RepSeq – A database of amino acid repeats present in lower eukaryotic pathogens
By Daniel P. Depledge, Ryan P. J. Lower, Deborah F. Smith. BMC Bioinformatics, 2007
787 citations recorded by the source corpus.
BackgroundAmino acid repeat-containing proteins have a broad range of functions and their identification is of relevance to many experimental biologists. In human-infective protozoan parasites (such as the Kinetoplastid and Plasmodium species), they are implicated in immune evasion and have been shown to influence virulence and pathogenicity. RepSeq http://repseq.gugbe.com is a new database of amino acid repeat-containing proteins found in lower eukaryotic pathogens. The RepSeq database is accessed via a web-based application which also provides links to related online tools and databases for further analyses.ResultsThe RepSeq algorithm typically identifies more than 98% of repeat-containing proteins and is capable of identifying both perfect and mismatch repeats. The proportion of proteins that contain repeat elements varies greatly between different families and even species (3–35% of the total protein content). The most common motif type is the Sequence Repeat Region (SRR) – a repeated motif containing multiple different amino acid types. Proteins containing Single Amino Acid Repeats (SAARs) and Di-Peptide Repeats (DPRs) typically account for 0.5–1.0% of the total protein number. Notable exceptions are P. falciparum and D. discoideum, in which 33.67% and 34.28% respectively of the predicted proteomes consist of repeat-containing proteins. These numbers are due to large insertions of low complexity single and multi-codon repeat regions.ConclusionThe RepSeq database provides a repository for repeat-containing proteins found in parasitic protozoa. The database allows for both individual and cross-species proteome analyses and also allows users to upload sequences of interest for analysis by the RepSeq algorithm. Identification of repeat-containing proteins provides researchers with a defined subset of proteins which can be analysed by expression profiling and functional characterisation, thereby facilitating study of pathogenicity and virulence factors in the parasitic protozoa. While primarily designed for kinetoplastid work, the RepSeq algorithm and database retain full functionality when used to analyse other species.
Subfields: Epidemiology, Molecular Biology, Parasitology
View Paper: https://www.semanticscholar.org/paper/97078e8522451e4f839d93f822e913cf257c08a5
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- CRISPR — a widespread system that provides acquired resistance against phages in bacteria and archaea (2008, background): “in 2000), and the most recent computational analyses revealed that CRISPRs are found in approximately 40% and 90% of sequenced bacterial and archaeal genomes, respectivel”
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- The human gut virome: inter-individual variation and dynamic response to diet. (2011, methodology): “Both direct repeat and spacer sequences were compared with previously sequenced CRISPR spacers and direct repeats (from CRISPRdb) (Grissa et al. 2007a) using BLAT (90% aligned at 90% identity), and to the nonredundant database (from NCBI) using BLASTn (90% aligned at 90% identity).”
- ICEberg 2.0: an updated database of bacterial integrative and conjugative elements (2018, neutral): “Using CRISPRTarget (30) with the cutoff score of 20 by default and the 125 497 CRISPRdbcollected non-redundant spacers (31), a total number of 831 targets of CRISPR spacers are found in 340 ICEs, in which 272 spacers are distributed on 104 experimentally validated ICEs (Supplementary Table S5).”
- Diversity, Activity, and Evolution of CRISPR Loci in Streptococcus thermophilus (2007, methodology): “addition, the CRISPR database CRISPRdb (9) and the CRISPR identification”
- CRISPR-Cas Systems: RNA-mediated Adaptive Immunity in Bacteria and Archaea (2013, methodology): “2009) and CRISPRdb databases (Grissa et al. 2007) 1 Discovery and Seminal Developments in the CRISPR Field 7”
- CRISPR/Cas system and its role in phage-bacteria interactions. (2010, methodology): “In these cases, only one locus is associated with a set of cas genes (32).”
- CRISPR-assisted editing of bacterial genomes (2013, background): “Heute ist bekannt, dass das Genom von etwa 45 % der bislang sequenzierten Bakterien und 83 % der Archaeen mindestens eine CRISPR-Struktur beinhaltet [2].”