Summary: La domain
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La domain Edit Wikipedia article
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| solution structure of the la domain of c-mpl binding protein | |||||||||
| Identifiers | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Symbol | La | ||||||||
| Pfam | PF05383 | ||||||||
| InterPro | IPR006630 | ||||||||
| SMART | TSPN | ||||||||
| PROSITE | PDOC00280 | ||||||||
| MEROPS | I75 | ||||||||
| SCOP | 2mpr | ||||||||
| SUPERFAMILY | 2mpr | ||||||||
| TCDB | 1.B.3 | ||||||||
| CDD | cd07323 | ||||||||
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In molecular biology, the La domain is a conserved protein domain.
Human 60 kDa SS-A/Ro ribonucleoproteins (RNPs) are composed of one of the four small Y RNAs and at least two proteins, Ro60 and La. The La protein is a 47 kDa polypeptide that frequently acts as an autoantigen in systemic lupus erythematosus and Sjogren's syndrome.[1] In the nucleus, La acts as a RNA polymerase III (RNAP III) transcription factor, while in the cytoplasm, La acts as a translation factor.[2] In the nucleus, La binds to the 3'UTR of nascent RNAP III transcripts to assist in folding and maturation.[3] In the cytoplasm, La recognises specific classes of mRNAs that contain a 5'-terminal oligopyrimidine (5'TOP) motif known to control protein synthesis.[4] The specific recognition is mediated by the N-terminal domain of La, which comprises a La motif and an RNA recognition motif (RRM). The La motif adopts an alpha/beta fold that comprises a winged-helix motif.[5]
Homologous La domain-containing proteins have been identified in a wide range of organisms except Archaea, bacteria and viruses.[6]
[edit] References
- ^ Izumi RE, Das S, Barat B, Raychaudhuri S, Dasgupta A (April 2004). "A peptide from autoantigen La blocks poliovirus and hepatitis C virus cap-independent translation and reveals a single tyrosine critical for La RNA binding and translation stimulation". J. Virol. 78 (7): 376376. PMC 371053. PMID 15016896. //www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=371053.
- ^ Intine RV, Tenenbaum SA, Sakulich AL, Keene JD, Maraia RJ (November 2003). "Differential phosphorylation and subcellular localization of La RNPs associated with precursor tRNAs and translation-related mRNAs". Mol. Cell 12 (5): 13017. DOI:10.1016/S1097-2765(03)00429-5. PMID 14636586.
- ^ Alfano C, Sanfelice D, Babon J, Kelly G, Jacks A, Curry S, Conte MR (April 2004). "Structural analysis of cooperative RNA binding by the La motif and central RRM domain of human La protein". Nat. Struct. Mol. Biol. 11 (4): 3239. DOI:10.1038/nsmb747. PMID 15004549.
- ^ Keene JD (December 2003). "Posttranscriptional generation of macromolecular complexes". Mol. Cell 12 (6): 13479. DOI:10.1016/S1097-2765(03)00496-9. PMID 14690589.
- ^ Kenan DJ, Keene JD (April 2004). "La gets its wings". Nat. Struct. Mol. Biol. 11 (4): 3035. DOI:10.1038/nsmb0404-303. PMID 15048103.
- ^ Lin-Marq N, Clarkson SG (January 1995). "A yeast RNA binding protein that resembles the human autoantigen La". J. Mol. Biol. 245 (2): 815. DOI:10.1006/jmbi.1994.0008. PMID 7799435.
This article incorporates text from the public domain Pfam and InterPro IPR006630
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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.
La domain Provide feedback
This presumed domain is found at the N-terminus of La RNA-binding proteins as well as other proteins [1]. The function of this region is uncertain.
Literature references
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Yoo CJ, Wolin SL; , Mol Cell Biol 1994;14:5412-5424.: La proteins from Drosophila melanogaster and Saccharomyces cerevisiae: a yeast homolog of the La autoantigen is dispensable for growth. PUBMED:8035818 EPMC:8035818
External database links
| PANDIT: | PF05383 |
| Pseudofam: | PF05383 |
| SCOP: | 1s7a |
| SYSTERS: | La |
This tab holds annotation information from the InterPro database.
InterPro entry IPR006630
Human Ro ribonucleoproteins (RNPs) are composed of one of the four small Y RNAs and at least two proteins, Ro60 and La. The La protein is a 47 kDa polypeptide that frequently acts as an autoantigen in systemic lupus erythematosus and Sjogren's syndrome [PUBMED:15016896]. In the nucleus, La acts as a RNA polymerase III (RNAP III) transcription factor, while in the cytoplasm, La acts as a translation factor [PUBMED:14636586]. In the nucleus, La binds to the 3'UTR of nascent RNAP III transcripts to assist in folding and maturation [PUBMED:15004549]. In the cytoplasm, La recognises specific classes of mRNAs that contain a 5'-terminal oligopyrimidine (5'TOP) motif known to control protein synthesis [PUBMED:14690589]. The specific recognition is mediated by the N-terminal domain of La, which comprises a La motif and a RNA recognition motif (RRM). The La motif adopts an alpha/beta fold that comprises a winged-helix motif [PUBMED:15048103].
Homologous La domain-containing proteins have been identified in a wide range of organisms except Archaea, bacteria and viruses [PUBMED:7799435].
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 (33) |
Full (1403) |
Representative proteomes | NCBI (1319) |
Meta (11) |
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| RP15 (260) |
RP35 (430) |
RP55 (669) |
RP75 (875) |
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| Jalview | ||||||||
| HTML | ||||||||
| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
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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 (33) |
Full (1403) |
Representative proteomes | NCBI (1319) |
Meta (11) |
||||
|---|---|---|---|---|---|---|---|---|
| RP15 (260) |
RP35 (430) |
RP55 (669) |
RP75 (875) |
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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: | Bateman A |
| Previous IDs: | none |
| Type: | Domain |
| Author: | Bateman A |
| Number in seed: | 33 |
| Number in full: | 1403 |
| Average length of the domain: | 58.80 aa |
| Average identity of full alignment: | 37 % |
| Average coverage of the sequence by the domain: | 10.47 % |
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: | 61 | ||||||||||||
| Family (HMM) version: | 12 | ||||||||||||
| 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 La domain has been found. There are 14 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