8tp5

H1 hemagglutinin (NC99) in complex with RBS-targeting Fab 1-1-1E04

Method: ELECTRON MICROSCOPY Dmax: 172.3 Å Quality: GOOD

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

Hemagglutinin HA1 chain

Influenza A virus (A/New Caledonia/20/1999(H1N1))

UniProt Q6WG00

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 × 12 其他Polymer 3 PDB declaration: 12-meric(12) Consistent with protein copy count Chain A; UniProt 18–339 Chain B; UniProt 344–514 Chain C; UniProt 18–339 Chain D; UniProt 344–514 Chain G; UniProt 18–339 Chain I; UniProt 344–514 Not recorded Heavy chain of Fab 1-1-1E04 × 3 Light chain of Fab 1-1-1E04 × 3 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 × 12 ELECTRON MICROSCOPY cryo-EM buffer:pH 7 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.90 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.

9 other PDB entries and 9 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q6WG00_9INFA
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 1–322; UniProt 18–339 Author chain C; PDBConstruct 1–322; UniProt 18–339 Author chain G; PDBConstruct 1–322; UniProt 18–339 Author chain B; PDBConstruct 1–171; UniProt 344–514 Author chain D; PDBConstruct 1–171; UniProt 344–514 Author chain I; PDBConstruct 1–171; UniProt 344–514

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 8tp5

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8tp5
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8tp5
Deposition date deposition_date2023-08-04
Structure title titleH1 hemagglutinin (NC99) in complex with RBS-targeting Fab 1-1-1E04
Keywords keywordsinfluenza, hemagglutinin, monoclonal antibody, immune complex, VIRAL PROTEIN, VIRAL PROTEIN-Immune System complex; VIRAL PROTEIN/Immune System
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier51.42
Radius of gyration Rg (electron density) rg_electron51.14
Forward intensity I(0) i0948833000.00
Molecular weight molecular_weight248540.0 kDa
Excluded volume excluded_volume307940 ų
Envelope volume envelope_volume417500 ų
Hydration-shell volume shell_volume72461 ų
Envelope diameter envelope_diameter170.9
Shell Rg shell_rg49.02
Envelope Rg envelope_rg51.06
Shape Rg shape_rg51.10
Total Rg total_rg51.18
Total atoms total_atoms17508
Residues n_residues2115
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 dmax172.3
Rg (real space) rg_real51.52
Rg uncertainty (real space) rg_real_error1.67
I(0) (real space) i0_real9.4880e+08
I(0) uncertainty (real space) i0_real_error1.7720e+07
Rg (reciprocal space) rg_reciprocal51.33
I(0) (reciprocal space) i0_reciprocal948600000.0000
Solution quality estimate total_estimate0.8614
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary61.1
Skewness Skewness skewness0.340
Kurtosis Kurtosis kurtosis-0.494
Angular range angular_range— – 0.1550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha78850000.0000
Real-space data points n_real_points32
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.903; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.947; Smooth: 0.538

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

8. Citations (1)

9. Files and Curves (10)