Summary: Bacterial antitoxin of type II TA system, VapB
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This is the Wikipedia entry entitled "Toxin-antitoxin system". More...
Toxin-antitoxin system Edit Wikipedia article
A toxin-antitoxin system is a plasmid stabilisation mechanism found in many prokaryotes.[1] Chromosomal toxin-antitoxin systems also exist and serve to respond to stresses, cause cell cycle arrest and bring about programmed cell death.[2] The systems involve a toxic protein which is inhibited via either a non-coding RNA (type I toxin-antitoxin) or by another protein (type II toxin-antitoxin).
Type I toxin-antitoxin system
Type II toxin antitoxin system
See also
References
- ^ Fozo EM, Makarova KS, Shabalina SA, Yutin N, Koonin EV, Storz G (2010). "Abundance of type I toxin-antitoxin systems in bacteria: searches for new candidates and discovery of novel families". Nucleic Acids Res. 38 (11): 3743–59. doi:10.1093/nar/gkq054. PMC 2887945. PMID 20156992. Retrieved 2010-08-11.
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ignored (help)CS1 maint: multiple names: authors list (link) - ^ Hayes F (2003). "Toxins-antitoxins: plasmid maintenance, programmed cell death, and cell cycle arrest". Science. 301 (5639): 1496–9. doi:10.1126/science.1088157. PMID 12970556. Retrieved 2010-08-11.
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Further Reading
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.
Bacterial antitoxin of type II TA system, VapB Provide feedback
VapB is the antitoxin of a bacterial toxin-antitoxin gene pair. The cognate toxin is VapC, PF05016. The family contains several related antitoxins from Cyanobacteria and Actinobacterial families. Antitoxins of this class carry an N-terminal ribbon-helix-helix domain, RHH, that is highly conserved across all type II bacterial antitoxins, which dimerises with the RHH domain of a second VapB molecule. A hinge section follows the RHH, with an additional pair of flexible alpha helices at the C-terminus. This C-terminus is the Toxin-binding region of the dimer, and so is specific to the cognate toxin, whereas the RHH domain has the specific function of lying across the RNA-binding groove of the toxin dimer and inactivating the active-site - a more general function of all antitoxins.
Literature references
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Pandey DP, Gerdes K;, Nucleic Acids Res. 2005;33:966-976.: Toxin-antitoxin loci are highly abundant in free-living but lost from host-associated prokaryotes. PUBMED:15718296 EPMC:15718296
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Ramage HR, Connolly LE, Cox JS;, PLoS Genet. 2009;5:e1000767.: Comprehensive functional analysis of Mycobacterium tuberculosis toxin-antitoxin systems: implications for pathogenesis, stress responses, and evolution. PUBMED:20011113 EPMC:20011113
Internal database links
SCOOP: | PSK_trans_fac RHH_1 |
This tab holds annotation information from the InterPro database.
InterPro entry IPR019239
VapB is the antitoxin of a bacterial toxin-antitoxin gene pair. The cognate toxin is VapC ( INTERPRO ). The family contains several related antitoxins from Cyanobacteria and Actinobacterial families. Antitoxins of this class carry an N-terminal ribbon-helix-helix domain, RHH, that is highly conserved across all type II bacterial antitoxins, which dimerises with the RHH domain of a second VapB molecule. A hinge section follows the RHH, with an additional pair of flexible alpha helices at the C terminus. This C terminus is the Toxin-binding region of the dimer, and so is specific to the cognate toxin, whereas the RHH domain has the specific function of lying across the RNA-binding groove of the toxin dimer and inactivating the active-site - a more general function of all antitoxins [ PUBMED:15718296 , PUBMED:20011113 ].
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
This family is a member of clan Met_repress (CL0057), which has the following description:
This superfamily contains many antitoxin families, all of which carry a ribbon-helix-helix DNA-binding motif with the beta-ribbon located in and recognising the major groove of operator DNA [1].
The clan contains the following 43 members:
Arc BrnA_antitoxin CcdA CopG_antitoxin DndE DUF1778 DUF1902 DUF2540 DUF2610 DUF6290 DUF6364 HicB HicB-like_2 HicB_lk_antitox MatP_C MetJ MobC MobC_2 Omega_Repress ParB_C ParD ParD_antitoxin ParD_like ParG Plasmid_stab_B PSK_trans_fac RelB RepB-RCR_reg Repressor_Mnt RHH_1 RHH_3 RHH_4 RHH_5 RHH_6 RHH_7 RHH_8 RHH_9 SeqA_N TraY VAPB_antitox VapB_antitoxin VirC2 VirD1Alignments
We store a range of different sequence alignments for families. As well as the seed alignment from which the family is built, we provide the full alignment, generated by searching the sequence database (reference proteomes) using the family HMM. We also generate alignments using four representative proteomes (RP) sets and the UniProtKB sequence database. More...
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We make a range of alignments for each Pfam-A family. You can see a description of each above. You can view these alignments in various ways but please note that some types of alignment are never generated while others may not be available for all families, most commonly because the alignments are too large to handle.
Seed (27) |
Full (1601) |
Representative proteomes | UniProt (7886) |
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RP15 (208) |
RP35 (776) |
RP55 (1743) |
RP75 (2954) |
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PP/heatmap | 1 |
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
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not generated,
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Seed (27) |
Full (1601) |
Representative proteomes | UniProt (7886) |
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RP15 (208) |
RP35 (776) |
RP55 (1743) |
RP75 (2954) |
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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.
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: | COGs (COG5450) |
Previous IDs: | DUF2191; VapB; |
Type: | Domain |
Sequence Ontology: | SO:0000417 |
Author: |
COGs, Finn RD |
Number in seed: | 27 |
Number in full: | 1601 |
Average length of the domain: | 47.7 aa |
Average identity of full alignment: | 31 % |
Average coverage of the sequence by the domain: | 66.2 % |
HMM information
HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 61295632 -E 1000 --cpu 4 HMM pfamseq
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Model details: |
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Model length: | 47 | ||||||||||||
Family (HMM) version: | 12 | ||||||||||||
Download: | download the raw HMM for this family |
Species distribution
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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 VapB_antitoxin domain has been found. There are 8 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 sequence.
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AlphaFold Structure Predictions
The list of proteins below match this family and have AlphaFold predicted structures. Click on the protein accession to view the predicted structure.