Summary: Cyclin-dependent kinase regulatory subunit
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This is the Wikipedia entry entitled "Cyclin-dependent kinase regulatory subunit family". More...
Cyclin-dependent kinase regulatory subunit family Edit Wikipedia article
| ckshs1: human cyclin dependent kinase subunit, type 1 in complex with phosphate | |||||||||
| Identifiers | |||||||||
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| Symbol | CKS | ||||||||
| Pfam | PF01111 | ||||||||
| InterPro | IPR000789 | ||||||||
| PROSITE | PDOC00728 | ||||||||
| SCOP | 1cks | ||||||||
| SUPERFAMILY | 1cks | ||||||||
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In molecular biology, the cyclin-dependent kinase regulatory subunit family is a family of proteins consisting of the regulatory subunits of cyclin-dependent protein kinases.
In eukaryotes, cyclin-dependent protein kinases interact with cyclins to regulate cell cycle progression, and are required for the G1 and G2 stages of cell division.[1] The proteins bind to a regulatory subunit, cyclin-dependent kinase regulatory subunit (CKS), which is essential for their function. This regulatory subunit is a small protein of 79 to 150 residues. In yeast (gene CKS1) and in fission yeast (gene suc1) a single isoform is known, while mammals have two highly related isoforms. The regulatory subunits exist as hexamers, formed by the symmetrical assembly of 3 interlocked homodimers, creating an unusual 12-stranded beta-barrel structure.[2] Through the barrel centre runs a 12A diameter tunnel, lined by 6 exposed helix pairs.[3] Six kinase units can be modelled to bind the hexameric structure, which may thus act as a hub for cyclin-dependent protein kinase multimerisation.[2][3]
This family includes the CKS1B and CKS2 genes in mammals.
[edit] References
- ^ Brizuela L, Draetta G, Beach D (November 1987). "p13suc1 acts in the fission yeast cell division cycle as a component of the p34cdc2 protein kinase". EMBO J. 6 (11): 350714. PMC 553810. PMID 3322810. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=553810.
- ^ a b Parge HE, Arvai AS, Murtari DJ, Reed SI, Tainer JA (October 1993). "Human CksHs2 atomic structure: a role for its hexameric assembly in cell cycle control". Science 262 (5132): 38795. doi:10.1126/science.8211159. PMID 8211159.
- ^ a b Tang Y, Reed SI (May 1993). "The Cdk-associated protein Cks1 functions both in G1 and G2 in Saccharomyces cerevisiae". Genes Dev. 7 (5): 82232. doi:10.1101/gad.7.5.822. PMID 8491379.
This article incorporates text from the public domain Pfam and InterPro IPR000789
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External database links
| HOMSTRAD: | cks |
| PANDIT: | PF01111 |
| PROSITE: | PDOC00728 |
| Pseudofam: | PF01111 |
| SCOP: | 1cks |
| SYSTERS: | CKS |
This tab holds annotation information from the InterPro database.
InterPro entry IPR000789
In eukaryotes, cyclin-dependent protein kinases interact with cyclins to regulate cell cycle progression, and are required for the G1 and G2 stages of cell division [PUBMED:3322810]. The proteins bind to a regulatory subunit, cyclin-dependent kinase regulatory subunit (CKS), which is essential for their function. This regulatory subunit is a small protein of 79 to 150 residues. In yeast (gene CKS1) and in fission yeast (gene suc1) a single isoform is known, while mammals have two highly related isoforms. The regulatory subunits exist as hexamers, formed by the symmetrical assembly of 3 interlocked homodimers, creating an unusual 12-stranded beta-barrel structure [PUBMED:8211159]. Through the barrel centre runs a 12A diameter tunnel, lined by 6 exposed helix pairs [PUBMED:8491379]. Six kinase units can be modelled to bind the hexameric structure, which may thus act as a hub for cyclin-dependent protein kinase multimerisation [PUBMED:8491379, PUBMED:8211159].
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Molecular function | cyclin-dependent protein kinase regulator activity (GO:0016538) |
| Biological process | cell cycle (GO:0007049) |
Domain organisation
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Alignments
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| Seed (33) |
Full (488) |
Representative proteomes | NCBI (442) |
Meta (1) |
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| RP15 (119) |
RP35 (178) |
RP55 (263) |
RP75 (323) |
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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
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| Seed (33) |
Full (488) |
Representative proteomes | NCBI (442) |
Meta (1) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (119) |
RP35 (178) |
RP55 (263) |
RP75 (323) |
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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: | Sarah Teichmann |
| Previous IDs: | none |
| Type: | Domain |
| Author: | Bateman A |
| Number in seed: | 33 |
| Number in full: | 488 |
| Average length of the domain: | 71.50 aa |
| Average identity of full alignment: | 58 % |
| Average coverage of the sequence by the domain: | 58.47 % |
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: | 70 | ||||||||||||
| Family (HMM) version: | 14 | ||||||||||||
| 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 CKS domain has been found. There are 20 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