1ZKX: Botulinum neurotoxin type E

Crystal structure of Glu158Ala/Thr159Ala/Asn160Ala- a triple mutant of Clostridium botulinum neurotoxin E catalytic domain. Determined by X-ray diffraction at 2.52 Å resolution. Released 5 Jul 2005.

Method
X-ray diffraction
Resolution
2.52 Å
Organism
Clostridium botulinum
Chains
2
Atoms
6,548
Mol. weight
95.39 kDa
Ligands
ZN
Released
5 Jul 2005

Explore 1ZKX in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

1ZKX contains 40 α-helices and 44 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.

Chain A: 21 helices, 22 β-strands

ElementResiduesLengthSheet
α-helix2-43
α-helix11-122
β-strand17-2151
β-strand29-3571
β-strand38-4471
α-helix51-544
β-strand6812
α-helix76-9217
α-helix97-10711
α-helix110-1123
β-strand131-13441
β-strand140-14341
β-strand147-15151
β-strand15512
β-strand160-16341
α-helix167-1693
α-helix172-1743
α-helix1801
β-strand181-18441
β-strand189-19133
β-strand192-19434
β-strand200-20234
α-helix203-2042
α-helix205-22016
β-strand231-23225
β-strand246-24725
α-helix248-2547
α-helix256-2616
α-helix264-28623
α-helix293-2953
α-helix296-30510
β-strand308-31036
β-strand316-31836
α-helix320-33011
α-helix335-3428
β-strand356-35943
α-helix3601
β-strand36917
β-strand37317
α-helix377-38610
β-strand38714
β-strand395-39623
α-helix403-4064
Chain B: 19 helices, 22 β-strands
ElementResiduesLengthSheet
α-helix11-122
β-strand17-2158
β-strand29-3578
β-strand38-4478
α-helix76-9419
α-helix97-10812
α-helix110-1123
β-strand131-13448
β-strand140-14348
β-strand147-15158
β-strand160-16348
β-strand16619
α-helix167-1693
β-strand17019
α-helix172-1743
β-strand181-18448
β-strand189-194610
β-strand200-202310
α-helix203-2042
α-helix205-22016
β-strand231-232211
β-strand246-247211
α-helix248-2547
α-helix256-2583
α-helix264-28724
α-helix293-2953
α-helix297-3059
β-strand308-310312
β-strand316-318312
α-helix320-33011
α-helix335-3428
β-strand355-358410
β-strand359113
β-strand369114
β-strand373114
α-helix377-38610
β-strand387110
α-helix392-3943
β-strand395113
α-helix396-3972
α-helix401-4077

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
botulinum neurotoxin type EA, Bprotein420Clostridium botulinumQ00496 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>1ZKX_1 botulinum neurotoxin type E (chains A, B)
PKINSFNYNDPVNDRTILYIKPGGCQEFYKSFNIMKNIWIIPERNVIGTTPQDFHPPTSL
KNGDSSYYDPNYLQSDEEKDRFLKIVTKIFNRINNNLSGGILLEELSKANPYLGNDNTPD
NQFHIGDASAVEIKFSNGSQDILLPNVIIMGAEPDLFAAASSNISLRNNYMPSNHGFGSI
AIVTFSPEYSFRFNDNSMNEFIQDPALTLMHELIHSLHGLYGAKGITTKYTITQKQNPLI
TNIRGTNIEEFLTFGGTDLNIITSAQSNDIYTNLLADYKKIASKLSKVQVSNPLLNPYKD
VFEAKYGLDKDASGIYSVNINKFNDIFKKLYSFTEFDLATKFQVKCRQTYIGQYKYFKLS
NLLNDSIYNISEGYNINNLKVNFRGQNANLNPRIITPITGRGLVKKIIRFCKNIVSVKGI

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn2

Water and common crystallization additives (CL) are not listed.

Primary citation

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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