9e3h

Cryo EM structure of pertussis toxin in complex with neutralizing Fab PERT-61

Method: ELECTRON MICROSCOPY Dmax: 133.1 Å Quality: GOOD

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

Pertussis toxin subunit 1

Bordetella pertussis

UniProt T1SR96

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 × 10 PDB declaration: decameric(10) Consistent with protein copy count Chain A; UniProt 1–269 Not recorded Pertussis toxin subunit 3 × 1 (P04979) Pertussis toxin subunit 4 × 2 (P0A3R5) Pertussis toxin subunit 5 × 1 (P04981) Islet-activating protein S2 × 1 (A0A0E8DFW5) PERT-61 HC × 2 PERT-61 LC × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 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.

4 other PDB entries and 4 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name T1SR96_BORPT
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–269; UniProt 1–269

Pertussis toxin subunit 3

Bordetella pertussis

UniProt P04979

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 × 10 PDB declaration: decameric(10) Consistent with protein copy count Chain C; UniProt 1–227 Not recorded Pertussis toxin subunit 1 × 1 (T1SR96) Pertussis toxin subunit 4 × 2 (P0A3R5) Pertussis toxin subunit 5 × 1 (P04981) Islet-activating protein S2 × 1 (A0A0E8DFW5) PERT-61 HC × 2 PERT-61 LC × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 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.

7 other PDB entries and 10 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TOX3_BORPE
Isoform
PDB entities 2
Chains and sequence ranges Author chain C; PDBConstruct 1–227; UniProt 1–227

Pertussis toxin subunit 4

Bordetella pertussis

UniProt P0A3R5

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 × 10 PDB declaration: decameric(10) Consistent with protein copy count Chain D; UniProt 1–152 Chain E; UniProt 1–152 Not recorded Pertussis toxin subunit 1 × 1 (T1SR96) Pertussis toxin subunit 3 × 1 (P04979) Pertussis toxin subunit 5 × 1 (P04981) Islet-activating protein S2 × 1 (A0A0E8DFW5) PERT-61 HC × 2 PERT-61 LC × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 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.

6 other PDB entries and 8 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TOX4_BORPE
Isoform
PDB entities 3
Chains and sequence ranges Author chain D; PDBConstruct 1–152; UniProt 1–152 Author chain E; PDBConstruct 1–152; UniProt 1–152

Pertussis toxin subunit 5

Bordetella pertussis

UniProt P04981

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 × 10 PDB declaration: decameric(10) Consistent with protein copy count Chain F; UniProt 1–133 Not recorded Pertussis toxin subunit 1 × 1 (T1SR96) Pertussis toxin subunit 3 × 1 (P04979) Pertussis toxin subunit 4 × 2 (P0A3R5) Islet-activating protein S2 × 1 (A0A0E8DFW5) PERT-61 HC × 2 PERT-61 LC × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 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.

7 other PDB entries and 10 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TOX5_BORPE
Isoform
PDB entities 4
Chains and sequence ranges Author chain F; PDBConstruct 1–133; UniProt 1–133

Islet-activating protein S2

Bordetella pertussis

UniProt A0A0E8DFW5

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 × 10 PDB declaration: decameric(10) Consistent with protein copy count Chain B; UniProt 1–226 Not recorded Pertussis toxin subunit 1 × 1 (T1SR96) Pertussis toxin subunit 3 × 1 (P04979) Pertussis toxin subunit 4 × 2 (P0A3R5) Pertussis toxin subunit 5 × 1 (P04981) PERT-61 HC × 2 PERT-61 LC × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 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.

4 other PDB entries and 4 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A0A0E8DFW5_BORPT
Isoform
PDB entities 5
Chains and sequence ranges Author chain B; PDBConstruct 1–226; UniProt 1–226

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 9e3h

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9e3h
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9e3h
Deposition date deposition_date2024-10-23
Structure title titleCryo EM structure of pertussis toxin in complex with neutralizing Fab PERT-61
Keywords keywordsPTx, mAb, Whooping, TOXIN, TOXIN-Immune System complex; TOXIN/Immune System
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier38.03
Radius of gyration Rg (electron density) rg_electron38.01
Forward intensity I(0) i0331196000.00
Molecular weight molecular_weight146830.0 kDa
Excluded volume excluded_volume183390 ų
Envelope volume envelope_volume235820 ų
Hydration-shell volume shell_volume53460 ų
Envelope diameter envelope_diameter145.1
Shell Rg shell_rg42.16
Envelope Rg envelope_rg38.03
Shape Rg shape_rg38.01
Total Rg total_rg38.27
Total atoms total_atoms10311
Residues n_residues1326
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 dmax133.1
Rg (real space) rg_real38.17
Rg uncertainty (real space) rg_real_error1.36
I(0) (real space) i0_real3.3120e+08
I(0) uncertainty (real space) i0_real_error6.5510e+06
Rg (reciprocal space) rg_reciprocal38.08
I(0) (reciprocal space) i0_reciprocal331200000.0000
Solution quality estimate total_estimate0.8568
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary44.4
Skewness Skewness skewness0.491
Kurtosis Kurtosis kurtosis0.043
Angular range angular_range— – 0.2100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha40900000.0000
Real-space data points n_real_points43
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.774; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.990; Smooth: 0.823

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)