1G9D: Clostridium botulinum neurotoxin B

Crystal structure of clostridium botulinum neurotoxin B complexed with an inhibitor (experiment 2). Determined by X-ray diffraction at 2.2 Å resolution. Released 13 Nov 2002.

Method
X-ray diffraction
Resolution
2.2 Å
Organism
Clostridium botulinum
Chains
1
Atoms
11,021
Mol. weight
151.63 kDa
Ligands
BAB, ZN
Released
13 Nov 2002

Explore 1G9D in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

1G9D contains 62 α-helices and 88 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: 62 helices, 88 β-strands

ElementResiduesLengthSheet
α-helix3-53
α-helix12-132
β-strand18-2251
α-helix24-263
β-strand33-3971
β-strand42-4431
α-helix55-584
β-strand63-6422
β-strand71-7223
β-strand7314
α-helix81-9818
α-helix102-11312
α-helix115-1173
β-strand12715
β-strand136-14051
α-helix1431
β-strand150-15451
β-strand157-16041
β-strand16514
β-strand170-17341
β-strand17516
β-strand18016
α-helix181-1833
β-strand190-19341
β-strand198-19927
β-strand201-20228
α-helix209-2113
β-strand219-22028
α-helix223-23816
β-strand24819
α-helix2491
β-strand250110
α-helix2511
β-strand257111
α-helix258-2592
β-strand26319
α-helix265-2717
α-helix275-2784
α-helix281-30424
β-strand30715
α-helix316-32611
β-strand330-331212
β-strand337-338212
α-helix341-3499
α-helix350-3545
α-helix357-3637
β-strand380-38237
β-strand392113
β-strand396113
α-helix400-4023
α-helix406-4116
β-strand41218
α-helix417-4193
β-strand420-42127
α-helix425-4273
β-strand428-42923
β-strand432-436514
β-strand445-449514
α-helix450-4523
β-strand454111
β-strand457110
α-helix459-4613
α-helix465-4673
β-strand470-472315
α-helix487-4915
α-helix501-5044
β-strand506-50721
α-helix508-5103
β-strand523-52422
β-strand526-530514
α-helix536-5416
β-strand553-555316
α-helix558-5636
β-strand567-569316
α-helix574-5818
α-helix586-60419
α-helix605-6084
β-strand609-611317
α-helix612-6143
β-strand616-619417
α-helix623-6275
α-helix638-6458
α-helix646-6494
α-helix662-6643
β-strand665-667315
α-helix668-6692
α-helix675-70228
α-helix703-7075
α-helix708-73831
α-helix742-7465
α-helix752-78534
α-helix787-81125
α-helix813-8164
α-helix822-8287
α-helix834-8374
α-helix839-8424
α-helix846-85712
α-helix859-8624
β-strand863-866418
β-strand867-869319
β-strand874-876319
β-strand883-886420
β-strand891-892218
β-strand897-900418
β-strand908-911420
β-strand925-932818
α-helix934-9374
α-helix938-9403
α-helix941-9466
β-strand948-956920
β-strand959-966820
β-strand969-975720
β-strand981-987720
β-strand1002-1008718
β-strand1012-1017618
β-strand1020-1026718
β-strand1038-1044720
β-strand1053-1061918
α-helix1064-10663
α-helix1067-107812
β-strand1082121
β-strand1084122
β-strand1090122
α-helix10911
β-strand1092-1093223
β-strand1096-1097224
β-strand1098-1101425
β-strand1107-1111524
β-strand1118-1122524
α-helix1123-11242
β-strand1125126
β-strand1136126
β-strand1144-1148524
β-strand1158-1159223
β-strand1161121
β-strand1165-1172824
β-strand1175-1180624
β-strand1181-1182227
β-strand1189-1191324
β-strand1193-1196424
β-strand1203-1204227
β-strand1207-1210424
β-strand1220125
β-strand1221-1225524
β-strand1233-12451324
β-strand1250-12591024
α-helix1261-12655
β-strand1279-1282425
β-strand1285128
β-strand1288128

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Botulinum neurotoxin type BAprotein1290Clostridium botulinumP10844 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>1G9D_1 BOTULINUM NEUROTOXIN TYPE B (chains A)
PVTINNFNYNDPIDNNNIIMMEPPFARGTGRYYKAFKITDRIWIIPERYTFGYKPEDFNK
SSGIFNRDVCEYYDPDYLNTNDKKNIFLQTMIKLFNRIKSKPLGEKLLEMIINGIPYLGD
RRVPLEEFNTNIASVTVNKLISNPGEVERKKGIFANLIIFGPGPVLNENETIDIGIQNHF
ASREGFGGIMQMKFCPEYVSVFNNVQENKGASIFNRRGYFSDPALILMHELIHVLHGLYG
IKVDDLPIVPNEKKFFMQSTDAIQAEELYTFGGQDPSIITPSTDKSIYDKVLQNFRGIVD
RLNKVLVCISDPNININIYKNKFKDKYKFVEDSEGKYSIDVESFDKLYKSLMFGFTETNI
AENYKIKTRASYFSDSLPPVKIKNLLDNEIYTIEEGFNISDKDMEKEYRGQNKAINKQAY
EEISKEHLAVYKIQMCKSVKAPGICIDVDNEDLFFIADKNSFSDDLSKNERIEYNTQSNY
IENDFPINELILDTDLISKIELPSENTESLTDFNVDVPVYEKQPAIKKIFTDENTIFQYL
YSQTFPLDIRDISLTSSFDDALLFSNKVYSFFSMDYIKTANKVVEAGLFAGWVKQIVNDF
VIEANKSNTMDKIADISLIVPYIGLALNVGNETAKGNFENAFEIAGASILLEFIPELLIP
VVGAFLLESYIDNKNKIIKTIDNALTKRNEKWSDMYGLIVAQWLSTVNTQFYTIKEGMYK
ALNYQAQALEEIIKYRYNIYSEKEKSNINIDFNDINSKLNEGINQAIDNINNFINGCSVS
YLMKKMIPLAVEKLLDFDNTLKKNLLNYIDENKLYLIGSAEYEKSKVNKYLKTIMPFDLS
IYTNDTILIEMFNKYNSEILNNIILNLRYKDNNLIDLSGYGAKVEVYDGVELNDKNQFKL
TSSANSKIRVTQNQNIIFNSVFLDFSVSFWIRIPKYKNDGIQNYIHNEYTIINCMKNNSG
WKISIRGNRIIWTLIDINGKTKSVFFEYNIREDISEYINRWFFVTITNNLNNAKIYINGK
LESNTDIKDIREVIANGEIIFKLDGDIDRTQFIWMKYFSIFNTELSQSNIEERYKIQSYS
EYLKDFWGNPLMYNKEYYMFNAGNKNSYIKLKKDSPVGEILTRSKYNQNSKYINYRDLYI
GEKFIIRRKSNSQSINDDIVRKEDYIYLDFFNLNQEWRVYTYKYFKKEEEKLFLAPISDS
DEFYNTIQIKEYDEQPTYSCQLLFKKDEESTDEIGLIGIHRFYESGIVFEEYKDYFCISK
WYLKEVKRKPYNLKLGCNWQFIPKDEGWTE

Ligands and cofactors

IDNameFormulaCopies
BABBIS(5-amidino-benzimidazolyl)methaneC17 H19 N82
ZNZinc ionZn2

Primary citation

A Novel Mechanism for Clostridium botulinum Neurotoxin Inhibition. Eswaramoorthy, S., Kumaran, D., Swaminathan, S. Biochemistry (2002) 41:9795-9802. DOI 10.1021/bi020060c · 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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