Summary: CD20-like family
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This is the Wikipedia entry entitled "CD20-like family". More...
CD20-like family Edit Wikipedia article
| CD20-like family | |||||||||
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crystal structure of rituximab fab in complex with an epitope peptide |
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| Identifiers | |||||||||
| Symbol | CD20 | ||||||||
| Pfam | PF04103 | ||||||||
| Pfam clan | CL0347 | ||||||||
| InterPro | IPR007237 | ||||||||
| TCDB | 1.A.37 | ||||||||
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In molecular biology, the CD20-like family of proteins includes the CD20 protein and the beta subunit of the high affinity receptor for IgE Fc, MS4A2. MS4A2 has a tetrameric structure consisting of a single IgE-binding alpha subunit, a single beta subunit, and two disulfide-linked gamma subunits. It has four putative transmembrane segments and a probable topology where both amino- and carboxy termini protrude into the cytoplasm.[1] This family also includes LR8 like proteins from humans (TMEM176B), mice and rats. The function of the human LR8 protein is unknown although it is known to be strongly expressed in the lung fibroblasts.[2] This family also includes sarcospan, a transmembrane component of dystrophin-associated glycoprotein. Loss of the sarcoglycan complex and sarcospan alone is sufficient to cause muscular dystrophy. The role of the sarcoglycan complex and sarcospan is thought to be to strengthen the dystrophin axis connecting the basement membrane with the cytoskeleton.[3]
[edit] References
- ^ Hupp K, Siwarski D, Mock BA, Kinet JP (December 1989). "Gene mapping of the three subunits of the high affinity FcR for IgE to mouse chromosomes 1 and 19". J. Immunol. 143 (11): 3787–91. PMID 2531187.
- ^ Lurton J, Rose TM, Raghu G, Narayanan AS (February 1999). "Isolation of a gene product expressed by a subpopulation of human lung fibroblasts by differential display". Am. J. Respir. Cell Mol. Biol. 20 (2): 327–31. PMID 9922225.
- ^ Araishi K, Sasaoka T, Imamura M, Noguchi S, Hama H, Wakabayashi E, Yoshida M, Hori T, Ozawa E (September 1999). "Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice". Hum. Mol. Genet. 8 (9): 1589–98. doi:10.1093/hmg/8.9.1589. PMID 10441321.
This article incorporates text from the public domain Pfam and InterPro IPR007237
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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.
CD20-like family Provide feedback
This family includes the CD20 protein and the beta subunit of the high affinity receptor for IgE Fc. The high affinity receptor for IgE is a tetrameric structure consisting of a single IgE-binding alpha subunit, a single beta subunit, and two disulfide-linked gamma subunits. The alpha subunit of Fc epsilon RI and most Fc receptors are homologous members of the Ig superfamily. By contrast, the beta and gamma subunits from Fc epsilon RI are not homologous to the Ig superfamily. Both molecules have four putative transmembrane segments and a probably topology where both amino- and carboxy termini protrude into the cytoplasm [1]. This family also includes LR8 like proteins from humans, mice and rats. The function of the human LR8 protein is unknown although it is known to be strongly expressed in the lung fibroblasts [2]. This family also includes sarcospan is a transmembrane component of dystrophin-associated glycoprotein. Loss of the sarcoglycan complex and sarcospan alone is sufficient to cause muscular dystrophy. The role of the sarcoglycan complex and sarcospan is thought to be to strengthen the dystrophin axis connecting the basement membrane with the cytoskeleton [3].
Literature references
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Hupp K, Siwarski D, Mock BA, Kinet JP; , J Immunol 1989;143:3787-3791.: Gene mapping of the three subunits of the high affinity FcR for IgE to mouse chromosomes 1 and 19. PUBMED:2531187 EPMC:2531187
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Lurton J, Rose TM, Raghu G, Narayanan AS; , Am J Respir Cell Mol Biol 1999;20:327-331.: Isolation of a gene product expressed by a subpopulation of human lung fibroblasts by differential display. PUBMED:9922225 EPMC:9922225
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Araishi K, Sasaoka T, Imamura M, Noguchi S, Hama H, Wakabayashi E, Yoshida M, Hori T, Ozawa E; , Hum Mol Genet. 1999;8:1589-1598.: Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice. PUBMED:10441321 EPMC:10441321
External database links
| PANDIT: | PF04103 |
| Pseudofam: | PF04103 |
| SYSTERS: | CD20 |
| Transporter classification: | 1.A.37 |
This tab holds annotation information from the InterPro database.
InterPro entry IPR007237
This family includes the CD20 protein and the beta subunit of the high affinity receptor for IgE Fc. The high affinity receptor for IgE is a tetrameric structure consisting of a single IgE-binding alpha subunit, a single beta subunit, and two disulphide-linked gamma subunits. The alpha subunit of Fc epsilon RI and most Fc receptors are homologous members of the Ig superfamily. By contrast, the beta and gamma subunits from Fc epsilon RI are not homologous to the Ig superfamily. Both molecules have four putative transmembrane segments and a probably topology where both amino- and carboxy termini protrude into the cytoplasm [PUBMED:2531187]. This family also includes LR8 like proteins from humans, mice and rats. The function of the human LR8 protein is unknown although it is known to be strongly expressed in the lung fibroblasts [PUBMED:9922225]. This family also includes sarcospan is a transmembrane component of dystrophin-associated glycoprotein. Loss of the sarcoglycan complex and sarcospan alone is sufficient to cause muscular dystrophy. The role of the sarcoglycan complex and sarcospan is thought to be to strengthen the dystrophin axis connecting the basement membrane with the cytoskeleton [PUBMED:10441321].
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 (80) |
Full (1022) |
Representative proteomes | NCBI (1008) |
Meta (0) |
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| RP15 (125) |
RP35 (173) |
RP55 (258) |
RP75 (533) |
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| Jalview | ||||||||
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| PP/heatmap | 1 | |||||||
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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 (80) |
Full (1022) |
Representative proteomes | NCBI (1008) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (125) |
RP35 (173) |
RP55 (258) |
RP75 (533) |
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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: | Pfam-B_1979 (rel 7.3), Pfam-B_10092 (rel 9.0) |
| Previous IDs: | none |
| Type: | Family |
| Author: | Bateman A, Moxon SJ, Pollington J, Finn RD |
| Number in seed: | 80 |
| Number in full: | 1022 |
| Average length of the domain: | 133.70 aa |
| Average identity of full alignment: | 19 % |
| Average coverage of the sequence by the domain: | 47.50 % |
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: | 150 | ||||||||||||
| Family (HMM) version: | 10 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
Sunburst controls
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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 CD20 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