8t5e

De novo design of high-affinity protein binders to bioactive helical peptides

Method: X-RAY DIFFRACTION Dmax: 51.2 Å Quality: GOOD

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

Bcl-2-like protein 11

OrganismNot specified

UniProt O43521

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 141–166 Not recorded Bim_fulldiff × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4;293 K;0.1 M Citric acid pH 2.5, 20% (w/v) PEG 6000 Resolution 3.00 Å R-free 0.264

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.

38 other PDB entries and 49 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name B2L11_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–26; UniProt 141–166

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 8t5e

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8t5e
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8t5e
Deposition date deposition_date2023-06-13
Structure title titleDe novo design of high-affinity protein binders to bioactive helical peptides
Keywords keywordsAlpha-helical peptides, protein design, diffusion, deep learning, DE NOVO PROTEIN; DE NOVO PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier16.43
Radius of gyration Rg (electron density) rg_electron14.98
Forward intensity I(0) i06265480.00
Molecular weight molecular_weight17753.0 kDa
Excluded volume excluded_volume22174 ų
Envelope volume envelope_volume25412 ų
Hydration-shell volume shell_volume14138 ų
Envelope diameter envelope_diameter50.8
Shell Rg shell_rg21.19
Envelope Rg envelope_rg15.42
Shape Rg shape_rg15.00
Total Rg total_rg16.09
Total atoms total_atoms1244
Residues n_residues152
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 dmax51.2
Rg (real space) rg_real16.32
Rg uncertainty (real space) rg_real_error0.27
I(0) (real space) i0_real6.2650e+06
I(0) uncertainty (real space) i0_real_error7.6470e+04
Rg (reciprocal space) rg_reciprocal16.33
I(0) (reciprocal space) i0_reciprocal6266000.0000
Solution quality estimate total_estimate0.8172
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary20.3
Skewness Skewness skewness0.165
Kurtosis Kurtosis kurtosis-0.379
Angular range angular_range— – 0.4850 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1611000.0000
Real-space data points n_real_points79
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.879; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.986; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)