Alan M Moses

Summary

Affiliation: Wellcome Trust Genome Campus
Country: UK

Publications

  1. ncbi Regulatory evolution in proteins by turnover and lineage-specific changes of cyclin-dependent kinase consensus sites
    Alan M Moses
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton CB10 1HH, United Kingdom
    Proc Natl Acad Sci U S A 104:17713-8. 2007
  2. ncbi Clustering of phosphorylation site recognition motifs can be exploited to predict the targets of cyclin-dependent kinase
    Alan M Moses
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, UK
    Genome Biol 8:R23. 2007
  3. ncbi Inferring selection on amino acid preference in protein domains
    Alan M Moses
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, UK
    Mol Biol Evol 26:527-36. 2009

Detail Information

Publications3

  1. ncbi Regulatory evolution in proteins by turnover and lineage-specific changes of cyclin-dependent kinase consensus sites
    Alan M Moses
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton CB10 1HH, United Kingdom
    Proc Natl Acad Sci U S A 104:17713-8. 2007
    ..Our results begin to explore the dynamics of regulatory evolution at the posttranslational level and show interesting similarities to recent observations of regulatory evolution at the level of transcription...
  2. ncbi Clustering of phosphorylation site recognition motifs can be exploited to predict the targets of cyclin-dependent kinase
    Alan M Moses
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, UK
    Genome Biol 8:R23. 2007
    ..Our data suggest that regulatory modules may exist in protein sequence as clusters of short sequence motifs...
  3. ncbi Inferring selection on amino acid preference in protein domains
    Alan M Moses
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, UK
    Mol Biol Evol 26:527-36. 2009
    ..Finally, we analyze a model for selection on amino acid preferences in protein domains and find that it is consistent with the quantitative effects that we observe...