Summary: Tetraspanin family
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Tetraspanin Edit Wikipedia article
| Tetraspanin family | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Tetraspanins have four transmembrane domains, two extracellular loops and contain a series of highly conserved amino acid residues. | |||||||||
| Identifiers | |||||||||
| Symbol | Tetraspanin | ||||||||
| Pfam | PF00335 | ||||||||
| Pfam clan | CL0347 | ||||||||
| InterPro | IPR000301 | ||||||||
| PROSITE | PDOC00371 | ||||||||
| SCOP | 1iv5 | ||||||||
| SUPERFAMILY | 1iv5 | ||||||||
| CDD | cd03127 | ||||||||
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Tetraspanins are a family of membrane proteins found in all multicellular eukaryotes.
Tetraspanins, also called tetraspans or the transmembrane 4 superfamily (TM4SF), have four transmembrane domains, intracellular N- and C-termini and two extracellular domains, one short (called the small extracellular domain or loop, SED/SEL or EC1) and one longer, typically 100 amino acid residues (the large extracellular domain/loop, LED/LEL or EC2). Although several protein families have four transmembrane domains, tetraspanins are defined by conserved domains listed in the Protein Families database under pfam00335.12.[1] The key features are four or more cysteine residues in the EC2 domain, with two in a highly conserved 'CCG' motif.
Research into this field is relatively recent (less than 20 years) and therefore there is much to learn about the function of specific tetraspanins. Generally, tetraspanins are often thought to act as scaffolding proteins, anchoring multiple proteins to one area of the cell membrane.[2]
Tetraspanins are highly conserved between species. Some tetraspanins can have N-linked glycosylations on the long extracellular loop (LEL, EC2) and palmitoylations at a CXXC motif in their transmembrane region.[3]
There are 34 tetraspanins in mammals, 33 of which have also been identified in humans. Tetraspanins display numerous properties that indicate their physiological importance in cell adhesion, motility, activation and proliferation, as well as their contribution to pathological conditions such as metastasis or viral infection.
A role for tetraspanins in platelets was demonstrated by the bleeding phenotypes of CD151- and TSSC6-deficient mice, which exhibit impaired "outside-in" signalling through αIIbβ3, the major platelet integrin. it is hypothesized that tetraspanins interact with and regulate other platelet receptors.[4]
Contents |
[edit] List of human tetraspanins
| Protein | Gene | Aliases |
|---|---|---|
| TSPAN1 | TSPAN1 | TSP-1 |
| TSPAN2 | TSPAN2 | TSP-2 |
| TSPAN3 | TSPAN3 | TSP-3 |
| TSPAN4 | TSPAN4 | TSP-4, NAG-2 |
| TSPAN5 | TSPAN5 | TSP-5 |
| TSPAN6 | TSPAN6 | TSP-6 |
| TSPAN7 | TSPAN5 | CD231/TALLA-1/A15 |
| TSPAN8 | TSPAN8 | CO-029 |
| TSPAN9 | TSPAN9 | NET-5 |
| TSPAN10 | TSPAN10 | OCULOSPANIN |
| TSPAN11 | TSPAN11 | CD151-like |
| TSPAN12 | TSPAN12 | NET-2 |
| TSPAN13 | TSPAN13 | NET-6 |
| TSPAN14 | TSPAN14 | |
| TSPAN15 | TSPAN15 | NET-7 |
| TSPAN16 | TSPAN16 | TM4-B |
| TSPAN17 | TSPAN17 | |
| TSPAN18 | TSPAN18 | |
| TSPAN19 | TSPAN19 | |
| TSPAN20 | UPK1B | UP1b, UPK1B |
| TSPAN21 | TSPAN21 | UP1a, UPK1A |
| TSPAN22 | PRPH2 | RDS, PRPH2 |
| TSPAN23 | TSPAN23 | ROM1 |
| TSPAN24 | CD151 | CD151 |
| TSPAN25 | CD53 | CD53 |
| TSPAN26 | CD37 | CD37 |
| TSPAN27 | CD82 | CD82 |
| TSPAN28 | CD81 | CD81 |
| TSPAN29 | CD9 | CD9 |
| TSPAN30 | CD63 | CD63 |
| TSPAN31 | TSPAN31 | SAS |
| TSPAN32 | TSPAN32 | TSSC6 |
| TSPAN33 | TSPAN33 | |
| TSPAN34 | TSPAN34 |
[edit] See also
[edit] Relevance to parasite vaccines
The schistosome worms make two tetraspanins: TSP-1 and TSP-2. TSP-2 antibodies are found in some people who seem to have immunity to schistosome infection (Schistosomiasis).[5]
[edit] External links
[edit] References
- ^ Pfam
- ^ Hemler ME (2005). "Tetraspanin functions and associated microdomains". Nat. Rev. Mol. Cell Biol. 6 (10): 801â11. doi:10.1038/nrm1736. PMID 16314869.
- ^ Wright MD, Tomlinson MG (1994). "The ins and outs of the transmembrane 4 superfamily". Immunol. Today 15 (12): 588â94. doi:10.1016/0167-5699(94)90222-4. PMID 7531445.
- ^ Goschnick MW, Lau LM, Wee JL, Liu YS, Hogarth PM, Robb LM, Hickey MJ, Wright MD, Jackson DE (2006). "Impaired "outside-in" integrin alphaIIbbeta3 signaling and thrombus stability in TSSC6-deficient mice". Blood 108 (6): 1911â8. doi:10.1182/blood-2006-02-004267. PMID 16720835.
- ^ Scientific American May 2008, referring to McManus & Loukas Clinical Microbiology reviews V21,N1,p225-242 (Jan 2008)
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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.
Tetraspanin family Provide feedback
No Pfam abstract.
External database links
| PANDIT: | PF00335 |
| PROSITE: | PDOC00371 PDOC00719 |
| Pseudofam: | PF00335 |
| SCOP: | 1iv5 |
| SYSTERS: | Tetraspannin |
This tab holds annotation information from the InterPro database.
InterPro entry IPR018499
Tetraspanins are a distinct family of proteins, containing four transmembrane domains: a small outer loop (EC1), a larger outer loop (EC2), a small inner loop (IL) and short cytoplasmic tails. They contain characteristic structural features, including 4-6 conserved extracellular cysteine residues, and polar residues within transmembrane domains. A fundamental role of tetraspanins appears to be organizing other proteins into a network of multimolecular membrane microdomains, sometimes called the `tetraspanin web'.
This entry represents tetraspanin proteins. It also recognises a number of peripherins. These are related retinal-specific memebers of the tetraspanin family which are located at the rims of the photoreceptor disks, where they may act jointly in disk morphogenesis [PUBMED:1610568].
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Cellular component | integral to membrane (GO:0016021) |
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 Tetraspannin (CL0347), which contains the following 3 members:
CD20 DUF4064 TetraspanninAlignments
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 (212) |
Full (4340) |
Representative proteomes | NCBI (3981) |
Meta (12) |
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| RP15 (761) |
RP35 (1047) |
RP55 (1771) |
RP75 (2488) |
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| Jalview | ||||||||
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| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
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not generated,
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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 (212) |
Full (4340) |
Representative proteomes | NCBI (3981) |
Meta (12) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (761) |
RP35 (1047) |
RP55 (1771) |
RP75 (2488) |
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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: | Bateman A & Pfam-B_3109 (Release 7.5) |
| Previous IDs: | transmembrane4; |
| Type: | Family |
| Author: | Bateman A, Finn RD |
| Number in seed: | 212 |
| Number in full: | 4340 |
| Average length of the domain: | 207.50 aa |
| Average identity of full alignment: | 17 % |
| Average coverage of the sequence by the domain: | 82.23 % |
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: | 221 | ||||||||||||
| Family (HMM) version: | 15 | ||||||||||||
| 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 Tetraspannin domain has been found. There are 4 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