Summary: Bacterial HORMA domain 2
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Bacterial HORMA domain 2 Provide feedback
Family of bacterial HORMA domains found in conserved genome contexts with Pch2/TRIP13 P-loop NTPases. Acts as a 'third component' in broad class of conflict systems reliant on the production of second messenger nucleotide or nucleotide derivatives. Together with Pch2/TRIP13, could act as co-effectors or in regulation of other effectors of the systems [1]. This domain found in bacterial proteins from the cyclic-oligonucleotide-based anti-phage signalling system (CBASS), such us CD-NTase-associated protein 7 from P. aeruginosa (Cap7), which is part of the type III-CBASS. CBSSs are a family of defence systems against bacteriophages [2,3].
Literature references
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Burroughs AM, Zhang D, Schaffer DE, Iyer LM, Aravind L;, Nucleic Acids Res. 2015;43:10633-10654.: Comparative genomic analyses reveal a vast, novel network of nucleotide-centric systems in biological conflicts, immunity and signaling. PUBMED:26590262 EPMC:26590262
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Millman A, Melamed S, Amitai G, Sorek R;, Nat Microbiol. 2020;5:1608-1615.: Diversity and classification of cyclic-oligonucleotide-based anti-phage signalling systems. PUBMED:32839535 EPMC:32839535
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Ye Q, Lau RK, Mathews IT, Birkholz EA, Watrous JD, Azimi CS, Pogliano J, Jain M, Corbett KD;, Mol Cell. 2020;77:709-722.: HORMA Domain Proteins and a Trip13-like ATPase Regulate Bacterial cGAS-like Enzymes to Mediate Bacteriophage Immunity. PUBMED:31932165 EPMC:31932165
Internal database links
SCOOP: | HORMA |
This tab holds annotation information from the InterPro database.
InterPro entry IPR040649
This entry represents the HORMA domain found in bacterial proteins from the cyclic-oligonucleotide-based anti-phage signalling system (CBASS), such us CD-NTase-associated protein 7 from Pseudomonas aeruginosa (Cap7, also known as Bacterial HORMA2 sensor protein), which is part of the type III-CBASS. CBSSs are a family of defence systems against bacteriophages which are ancestry related with the cGASâSTING innate immune pathway in animals. CBASSs are composed of an oligonucleotide cyclase, which generates signalling cyclic oligonucleotides in response to phage infection, and an effector that is activated by the cyclic oligonucleotides and promotes cell death [ PUBMED:32839535 , PUBMED:31932165 ]. Cap7 is essential for phage defence and it is the sensor protein in the type III-CBASS. It binds to a closure peptide (consensus Glu-Val-Met-Glu-Phe-Asn-Pro), and forms the CdnD:Cap7:Cap8 complex, which allows it to activate the oligonucleotide cyclase CdnD for second messenger synthesis. The oligonucleotide cyclase becomes active only when physically bound by the HORMA-domain protein [ PUBMED:32839535 ].
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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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 (5) |
Full (53) |
Representative proteomes | UniProt (220) |
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RP15 (7) |
RP35 (23) |
RP55 (54) |
RP75 (96) |
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PP/heatmap | 1 |
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
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Seed (5) |
Full (53) |
Representative proteomes | UniProt (220) |
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RP15 (7) |
RP35 (23) |
RP55 (54) |
RP75 (96) |
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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.
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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: | Laks |
Previous IDs: | none |
Type: | Domain |
Sequence Ontology: | SO:0000417 |
Author: |
Iyer LM |
Number in seed: | 5 |
Number in full: | 53 |
Average length of the domain: | 165.7 aa |
Average identity of full alignment: | 48 % |
Average coverage of the sequence by the domain: | 98.78 % |
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: | 166 | ||||||||||||
Family (HMM) version: | 4 | ||||||||||||
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 bacHORMA_2 domain has been found. There are 9 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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