8z7n

Structure of HIV-1 CH119 SOSIP.664 trimer in complex with CD4 molecules

Method: ELECTRON MICROSCOPY Dmax: 174.1 Å Quality: GOOD

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

Envelope glycoprotein gp160

Human immunodeficiency virus 1

UniProt A1EAH4

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 × 9 PDB declaration: nonameric(9) Consistent with protein copy count Chain A; UniProt 29–506 Chain B; UniProt 510–662 Chain D; UniProt 29–506 Chain E; UniProt 510–662 Chain G; UniProt 29–506 Chain H; UniProt 510–662 Mutation:A507C Mutation:I48P,T94C T-cell surface glycoprotein CD4 × 3 (P01730) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 18 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.58 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.

No other PDB entry for the same UniProt protein was found.

View Construct and Data Evidence
UniProt name A1EAH4_9HIV1
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 36–513; UniProt 29–506 Author chain D; PDBConstruct 36–513; UniProt 29–506 Author chain G; PDBConstruct 36–513; UniProt 29–506 Author chain B; PDBConstruct 1–153; UniProt 510–662 Author chain E; PDBConstruct 1–153; UniProt 510–662 Author chain H; PDBConstruct 1–153; UniProt 510–662

T-cell surface glycoprotein CD4

Homo sapiens

UniProt P01730

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 × 9 PDB declaration: nonameric(9) Consistent with protein copy count Chain C; UniProt 1–392 Chain F; UniProt 1–392 Chain I; UniProt 1–392 Not recorded Envelope glycoprotein gp160 × 3 (A1EAH4) Envelope glycoprotein gp160 × 3 (A1EAH4) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 18 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.58 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.

78 other PDB entries and 99 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CD4_HUMAN
Isoform
PDB entities 3
Chains and sequence ranges Author chain C; PDBConstruct 1–392; UniProt 1–392 Author chain F; PDBConstruct 1–392; UniProt 1–392 Author chain I; PDBConstruct 1–392; UniProt 1–392

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 8z7n

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8z7n
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8z7n
Deposition date deposition_date2024-04-20
Structure title titleStructure of HIV-1 CH119 SOSIP.664 trimer in complex with CD4 molecules
Keywords keywordsHIV-1, CRF_07BC, Env, CD4, VIRUS; VIRUS
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier50.69
Radius of gyration Rg (electron density) rg_electron50.41
Forward intensity I(0) i0839715000.00
Molecular weight molecular_weight237380.0 kDa
Excluded volume excluded_volume296210 ų
Envelope volume envelope_volume441150 ų
Hydration-shell volume shell_volume75094 ų
Envelope diameter envelope_diameter180.7
Shell Rg shell_rg51.73
Envelope Rg envelope_rg50.50
Shape Rg shape_rg50.38
Total Rg total_rg50.55
Total atoms total_atoms16641
Residues n_residues2094
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 dmax174.1
Rg (real space) rg_real50.73
Rg uncertainty (real space) rg_real_error1.81
I(0) (real space) i0_real8.3970e+08
I(0) uncertainty (real space) i0_real_error1.5900e+07
Rg (reciprocal space) rg_reciprocal50.66
I(0) (reciprocal space) i0_reciprocal839600000.0000
Solution quality estimate total_estimate0.8562
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary67.4
Skewness Skewness skewness0.341
Kurtosis Kurtosis kurtosis-0.174
Angular range angular_range— – 0.1550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha56630000.0000
Real-space data points n_real_points32
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.815; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.984; Smooth: 0.696

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)