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PDBsum entry 3v0b

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protein metals Protein-protein interface(s) links
Toxin PDB id
3v0b

 

 

 

 

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Contents
Protein chains
1280 a.a.
1150 a.a.
Metals
_CA
_ZN
PDB id:
3v0b
Name: Toxin
Title: 3.9 angstrom crystal structure of bont/ai in complex with ntnha
Structure: Bont/a. Chain: a. Fragment: inactive full length bont/a1. Synonym: bont/a1, botulinum neurotoxin type a, neurotoxin a, neurotoxin bont. Engineered: yes. Mutation: yes. Ntnh. Chain: b.
Source: Clostridium botulinum. Organism_taxid: 1491. Gene: bont/a, bont/a, bonta. Expressed in: escherichia coli. Expression_system_taxid: 562. Gene: ant, ntnh. Expression_system_taxid: 562
Resolution:
3.90Å     R-factor:   0.253     R-free:   0.280
Authors: S.Gu,S.Rumpel,J.Zhou,J.Strotmeier,H.Bigalke,K.Perry,C.B.Shoemaker, A.Rummel,R.Jin
Key ref: S.Gu et al. (2012). Botulinum neurotoxin is shielded by NTNHA in an interlocked complex. Science, 335, 977-981. PubMed id: 22363010
Date:
07-Dec-11     Release date:   14-Mar-12    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
P0DPI1  (BXA1_CLOBH) -  Botulinum neurotoxin type A from Clostridium botulinum (strain Hall / ATCC 3502 / NCTC 13319 / Type A)
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1296 a.a.
1280 a.a.*
Protein chain
Pfam   ArchSchema ?
Q45914  (BXAN_CLOBO) -  Non-toxic nonhemagglutinin type A from Clostridium botulinum
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1193 a.a.
1150 a.a.
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 4 residue positions (black crosses)

 Enzyme reactions 
   Enzyme class: Chain A: E.C.3.4.24.69  - bontoxilysin.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: Limited hydrolysis of proteins of the neuroexocytosis apparatus, synaptobrevins, SNAP25 or syntaxin. No detected action on small molecule substrates.
      Cofactor: Zn(2+)

 

 
Science 335:977-981 (2012)
PubMed id: 22363010  
 
 
Botulinum neurotoxin is shielded by NTNHA in an interlocked complex.
S.Gu, S.Rumpel, J.Zhou, J.Strotmeier, H.Bigalke, K.Perry, C.B.Shoemaker, A.Rummel, R.Jin.
 
  ABSTRACT  
 
No abstract given.

 

 

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