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1.
Nucleic Acids Res ; 38(Database issue): D167-80, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19920119

ABSTRACT

Linear motifs are short segments of multidomain proteins that provide regulatory functions independently of protein tertiary structure. Much of intracellular signalling passes through protein modifications at linear motifs. Many thousands of linear motif instances, most notably phosphorylation sites, have now been reported. Although clearly very abundant, linear motifs are difficult to predict de novo in protein sequences due to the difficulty of obtaining robust statistical assessments. The ELM resource at http://elm.eu.org/ provides an expanding knowledge base, currently covering 146 known motifs, with annotation that includes >1300 experimentally reported instances. ELM is also an exploratory tool for suggesting new candidates of known linear motifs in proteins of interest. Information about protein domains, protein structure and native disorder, cellular and taxonomic contexts is used to reduce or deprecate false positive matches. Results are graphically displayed in a 'Bar Code' format, which also displays known instances from homologous proteins through a novel 'Instance Mapper' protocol based on PHI-BLAST. ELM server output provides links to the ELM annotation as well as to a number of remote resources. Using the links, researchers can explore the motifs, proteins, complex structures and associated literature to evaluate whether candidate motifs might be worth experimental investigation.


Subject(s)
Amino Acid Motifs/genetics , Computational Biology/methods , Databases, Genetic , Databases, Nucleic Acid , Eukaryotic Cells/chemistry , Amino Acid Sequence , Animals , Computational Biology/trends , Databases, Protein , Humans , Information Storage and Retrieval/methods , Internet , Molecular Sequence Data , Protein Structure, Tertiary , Sequence Homology, Amino Acid , Software
2.
Nucleic Acids Res ; 31(13): 3625-30, 2003 Jul 01.
Article in English | MEDLINE | ID: mdl-12824381

ABSTRACT

Multidomain proteins predominate in eukaryotic proteomes. Individual functions assigned to different sequence segments combine to create a complex function for the whole protein. While on-line resources are available for revealing globular domains in sequences, there has hitherto been no comprehensive collection of small functional sites/motifs comparable to the globular domain resources, yet these are as important for the function of multidomain proteins. Short linear peptide motifs are used for cell compartment targeting, protein-protein interaction, regulation by phosphorylation, acetylation, glycosylation and a host of other post-translational modifications. ELM, the Eukaryotic Linear Motif server at http://elm.eu.org/, is a new bioinformatics resource for investigating candidate short non-globular functional motifs in eukaryotic proteins, aiming to fill the void in bioinformatics tools. Sequence comparisons with short motifs are difficult to evaluate because the usual significance assessments are inappropriate. Therefore the server is implemented with several logical filters to eliminate false positives. Current filters are for cell compartment, globular domain clash and taxonomic range. In favourable cases, the filters can reduce the number of retained matches by an order of magnitude or more.


Subject(s)
Amino Acid Motifs , Eukaryotic Cells/chemistry , Sequence Analysis, Protein/methods , Software , Internet , Protein Structure, Tertiary , Proteins/chemistry , Proteins/physiology , User-Computer Interface
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