Streptococcal pyrogenic exotoxin A1. Determined by X-ray diffraction at 2.57 Å resolution. Released 24 Nov 1999.
Explore 1B1Z in 3D Show helices and sheets RCSB PDB PDBe
1B1Z contains 34 α-helices and 74 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 |
|---|---|---|---|
| α-helix | 6-8 | 3 | |
| α-helix | 10-11 | 2 | |
| α-helix | 12-14 | 3 | |
| α-helix | 19-26 | 8 | |
| α-helix | 28-29 | 2 | |
| β-strand | 30-36 | 7 | 1 |
| β-strand | 39 | 1 | 2 |
| β-strand | 45-48 | 4 | 2 |
| β-strand | 52 | 1 | 3 |
| β-strand | 55 | 1 | 3 |
| β-strand | 57-61 | 5 | 2 |
| α-helix | 65-71 | 7 | |
| β-strand | 75-80 | 6 | 1 |
| β-strand | 83 | 1 | 2 |
| β-strand | 96-100 | 5 | 2 |
| β-strand | 103-105 | 3 | 1 |
| β-strand | 110-123 | 14 | 4 |
| β-strand | 126-137 | 12 | 4 |
| β-strand | 139-141 | 3 | 5 |
| α-helix | 142-157 | 16 | |
| β-strand | 169-175 | 7 | 4 |
| β-strand | 182-185 | 4 | 4 |
| α-helix | 194-197 | 4 | |
| α-helix | 198-201 | 4 | |
| β-strand | 206-208 | 3 | 5 |
| β-strand | 213-219 | 7 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 6-8 | 3 | |
| α-helix | 10-11 | 2 | |
| α-helix | 12-14 | 3 | |
| α-helix | 19-26 | 8 | |
| α-helix | 28-29 | 2 | |
| β-strand | 30-35 | 6 | 6 |
| β-strand | 39 | 1 | 7 |
| β-strand | 45-48 | 4 | 7 |
| β-strand | 52 | 1 | 8 |
| β-strand | 55 | 1 | 8 |
| β-strand | 57-61 | 5 | 7 |
| α-helix | 65-71 | 7 | |
| β-strand | 76-80 | 5 | 6 |
| β-strand | 83 | 1 | 7 |
| β-strand | 96-100 | 5 | 7 |
| β-strand | 103-105 | 3 | 6 |
| β-strand | 110-123 | 14 | 9 |
| β-strand | 126-137 | 12 | 9 |
| β-strand | 139-141 | 3 | 10 |
| α-helix | 142-157 | 16 | |
| β-strand | 169-175 | 7 | 9 |
| β-strand | 182-185 | 4 | 9 |
| α-helix | 194-197 | 4 | |
| α-helix | 198-201 | 4 | |
| β-strand | 206-208 | 3 | 10 |
| β-strand | 213-219 | 7 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 6-8 | 3 | |
| α-helix | 10-11 | 2 | |
| α-helix | 12-14 | 3 | |
| α-helix | 19-26 | 8 | |
| α-helix | 28-29 | 2 | |
| β-strand | 30-36 | 7 | 11 |
| β-strand | 39 | 1 | 12 |
| β-strand | 45-48 | 4 | 12 |
| β-strand | 52 | 1 | 13 |
| β-strand | 55 | 1 | 13 |
| β-strand | 57-61 | 5 | 12 |
| α-helix | 65-71 | 7 | |
| β-strand | 75-80 | 6 | 11 |
| β-strand | 83 | 1 | 12 |
| β-strand | 96-100 | 5 | 12 |
| β-strand | 103-105 | 3 | 11 |
| β-strand | 110-123 | 14 | 14 |
| β-strand | 126-137 | 12 | 14 |
| β-strand | 139-141 | 3 | 15 |
| α-helix | 142-157 | 16 | |
| β-strand | 161 | 1 | 16 |
| β-strand | 163 | 1 | 16 |
| β-strand | 169-175 | 7 | 14 |
| α-helix | 180-181 | 2 | |
| β-strand | 182-185 | 4 | 14 |
| α-helix | 194-197 | 4 | |
| α-helix | 198-201 | 4 | |
| β-strand | 206-208 | 3 | 15 |
| β-strand | 213-219 | 7 | 14 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 12-14 | 3 | |
| α-helix | 19-26 | 8 | |
| β-strand | 30-36 | 7 | 17 |
| β-strand | 39 | 1 | 18 |
| β-strand | 45-48 | 4 | 18 |
| β-strand | 52 | 1 | 19 |
| β-strand | 55 | 1 | 19 |
| β-strand | 57-61 | 5 | 18 |
| α-helix | 65-71 | 7 | |
| β-strand | 75-80 | 6 | 17 |
| β-strand | 83 | 1 | 18 |
| β-strand | 96-100 | 5 | 18 |
| β-strand | 103-105 | 3 | 17 |
| β-strand | 110 | 1 | 20 |
| β-strand | 117-120 | 4 | 21 |
| β-strand | 123 | 1 | 21 |
| β-strand | 126 | 1 | 21 |
| β-strand | 130-133 | 4 | 21 |
| β-strand | 137 | 1 | 20 |
| β-strand | 139-141 | 3 | 22 |
| α-helix | 142-157 | 16 | |
| β-strand | 170-176 | 7 | 21 |
| β-strand | 182-185 | 4 | 21 |
| α-helix | 194-197 | 4 | |
| α-helix | 198-201 | 4 | |
| β-strand | 206-208 | 3 | 22 |
| β-strand | 212-218 | 7 | 21 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Protein (TOXIN) | A, B, C, D | protein | 219 | Streptococcus pyogenes | P0DJY7 (AlphaFold model) |
>1B1Z_1 PROTEIN (TOXIN) (chains A, B, C, D) DPDPSQLHRSSLVKNLQNIYFLYEGDPVTHENVKSVDQLLSHDLIYNVSGPNYDKLKTEL KNQEMATLFKDKNVDIYGVEYYHLCYLCENAERSACIYGGVTNHEGNHLEIPKKIVVKVS IDGIQSLSFDIETNKKMVTAQELDYKVRKYLTDNKQLYTNGPSKYETGYIKFIPKNKESF WFDFFPEPEFTQSKYLMIYKDNETLDSNTSQIEVYLTTK
Structural basis for the recognition of superantigen streptococcal pyrogenic exotoxin A (SpeA1) by MHC class II molecules and T-cell receptors. Papageorgiou, A.C., Collins, C.M., Gutman, D.M. et al. EMBO J (1999) 18:9-21. DOI 10.1093/emboj/18.1.9 · PubMed
Other PDB entries of the same protein (UniProt P0DJY7 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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