4pa1

Crystal Structure of Catalytic Core domain of FIV Integrase

Method: X-RAY DIFFRACTION Dmax: 53.0 Å Quality: REASONABLE

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

Integrase

Feline immunodeficiency virus

UniProt P16088

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 904–1052 Fragment:catalytic domain No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8.5;293 K;30% PEG 4000, 200 mM MgCl2, 100 mM TrisHCl pH 8.5 Resolution 1.84 Å R-free 0.222
2 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 904–1052 Fragment:catalytic domain No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8.5;293 K;30% PEG 4000, 200 mM MgCl2, 100 mM TrisHCl pH 8.5 Resolution 1.84 Å R-free 0.222
3 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 904–1052 Fragment:catalytic domain No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8.5;293 K;30% PEG 4000, 200 mM MgCl2, 100 mM TrisHCl pH 8.5 Resolution 1.84 Å R-free 0.222

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.

19 other PDB entries and 26 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name POL_FIVPE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–151; UniProt 904–1052

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 4pa1

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4pa1
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4pa1
Deposition date deposition_date2014-04-07
Structure title titleCrystal Structure of Catalytic Core domain of FIV Integrase
Keywords keywordsRetrovirus, FIV, Integrase, VIRAL PROTEIN; VIRAL PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier16.58
Radius of gyration Rg (electron density) rg_electron15.38
Forward intensity I(0) i05522220.00
Molecular weight molecular_weight16892.0 kDa
Excluded volume excluded_volume21180 ų
Envelope volume envelope_volume24528 ų
Hydration-shell volume shell_volume13616 ų
Envelope diameter envelope_diameter56.0
Shell Rg shell_rg21.15
Envelope Rg envelope_rg15.69
Shape Rg shape_rg15.35
Total Rg total_rg16.57
Total atoms total_atoms1188
Residues n_residues151
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 dmax53.0
Rg (real space) rg_real16.48
Rg uncertainty (real space) rg_real_error0.37
I(0) (real space) i0_real5.5220e+06
I(0) uncertainty (real space) i0_real_error5.8310e+04
Rg (reciprocal space) rg_reciprocal16.49
I(0) (reciprocal space) i0_reciprocal5522000.0000
Solution quality estimate total_estimate0.6601
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary21.3
Skewness Skewness skewness0.143
Kurtosis Kurtosis kurtosis-0.404
Angular range angular_range— – 0.4800 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha839500.0000
Real-space data points n_real_points78
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.856; Stabil: 1.000; Sysdev: 0.338; Positv: 1.000; Valcen: 0.997; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd4pa1a1
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.55 — Ribonuclease H-like motif
Superfamily Superfamily superfamilyc.55.3 — Ribonuclease H-like
Family Family familyc.55.3.0 — automated matches
Domain ID domain_idd4pa1a2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (1 domains)

Domain ID domain_id4pa1A00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology420 — Nucleotidyltransferase; domain 5
Homologous superfamily homologous superfamily10 — Ribonuclease H-like superfamily/Ribonuclease H

8. Citations (1)

9. Files and Curves (10)