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Methods Mol Biol ; 409: 341-53, 2007.
Article in English | MEDLINE | ID: mdl-18450013

ABSTRACT

An iterative approach to resolving protein-peptide binding motifs is appropriate when the length of the binding protein is variable and a variety of amino acid residues may successfully occupy multiple positions. This chapter describes an iterative algorithm that first aligns binding peptides of variable lengths and then extracts a quantitative motif from the resulting alignment. Numerous examples are presented to illustrate the utility of the iterative process.


Subject(s)
Histocompatibility Antigens Class II/chemistry , Histocompatibility Antigens Class II/metabolism , Algorithms , Amino Acid Motifs , Amino Acid Sequence , Computational Biology , Computer Simulation , Databases, Protein , HLA-DR1 Antigen/chemistry , HLA-DR1 Antigen/metabolism , Humans , Immunogenetics , Models, Molecular , Peptides/chemistry , Peptides/immunology , Peptides/metabolism , Protein Binding
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