Summary: Cache domain
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Cache domain Edit Wikipedia article
Cache domain | |||||||||
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Identifiers | |||||||||
Symbol | Cache_1 | ||||||||
Pfam | PF02743 | ||||||||
Pfam clan | CL0165 | ||||||||
InterPro | IPR004010 | ||||||||
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Cache domain (type 2) | |||||||||
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Identifiers | |||||||||
Symbol | Cache_2 | ||||||||
Pfam | PF08269 | ||||||||
Pfam clan | CL0165 | ||||||||
InterPro | IPR013163 | ||||||||
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In molecular biology, the cache domain is an extracellular protein domain that is predicted to have a role in small-molecule recognition in a wide range of proteins, including the animal dihydropyridine-sensitive voltage-gated Ca2+ channel alpha-2delta subunit, and various bacterial chemotaxis receptors. The name Cache comes from CAlcium channels and CHEmotaxis receptors. This domain consists of an N-terminal part with three predicted strands and an alpha-helix, and a C-terminal part with a strand dyad followed by a relatively unstructured region. The N-terminal portion of the (unpermuted) Cache domain contains three predicted strands that could form a sheet analogous to that present in the core of the PAS domain structure. Cache domains are particularly widespread in bacteria such as Vibrio cholerae. The animal calcium channel alpha-2delta subunits might have acquired a part of their extracellular domains from a bacterial source.[1] The Cache domain appears to have arisen from the GAF-PAS fold despite their divergent functions.[2]
References
- ^ Anantharaman V, Aravind L (November 2000). "Cache - a signaling domain common to animal Ca(2+)-channel subunits and a class of prokaryotic chemotaxis receptors". Trends Biochem. Sci. 25 (11): 535–7. doi:10.1016/s0968-0004(00)01672-8. PMID 11084361.
- ^ Anantharaman V, Koonin EV, Aravind L (April 2001). "Regulatory potential, phyletic distribution and evolution of ancient, intracellular small-molecule-binding domains". J. Mol. Biol. 307 (5): 1271–92. doi:10.1006/jmbi.2001.4508. PMID 11292341.
This article incorporates text from the public domain Pfam and InterPro IPR004010
This article incorporates text from the public domain Pfam and InterPro IPR013163
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.
Cache domain Provide feedback
Double Cache domain 2 (dCache_2) may be a result of single Cache domain 2 (sCache_2) duplication [2].
Literature references
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Anantharaman V, Aravind L; , Trends Biochem Sci 2000;25:535-537.: Cache - a signaling domain common to animal Ca(2+)-channel subunits and a class of prokaryotic chemotaxis receptors. PUBMED:11084361 EPMC:11084361
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Upadhyay AA, Fleetwood AD, Adebali O, Finn RD, Zhulin IB;, PLoS Comput Biol. 2016;12:e1004862.: Cache Domains That are Homologous to, but Different from PAS Domains Comprise the Largest Superfamily of Extracellular Sensors in Prokaryotes. PUBMED:27049771 EPMC:27049771
Internal database links
SCOOP: | Cache_3-Cache_2 dCache_1 HAMP sCache_2 sCache_3_2 sCache_3_3 |
Similarity to PfamA using HHSearch: | dCache_1 sCache_2 sCache_2 Cache_3-Cache_2 Cache_3-Cache_2 |
This tab holds annotation information from the InterPro database.
InterPro entry IPR004010
Cache is an extracellular domain that is predicted to have a role in small-molecule recognition in a wide range of proteins, including the animal dihydropyridine-sensitive voltage-gated Ca2 channel alpha-2delta subunit, and various bacterial chemotaxis receptors. The name Cache comes from CAlcium channels and CHEmotaxis receptors.
The Cache domain, also known as the extracellular PAS domain, consists of an N-terminal part with three predicted strands and an alpha-helix, and a C-terminal part with a strand dyad followed by a relatively unstructured region. The N-terminal portion of the Cache domain containing the three predicted strands could form a sheet analogous to that present in the core of the PAS domain structure. Cache domains are particularly widespread in bacteria, such as Vibrio cholerae. The animal calcium channel alpha-2delta subunits might have acquired a part of their extracellular domains from a bacterial source [ PUBMED:11084361 ]. The Cache domain appears to have arisen from the GAF-PAS fold, despite their divergent functions [ PUBMED:11292341 , PUBMED:27049771 ].
This entry represents the double Cache domain 2 (dCache_2), which may be a result of single Cache domain 2 (sCache_2) duplication [ PUBMED:27049771 ].
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 Cache (CL0165), which has the following description:
The Cache domain an extracellular domain that is thought to have a role in small-molecule recognition in a wide range of proteins, including the animal Ca(2+)-channel subunits and a class of prokaryotic chemotaxis receptors [1]. It is homologous to, but sufficiently different from the most common intracellular sensor module, the PAS domain. Furthermore, it is suggested that it might have originated from a simpler intracellular PAS/GAF ancestor as a benefit of extracellular sensing [2].
The clan contains the following 25 members:
2CSK_N ArlS_N Cache_3-Cache_2 CHASE CHASE4 CHASE7 CHASE8 dCache_1 dCache_2 dCache_3 Diacid_rec DUF4153 DUF4173 GAPES1 LuxQ-periplasm PhoQ_Sensor sCache_2 sCache_3_2 sCache_3_3 sCache_4 sCache_like SMP_2 Stimulus_sens_1 VGCC_alpha2 YkuI_CAlignments
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Seed (38) |
Full (1333) |
Representative proteomes | UniProt (6564) |
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RP15 (231) |
RP35 (717) |
RP55 (1382) |
RP75 (2425) |
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HTML | |||||||
PP/heatmap | 1 |
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
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Seed (38) |
Full (1333) |
Representative proteomes | UniProt (6564) |
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RP15 (231) |
RP35 (717) |
RP55 (1382) |
RP75 (2425) |
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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.
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Curation and family details
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Curation
Seed source: | Pfam-B_865 (release 17.0) |
Previous IDs: | Cache_2; |
Type: | Domain |
Sequence Ontology: | SO:0000417 |
Author: |
Finn RD |
Number in seed: | 38 |
Number in full: | 1333 |
Average length of the domain: | 214.90 aa |
Average identity of full alignment: | 18 % |
Average coverage of the sequence by the domain: | 36.02 % |
HMM information
HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 57096847 -E 1000 --cpu 4 HMM pfamseq
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Model details: |
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Model length: | 297 | ||||||||||||
Family (HMM) version: | 13 | ||||||||||||
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 dCache_2 domain has been found. There are 2 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 sequence.
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