4EL4: Botulinum neurotoxin A light chain

Crystal structure of the catalytic domain of botulinum neurotoxin BoNT/A C134S/C165S double mutant. Determined by X-ray diffraction at 1.2 Å resolution. Released 15 Aug 2012.

Method
X-ray diffraction
Resolution
1.2 Å
Organism
Clostridium botulinum
Chains
1
Atoms
4,195
Mol. weight
51.32 kDa
Ligands
ZN
Released
15 Aug 2012

Explore 4EL4 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4EL4 contains 18 α-helices and 25 β-strands across 1 chain. 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: 18 helices, 25 β-strands

ElementResiduesLengthSheet
α-helix13-142
β-strand19-2351
β-strand33-3971
β-strand42-4871
β-strand7312
α-helix81-9919
α-helix102-11312
α-helix115-1173
β-strand11913
β-strand126-12724
β-strand12813
α-helix131-1333
β-strand134-13851
β-strand144-14851
β-strand151-15551
β-strand15912
β-strand164-16631
β-strand184-18741
β-strand192-19655
α-helix200-2034
β-strand213-21425
α-helix215-2162
α-helix217-23216
β-strand242-24436
α-helix249-2535
β-strand257-25936
α-helix260-2667
α-helix268-2736
α-helix276-29924
β-strand302-30324
α-helix310-32112
β-strand324-32527
β-strand331-33227
α-helix335-3439
α-helix344-3485
α-helix351-3588
β-strand372-37545
β-strand38518
β-strand38918
α-helix402-4043
β-strand40515
α-helix410-4123
β-strand414-41855

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Botulinum neurotoxin A light chainAprotein445Clostridium botulinumP0DPI1 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>4EL4_1 Botulinum neurotoxin A light chain (chains A)
MGSSHHHHHHSSGLVPRGSHMPFVNKQFNYKDPVNGVDIAYIKIPNAGQMQPVKAFKIHN
KIWVIPERDTFTNPEEGDLNPPPEAKQVPVSYYDSTYLSTDNEKDNYLKGVTKLFERIYS
TDLGRMLLTSIVRGIPFWGGSTIDTELKVIDTNSINVIQPDGSYRSEELNLVIIGPSADI
IQFESKSFGHEVLNLTRNGYGSTQYIRFSPDFTFGFEESLEVDTNPLLGAGKFATDPAVT
LAHELIHAGHRLYGIAINPNRVFKVNTNAYYEMSGLEVSFEELRTFGGHDAKFIDSLQEN
EFRLYYYNKFKDIASTLNKAKSIVGTTASLQYMKNVFKEKYLLSEDTSGKFSVDKLKFDK
LYKMLTEIYTEDNFVKFFKVLNRKTYLNFDKAVFKINIVPKVNYTIYDGFNLRNTNLAAN
FNGQNTEINNMNFTKLKNFTGLFEF

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn1

Water and common crystallization additives (GOL, IMD, EDO) are not listed.

Primary citation

Structural Framework for Covalent Inhibition of Clostridium botulinum Neurotoxin A by Targeting Cys165. Stura, E.A., Le Roux, L., Guitot, K. et al. J Biol Chem (2012) 287:33607-33614. DOI 10.1074/jbc.M112.396697 · PubMed

Other PDB entries of the same protein (UniProt P0DPI1 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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