5ajk

Crystal structure of variola virus virulence factor F1L in complex with human Bak BH3 domain

Method: X-RAY DIFFRACTION Dmax: 109.7 Å Quality: EXCELLENT

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

HOMOLOG OF VACCINIA VIRUS CDS F1L

VARIOLA VIRUS

UniProt Q85365

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 39–201 Chain C; UniProt 39–201 Fragment:RESIDUES 39-201 BCL-2 HOMOLOGOUS ANTAGONIST/KILLER × 2 (Q16611) CL CHLORIDE ION × 2 ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.2;1.7 M MGSO4, 0.1 M NA-ACETATE PH 5.2 Resolution 2.55 Å R-free 0.240
2 Protein heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain E; UniProt 39–201 Chain K; UniProt 39–201 Fragment:RESIDUES 39-201 BCL-2 HOMOLOGOUS ANTAGONIST/KILLER × 2 (Q16611) ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.2;1.7 M MGSO4, 0.1 M NA-ACETATE PH 5.2 Resolution 2.55 Å R-free 0.240
3 Protein heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain G; UniProt 39–201 Chain I; UniProt 39–201 Fragment:RESIDUES 39-201 BCL-2 HOMOLOGOUS ANTAGONIST/KILLER × 2 (Q16611) ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.2;1.7 M MGSO4, 0.1 M NA-ACETATE PH 5.2 Resolution 2.55 Å R-free 0.240

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 Q85365_VARV
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 6–168; UniProt 39–201 Author chain C; PDBConstruct 6–168; UniProt 39–201 Author chain E; PDBConstruct 6–168; UniProt 39–201 Author chain G; PDBConstruct 6–168; UniProt 39–201 Author chain I; PDBConstruct 6–168; UniProt 39–201 Author chain K; PDBConstruct 6–168; UniProt 39–201

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain B; UniProt 67–92 Chain D; UniProt 67–92 Fragment:RESIDUES 67-92 HOMOLOG OF VACCINIA VIRUS CDS F1L × 2 (Q85365) CL CHLORIDE ION × 2 ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.2;1.7 M MGSO4, 0.1 M NA-ACETATE PH 5.2 Resolution 2.55 Å R-free 0.240
2 Protein heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain F; UniProt 67–92 Chain L; UniProt 67–92 Fragment:RESIDUES 67-92 HOMOLOG OF VACCINIA VIRUS CDS F1L × 2 (Q85365) ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.2;1.7 M MGSO4, 0.1 M NA-ACETATE PH 5.2 Resolution 2.55 Å R-free 0.240
3 Protein heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain H; UniProt 67–92 Chain J; UniProt 67–92 Fragment:RESIDUES 67-92 HOMOLOG OF VACCINIA VIRUS CDS F1L × 2 (Q85365) ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.2;1.7 M MGSO4, 0.1 M NA-ACETATE PH 5.2 Resolution 2.55 Å R-free 0.240

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 101 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 B; PDBConstruct 1–26; UniProt 67–92 Author chain D; PDBConstruct 1–26; UniProt 67–92 Author chain F; PDBConstruct 1–26; UniProt 67–92 Author chain H; PDBConstruct 1–26; UniProt 67–92 Author chain J; PDBConstruct 1–26; UniProt 67–92 Author chain L; PDBConstruct 1–26; UniProt 67–92

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 5ajk

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5ajk
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5ajk
Deposition date deposition_date2015-02-25
Structure title titleCrystal structure of variola virus virulence factor F1L in complex with human Bak BH3 domain
Keywords keywordsBCL-2, APOPTOSIS, POXVIRUS, BID; APOPTOSIS
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier34.63
Radius of gyration Rg (electron density) rg_electron33.81
Forward intensity I(0) i0215302000.00
Molecular weight molecular_weight114110.0 kDa
Excluded volume excluded_volume141310 ų
Envelope volume envelope_volume185770 ų
Hydration-shell volume shell_volume45783 ų
Envelope diameter envelope_diameter114.4
Shell Rg shell_rg40.58
Envelope Rg envelope_rg33.05
Shape Rg shape_rg33.81
Total Rg total_rg34.31
Total atoms total_atoms15718
Residues n_residues978
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 dmax109.7
Rg (real space) rg_real34.54
Rg uncertainty (real space) rg_real_error0.64
I(0) (real space) i0_real2.1530e+08
I(0) uncertainty (real space) i0_real_error3.3260e+06
Rg (reciprocal space) rg_reciprocal34.60
I(0) (reciprocal space) i0_reciprocal215300000.0000
Solution quality estimate total_estimate0.9028
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary45.3
Skewness Skewness skewness0.199
Kurtosis Kurtosis kurtosis-0.499
Angular range angular_range— – 0.2300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha80600000.0000
Real-space data points n_real_points47
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.939; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.918

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)