4uf1

Deerpox virus DPV022 in complex with Bak BH3

Method: X-RAY DIFFRACTION Dmax: 67.9 Å Quality: GOOD

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

Antiapoptotic membrane protein

Deerpox virus (strain W-1170-84)

UniProt Q08FF8

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 1–155 Fragment:BCL-2, UNP RESIDUES 1-155 Bcl-2 homologous antagonist/killer × 2 (Q16611) SO4 SULFATE ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.5;17% PEG 8000, 0.2M MES PH 5.5, 0.2M AMMONIUM SULPHATE Resolution 2.30 Å R-free 0.206

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.

2 other PDB entries and 2 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q08FF8_DPV84
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 14–168; UniProt 1–155

Bcl-2 homologous antagonist/killer

OrganismNot specified

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 Fragment:BH3, UNP RESIDUES 67-92 Antiapoptotic membrane protein × 2 (Q08FF8) SO4 SULFATE ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.5;17% PEG 8000, 0.2M MES PH 5.5, 0.2M AMMONIUM SULPHATE Resolution 2.30 Å R-free 0.206

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 2
Chains and sequence ranges Author chain B; 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 4uf1

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4uf1
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4uf1
Deposition date deposition_date2014-12-23
Structure title titleDeerpox virus DPV022 in complex with Bak BH3
Keywords keywordsVIRAL PROTEIN, DEERPOX VIRUS, APOPTOSIS, BCL-2, BAK BH3; VIRAL PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier18.66
Radius of gyration Rg (electron density) rg_electron17.61
Forward intensity I(0) i06206640.00
Molecular weight molecular_weight18201.0 kDa
Excluded volume excluded_volume22945 ų
Envelope volume envelope_volume28999 ų
Hydration-shell volume shell_volume14657 ų
Envelope diameter envelope_diameter68.5
Shell Rg shell_rg22.80
Envelope Rg envelope_rg18.11
Shape Rg shape_rg17.60
Total Rg total_rg18.62
Total atoms total_atoms2577
Residues n_residues157
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 dmax67.9
Rg (real space) rg_real18.68
Rg uncertainty (real space) rg_real_error0.54
I(0) (real space) i0_real6.2070e+06
I(0) uncertainty (real space) i0_real_error7.9420e+04
Rg (reciprocal space) rg_reciprocal18.68
I(0) (reciprocal space) i0_reciprocal6207000.0000
Solution quality estimate total_estimate0.8324
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary21.4
Skewness Skewness skewness0.433
Kurtosis Kurtosis kurtosis0.142
Angular range angular_range— – 0.4250 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha691700.0000
Real-space data points n_real_points74
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.635; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.954; Smooth: 0.957

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id4uf1A00
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)