Summary: Endonuclease-reverse transcriptase
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This is the Wikipedia entry entitled "Endonuclease/Exonuclease/phosphatase family". More...
Endonuclease/Exonuclease/phosphatase family Edit Wikipedia article
| Endonuclease/Exonuclease/phosphatase family | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Structure of the multifunctional DNA-repair enzyme exonuclease III.[1] | |||||||||
| Identifiers | |||||||||
| Symbol | Exo_endo_phos | ||||||||
| Pfam | PF03372 | ||||||||
| InterPro | IPR005135 | ||||||||
| PROSITE | PDOC00598 | ||||||||
| SCOP | 1ako | ||||||||
| SUPERFAMILY | 1ako | ||||||||
| OPM superfamily | 148 | ||||||||
| OPM protein | 1zwx | ||||||||
| CDD | cd08372 | ||||||||
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Endonuclease/Exonuclease/phosphatase family is a structural domain found in the large family of proteins including magnesium dependent endonucleases and many phosphatases involved in intracellular signaling.[2]
Contents |
[edit] Examples
- AP endonuclease proteins EC 4.2.99.18,
- DNase I proteins EC 3.1.21.1,
- Synaptojanin, an inositol-1,4,5-trisphosphate phosphatase EC 3.1.3.56
- Sphingomyelinase EC 3.1.4.12 and Nocturnin O35710.
[edit] Subfamilies
- Inositol polyphosphate related phosphatase IPR000300
[edit] Human proteins containing this domain
2'-PDE; 2-PDE; ANGEL1; ANGEL2; APEX1; APEX2; CCRN4L; CNOT6; CNOT6L; DNASE1; DNASE1L1; DNASE1L2; DNASE1L3; INPP5A; INPP5B; INPP5D; INPP5E; INPPL1; KIAA1706; OCRL; PIB5PA; SKIP; SMPD2; SMPD3; SYNJ1; SYNJ2; TTRAP;
[edit] Notes
- ^ Mol CD, Kuo CF, Thayer MM, Cunningham RP, Tainer JA (March 1995). "Structure and function of the multifunctional DNA-repair enzyme exonuclease III". Nature 374 (6520): 381â6. doi:10.1038/374381a0. PMID 7885481.
- ^ Dlaki M (2000). "Functionally unrelated signalling proteins contain a fold similar to Mg2+-dependent endonucleases". Trends Biochem. Sci. 25 (6): 272â273. doi:10.1016/S0968-0004(00)01582-6. PMID 10838565.
[edit] References
- DlakiÄ M (June 2000). "Functionally unrelated signalling proteins contain a fold similar to Mg2+-dependent endonucleases". Trends Biochem. Sci. 25 (6): 272â3. doi:10.1016/S0968-0004(00)01582-6. PMID 10838565. http://linkinghub.elsevier.com/retrieve/pii/S0968-0004(00)01582-6.
- Mol CD, Kuo CF, Thayer MM, Cunningham RP, Tainer JA (March 1995). "Structure and function of the multifunctional DNA-repair enzyme exonuclease III". Nature 374 (6520): 381â6. doi:10.1038/374381a0. PMID 7885481.
- Lahm A, Suck D (December 1991). "DNase I-induced DNA conformation. 2 A structure of a DNase I-octamer complex". J. Mol. Biol. 222 (3): 645â67. doi:10.1016/0022-2836(91)90502-W. PMID 1748997. http://linkinghub.elsevier.com/retrieve/pii/0022-2836(91)90502-W.
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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.
Endonuclease-reverse transcriptase Provide feedback
This domain represents the endonuclease region of retrotransposons from a range of bacteria, archaea and eukaryotes. These are enzymes largely from class EC:2.7.7.49.
Literature references
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Mizrokhi LJ, Mazo AM;, Proc Natl Acad Sci U S A. 1990;87:9216-9220.: Evidence for horizontal transmission of the mobile element jockey between distant Drosophila species. PUBMED:1701254 EPMC:1701254
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Loreto EL, Carareto CM, Capy P;, Heredity. 2008;100:545-554.: Revisiting horizontal transfer of transposable elements in Drosophila. PUBMED:18431403 EPMC:18431403
Internal database links
| SCOOP: | DUF4544 |
| Similarity to PfamA using HHSearch: | Exo_endo_phos |
External database links
| PANDIT: | PF14529 |
| Pseudofam: | PF14529 |
| SYSTERS: | Exo_endo_phos_2 |
This tab holds annotation information from the InterPro database.
No InterPro data for this Pfam family.
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 DNase_I-like (CL0530), which contains the following 2 members:
Exo_endo_phos Exo_endo_phos_2Alignments
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 using the family HMM. We also generate alignments using four representative proteomes (RP) sets, the NCBI sequence database, and our metagenomics sequence database. More...
View options
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 (204) |
Full (2004) |
Representative proteomes | NCBI (5329) |
Meta (1737) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (649) |
RP35 (1047) |
RP55 (1503) |
RP75 (1603) |
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| Jalview | ||||||||
| HTML | ||||||||
| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
available,
not generated,
— not available.
Format an alignment
Download options
We make all of our alignments available in Stockholm format. You can download them here as raw, plain text files or as gzip-compressed files.
| Seed (204) |
Full (2004) |
Representative proteomes | NCBI (5329) |
Meta (1737) |
||||
|---|---|---|---|---|---|---|---|---|
| RP15 (649) |
RP35 (1047) |
RP55 (1503) |
RP75 (1603) |
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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
This family is new in this Pfam release.
| Seed source: | CATH:1wduB00 |
| Previous IDs: | none |
| Type: | Domain |
| Author: | Coggill P |
| Number in seed: | 204 |
| Number in full: | 2004 |
| Average length of the domain: | 121.10 aa |
| Average identity of full alignment: | 19 % |
| Average coverage of the sequence by the domain: | 18.41 % |
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: | 119 | ||||||||||||
| Family (HMM) version: | 1 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
Sunburst controls
ShowThis visualisation provides a simple graphical representation of the distribution of this family across species. You can find the original interactive tree in the adjacent tab. More...
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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 Exo_endo_phos_2 domain has been found. There are 3 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