7p0s

ORF virus encoded Bcl-2 homolog ORFV125 in complex with Puma BH3 peptide

Method: X-RAY DIFFRACTION Dmax: 75.8 Å Quality: GOOD

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

Apoptosis inhibitor

Orf virus

UniProt A0A0R8HV90

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 1–143 Chain B; UniProt 1–143 Not recorded Bcl-2-binding component 3, isoforms 1/2 × 2 (Q9BXH1) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.2 M Magnesium acetate, 25% PEG 3350 Resolution 2.50 Å R-free 0.286

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.

3 other PDB entries and 4 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A0A0R8HV90_ORFV
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 6–148; UniProt 1–143 Author chain B; PDBConstruct 6–148; UniProt 1–143

Bcl-2-binding component 3, isoforms 1/2

OrganismNot specified

UniProt Q9BXH1

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 C; UniProt 130–155 Chain U; UniProt 130–155 Not recorded Apoptosis inhibitor × 2 (A0A0R8HV90) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.2 M Magnesium acetate, 25% PEG 3350 Resolution 2.50 Å R-free 0.286

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.

9 other PDB entries and 9 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BBC3_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain C; PDBConstruct 1–26; UniProt 130–155 Author chain U; PDBConstruct 1–26; UniProt 130–155

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 7p0s

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7p0s
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7p0s
Deposition date deposition_date2021-06-30
Structure title titleORF virus encoded Bcl-2 homolog ORFV125 in complex with Puma BH3 peptide
Keywords keywordsORF virus, Bcl-2, Apoptosis; APOPTOSIS
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier22.37
Radius of gyration Rg (electron density) rg_electron21.12
Forward intensity I(0) i023436300.00
Molecular weight molecular_weight35289.0 kDa
Excluded volume excluded_volume43578 ų
Envelope volume envelope_volume53237 ų
Hydration-shell volume shell_volume21387 ų
Envelope diameter envelope_diameter77.2
Shell Rg shell_rg27.42
Envelope Rg envelope_rg21.44
Shape Rg shape_rg21.14
Total Rg total_rg21.88
Total atoms total_atoms4921
Residues n_residues316
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 dmax75.8
Rg (real space) rg_real22.36
Rg uncertainty (real space) rg_real_error0.56
I(0) (real space) i0_real2.3440e+07
I(0) uncertainty (real space) i0_real_error2.9720e+05
Rg (reciprocal space) rg_reciprocal22.36
I(0) (reciprocal space) i0_reciprocal23440000.0000
Solution quality estimate total_estimate0.8764
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.1
Skewness Skewness skewness0.347
Kurtosis Kurtosis kurtosis-0.408
Angular range angular_range— – 0.3550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7684000.0000
Real-space data points n_real_points67
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.802; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.986; Smooth: 0.999

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)