Summary: LisH
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This is the Wikipedia entry entitled "LisH domain". More...
LisH domain Edit Wikipedia article
| n-terminal domain of lissencephaly-1 protein (lis-1) | |||||||||
| Identifiers | |||||||||
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| Symbol | LisH | ||||||||
| Pfam | PF08513 | ||||||||
| InterPro | IPR013720 | ||||||||
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In molecular biology, the LisH domain (lis homology domain) is a protein domain found in a large number of eukaryotic proteins, from metazoa, fungi and plants that have a wide range of functions. The recently solved structure of the LisH domain in the N-terminal region of LIS1 depicted it as a novel dimerisation motif, and that other structural elements are likely to play an important role in dimerisation.[1][2][3]
The LisH domain is found in the Saccharomyces cerevisiae SIF2 protein, a component of the SET3 complex which is responsible for repressing meiotic genes In SIF2 the LisH domain has been shown to mediate dimer and tetramer formation.[4] It has been shown that the LisH domain helps mediate interaction with components of the SET3 complex.[4]
[edit] References
- ^ Kim MH, Cooper DR, Oleksy A, Devedjiev Y, Derewenda U, Reiner O, Otlewski J, Derewenda ZS (June 2004). "The structure of the N-terminal domain of the product of the lissencephaly gene Lis1 and its functional implications". Structure 12 (6): 987–98. doi:10.1016/j.str.2004.03.024. PMID 15274919.
- ^ Mateja A, Cierpicki T, Paduch M, Derewenda ZS, Otlewski J (March 2006). "The dimerization mechanism of LIS1 and its implication for proteins containing the LisH motif". J. Mol. Biol. 357 (2): 621–31. doi:10.1016/j.jmb.2006.01.002. PMID 16445939.
- ^ Gerlitz G, Darhin E, Giorgio G, Franco B, Reiner O (November 2005). "Novel functional features of the Lis-H domain: role in protein dimerization, half-life and cellular localization". Cell Cycle 4 (11): 1632–40. PMID 16258276.
- ^ a b Cerna D, Wilson DK (2005). "The structure of Sif2p, a WD repeat protein functioning in the SET3 corepressor complex.". J Mol Biol 351 (4): 923–35. doi:10.1016/j.jmb.2005.06.025. PMID 16051270. http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16051270.
This article incorporates text from the public domain Pfam and InterPro IPR013720
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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.
LisH Provide feedback
The LisH (lis homology) domain mediates protein dimerisation and tetramerisation. The LisH domain is found in Sif2, a component of the Set3 complex which is responsible for repressing meiotic genes. It has been shown that the LisH domain helps mediate interaction with components of the Set3 complex [1].
Literature references
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Cerna D, Wilson DK; , J Mol Biol 2005;351:923-935.: The structure of Sif2p, a WD repeat protein functioning in the SET3 corepressor complex. PUBMED:16051270 EPMC:16051270
External database links
| PANDIT: | PF08513 |
| Pseudofam: | PF08513 |
| SYSTERS: | LisH |
This tab holds annotation information from the InterPro database.
InterPro entry IPR013720
The LisH motif is found in a large number of eukaryotic proteins, from metazoa, fungi and plants that have a wide range of functions. The recently solved structure of the LisH domain in the N-terminal region of LIS1 depicted it as a novel dimerization motif, and that other structural elements are likely to play an important role in dimerisation [PUBMED:15274919, PUBMED:16445939, PUBMED:16258276].
The LisH (lis homology) domain mediates protein dimerisation and tetramerisation. The LisH domain is found in Sif2, a component of the Set3 complex which is responsible for repressing meiotic genes. It has been shown that the LisH domain helps mediate interaction with components of the Set3 complex [PUBMED:16051270].
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...
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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 (58) |
Full (1365) |
Representative proteomes | NCBI (1281) |
Meta (4) |
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| RP15 (243) |
RP35 (438) |
RP55 (680) |
RP75 (874) |
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| Jalview | ||||||||
| HTML | ||||||||
| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
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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 (58) |
Full (1365) |
Representative proteomes | NCBI (1281) |
Meta (4) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (243) |
RP35 (438) |
RP55 (680) |
RP75 (874) |
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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_8344 (release 17.0) |
| Previous IDs: | none |
| Type: | Domain |
| Author: | Mistry J, Wood V |
| Number in seed: | 58 |
| Number in full: | 1365 |
| Average length of the domain: | 26.50 aa |
| Average identity of full alignment: | 35 % |
| Average coverage of the sequence by the domain: | 4.96 % |
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: | 27 | ||||||||||||
| Family (HMM) version: | 6 | ||||||||||||
| 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 LisH 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