Spider toxin

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search
Spider toxin
File:1IVA.pdb.png
Solution structure of omega-agatoxin-Aa4a from Agelenopsis aperta.[1]
Identifiers
SymbolToxin_9
PfamPF02819
Pfam clanCL0083
InterProIPR004169
SCOP21oav / SCOPe / SUPFAM
OPM superfamily112
OPM protein1agg
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
Delta Atracotoxin
Identifiers
SymbolAtracotoxin
PfamPF05353
InterProIPR008017
SCOP21qdp / SCOPe / SUPFAM
OPM protein1vtx
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
Spider toxin CSTX family
Identifiers
SymbolToxin_35
PfamPF10530
InterProIPR011142
PROSITEPDOC60029
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
Spider potassium channel inhibitory toxin
Identifiers
SymbolToxin_12
PfamPF07740
Pfam clanCL0083
InterProIPR011696
SCOP21d1h / SCOPe / SUPFAM
OPM superfamily112
OPM protein1qk6
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

Spider toxins are a family of proteins produced by spiders which function as neurotoxins. The mechanism of many spider toxins is through blockage of calcium channels.

A remotely related group of atracotoxins operate by opening sodium channels. Delta atracotoxin from the venom of the Sydney funnel-web spider produces potentially fatal neurotoxic symptoms in primates by slowing the inactivation of voltage-gated sodium channels.[2] The structure of atracotoxin comprises a core beta region containing a triple-stranded a thumb-like extension protruding from the beta region and a C-terminal helix. The beta region contains a cystine knot motif, a feature seen in other neurotoxic polypeptides[2] and other spider toxins, of the CSTX family.

Spider potassium channel inhibitory toxins is another group of spider toxins. A representative of this group is hanatoxin, a 35 amino acid peptide toxin which was isolated from Chilean rose tarantula (Grammostola rosea, syn. G. spatulata) venom. It inhibits the drk1 voltage-gated potassium channel by altering the energetics of gating.[3] See also Huwentoxin-1.[4]

See also

[edit | edit source]

References

[edit | edit source]
  1. ^ PDB: 1IVA​; Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  2. ^ a b Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  3. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  4. ^ InterProIPR013140

Further reading

[edit | edit source]
  • Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
This article incorporates text from the public domain Pfam and InterPro: IPR008017