8gsv

Crystal structure of human BAK in complex with the Pxt1 BH3 domain

Method: X-RAY DIFFRACTION Dmax: 129.0 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 × 24 PDB declaration: 24-meric(24) Consistent with protein copy count Chain A; UniProt 23–185 Chain C; UniProt 23–185 Chain E; UniProt 23–185 Chain G; UniProt 23–185 Chain I; UniProt 23–185 Chain K; UniProt 23–185 Chain M; UniProt 23–185 Chain O; UniProt 23–185 Chain Q; UniProt 23–185 Chain S; UniProt 23–185 Chain U; UniProt 23–185 Chain W; UniProt 23–185 Mutation:C166S Peroxisomal testis-specific protein 1 × 12 (Q8NFP0) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;291 K;0.1 M Sodium citrate(pH 4.8) and 17 % PEG 3000 Resolution 2.20 Å R-free 0.266

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 4–166; UniProt 23–185 Author chain C; PDBConstruct 4–166; UniProt 23–185 Author chain E; PDBConstruct 4–166; UniProt 23–185 Author chain G; PDBConstruct 4–166; UniProt 23–185 Author chain I; PDBConstruct 4–166; UniProt 23–185 Author chain K; PDBConstruct 4–166; UniProt 23–185 Author chain M; PDBConstruct 4–166; UniProt 23–185 Author chain O; PDBConstruct 4–166; UniProt 23–185 Author chain Q; PDBConstruct 4–166; UniProt 23–185 Author chain S; PDBConstruct 4–166; UniProt 23–185 Author chain U; PDBConstruct 4–166; UniProt 23–185 Author chain W; PDBConstruct 4–166; UniProt 23–185

Peroxisomal testis-specific protein 1

Homo sapiens

UniProt Q8NFP0

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 × 24 PDB declaration: 24-meric(24) Consistent with protein copy count Chain B; UniProt 76–101 Chain D; UniProt 76–101 Chain F; UniProt 76–101 Chain H; UniProt 76–101 Chain J; UniProt 76–101 Chain L; UniProt 76–101 Chain N; UniProt 76–101 Chain P; UniProt 76–101 Chain R; UniProt 76–101 Chain T; UniProt 76–101 Chain V; UniProt 76–101 Chain X; UniProt 76–101 Not recorded Bcl-2 homologous antagonist/killer × 12 (Q16611) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;291 K;0.1 M Sodium citrate(pH 4.8) and 17 % PEG 3000 Resolution 2.20 Å R-free 0.266

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.

1 other PDB entries and 1 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PXT1_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 4–29; UniProt 76–101 Author chain D; PDBConstruct 4–29; UniProt 76–101 Author chain F; PDBConstruct 4–29; UniProt 76–101 Author chain H; PDBConstruct 4–29; UniProt 76–101 Author chain J; PDBConstruct 4–29; UniProt 76–101 Author chain L; PDBConstruct 4–29; UniProt 76–101 Author chain N; PDBConstruct 4–29; UniProt 76–101 Author chain P; PDBConstruct 4–29; UniProt 76–101 Author chain R; PDBConstruct 4–29; UniProt 76–101 Author chain T; PDBConstruct 4–29; UniProt 76–101 Author chain V; PDBConstruct 4–29; UniProt 76–101 Author chain X; PDBConstruct 4–29; UniProt 76–101

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 8gsv

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id8gsv
Deposition date deposition_date2022-09-07
Structure title titleCrystal structure of human BAK in complex with the Pxt1 BH3 domain
Keywords keywordsPeroxisomal testis-specific 1, Pxt1, Bak, BH3, apoptosis; APOPTOSIS
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier43.26
Radius of gyration Rg (electron density) rg_electron42.49
Forward intensity I(0) i0871020000.00
Molecular weight molecular_weight241470.0 kDa
Excluded volume excluded_volume300980 ų
Envelope volume envelope_volume417630 ų
Hydration-shell volume shell_volume79216 ų
Envelope diameter envelope_diameter129.8
Shell Rg shell_rg50.91
Envelope Rg envelope_rg40.55
Shape Rg shape_rg42.49
Total Rg total_rg42.86
Total atoms total_atoms17052
Residues n_residues2112
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 dmax129.0
Rg (real space) rg_real42.92
Rg uncertainty (real space) rg_real_error0.69
I(0) (real space) i0_real8.7100e+08
I(0) uncertainty (real space) i0_real_error1.5790e+07
Rg (reciprocal space) rg_reciprocal43.26
I(0) (reciprocal space) i0_reciprocal871400000.0000
Solution quality estimate total_estimate0.8970
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary60.9
Skewness Skewness skewness-0.065
Kurtosis Kurtosis kurtosis-0.601
Angular range angular_range— – 0.1800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha56290000.0000
Real-space data points n_real_points37
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.925; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.961; Smooth: 0.919

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 12 domains

CATH v4.4 (12 domains)

Domain ID domain_id8gsvA01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id8gsvC01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id8gsvE01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id8gsvG01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id8gsvI01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id8gsvK01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id8gsvM01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id8gsvO01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id8gsvQ01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id8gsvS01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id8gsvU01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like
Domain ID domain_id8gsvW01
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)