9pgu

HIV Capsid Hexamer bound to Compound 40

Method: X-RAY DIFFRACTION Dmax: 106.8 Å Quality: EXCELLENT

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

HIV-1 capsid

Human immunodeficiency virus 1

UniProt B6DRA0

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 × 6 PDB declaration: hexameric(6) Consistent with protein copy count Chain A; UniProt 133–363 Chain B; UniProt 133–363 Chain C; UniProt 133–363 Chain D; UniProt 133–363 Chain E; UniProt 133–363 Chain F; UniProt 133–363 Not recorded A1CH6 (5M)-5-{2-[(1S)-2-(3,5-difluorophenyl)-1-{2-[(3bS,4aR)-5,5-difluoro-3-(trifluoromethyl)-3b,4,4a,5-tetrahydro-1H-cyclopropa[3,4]cyclopenta[1,2-c]pyrazol-1-yl]acetamido}ethyl]pyridin-3-yl}-2-fluorobenzamide × 6 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.5;293.15 K;7% peg 8000, 0.1M sodium malonate, pH 6.5 Resolution 3.36 Å R-free 0.262

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.

70 other PDB entries and 103 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name B6DRA0_9HIV1
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–232; UniProt 133–363 Author chain B; PDBConstruct 2–232; UniProt 133–363 Author chain C; PDBConstruct 2–232; UniProt 133–363 Author chain D; PDBConstruct 2–232; UniProt 133–363 Author chain E; PDBConstruct 2–232; UniProt 133–363 Author chain F; PDBConstruct 2–232; UniProt 133–363

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 9pgu

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9pgu
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9pgu
Deposition date deposition_date2025-07-08
Structure title titleHIV Capsid Hexamer bound to Compound 40
Keywords keywordsCapsid, p24, HIV-1, 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_guinier35.59
Radius of gyration Rg (electron density) rg_electron34.85
Forward intensity I(0) i0585628000.00
Molecular weight molecular_weight129770.0 kDa
Excluded volume excluded_volume124840 ų
Envelope volume envelope_volume229870 ų
Hydration-shell volume shell_volume52918 ų
Envelope diameter envelope_diameter109.8
Shell Rg shell_rg43.06
Envelope Rg envelope_rg34.36
Shape Rg shape_rg34.86
Total Rg total_rg35.26
Total atoms total_atoms9765
Residues n_residues1239
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 dmax106.8
Rg (real space) rg_real35.38
Rg uncertainty (real space) rg_real_error0.60
I(0) (real space) i0_real5.8560e+08
I(0) uncertainty (real space) i0_real_error9.3370e+06
Rg (reciprocal space) rg_reciprocal35.52
I(0) (reciprocal space) i0_reciprocal585700000.0000
Solution quality estimate total_estimate0.9063
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary43.7
Skewness Skewness skewness0.070
Kurtosis Kurtosis kurtosis-0.618
Angular range angular_range— – 0.2200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha25080000.0000
Real-space data points n_real_points45
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.968; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.983; Smooth: 0.890

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)