9cpn

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

Method: X-RAY DIFFRACTION Dmax: 137.6 Å Quality: REASONABLE

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 Other combination Heteromer Protein × 2 其他Polymer 1 PDB declaration: dimeric(2) Consistent with protein copy count Chain E; UniProt 68–89 Not recorded Induced myeloid leukemia cell differentiation protein Mcl-1 × 1 alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;295 K;15-25% PEG 4000, 0.2 M lithium sulfate, 0.1 M TRIS pH 8.5 Resolution 1.89 Å R-free 0.243
2 Other combination Heteromer Protein × 2 其他Polymer 1 PDB declaration: dimeric(2) Consistent with protein copy count Chain F; UniProt 68–89 Not recorded Induced myeloid leukemia cell differentiation protein Mcl-1 × 1 alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;295 K;15-25% PEG 4000, 0.2 M lithium sulfate, 0.1 M TRIS pH 8.5 Resolution 1.89 Å R-free 0.243
3 Other combination Heteromer Protein × 2 其他Polymer 1 PDB declaration: dimeric(2) Consistent with protein copy count Chain G; UniProt 68–89 Not recorded Induced myeloid leukemia cell differentiation protein Mcl-1 × 1 alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;295 K;15-25% PEG 4000, 0.2 M lithium sulfate, 0.1 M TRIS pH 8.5 Resolution 1.89 Å R-free 0.243
4 Other combination Heteromer Protein × 2 其他Polymer 1 PDB declaration: dimeric(2) Consistent with protein copy count Chain H; UniProt 68–89 Not recorded Induced myeloid leukemia cell differentiation protein Mcl-1 × 1 alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;295 K;15-25% PEG 4000, 0.2 M lithium sulfate, 0.1 M TRIS pH 8.5 Resolution 1.89 Å R-free 0.243

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 100 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BAK_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain E; PDBConstruct 1–22; UniProt 68–89 Author chain F; PDBConstruct 1–22; UniProt 68–89 Author chain G; PDBConstruct 1–22; UniProt 68–89 Author chain H; PDBConstruct 1–22; UniProt 68–89

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 9cpn

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9cpn
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_guinier44.87
Radius of gyration Rg (electron density) rg_electron44.43
Forward intensity I(0) i0778614000.00
Molecular weight molecular_weight233840.0 kDa
Excluded volume excluded_volume293800 ų
Envelope volume envelope_volume384060 ų
Hydration-shell volume shell_volume72030 ų
Envelope diameter envelope_diameter145.3
Shell Rg shell_rg48.97
Envelope Rg envelope_rg43.80
Shape Rg shape_rg44.42
Total Rg total_rg44.67
Total atoms total_atoms32621
Residues n_residues2126
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 dmax137.6
Rg (real space) rg_real45.44
Rg uncertainty (real space) rg_real_error0.42
I(0) (real space) i0_real7.6390e+08
I(0) uncertainty (real space) i0_real_error1.1560e+07
Rg (reciprocal space) rg_reciprocal44.87
I(0) (reciprocal space) i0_reciprocal778700000.0000
Solution quality estimate total_estimate0.7057
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary55.0
Skewness Skewness skewness0.228
Kurtosis Kurtosis kurtosis-0.491
Angular range angular_range— – 0.1750 −1
Current regularization parameter α current_alpha2.1580
Highest regularization parameter α highest_alpha73380000.0000
Real-space data points n_real_points36
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.984; Stabil: 0.918; Sysdev: 0.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.491

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)