Summary: Mitochondrial small ribosomal subunit Rsm22
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Mitochondrial small ribosomal subunit Rsm22 Provide feedback
Rsm22 has been identified as a mitochondrial small ribosomal subunit  and is a methyltransferase. In Schizosaccharomyces pombe, Rsm22 is tandemly fused to Cox11 (a factor required for copper insertion into cytochrome oxidase) and the two proteins are proteolytically cleaved after import into the mitochondria .
Khalimonchuk O, Ott M, Funes S, Ostermann K, Rodel G, Herrmann JM; , Eukaryot Cell. 2006;5:997-1006.: Sequential processing of a mitochondrial tandem protein: insights into protein import in Schizosaccharomyces pombe. PUBMED:16835444 EPMC:16835444
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This tab holds annotation information from the InterPro database.
InterPro entry IPR015324
Ribosomes are the particles that catalyse mRNA-directed protein synthesis in all organisms. The codons of the mRNA are exposed on the ribosome to allow tRNA binding. This leads to the incorporation of amino acids into the growing polypeptide chain in accordance with the genetic information. Incoming amino acid monomers enter the ribosomal A site in the form of aminoacyl-tRNAs complexed with elongation factor Tu (EF-Tu) and GTP. The growing polypeptide chain, situated in the P site as peptidyl-tRNA, is then transferred to aminoacyl-tRNA and the new peptidyl-tRNA, extended by one residue, is translocated to the P site with the aid the elongation factor G (EF-G) and GTP as the deacylated tRNA is released from the ribosome through one or more exit sites [PUBMED:11297922, PUBMED:11290319]. About 2/3 of the mass of the ribosome consists of RNA and 1/3 of protein. The proteins are named in accordance with the subunit of the ribosome which they belong to - the small (S1 to S31) and the large (L1 to L44). Usually they decorate the rRNA cores of the subunits.
Many ribosomal proteins, particularly those of the large subunit, are composed of a globular, surfaced-exposed domain with long finger-like projections that extend into the rRNA core to stabilise its structure. Most of the proteins interact with multiple RNA elements, often from different domains. In the large subunit, about 1/3 of the 23S rRNA nucleotides are at least in van der Waal's contact with protein, and L22 interacts with all six domains of the 23S rRNA. Proteins S4 and S7, which initiate assembly of the 16S rRNA, are located at junctions of five and four RNA helices, respectively. In this way proteins serve to organise and stabilise the rRNA tertiary structure. While the crucial activities of decoding and peptide transfer are RNA based, proteins play an active role in functions that may have evolved to streamline the process of protein synthesis. In addition to their function in the ribosome, many ribosomal proteins have some function 'outside' the ribosome [PUBMED:11290319, PUBMED:11114498].
Rsm22 has been identified as a mitochondrial small ribosomal subunit [PUBMED:16835444] and is a methyltransferase. In Schizosaccharomyces pombe (Fission yeast), Rsm22 is tandemly fused to Cox11 (a factor required for copper insertion into cytochrome oxidase) and the two proteins are proteolytically cleaved after import into the mitochondria [PUBMED:16835444]. This entry consists of mitochondrial Rsm22 and homologous sequences from bacteria.
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|Molecular function||methyltransferase activity (GO:0008168)|
|Biological process||translation (GO:0006412)|
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|Seed source:||Pfam-B_8789 (release 20.0)|
|Author:||Mistry J, Wood V|
|Number in seed:||7|
|Number in full:||679|
|Average length of the domain:||228.70 aa|
|Average identity of full alignment:||20 %|
|Average coverage of the sequence by the domain:||53.83 %|
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build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
|Family (HMM) version:||5|
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