Summary: Latrophilin/CL-1-like GPS domain
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Latrophilin/CL-1-like GPS domain Provide feedback
Domain present in latrophilin/CL-1, sea urchin REJ and polycystin.
Literature references
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Krasnoperov V, Bittner MA, Holz RW, Chepurny O, Petrenko AG; , J Biol Chem 1999;274:3590-3596.: Structural requirements for alpha-latrotoxin binding and alpha- latrotoxin-stimulated secretion. A study with calcium-independent receptor of alpha-latrotoxin (CIRL) deletion mutants. PUBMED:9920906 EPMC:9920906
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Sugita S, Ichtchenko K, Khvotchev M, Sudhof TC; , J Biol Chem 1998;273:32715-32724.: alpha-Latrotoxin receptor CIRL/latrophilin 1 (CL1) defines an unusual family of ubiquitous G-protein-linked receptors. G-protein coupling not required for triggering exocytosis. PUBMED:9830014 EPMC:9830014
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Ponting CP, Hofmann K, Bork P; , Curr Biol 1999;26:585-588.: A latrophilin/CL-1-like GPS domain in polycystin-1. PUBMED:10469603 EPMC:10469603
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Wei W, Hackmann K, Xu H, Germino G, Qian F; , J Biol Chem. 2007;282:21729-21737.: Characterization of cis-autoproteolysis of polycystin-1, the product of human polycystic kidney disease 1 gene. PUBMED:17525154 EPMC:17525154
External database links
| MEROPS: | T6 |
| PANDIT: | PF01825 |
| Pseudofam: | PF01825 |
| SMART: | GPS |
| SYSTERS: | GPS |
This tab holds annotation information from the InterPro database.
InterPro entry IPR000203
This domain has been termed the GPS domain (for GPCR proteolytic site), because it contains a cleavage site in SWISSPROT latrophilin [PUBMED:9920906]. However this region in latrophilin is found in many otherwise unrelated cell surface receptors [PUBMED:10469603]. There is no evidence currently that this domain provides a cleavage site in any of the other receptors. However the peptide bond that is cleaved in latrophilin is between Leu and Thr residues that are conserved in some of the other receptors [PUBMED:10469603].
GPS domains are about 50 residues long and contain either 2 or 4 cysteine residues that are likely to form disulphide bridges. Based on conservation of these cysteines the following pairing can be predicted.
+-----------------+
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+-----------------+---------------+ |
| | | |
XXXCXXXXXXXXXXXXXXXXXCXXXXXXXXXXXXXXXCXCXXLTXXXXXXX
^
cleavage site
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Cellular component | membrane (GO:0016020) |
| Biological process | neuropeptide signaling pathway (GO:0007218) |
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
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 (139) |
Full (2565) |
Representative proteomes | NCBI (2317) |
Meta (28) |
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| RP15 (524) |
RP35 (628) |
RP55 (925) |
RP75 (1472) |
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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:
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 (139) |
Full (2565) |
Representative proteomes | NCBI (2317) |
Meta (28) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (524) |
RP35 (628) |
RP55 (925) |
RP75 (1472) |
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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: | SMART |
| Previous IDs: | none |
| Type: | Family |
| Author: | Bateman A |
| Number in seed: | 139 |
| Number in full: | 2565 |
| Average length of the domain: | 46.70 aa |
| Average identity of full alignment: | 35 % |
| Average coverage of the sequence by the domain: | 3.56 % |
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: | 44 | ||||||||||||
| Family (HMM) version: | 16 | ||||||||||||
| 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 GPS 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