Summary: Scorpion toxin-like domain
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This is the Wikipedia entry entitled "Scorpion toxin". More...
Scorpion toxin Edit Wikipedia article
| Scorpion long-chain toxin | |||||||||
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| Crystal structure of toxin II from the scorpion Androctonus australis Hector.[1] | |||||||||
| Identifiers | |||||||||
| Symbol | Toxin_3 | ||||||||
| Pfam | PF00537 | ||||||||
| InterPro | IPR002061 | ||||||||
| SCOP | 2sn3 | ||||||||
| SUPERFAMILY | 2sn3 | ||||||||
| OPM superfamily | 61 | ||||||||
| OPM protein | 1djt | ||||||||
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| Scorpion short toxin | |||||||||
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| Agitoxin-2. Disulphide bonds are highlighted. PDB 1agt [2] | |||||||||
| Identifiers | |||||||||
| Symbol | Toxin_2 | ||||||||
| Pfam | PF00451 | ||||||||
| Pfam clan | CL0054 | ||||||||
| InterPro | IPR001947 | ||||||||
| PROSITE | PDOC00875 | ||||||||
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Scorpion toxins are proteins found in the venom of scorpions. Their toxic effect may be mammal or insect specific, and acts by binding to sodium channels, inhibiting the inactivation of activated channels and blocking neuronal transmission.
The family includes related short- and long-chain scorpion toxins. It also contains a group of proteinase inhibitors from the plants Arabidopsis thaliana and Brassica spp.
The Brassica napus (Oil seed rape) and Sinapis alba (White mustard) inhibitors,[3][4] inhibit the catalytic activity of bovine beta-trypsin and bovine alpha-chymotrypsin, which belong to MEROPS peptidase family S1 (IPR001254).[5]
This group of proteins is now used in the creation of insecticides, vaccines, and protein engineering scaffolds.
Contents |
[edit] Structure
The complete covalent structure of several such toxins has been deduced: They comprise around 66 amino acid residues forming a three stranded anti-parallel beta sheet over which lies an alpha helix of approximately three turns. Four disulfide bridges cross-link the structure of the long-chain toxins whereas the short toxins contain only three.[6][7] BmKAEP, an anti-epilepsy peptide isolated from the venom of the Manchurian scorpion,[8] shows similarity to both scorpion neurotoxins and anti-insect toxins.
[edit] Function
The toxin's molecular function is to inhibit ion channels. Scorpion toxins are used in insecticides, vaccines, and protein engineering scaffolds. The toxins are now used to treat cancer patients by injecting fluorescent scorpion toxin into cancerous tissue to show tumor boundaries. Scorpion toxin genes are also used to kill insect pests by creating hypervirulent fungus in the insect through gene insertion.
[edit] Subfamilies
[edit] References
- ^ PDB 1PTX; Housset D, Habersetzer-Rochat C, Astier JP, Fontecilla-Camps JC (April 1994). "Crystal structure of toxin II from the scorpion Androctonus australis Hector refined at 1.3 A resolution". J. Mol. Biol. 238 (1): 88â103. doi:10.1006/jmbi.1994.1270. PMID 8145259.
- ^ Krezel, A. M.; Kasibhatla, C.; Hidalgo, P.; MacKinnon, R.; Wagner, G. (1995). "Solution structure of the potassium channel inhibitor agitoxin 2: Caliper for probing channel geometry". Protein Science 4 (8): 1478â1489. doi:10.1002/pro.5560040805. PMC 2143198. PMID 8520473. //www.ncbi.nlm.nih.gov/pmc/articles/PMC2143198/.
- ^ Ronchi S, Ceciliani F, Ascenzi P, Bortolotti F, Menegatti E, Palmieri S (1994). "Purification, inhibitory properties, amino acid sequence and identification of the reactive site of a new serine proteinase inhibitor from oil-rape (Brassica napus) seed". FEBS Lett. 342 (2): 221â224. doi:10.1016/0014-5793(94)80505-9. PMID 8143882.
- ^ Bolognesi M, Ronchi S, Tedeschi G, Ascenzi P, Bortolotti F, Menegatti E, Palmieri S, Thomas RM (1992). "Purification, inhibitory properties and amino acid sequence of a new serine proteinase inhibitor from white mustard (Sinapis alba L.) seed". FEBS Lett. 301 (1): 10â14. doi:10.1016/0014-5793(92)80199-Q. PMID 1451776.
- ^ Rawlings ND, Barrett AJ, Tolle DP (2004). "Evolutionary families of peptidase inhibitors". Biochem. J. 378 (Pt 3): 705â16. doi:10.1042/BJ20031825. PMC 1224039. PMID 14705960. //www.ncbi.nlm.nih.gov/pmc/articles/PMC1224039/.
- ^ Granier C, Kopeyan C, Rochat H, Mansuelle P, Sampieri F, Brando T, Bahraoui EM (1990). "Primary structure of scorpion anti-insect toxins isolated from the venom of Leiurus quinquestriatus quinquestriatus". FEBS Lett. 261 (2): 423â426. doi:10.1016/0014-5793(90)80607-K. PMID 2311768.
- ^ Rochat H, Gregoire J (1983). "Covalent structure of toxins I and II from the scorpion Buthus occitanus tunetanus". Toxicon 21 (1): 153â162. doi:10.1016/0041-0101(83)90058-2. PMID 6845379.
- ^ Zhou XH, Yang D, Zhang JH, Liu CM, Lei KJ (1989). "Purification and N-terminal partial sequence of anti-epilepsy peptide from venom of the scorpion Buthus martensii Karsch". Biochem. J. 257 (2): 509â517. PMC 1135608. PMID 2930463. //www.ncbi.nlm.nih.gov/pmc/articles/PMC1135608/.
[edit] External links
This article incorporates text from the public domain Pfam and InterPro IPR002061
This page is based on a Wikipedia article. The text is available under the Creative Commons Attribution/Share-Alike License.
This tab holds the annotation information that is stored in the Pfam database. As we move to using Wikipedia as our main source of annotation, the contents of this tab will be gradually replaced by the Wikipedia tab.
Scorpion toxin-like domain Provide feedback
This family contains both neurotoxins and plant defensins. The mustard trypsin inhibitor, MTI-2, is plant defensin. It is a potent inhibitor of trypsin with no activity towards chymotrypsin. MTI-2 is toxic for Lepidopteran insects, but has low activity against aphids [1]. Brazzein is plant defensin-like protein. It is pH-stable, heat-stable and intensely sweet protein [2]. The scorpion toxin (a neurotoxin) binds to sodium channels and inhibits the activation mechanisms of the channels, thereby blocking neuronal transmission. Scorpion toxins bind to sodium channels and inhibit the activation mechanisms of the channels, thereby blocking neuronal transmission
Literature references
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Ceci LR, Volpicella M, Rahbe Y, Gallerani R, Beekwilder J, Jongsma MA; , Plant J 2003;33:557-566.: Selection by phage display of a variant mustard trypsin inhibitor toxic against aphids. PUBMED:12581313 EPMC:12581313
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Assadi-Porter FM, Aceti DJ, Markley JL; , Arch Biochem Biophys 2000;376:259-265.: Sweetness determinant sites of brazzein, a small, heat-stable, sweet-tasting protein. PUBMED:10775411 EPMC:10775411
External database links
| HOMSTRAD: | scorptoxin |
| PANDIT: | PF00537 |
| Pseudofam: | PF00537 |
| SCOP: | 2sn3 |
| SYSTERS: | Toxin_3 |
This tab holds annotation information from the InterPro database.
InterPro entry IPR002061
This family contains both neurotoxins and plant defensins. The mustard trypsin inhibitor, MTI-2, is a plant defensin. It is a potent inhibitor of trypsin with no activity towards chymotrypsin. MTI-2 is toxic for Lepidopteran insects, but has low activity against aphids [PUBMED:2581313]. Brazzein is a plant defensin-like protein. It is pH-stable, heat-stable and intensely sweet protein [PUBMED:10775411]. The scorpion toxin (a neurotoxin) binds to sodium channels and inhibits the activation mechanisms of the channels, thereby blocking neuronal transmission.
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Cellular component | extracellular region (GO:0005576) |
| Molecular function | ion channel inhibitor activity (GO:0008200) |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Pfam Clan
Alignments
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| Seed (33) |
Full (487) |
Representative proteomes | NCBI (598) |
Meta (0) |
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| RP15 (7) |
RP35 (7) |
RP55 (7) |
RP75 (15) |
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| Jalview | ||||||||
| HTML | ||||||||
| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
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| Seed (33) |
Full (487) |
Representative proteomes | NCBI (598) |
Meta (0) |
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| RP15 (7) |
RP35 (7) |
RP55 (7) |
RP75 (15) |
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| Raw Stockholm | ||||||||
| Gzipped | ||||||||
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
External links
MyHits provides a collection of tools to handle multiple sequence alignments. For example, one can refine a seed alignment (sequence addition or removal, re-alignment or manual edition) and then search databases for remote homologs using HMMER3.
HMM logo
HMM logos is one way of visualising profile HMMs. Logos provide a quick overview of the properties of an HMM in a graphical form. You can see a more detailed description of HMM logos and find out how you can interpret them here. More...
Trees
This page displays the phylogenetic tree for this family's seed alignment. We use FastTree to calculate neighbour join trees with a local bootstrap based on 100 resamples (shown next to the tree nodes). FastTree calculates approximately-maximum-likelihood phylogenetic trees from our seed alignment.
Note: You can also download the data file for the tree.
Curation and family details
This section shows the detailed information about the Pfam family. You can see the definitions of many of the terms in this section in the glossary and a fuller explanation of the scoring system that we use in the scores section of the help pages.
Curation
| Seed source: | Pfam-B_8170 (release 8.0) |
| Previous IDs: | toxin_3; |
| Type: | Domain |
| Author: | Bateman A, Moxon SJ, Finn RD |
| Number in seed: | 33 |
| Number in full: | 487 |
| Average length of the domain: | 53.00 aa |
| Average identity of full alignment: | 38 % |
| Average coverage of the sequence by the domain: | 69.05 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
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| Model details: |
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| Model length: | 54 | ||||||||||||
| Family (HMM) version: | 13 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Interactions
There is 1 interaction for this family. More...
Toxin_3Structures
For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the PDBe group, to allow us to map Pfam domains onto UniProt sequences and three-dimensional protein structures. The table below shows the structures on which the Toxin_3 domain has been found. There are 78 instances of this domain found in the PDB. Note that there may be multiple copies of the domain in a single PDB structure, since many structures contain multiple copies of the same protein seqence.
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Archea
Eukaryota
Bacteria
Other sequences
Viruses
Unclassified
Viroids
Unclassified sequence