Quality: GOOD

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

Beclin-1

OrganismNot specified

UniProt Q14457

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 141–171 Not recorded SO4 SULFATE ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:EVAPORATION;pH 5.6;293 K;250mM potassium sodium tartrate tetrahydrate, 2.2 M ammonium sulfate, 100mM sodium citrate tribasic dihydrate (pH 5.6) Resolution 1.95 Å R-free 0.216

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 50 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BECN1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–31; UniProt 141–171

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 5efm

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5efm
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5efm
Deposition date deposition_date2015-10-23
Structure title titleBeclin 1 Flexible-helical Domian (FHD) (141-171)
Keywords keywordsflexible helix, APOPTOSIS; APOPTOSIS
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier9.14
Radius of gyration Rg (electron density) rg_electron7.74
Forward intensity I(0) i0166416.00
Molecular weight molecular_weight1978.0 kDa
Excluded volume excluded_volume2331 ų
Envelope volume envelope_volume2815 ų
Hydration-shell volume shell_volume3663 ų
Envelope diameter envelope_diameter28.6
Shell Rg shell_rg11.79
Envelope Rg envelope_rg8.20
Shape Rg shape_rg7.72
Total Rg total_rg9.31
Total atoms total_atoms135
Residues n_residues15
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 dmax31.9
Rg (real space) rg_real9.18
Rg uncertainty (real space) rg_real_error0.40
I(0) (real space) i0_real1.6640e+05
I(0) uncertainty (real space) i0_real_error1.7460e+03
Rg (reciprocal space) rg_reciprocal9.18
I(0) (reciprocal space) i0_reciprocal166400.0000
Solution quality estimate total_estimate0.8626
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary10.5
Skewness Skewness skewness0.428
Kurtosis Kurtosis kurtosis-0.109
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha14940.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.812; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.875; Smooth: 0.901

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)