Ssu72 Results: Difference between revisions

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==Function==
==Function==
===BLAST results===
===BLAST results===
Running a protein BLAST search on the Drosophila Ssu72 protein returned a large number of highly relevant (bit score > 200) sequences that were of a very similar length (see Figure 1). However, the first 27 of those sequences were not considered relevant for a number of reasons. For instance, some were merely homologous proteins in other closely related Drosophila species that had been identified in a similar manner to this one and for which there were no PubMed publications available and thus no information that could be used to easily infer function. Others had not been functionally characterised by experimentation or structural analysis, because they had been identified by high-throughput sequencing and minimal, if any, human input. Some BLAST hits were labelled as hypothetical proteins and therefore not necessarily even protein coding or biologically present. The first relevant protein identified was 'SSU72 RNA polymerase II CTD phosphatase homolog (S. cerevisiae)', the human Ssu72 protein, for which there were a small number of articles available on PubMed (see Figure 2), as well as expression data from SymAtlas (see Figure 3). This protein was also found to have  
Running a protein BLAST search on 'serine phosphatase of RNA polymerase II CTD (SSU72 superfamily)' from Drosophila melenogaster (the 'Drosophila Ssu72 protein') returned a large number of highly relevant (bit score > 200) sequences that were of a very similar length (see Figure 1) to that of the query. However, the first 27 of those sequences were not considered relevant, for the purposes of this paper, for a number of reasons. For instance, some were merely homologous proteins in other closely related Drosophila species that had been identified in a similar manner to this one and for which there were no PubMed publications available and thus no information that could be used to easily infer function. Similarly, other proteins, in more distantly related organisms, had not been functionally characterised by experimentation or structural analysis, because they had been identified by high-throughput sequencing and minimal, if any, human input. Some BLAST hits were labelled as hypothetical proteins and therefore not necessarily protein coding or biologically present. The first relevant protein identified was 'SSU72 RNA polymerase II CTD phosphatase homolog (S. cerevisiae)', the human Ssu72 protein, for which there were a small number of articles available on PubMed (see Figure 2), as well as expression data from SymAtlas (see Figure 3). This protein was also found to have a 60.21% sequence identity with the Drosophila Ssu72 protein, with no gaps in the alignment.





Revision as of 12:52, 11 June 2009

Function

BLAST results

Running a protein BLAST search on 'serine phosphatase of RNA polymerase II CTD (SSU72 superfamily)' from Drosophila melenogaster (the 'Drosophila Ssu72 protein') returned a large number of highly relevant (bit score > 200) sequences that were of a very similar length (see Figure 1) to that of the query. However, the first 27 of those sequences were not considered relevant, for the purposes of this paper, for a number of reasons. For instance, some were merely homologous proteins in other closely related Drosophila species that had been identified in a similar manner to this one and for which there were no PubMed publications available and thus no information that could be used to easily infer function. Similarly, other proteins, in more distantly related organisms, had not been functionally characterised by experimentation or structural analysis, because they had been identified by high-throughput sequencing and minimal, if any, human input. Some BLAST hits were labelled as hypothetical proteins and therefore not necessarily protein coding or biologically present. The first relevant protein identified was 'SSU72 RNA polymerase II CTD phosphatase homolog (S. cerevisiae)', the human Ssu72 protein, for which there were a small number of articles available on PubMed (see Figure 2), as well as expression data from SymAtlas (see Figure 3). This protein was also found to have a 60.21% sequence identity with the Drosophila Ssu72 protein, with no gaps in the alignment.


Literature review

The function of the human Ssu72 protein, for which there exist a number of mammalian homologues, was first thought to be . Therefore, a ProFunc analysis was carried out on our candidate protein, Drosophila Ssu72, with the purpose of comparing components of its primary and secondary structure with proteins that do not necessarily have a high level of overall sequence similarity.

Evolution

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Structure

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Abstract | Introduction | Results | Discussion | Conclusion | Method | References