Crystal structure of Glu335Gln mutant of Clostridium botulinum neurotoxin E catalytic domain. Determined by X-ray diffraction at 2.6 Å resolution. Released 5 Jul 2005.
Explore 1ZL5 in 3D Show helices and sheets RCSB PDB PDBe
1ZL5 contains 38 α-helices and 45 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 | 2-4 | 3 | |
| α-helix | 11-12 | 2 | |
| β-strand | 17-21 | 5 | 1 |
| β-strand | 29-35 | 7 | 1 |
| β-strand | 38-41 | 4 | 1 |
| α-helix | 51-54 | 4 | |
| β-strand | 68 | 1 | 2 |
| α-helix | 76-93 | 18 | |
| α-helix | 97-108 | 12 | |
| α-helix | 110-112 | 3 | |
| β-strand | 131-134 | 4 | 1 |
| β-strand | 140-143 | 4 | 1 |
| β-strand | 147-150 | 4 | 1 |
| β-strand | 155 | 1 | 2 |
| β-strand | 160-163 | 4 | 1 |
| β-strand | 166 | 1 | 3 |
| β-strand | 170 | 1 | 3 |
| α-helix | 172-174 | 3 | |
| β-strand | 181-184 | 4 | 1 |
| β-strand | 189-194 | 6 | 4 |
| β-strand | 200-202 | 3 | 4 |
| α-helix | 205-220 | 16 | |
| α-helix | 224-227 | 4 | |
| β-strand | 231-232 | 2 | 5 |
| β-strand | 246-247 | 2 | 5 |
| α-helix | 248-254 | 7 | |
| α-helix | 256-259 | 4 | |
| α-helix | 264-285 | 22 | |
| α-helix | 293-295 | 3 | |
| α-helix | 296-305 | 10 | |
| β-strand | 308-310 | 3 | 6 |
| β-strand | 316-318 | 3 | 6 |
| α-helix | 320-331 | 12 | |
| α-helix | 335-342 | 8 | |
| β-strand | 355-359 | 5 | 4 |
| β-strand | 369 | 1 | 7 |
| β-strand | 373 | 1 | 7 |
| α-helix | 377-383 | 7 | |
| β-strand | 387 | 1 | 4 |
| α-helix | 392-394 | 3 | |
| β-strand | 395-396 | 2 | 4 |
| α-helix | 403-406 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 2-4 | 3 | |
| α-helix | 11-12 | 2 | |
| β-strand | 17-21 | 5 | 8 |
| β-strand | 29-35 | 7 | 8 |
| β-strand | 38-44 | 7 | 8 |
| α-helix | 51-53 | 3 | |
| α-helix | 76-94 | 19 | |
| α-helix | 97-107 | 11 | |
| α-helix | 110-112 | 3 | |
| β-strand | 131-134 | 4 | 8 |
| β-strand | 140-143 | 4 | 8 |
| β-strand | 147-151 | 5 | 8 |
| β-strand | 160-163 | 4 | 8 |
| β-strand | 166 | 1 | 9 |
| β-strand | 170 | 1 | 9 |
| α-helix | 172-174 | 3 | |
| β-strand | 181-184 | 4 | 8 |
| β-strand | 189-194 | 6 | 10 |
| β-strand | 200-202 | 3 | 10 |
| α-helix | 203-204 | 2 | |
| α-helix | 205-220 | 16 | |
| β-strand | 231 | 1 | 11 |
| β-strand | 247 | 1 | 11 |
| α-helix | 248-254 | 7 | |
| α-helix | 256-259 | 4 | |
| α-helix | 264-287 | 24 | |
| α-helix | 293-295 | 3 | |
| α-helix | 297-305 | 9 | |
| β-strand | 308-310 | 3 | 12 |
| β-strand | 316-318 | 3 | 12 |
| α-helix | 320-332 | 13 | |
| α-helix | 335-342 | 8 | |
| β-strand | 355-358 | 4 | 10 |
| β-strand | 359 | 1 | 13 |
| β-strand | 369 | 1 | 14 |
| β-strand | 373 | 1 | 14 |
| α-helix | 377-380 | 4 | |
| β-strand | 387 | 1 | 10 |
| α-helix | 392-394 | 3 | |
| β-strand | 395 | 1 | 13 |
| α-helix | 401-407 | 7 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| botulinum neurotoxin type E | A, B | protein | 420 | Clostridium botulinum | Q00496 (AlphaFold model) |
>1ZL5_1 botulinum neurotoxin type E (chains A, B) PKINSFNYNDPVNDRTILYIKPGGCQEFYKSFNIMKNIWIIPERNVIGTTPQDFHPPTSL KNGDSSYYDPNYLQSDEEKDRFLKIVTKIFNRINNNLSGGILLEELSKANPYLGNDNTPD NQFHIGDASAVEIKFSNGSQDILLPNVIIMGAEPDLFETNSSNISLRNNYMPSNHGFGSI AIVTFSPEYSFRFNDNSMNEFIQDPALTLMHELIHSLHGLYGAKGITTKYTITQKQNPLI TNIRGTNIEEFLTFGGTDLNIITSAQSNDIYTNLLADYKKIASKLSKVQVSNPLLNPYKD VFEAKYGLDKDASGIYSVNINKFNDIFKKLYSFTQFDLATKFQVKCRQTYIGQYKYFKLS NLLNDSIYNISEGYNINNLKVNFRGQNANLNPRIITPITGRGLVKKIIRFCKNIVSVKGI
Analysis of Active Site Residues of Botulinum Neurotoxin E by Mutational, Functional, and Structural Studies: Glu335Gln Is an Apoenzyme. Agarwal, R., Binz, T., Swaminathan, S. Biochemistry (2005) 44:8291-8302. DOI 10.1021/bi050253a · PubMed
Other PDB entries of the same protein (UniProt Q00496 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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