6x5b

Symmetric model of CD4- and 17-bound B41 HIV-1 Env SOSIP in complex with small molecule GO52

Method: ELECTRON MICROSCOPY Dmax: 152.4 Å Quality: GOOD

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

Envelope glycoprotein gp120

Human immunodeficiency virus 1

UniProt B3UES2

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Other combination Heteromer Protein × 15 其他Polymer 6 PDB declaration: pentadecameric(15) Consistent with protein copy count Chain A; UniProt 29–517 Chain D; UniProt 29–517 Chain J; UniProt 29–517 Mutation:A501C, E510R, K511R, 512R, 513R Envelope glycoprotein gp41 × 3 (B3UEZ6) 17b Fab light chain × 3 T-cell surface glycoprotein CD4 × 3 (P01730) 17b Fab heavy chain × 3 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 3 ;alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose ; × 3 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 27 UOV N-(4'-methyl[1,1'-biphenyl]-4-yl)-1-oxa-7-azaspiro[3.5]nonane-7-carboxamide × 3 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4;Detergent diluted into sample shortly before application to grid cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.60 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.

16 other PDB entries and 16 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name B3UES2_9HIV1
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 36–524; UniProt 29–517 Author chain D; PDBConstruct 36–524; UniProt 29–517 Author chain J; PDBConstruct 36–524; UniProt 29–517

Envelope glycoprotein gp41

Human immunodeficiency virus 1

UniProt B3UEZ6

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Other combination Heteromer Protein × 15 其他Polymer 6 PDB declaration: pentadecameric(15) Consistent with protein copy count Chain B; UniProt 516–668 Chain E; UniProt 516–668 Chain K; UniProt 516–668 Mutation:I559P, T605C Envelope glycoprotein gp120 × 3 (B3UES2) 17b Fab light chain × 3 T-cell surface glycoprotein CD4 × 3 (P01730) 17b Fab heavy chain × 3 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 3 ;alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose ; × 3 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 27 UOV N-(4'-methyl[1,1'-biphenyl]-4-yl)-1-oxa-7-azaspiro[3.5]nonane-7-carboxamide × 3 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4;Detergent diluted into sample shortly before application to grid cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.60 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.

14 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name B3UEZ6_9HIV1
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–153; UniProt 516–668 Author chain E; PDBConstruct 1–153; UniProt 516–668 Author chain K; PDBConstruct 1–153; UniProt 516–668

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 Other combination Heteromer Protein × 15 其他Polymer 6 PDB declaration: pentadecameric(15) Consistent with protein copy count Chain C; UniProt 25–203 Chain G; UniProt 25–203 Chain N; UniProt 25–203 Not recorded Envelope glycoprotein gp120 × 3 (B3UES2) Envelope glycoprotein gp41 × 3 (B3UEZ6) 17b Fab light chain × 3 17b Fab heavy chain × 3 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 3 ;alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose ; × 3 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 27 UOV N-(4'-methyl[1,1'-biphenyl]-4-yl)-1-oxa-7-azaspiro[3.5]nonane-7-carboxamide × 3 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4;Detergent diluted into sample shortly before application to grid cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.60 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 4
Chains and sequence ranges Author chain C; PDBConstruct 20–198; UniProt 25–203 Author chain G; PDBConstruct 20–198; UniProt 25–203 Author chain N; PDBConstruct 20–198; UniProt 25–203

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 6x5b

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6x5b
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6x5b
Deposition date deposition_date2020-05-25
Structure title titleSymmetric model of CD4- and 17-bound B41 HIV-1 Env SOSIP in complex with small molecule GO52
Keywords keywordsHIV-1, Env, CD4, receptor-bound state, small molecule, VIRAL PROTEIN, VIRAL PROTEIN-Immune System complex; VIRAL PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier49.91
Radius of gyration Rg (electron density) rg_electron49.43
Forward intensity I(0) i01215010000.00
Molecular weight molecular_weight287990.0 kDa
Excluded volume excluded_volume359350 ų
Envelope volume envelope_volume519070 ų
Hydration-shell volume shell_volume84668 ų
Envelope diameter envelope_diameter152.7
Shell Rg shell_rg56.15
Envelope Rg envelope_rg48.07
Shape Rg shape_rg49.42
Total Rg total_rg49.66
Total atoms total_atoms20232
Residues n_residues2436
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 dmax152.4
Rg (real space) rg_real49.63
Rg uncertainty (real space) rg_real_error1.14
I(0) (real space) i0_real1.2150e+09
I(0) uncertainty (real space) i0_real_error2.3050e+07
Rg (reciprocal space) rg_reciprocal50.13
I(0) (reciprocal space) i0_reciprocal1216000000.0000
Solution quality estimate total_estimate0.8909
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary71.4
Skewness Skewness skewness-0.104
Kurtosis Kurtosis kurtosis-0.637
Angular range angular_range— – 0.1600 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha78850000.0000
Real-space data points n_real_points33
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.890; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.973; Smooth: 0.934

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (9)

8. Citations (2)

9. Files and Curves (10)