4fiv

FIV PROTEASE COMPLEXED WITH AN INHIBITOR LP-130

Method: X-RAY DIFFRACTION Dmax: 48.6 Å Quality: GOOD

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

FELINE IMMUNODEFICIENCY VIRUS PROTEASE

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 42–154 Not recorded LP1 4-[2-(2-ACETYLAMINO-3-NAPHTALEN-1-YL-PROPIONYLAMINO)-4-METHYL-PENTANOYLAMINO]-3-HYDROXY-6-METHYL-HEPTANOIC ACID [1-(1-CARBAMOYL-2-NAPHTHALEN-1-YL-ETHYLCARBAMOYL)-PROPYL]-AMIDE × 2 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7.2;pH 7.2 Resolution 1.80 Å

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 28 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 1–113; UniProt 42–154

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 4fiv

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id4fiv
Deposition date deposition_date1998-07-15
Structure title titleFIV PROTEASE COMPLEXED WITH AN INHIBITOR LP-130
Keywords keywordsASPARTIC PROTEASE, FIV, RETROPEPSIN, RETROVIRUS, CAT; ASPARTIC PROTEASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier15.20
Radius of gyration Rg (electron density) rg_electron13.85
Forward intensity I(0) i03493460.00
Molecular weight molecular_weight13494.0 kDa
Excluded volume excluded_volume17105 ų
Envelope volume envelope_volume19393 ų
Hydration-shell volume shell_volume11972 ų
Envelope diameter envelope_diameter47.5
Shell Rg shell_rg19.58
Envelope Rg envelope_rg14.16
Shape Rg shape_rg13.81
Total Rg total_rg15.22
Total atoms total_atoms949
Residues n_residues113
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 dmax48.6
Rg (real space) rg_real15.11
Rg uncertainty (real space) rg_real_error0.20
I(0) (real space) i0_real3.4930e+06
I(0) uncertainty (real space) i0_real_error3.4540e+04
Rg (reciprocal space) rg_reciprocal15.12
I(0) (reciprocal space) i0_reciprocal3493000.0000
Solution quality estimate total_estimate0.8853
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary18.4
Skewness Skewness skewness0.172
Kurtosis Kurtosis kurtosis-0.372
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha751500.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.843; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.996; Smooth: 0.979

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd4fiva_
Class classb — All beta proteins
Fold Fold foldb.50 — Acid proteases
Superfamily Superfamily superfamilyb.50.1 — Acid proteases
Family Family familyb.50.1.1 — Retroviral protease (retropepsin)

CATH v4.4 (1 domains)

Domain ID domain_id4fivA00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology70 — Cathepsin D, subunit A; domain 1
Homologous superfamily homologous superfamily10 — Acid Proteases

8. Citations (1)

9. Files and Curves (10)