8uky

Crystal structure of BAK in complex with inhibiting antibody 14G6

Method: X-RAY DIFFRACTION Dmax: 151.0 Å Quality: GOOD

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

Bcl-2 homologous antagonist/killer

Homo sapiens

UniProt Q16611

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain C; UniProt 23–186 Not recorded 14G6 Fab light chain × 1 14G6 Fab heavy chain × 1 SO4 SULFATE ION × 1 CCN ACETONITRILE × 3 PEG DI(HYDROXYETHYL)ETHER × 3 144 TRIS-HYDROXYMETHYL-METHYL-AMMONIUM × 1 PGE TRIETHYLENE GLYCOL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.09 M Bis-Tris chloride, pH 5.5, 22.5% PEG3350, 4% acetonitrile Resolution 2.40 Å R-free 0.252
2 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain D; UniProt 23–186 Not recorded 14G6 Fab light chain × 1 14G6 Fab heavy chain × 1 SO4 SULFATE ION × 2 PEG DI(HYDROXYETHYL)ETHER × 5 144 TRIS-HYDROXYMETHYL-METHYL-AMMONIUM × 1 PGE TRIETHYLENE GLYCOL × 1 EDO 1,2-ETHANEDIOL × 2 1PE PENTAETHYLENE GLYCOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.09 M Bis-Tris chloride, pH 5.5, 22.5% PEG3350, 4% acetonitrile Resolution 2.40 Å R-free 0.252

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.

53 other PDB entries and 102 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BAK_HUMAN
Isoform
PDB entities 3
Chains and sequence ranges Author chain C; PDBConstruct 7–170; UniProt 23–186 Author chain D; PDBConstruct 7–170; UniProt 23–186

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 8uky

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id8uky
Deposition date deposition_date2023-10-15
Structure title titleCrystal structure of BAK in complex with inhibiting antibody 14G6
Keywords keywordsBAK, APOPTOSIS-INHIBITOR complex, BCL2, antibody; APOPTOSIS/INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier41.75
Radius of gyration Rg (electron density) rg_electron41.91
Forward intensity I(0) i0256437000.00
Molecular weight molecular_weight128730.0 kDa
Excluded volume excluded_volume160350 ų
Envelope volume envelope_volume221820 ų
Hydration-shell volume shell_volume46793 ų
Envelope diameter envelope_diameter150.1
Shell Rg shell_rg43.69
Envelope Rg envelope_rg41.48
Shape Rg shape_rg41.85
Total Rg total_rg42.20
Total atoms total_atoms9063
Residues n_residues1157
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 dmax151.0
Rg (real space) rg_real42.02
Rg uncertainty (real space) rg_real_error1.95
I(0) (real space) i0_real2.5640e+08
I(0) uncertainty (real space) i0_real_error4.7010e+06
Rg (reciprocal space) rg_reciprocal41.76
I(0) (reciprocal space) i0_reciprocal256400000.0000
Solution quality estimate total_estimate0.8389
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary43.7
Skewness Skewness skewness0.501
Kurtosis Kurtosis kurtosis-0.194
Angular range angular_range— – 0.1900 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha24430000.0000
Real-space data points n_real_points39
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.735; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.870; Smooth: 0.825

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (11)

8. Citations (1)

9. Files and Curves (10)