2  structures 3  species 0  interactions 3  sequences 1  architecture

Family: Toxin_30 (PF08117)

Summary

Ptu family Add an annotation

This family consists of toxic peptides that are isolated from the saliva of assassin bugs. The saliva contains a complex mixture of proteins that are used by the bug either to immobilise the prey or to digest it. One of the proteins (Ptu1) has been purified and shown to block reversibly the N-type calcium channels and to be less specific for the L- and P/Q- type calcium channels expressed in BHK cells [1].


Literature references

  1. Bernard C, Corzo G, Mosbah A, Nakajima T, Darbon H; , Biochemistry 2001;40:12795-12800.: Solution structure of Ptu1, a toxin from the assassin bug Peirates turpis that blocks the voltage-sensitive calcium channel N-type. PUBMED:11669615


InterPro entry IPR012325

Assassin bugs (Arthropoda:Insecta:Hemiptera:Reduviidae), sometimes known as conenoses or kissing bugs, are one of the largest and morphologically diverse families of true bugs feeding on crickets, caterpillars and other insects. Some assassin bug species are bloodsucking parasites of mammals, even of human. They can be commonly found throughout most of the world and their size varies from a few millimetres to as much as 3 or 4 centimetres. The toxic saliva of the predatory assassin bugs contains a complex mixture of small and large peptides for diverse uses such as immobilizing and pre-digesting their prey, and defence against competitors and predators. Assassin bug toxins are small peptides with disulphide connectivity that target ion-channels. They are relatively homologous to the calcium channel blockers omega-conotoxins from marine cone snails and belong to the four-loop cysteine scaffold structural class PUBMED:11423127, PUBMED:11669615.

One of these small proteins, Ptu1, blocks reversibly the N-type calcium channels, but at the same time is less specific for the L- or P/Q-type calcium channels PUBMED:11423127. Ptu1 is 34 amino acid residues long and is cross-linked by three disulphide bridges. Ptu1 contains a beta-sheet region made of two antiparallel beta-strands and consists of a compact disulphide-bonded core from which four loops emerge as well as N- and C-termini PUBMED:11669615. Some assassin bug toxins are listed below:

Clan

This family is a member of clan Omega_toxin (CL0083), which contains the following 16 members:

Albumin_I Conotoxin Mu-conotoxin Omega-toxin Toxin_11 Toxin_12 Toxin_16 Toxin_18 Toxin_21 Toxin_22 Toxin_24 Toxin_27 Toxin_30 Toxin_7 Toxin_9 UPF0506

Gene Ontology

External database links

Domain organisation

Below is a listing of the unique domain organisations or architectures in which this domain is found. More...

Loading domain graphics...

Alignments

There are various ways to view or download the sequence alignments that we store. You can use a sequence viewer to look at either the seed or full alignment for the family, or you can look at a plain text version of the sequence in a variety of different formats. More...

View options

Alignment:
Viewer:  

Formatting options

Alignment:
Format:
Order:
Sequence:
Gaps:
Download/view:

Download options

Very large alignments can often cause problems for the formatting tool above. If you find that downloading or viewing a large alignment is problematic, you can also download a gzip-compressed, Stockholm-format file containing the seed or full alignment for this family.

You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.

The main seed and full alignments are generated using sequences from the UniProt sequence database. However, we also generate alignments using sequences from the NCBI sequence database and the "metaseq" metagenomics dataset.

You can view alignments from these two additional datasets using the form above, or you can download alignments of NCBI or metagenomics sequences, as gzip-compressed files.

Pfam alignments:
Full length sequences

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 HMMER2.

Pfam alignments:

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. 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 or full alignments.

Note: You can also download the data files for the seed, full, NCBI or metagenomics trees.

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 View help on the curation process

Seed source: Short protein clustering
Previous IDs: none
Type: Family
Author: Lee SC
Number in seed: 2
Number in full: 3
Average length of the domain: 34.70 aa
Average identity of full alignment: 55 %
Average coverage of the sequence by the domain: 99.05 %

HMM information View help on HMM parameters

HMM build commands:
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 9421015 -E 1000 HMM pfamseq
Model details:
Parameter Sequence Domain
Gathering cut-off 24.5 24.5
Trusted cut-off 24.9 79.1
Noise cut-off 24.2 23.5
Model length: 35
Family (HMM) version: 4
Download: download the raw HMM for this family

Species distribution

Tree controls

Hide

The tree shows the occurrence of this domain across different species. More...

Loading...

Structures

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_30 domain has been found.

Loading structure mapping...