7NA9: BoNT/B-LC-JSG-C1

Crystal structure of BoNT/B-LC-JSG-C1. Determined by X-ray diffraction at 1.76 Å resolution. Released 22 Dec 2021.

Method
X-ray diffraction
Resolution
1.76 Å
Organisms
Clostridium botulinum, Vicugna pacos
Chains
2
Atoms
5,173
Mol. weight
66.16 kDa
Ligands
ZN
Released
22 Dec 2021

Explore 7NA9 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7NA9 contains 28 α-helices and 38 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: 22 helices, 26 β-strands

ElementResiduesLengthSheet
α-helix13-142
β-strand19-2351
α-helix25-273
β-strand34-4071
β-strand43-4641
α-helix56-594
β-strand7412
α-helix82-10019
α-helix103-11412
α-helix116-1183
β-strand128-12923
β-strand137-14261
β-strand150-15561
β-strand158-16141
β-strand16612
β-strand171-17331
β-strand176-17724
β-strand180-18124
α-helix182-1843
β-strand191-19441
β-strand199-20025
β-strand202-20326
α-helix207-2093
α-helix214-2163
β-strand220-22126
α-helix224-23916
α-helix243-2453
β-strand248-24927
β-strand264-26527
α-helix266-2727
α-helix276-2794
α-helix282-30524
β-strand308-30923
α-helix317-32711
β-strand331-33228
β-strand338-33928
α-helix342-3509
α-helix351-3555
α-helix358-3658
β-strand381-38335
β-strand39319
β-strand39719
α-helix401-4033
α-helix407-4126
β-strand41316
α-helix418-4203
β-strand421-42225
α-helix426-43712
Chain D: 6 helices, 12 β-strands
ElementResiduesLengthSheet
α-helix-1-13
β-strand3-7510
β-strand11-13311
β-strand18-25810
β-strand34-39612
α-helix44-452
β-strand46-51612
β-strand58-60312
β-strand68-73610
α-helix74-763
β-strand78-83610
α-helix88-903
β-strand92-98712
α-helix107-1104
α-helix113-1153
β-strand118-119212
β-strand123-125312
β-strand126-128311

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Botulinum neurotoxin type BAprotein446Clostridium botulinumP10844 (AlphaFold model)
Jsg-C1Dprotein134Vicugna pacos
Sequence of entity 1 (A), FASTA
>7NA9_1 Botulinum neurotoxin type B (chains A)
GPLGSMPVTINNFNYNDPIDNNNIIMMEPPFARGTGRYYKAFKITDRIWIIPERYTFGYK
PEDFNKSSGIFNRDVCEYYDPDYLNTNDKKNIFLQTMIKLFNRIKSKPLGEKLLEMIING
IPYLGDRRVPLEEFNTNIASVTVNKLISNPGEVERKKGIFANLIIFGPGPVLNENETIDI
GIQNHFASREGFGGIMQMKFCPEYVSVFNNVQENKGASIFNRRGYFSDPALILMHELIHV
LHGLYGIKVDDLPIVPNEKKFFMQSTDAIQAEELYTFGGQDPSIITPSTDKSIYDKVLQN
FRGIVDRLNKVLVCISDPNININIYKNKFKDKYKFVEDSEGKYSIDVESFDKLYKSLMFG
FTETNIAENYKIKTRASYFSDSLPPVKIKNLLDNEIYTIEEGFNISDKDMEKEYRGQNKA
INKQAYEEISKEHLAVYKIQMCKSVK
Sequence of entity 2 (D), FASTA
>7NA9_2 JSG-C1 (chains D)
GPLGSQVQLVESGGGLVQTGGSLRLSCAASGRTFRRNTMGWFRQAPGKVREFVAAISWSG
DRTYCADSVKGRFTISRDNAKNTVDLLMNSLKPEDTAIYYCAADGTASVFNSYASADRNK
YNYWGQGTQVTVSS

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn1

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

Primary citation

Probing the structure and function of the protease domain of botulinum neurotoxins using single-domain antibodies. Lam, K.H., Tremblay, J.M., Perry, K. et al. PLoS Pathog (2022) 18:e1010169-e1010169. DOI 10.1371/journal.ppat.1010169 · PubMed

Other PDB entries of the same protein (UniProt P10844 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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