9cpe

Structural basis of BAK sequestration by MCL-1 and consequences for apoptosis initiation

Method: X-RAY DIFFRACTION Dmax: 48.8 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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 20–186 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;295 K;15-25% PEG 3350, 0.1 M sodium acetate, 0.1M HEPES pH 7.5 Resolution 1.49 Å R-free 0.212

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 103 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 1–167; UniProt 20–186

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 9cpe

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9cpe
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9cpe
Deposition date deposition_date2024-07-18
最后修订 last_revision2025-06-04
Structure title titleStructural basis of BAK sequestration by MCL-1 and consequences for apoptosis initiation
Keywords keywordsAnti-apoptosis, Mitochondrial poration, BCL-2 family, Cell fate, APOPTOSIS; APOPTOSIS
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier16.14
Radius of gyration Rg (electron density) rg_electron14.68
Forward intensity I(0) i06081970.00
Molecular weight molecular_weight17676.0 kDa
Excluded volume excluded_volume22036 ų
Envelope volume envelope_volume24692 ų
Hydration-shell volume shell_volume14051 ų
Envelope diameter envelope_diameter48.6
Shell Rg shell_rg20.72
Envelope Rg envelope_rg14.93
Shape Rg shape_rg14.65
Total Rg total_rg15.89
Total atoms total_atoms2453
Residues n_residues156
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 dmax48.8
Rg (real space) rg_real16.00
Rg uncertainty (real space) rg_real_error0.21
I(0) (real space) i0_real6.0820e+06
I(0) uncertainty (real space) i0_real_error6.3510e+04
Rg (reciprocal space) rg_reciprocal16.01
I(0) (reciprocal space) i0_reciprocal6082000.0000
Solution quality estimate total_estimate0.8979
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary22.2
Skewness Skewness skewness0.037
Kurtosis Kurtosis kurtosis-0.459
Angular range angular_range— – 0.4950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1398000.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.897; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.982; Smooth: 0.997

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)