Summary: Telomere repeat binding factor (TRF)
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Telomere repeat binding factor (TRF) Provide feedback
Telomere repeat binding factor (TRF) family proteins are important for the regulation of telomere stability. The two related human TRF proteins hTRF1 and hTRF2 form homodimers and bind directly to telomeric TTAGGG repeats via the myb DNA binding domain PF00249 at the carboxy terminus [1]. TRF1 is implicated in telomere length regulation and TRF2 in telomere protection [1]. Other telomere complex associated proteins are recruited through their interaction with either TRF1 or TRF2. The fission yeast protein Taz1p (telomere-associated in Schizosaccharomyces pombe) has similarity to both hTRF1 and hTRF2 and may perform the dual functions of TRF1 and TRF2 at fission yeast telomeres [2]. This domain is composed of multiple alpha helices [3] arranged in a solenoid conformation similar to TPR repeats. The fungal members have now also been found to carry two double strand telomeric repeat binding factors [4].
Literature references
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Ye JZ, Donigian JR, van Overbeek M, Loayza D, Luo Y, Krutchinsky AN, Chait BT, de Lange T; , J Biol Chem 2004;279:47264-47271.: TIN2 binds TRF1 and TRF2 simultaneously and stabilizes the TRF2 complex on telomeres. PUBMED:15316005 EPMC:15316005
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Cooper JP, Nimmo ER, Allshire RC, Cech TR; , Nature 1997;385:744-747.: Regulation of telomere length and function by a Myb-domain protein in fission yeast. PUBMED:9034194 EPMC:9034194
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Fairall L, Chapman L, Moss H, de Lange T, Rhodes D; , Mol Cell 2001;8:351-361.: Structure of the TRFH dimerization domain of the human telomeric proteins TRF1 and TRF2. PUBMED:11545737 EPMC:11545737
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Pitt CW, Valente LP, Rhodes D, Simonsson T; , J Biol Chem. 2008;283:2693-2701.: Identification and characterization of an essential telomeric repeat binding factor in fission yeast. PUBMED:17977837 EPMC:17977837
External database links
| PANDIT: | PF08558 |
| Pseudofam: | PF08558 |
| SCOP: | 1h6p |
| SYSTERS: | TRF |
This tab holds annotation information from the InterPro database.
InterPro entry IPR013867
Telomeres function to shield chromosome ends from degradation and end-to-end fusions, as well as preventing the activation of DNA damage checkpoints. Telomeric repeat binding factor (TRF) proteins TRF1 and TRF2 are major components of vertebrate telomeres required for regulation of telomere stability. TRF1 and TRF2 bind to telomeric DNA as homodimers. Dimerisation involves the TRF homology (TRFH) subdomain contained within the dimerisation domain. The TRFH subdomain is important not only for dimerisation, but for DNA binding, telomere localisation, and interactions with other telomeric proteins. The dimerisation domains of TRF1 and TRF2 show the same multi-helical structure, arranged in a solenoid conformation similar to TPR repeats, which can be divided into an alpha-alpha superhelix and a long alpha hairpin [PUBMED:11545737].
The two related human TRF proteins hTRF1 and hTRF2 form homodimers and bind directly to telomeric TTAGGG repeats via the myb DNA binding domain INTERPRO at the carboxy terminus [PUBMED:15316005]. TRF1 is implicated in telomere length regulation and TRF2 in telomere protection [PUBMED:15316005]. Other telomere complex associated proteins are recruited through their interaction with either TRF1 or TRF2. The fission yeast protein Taz1p (telomere-associated in Schizosaccharomyces pombe (Fission yeast) has similarity to both hTRF1 and hTRF2 and may perform the dual functions of TRF1 and TRF2 at fission yeast telomeres [PUBMED:9034194].
This entry represents dimerisation domain.
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Molecular function | telomeric DNA binding (GO:0042162) |
| protein homodimerization activity (GO:0042803) |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Alignments
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| Seed (27) |
Full (262) |
Representative proteomes | NCBI (253) |
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| RP15 (15) |
RP35 (46) |
RP55 (92) |
RP75 (139) |
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| PP/heatmap | 1 | |||||||
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1Cannot generate PP/Heatmap alignments for seeds; no PP data available
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| Seed (27) |
Full (262) |
Representative proteomes | NCBI (253) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (15) |
RP35 (46) |
RP55 (92) |
RP75 (139) |
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| 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.
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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: | Pfam-B_8956 (release 18.0) |
| Previous IDs: | none |
| Type: | Domain |
| Author: | Daub J, Wood V |
| Number in seed: | 27 |
| Number in full: | 262 |
| Average length of the domain: | 216.50 aa |
| Average identity of full alignment: | 25 % |
| Average coverage of the sequence by the domain: | 37.59 % |
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: | 239 | ||||||||||||
| Family (HMM) version: | 5 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Interactions
There is 1 interaction for this family. More...
TRFStructures
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 TRF domain has been found. There are 11 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