Clostridium botulinum Neurotoxin Serotype A Light Chain, Residues 1-424. Determined by X-ray diffraction at 2.0 Å resolution. Released 5 Jun 2007.
Explore 2IMC in 3D Show helices and sheets RCSB PDB PDBe
2IMC contains 37 α-helices and 50 β-strands across 2 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 | 13-14 | 2 | |
| β-strand | 19-23 | 5 | 1 |
| β-strand | 33-39 | 7 | 1 |
| β-strand | 42-48 | 7 | 1 |
| α-helix | 54-56 | 3 | |
| α-helix | 60-63 | 4 | |
| β-strand | 73 | 1 | 2 |
| α-helix | 81-99 | 19 | |
| α-helix | 102-113 | 12 | |
| α-helix | 115-117 | 3 | |
| β-strand | 119 | 1 | 3 |
| β-strand | 126-127 | 2 | 4 |
| β-strand | 128 | 1 | 3 |
| α-helix | 131-133 | 3 | |
| β-strand | 134-138 | 5 | 1 |
| α-helix | 139 | 1 | |
| β-strand | 144-148 | 5 | 1 |
| β-strand | 151-155 | 5 | 1 |
| β-strand | 159 | 1 | 2 |
| β-strand | 164-166 | 3 | 1 |
| β-strand | 184-187 | 4 | 1 |
| β-strand | 192-194 | 3 | 5 |
| β-strand | 195-198 | 4 | 6 |
| β-strand | 211-214 | 4 | 6 |
| α-helix | 217-232 | 16 | |
| α-helix | 236-238 | 3 | |
| α-helix | 260-266 | 7 | |
| α-helix | 268-272 | 5 | |
| α-helix | 276-298 | 23 | |
| β-strand | 302-303 | 2 | 4 |
| α-helix | 310-321 | 12 | |
| β-strand | 324-325 | 2 | 7 |
| β-strand | 331-332 | 2 | 7 |
| α-helix | 335-343 | 9 | |
| α-helix | 344-348 | 5 | |
| α-helix | 351-358 | 8 | |
| α-helix | 368-370 | 3 | |
| β-strand | 373-375 | 3 | 5 |
| β-strand | 385 | 1 | 8 |
| β-strand | 389 | 1 | 8 |
| α-helix | 399-404 | 6 | |
| β-strand | 405 | 1 | 6 |
| α-helix | 410-412 | 3 | |
| β-strand | 414-417 | 4 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 19-23 | 5 | 9 |
| α-helix | 30-32 | 3 | |
| β-strand | 33-39 | 7 | 9 |
| β-strand | 42-48 | 7 | 9 |
| β-strand | 73 | 1 | 10 |
| α-helix | 81-99 | 19 | |
| α-helix | 102-113 | 12 | |
| α-helix | 115-117 | 3 | |
| β-strand | 119 | 1 | 11 |
| β-strand | 126-127 | 2 | 12 |
| β-strand | 128 | 1 | 11 |
| α-helix | 131-133 | 3 | |
| β-strand | 134-138 | 5 | 9 |
| α-helix | 139 | 1 | |
| β-strand | 144-148 | 5 | 9 |
| β-strand | 151-155 | 5 | 9 |
| β-strand | 159 | 1 | 10 |
| β-strand | 164-166 | 3 | 9 |
| β-strand | 184-187 | 4 | 9 |
| β-strand | 192-194 | 3 | 13 |
| β-strand | 195-197 | 3 | 14 |
| β-strand | 212-214 | 3 | 14 |
| α-helix | 217-232 | 16 | |
| α-helix | 236-238 | 3 | |
| β-strand | 242 | 1 | 15 |
| β-strand | 259 | 1 | 15 |
| α-helix | 260-266 | 7 | |
| α-helix | 268-273 | 6 | |
| α-helix | 276-298 | 23 | |
| β-strand | 302-303 | 2 | 12 |
| α-helix | 310-321 | 12 | |
| β-strand | 324-325 | 2 | 16 |
| β-strand | 331-332 | 2 | 16 |
| α-helix | 335-343 | 9 | |
| α-helix | 344-348 | 5 | |
| α-helix | 351-358 | 8 | |
| β-strand | 373-375 | 3 | 13 |
| β-strand | 385 | 1 | 17 |
| β-strand | 389 | 1 | 17 |
| α-helix | 402-404 | 3 | |
| β-strand | 405 | 1 | 14 |
| α-helix | 410-412 | 3 | |
| β-strand | 414-415 | 2 | 13 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Botulinum neurotoxin A light-chain | A, B | protein | 444 | Clostridium botulinum | P0DPI1 (AlphaFold model) |
>2IMC_1 Botulinum neurotoxin A light-chain (chains A, B) MGSSHHHHHHSSGLVPRGSHMQFVNKQFNYKDPVNGVDIAYIKIPNVGQMQPVKAFKIHN KIWVIPERDTFTNPEEGDLNPPPEAKQVPVSYYDSTYLSTDNEKDNYLKGVTKLFERIYS TDLGRMLLTSIVRGIPFWGGSTIDTELKVIDTNCINVIQPDGSYRSEELNLVIIGPSADI IQFECKSFGHEVLNLTRNGYGSTQYIRFSPDFTFGFEESLEVDTNPLLGAGKFATDPAVT LAHELIHAGHRLYGIAINPNRVFKVNTNAYYEMSGLEVSFEELRTFGGHDAKFIDSLQEN EFRLYYYNKFKDIASTLNKAKSIVGTTASLQYMKNVFKEKYLLSEDTSGKFSVDKLKFDK LYKMLTEIYTEDNFVKFFKVLNRKTYLNFDKAVFKINIVPKVNYTIYDGFNLRNTNLAAN FNGQNTEINNMNFTKLKNFTGLFE
| ID | Name | Formula | Copies |
|---|---|---|---|
| ZN | Zinc ion | Zn | 2 |
Structures of Clostridium botulinum Neurotoxin Serotype A Light Chain Complexed with Small-Molecule Inhibitors Highlight Active-Site Flexibility. Silvaggi, N.R., Boldt, G.E., Hixon, M.S. et al. Chem Biol (2007) 14:533-542. DOI 10.1016/j.chembiol.2007.03.014 · PubMed
Other PDB entries of the same protein (UniProt P0DPI1 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 2IMC directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.