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Multiple Alignment and Phylogenetic Trees Csc 487/687 Computing for Bioinformatics Multiple Sequence Alignment • One amino acid sequence plays coy; a pair of homologous sequences whisper; many aligned sequences shout out loud. • Very informative Definition • A global alignment of a set of sequences is obtained by – inserting into each sequence gap characters • so that – the resulting sequences are of the same length • and so that – no “column” has only gap characters Example: Chromo domains aligned Use of alignments • High sequence similarity usually means significant structural and/or functional similarity. The reverse does not need to be true • Homolog proteins (common ancestor) can vary significantly in large parts of the sequences, but still retain common 2D-patterns, 3D-patterns or common active site or binding site. • Comparison of several sequences in a family can reveal what is common for the family. Something common for several sequences can be significant when regarding all of the sequences, but need not if regarding only two. • Multiple alignment can be used to derive evolutionary history. Use of alignments • Predict features of aligned objects – conserved positions • structurally/functionally important Conserved positions Use of alignments • Predict features of aligned objects – conserved positions • structurally/functionally important – patterns of hydrophobicity/hydrophilicity • secondary structure elements Helix pattern Use of alignments • Predict features of aligned objects – conserved positions • structurally/functionally important – patterns of hydrophobicity/hydrophilicity • secondary structure elements – “gappy” regions • loops/variable regions Loop? Loop? Loop? Use of Alignments - make patterns/profiles • Can make a profile or a pattern that can be used to match against a sequence database and identify new family members • Profiles/patterns can be used to predict family membership of new sequences • Databases of profiles/patterns – PROSITE – PFAM – PRINTS – ... Prosite: Motifs for classification Protein sequence Prosite pattern 1 Prosite pattern 2 Prosite pattern n Family 1 Family 2 Family n Pattern Regular expression Profile Pattern from alignment [FYL]-x-[LIVMC]-[KR]-W-x-[GDNR]-[FYWLE]-x(5,6)-[ST]-W-[ES]-[PSTDN]-x(3)-[LIVMC] Alignment problem Given a set of sequences, produce a multiple alignment which corresponds as well as possible to the biological relationships between the corresponding bio-molecules For homologous proteins • Two residues should be aligned (on top of each other) – if they are homologous (evolved from the same residue in a common ancestor protein) – if they are structurally equivalent Automatic approach • Need a way of scoring alignments – fitness function which for an alignment quantifies its “goodness” • Need an algorithm for finding alignments with good scores • Not all methods provide a scoring function for the final alignment! Analysis of fitness function • One can test whether the alignments optimal under a given fitness function correspond well to the biological relationships between the sequences • For example, if the structure of (some of) the proteins are known. Align by use of dynamic programming • Dynamic programming finds best alignment of k sequences with given scoring scheme • For two sequences there are three different column types • For three sequences there are seven different column types x means an amino acid, - a blank Sequence1 x - x x - - x Sequence2 x x - x - x Sequence3 x x x - x - x • Time complexity of O(nk) (sequence lengths = n) Use of dynamic programming • Dynamic programming finds best alignment of k sequences given scoring scheme Algorithm for dynamic programming