Summary: FHA domain
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This is the Wikipedia entry entitled "Forkhead-associated domain". More...
Forkhead-associated domain Edit Wikipedia article
| solution structure of the fha domain of human ubiquitin ligase protein rnf8 | |||||||||
| Identifiers | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Symbol | FHA | ||||||||
| Pfam | PF00498 | ||||||||
| Pfam clan | CL0357 | ||||||||
| InterPro | IPR000253 | ||||||||
| PROSITE | PDOC50006 | ||||||||
| SCOP | 1qu5 | ||||||||
| SUPERFAMILY | 1qu5 | ||||||||
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In molecular biology, the forkhead-associated domain (FHA domain) is a phosphopeptide recognition domain found in many regulatory proteins.[1] It displays specificity for phosphothreonine-containing epitopes but will also recognise phosphotyrosine with relatively high affinity. It spans approximately 80-100 amino acid residues folded into an 11-stranded beta sandwich, which sometimes contains small helical insertions between the loops connecting the strands.[2]
To date, genes encoding FHA-containing proteins have been identified in eubacterial and eukaryotic but not archaeal genomes. The domain is present in a diverse range of proteins, such as kinases, phosphatases, kinesins, transcription factors, RNA-binding proteins and metabolic enzymes which partake in many different cellular processes - DNA repair, signal transduction, vesicular transport and protein degradation are just a few examples.
[edit] References
- ^ Hofmann K, Bucher P (September 1995). "The FHA domain: a putative nuclear signalling domain found in protein kinases and transcription factors". Trends Biochem. Sci. 20 (9): 3479. DOI:10.1016/S0968-0004(00)89072-6. PMID 7482699.
- ^ Durocher D, Jackson SP (February 2002). "The FHA domain". FEBS Lett. 513 (1): 5866. DOI:10.1016/S0014-5793(01)03294-X. PMID 11911881.
[edit] External links
- Eukaryotic Linear Motif resource motif class LIG_FHA_1
- Eukaryotic Linear Motif resource motif class LIG_FHA_2
This article incorporates text from the public domain Pfam and InterPro IPR000253
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.
FHA domain Provide feedback
The FHA (Forkhead-associated) domain is a phosphopeptide binding motif [2].
Literature references
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Hofmann K, Bucher, P; , Trends Biochem Sci 1995;20:347-349.: The FHA domain: a putative nuclear signalling domain found in protein kinases and transcription factors. PUBMED:7482699 EPMC:7482699
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Durocher D, Henckel J, Fersht AR, Jackson SP; , Mol Cell. 1999;4:387-394.: The FHA domain is a modular phosphopeptide recognition motif. PUBMED:10518219 EPMC:10518219
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Pallen M, Chaudhuri R, Khan A; , Trends Microbiol 2002;10:556-563.: Bacterial FHA domains: neglected players in the phospho-threonine signalling game? PUBMED:12564991 EPMC:12564991
External database links
| HOMSTRAD: | FHA |
| PANDIT: | PF00498 |
| PROSITE: | PDOC50006 |
| Pseudofam: | PF00498 |
| SCOP: | 1qu5 |
| SYSTERS: | FHA |
This tab holds annotation information from the InterPro database.
InterPro entry IPR000253
The forkhead-associated (FHA) domain [PUBMED:7482699] is a phosphopeptide recognition domain found in many regulatory proteins. It displays specificity for phosphothreonine-containing epitopes but will also recognise phosphotyrosine with relatively high affinity. It spans approximately 80-100 amino acid residues folded into an 11-stranded beta sandwich, which sometimes contain small helical insertions between the loops connecting the strands [PUBMED:11911881].
To date, genes encoding FHA-containing proteins have been identified in eubacterial and eukaryotic but not archaeal genomes. The domain is present in a diverse range of proteins, such as kinases, phosphatases, kinesins, transcription factors, RNA-binding proteins and metabolic enzymes which partake in many different cellular processes - DNA repair, signal transduction, vesicular transport and protein degradation are just a few examples.
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Molecular function | protein binding (GO:0005515) |
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
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 (221) |
Full (10726) |
Representative proteomes | NCBI (10014) |
Meta (968) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (1945) |
RP35 (3258) |
RP55 (4503) |
RP75 (5327) |
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| Jalview | ||||||||
| HTML | ||||||||
| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
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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 (221) |
Full (10726) |
Representative proteomes | NCBI (10014) |
Meta (968) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (1945) |
RP35 (3258) |
RP55 (4503) |
RP75 (5327) |
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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
| Seed source: | Prosite |
| Previous IDs: | none |
| Type: | Family |
| Author: | Finn RD, Durocher D |
| Number in seed: | 221 |
| Number in full: | 10726 |
| Average length of the domain: | 70.70 aa |
| Average identity of full alignment: | 25 % |
| Average coverage of the sequence by the domain: | 13.00 % |
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: | 68 | ||||||||||||
| Family (HMM) version: | 21 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Interactions
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 FHA domain has been found. There are 93 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