Pertussis toxin S1 subunit bound to BaAD. Determined by X-ray diffraction at 1.0 Å resolution. Released 13 Apr 2022.
Explore 7SNE in 3D Show helices and sheets RCSB PDB PDBe
7SNE contains 26 α-helices and 48 β-strands across 4 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 6-11 | 6 | 1 |
| α-helix | 15-21 | 7 | |
| β-strand | 23-24 | 2 | 2 |
| β-strand | 29 | 1 | 3 |
| α-helix | 32-36 | 5 | |
| β-strand | 48 | 1 | 3 |
| β-strand | 50-54 | 5 | 1 |
| α-helix | 57-76 | 20 | |
| β-strand | 84-92 | 9 | 1 |
| β-strand | 97-99 | 3 | 1 |
| α-helix | 100-111 | 12 | |
| β-strand | 129-133 | 5 | 1 |
| β-strand | 135-136 | 2 | 2 |
| α-helix | 138-140 | 3 | |
| β-strand | 141-149 | 9 | 1 |
| β-strand | 156-162 | 7 | 1 |
| β-strand | 174 | 1 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 2-4 | 3 | |
| β-strand | 6-11 | 6 | 4 |
| α-helix | 15-21 | 7 | |
| β-strand | 23-24 | 2 | 5 |
| β-strand | 29 | 1 | 6 |
| α-helix | 32-36 | 5 | |
| β-strand | 48 | 1 | 6 |
| β-strand | 50-54 | 5 | 4 |
| α-helix | 57-77 | 21 | |
| β-strand | 84-92 | 9 | 4 |
| β-strand | 97-99 | 3 | 4 |
| α-helix | 100-111 | 12 | |
| α-helix | 114-119 | 6 | |
| β-strand | 129-133 | 5 | 4 |
| β-strand | 135-136 | 2 | 5 |
| α-helix | 138-140 | 3 | |
| β-strand | 141-149 | 9 | 4 |
| β-strand | 156-162 | 7 | 4 |
| β-strand | 174 | 1 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 2-4 | 3 | |
| β-strand | 6-11 | 6 | 7 |
| α-helix | 15-21 | 7 | |
| β-strand | 23-24 | 2 | 8 |
| β-strand | 29 | 1 | 9 |
| α-helix | 32-36 | 5 | |
| β-strand | 48 | 1 | 9 |
| β-strand | 50-54 | 5 | 7 |
| α-helix | 57-76 | 20 | |
| β-strand | 84-92 | 9 | 7 |
| β-strand | 97-99 | 3 | 7 |
| α-helix | 100-111 | 12 | |
| α-helix | 114-116 | 3 | |
| β-strand | 129-133 | 5 | 7 |
| β-strand | 135-136 | 2 | 8 |
| α-helix | 138-140 | 3 | |
| β-strand | 141-149 | 9 | 7 |
| β-strand | 156-162 | 7 | 7 |
| β-strand | 174 | 1 | 7 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 2-4 | 3 | |
| β-strand | 6-11 | 6 | 10 |
| α-helix | 15-21 | 7 | |
| β-strand | 23-24 | 2 | 11 |
| β-strand | 29 | 1 | 12 |
| α-helix | 32-36 | 5 | |
| β-strand | 48 | 1 | 12 |
| β-strand | 50-54 | 5 | 10 |
| α-helix | 57-77 | 21 | |
| β-strand | 84-92 | 9 | 10 |
| β-strand | 97-99 | 3 | 10 |
| α-helix | 100-111 | 12 | |
| α-helix | 114-116 | 3 | |
| β-strand | 129-133 | 5 | 10 |
| β-strand | 135-136 | 2 | 11 |
| α-helix | 138-140 | 3 | |
| β-strand | 141-149 | 9 | 10 |
| β-strand | 156-162 | 7 | 10 |
| β-strand | 174 | 1 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Pertussis toxin subunit 1 | A, B, C, D | protein | 184 | Bordetella pertussis | P04977 (AlphaFold model) |
>7SNE_1 Pertussis toxin subunit 1 (chains A, B, C, D) GPGDPPATVYRYDSRPPEDVFQNGFTAWGNNDNVLEHLTGRSSQVGSSNSAFVSTSSSRR YTEVYLEHRMQEAVEAERAGRGTGHFIGYIYEVRADNNFYGAASSYFEYVDTYGDNAGRI LAGALATYQSEYLAHRRIPPENIRRVTRVYHNGITGETTTTEYSNARYVSQQTRANPNPY TSRR
| ID | Name | Formula | Copies |
|---|---|---|---|
| 9XR | [(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl… | C22 H29 N7 O14 P2 | 4 |
Crystal structures of pertussis toxin with NAD + and analogs provide structural insights into the mechanism of its cytosolic ADP-ribosylation activity. Sakari, M., Tran, M.T., Rossjohn, J. et al. J Biol Chem (2022) 298:101892-101892. DOI 10.1016/j.jbc.2022.101892 · PubMed
Other PDB entries of the same protein (UniProt P04977 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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