6uxo

Crystal structure of BAK core domain BH3-groove-dimer in complex with DDM

Method: X-RAY DIFFRACTION Dmax: 109.6 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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 68–148 Chain B; UniProt 68–148 Fragment:Core/dimerisation domain, residues 68-148 LMT DODECYL-BETA-D-MALTOSIDE × 3 SO4 SULFATE ION × 6 ACT ACETATE ION × 1 EDO 1,2-ETHANEDIOL × 6 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4.6;293 K;ammonium sulfate, n-Dodecyl-b-D-maltoside, sodium acetate Resolution 1.80 Å R-free 0.250
2 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 68–148 Chain D; UniProt 68–148 Fragment:Core/dimerisation domain, residues 68-148 LMT DODECYL-BETA-D-MALTOSIDE × 4 SO4 SULFATE ION × 7 ACT ACETATE ION × 1 EDO 1,2-ETHANEDIOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4.6;293 K;ammonium sulfate, n-Dodecyl-b-D-maltoside, sodium acetate Resolution 1.80 Å R-free 0.250
3 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain E; UniProt 68–148 Chain F; UniProt 68–148 Fragment:Core/dimerisation domain, residues 68-148 LMT DODECYL-BETA-D-MALTOSIDE × 5 SO4 SULFATE ION × 5 ACT ACETATE ION × 1 EDO 1,2-ETHANEDIOL × 7 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4.6;293 K;ammonium sulfate, n-Dodecyl-b-D-maltoside, sodium acetate Resolution 1.80 Å R-free 0.250
4 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain G; UniProt 68–148 Chain H; UniProt 68–148 Fragment:Core/dimerisation domain, residues 68-148 LMT DODECYL-BETA-D-MALTOSIDE × 4 SO4 SULFATE ION × 7 ACT ACETATE ION × 1 EDO 1,2-ETHANEDIOL × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4.6;293 K;ammonium sulfate, n-Dodecyl-b-D-maltoside, sodium acetate Resolution 1.80 Å R-free 0.250
5 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain I; UniProt 68–148 Chain J; UniProt 68–148 Fragment:Core/dimerisation domain, residues 68-148 LMT DODECYL-BETA-D-MALTOSIDE × 5 SO4 SULFATE ION × 6 ACT ACETATE ION × 1 EDO 1,2-ETHANEDIOL × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4.6;293 K;ammonium sulfate, n-Dodecyl-b-D-maltoside, sodium acetate Resolution 1.80 Å R-free 0.250
6 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain K; UniProt 68–148 Chain L; UniProt 68–148 Fragment:Core/dimerisation domain, residues 68-148 LMT DODECYL-BETA-D-MALTOSIDE × 3 SO4 SULFATE ION × 4 ACT ACETATE ION × 1 EDO 1,2-ETHANEDIOL × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4.6;293 K;ammonium sulfate, n-Dodecyl-b-D-maltoside, sodium acetate Resolution 1.80 Å R-free 0.250

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 98 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BAK_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 5–85; UniProt 68–148 Author chain B; PDBConstruct 5–85; UniProt 68–148 Author chain C; PDBConstruct 5–85; UniProt 68–148 Author chain D; PDBConstruct 5–85; UniProt 68–148 Author chain E; PDBConstruct 5–85; UniProt 68–148 Author chain F; PDBConstruct 5–85; UniProt 68–148 Author chain G; PDBConstruct 5–85; UniProt 68–148 Author chain H; PDBConstruct 5–85; UniProt 68–148 Author chain I; PDBConstruct 5–85; UniProt 68–148 Author chain J; PDBConstruct 5–85; UniProt 68–148 Author chain K; PDBConstruct 5–85; UniProt 68–148 Author chain L; PDBConstruct 5–85; UniProt 68–148

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 6uxo

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6uxo
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6uxo
Deposition date deposition_date2019-11-07
Structure title titleCrystal structure of BAK core domain BH3-groove-dimer in complex with DDM
Keywords keywordsPore-forming Protein, APOPTOSIS; APOPTOSIS
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier32.57
Radius of gyration Rg (electron density) rg_electron32.27
Forward intensity I(0) i0241344000.00
Molecular weight molecular_weight124250.0 kDa
Excluded volume excluded_volume155310 ų
Envelope volume envelope_volume195940 ų
Hydration-shell volume shell_volume49204 ų
Envelope diameter envelope_diameter118.6
Shell Rg shell_rg40.38
Envelope Rg envelope_rg32.35
Shape Rg shape_rg32.27
Total Rg total_rg32.90
Total atoms total_atoms8693
Residues n_residues955
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 dmax109.6
Rg (real space) rg_real32.47
Rg uncertainty (real space) rg_real_error0.74
I(0) (real space) i0_real2.4130e+08
I(0) uncertainty (real space) i0_real_error3.7960e+06
Rg (reciprocal space) rg_reciprocal32.52
I(0) (reciprocal space) i0_reciprocal241400000.0000
Solution quality estimate total_estimate0.8777
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary38.0
Skewness Skewness skewness0.292
Kurtosis Kurtosis kurtosis-0.360
Angular range angular_range— – 0.2450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha34040000.0000
Real-space data points n_real_points50
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.817; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.955

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

7. Fold Classification (SCOP + CATH) 12 domains

CATH v4.4 (12 domains)

Domain ID domain_id6uxoA01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id6uxoB01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id6uxoC01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id6uxoD01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id6uxoE01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id6uxoF01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id6uxoG01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id6uxoH01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id6uxoI01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id6uxoJ01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id6uxoK01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id6uxoL01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like

8. Citations (1)

9. Files and Curves (10)