skbio.alignment.global_pairwise_align_protein#

skbio.alignment.global_pairwise_align_protein(seq1, seq2, gap_open_penalty=11, gap_extend_penalty=1, substitution_matrix=None, penalize_terminal_gaps=False)[source]#

Globally align pair of protein seqs or alignments with Needleman-Wunsch.

Parameters:

seq1Protein or TabularMSA[Protein]: The first unaligned sequence(s).
seq2Protein or TabularMSA[Protein]: The second unaligned sequence(s).
gap_open_penaltyint or float, optional: Penalty for opening a gap (this is substracted from previous best alignment score, so is typically positive).
gap_extend_penaltyint or float, optional: Penalty for extending a gap (this is substracted from previous best alignment score, so is typically positive).
substitution_matrix: 2D dict (or similar), optional: Lookup for substitution scores (these values are added to the previous best alignment score); default is BLOSUM 50.
penalize_terminal_gaps: bool, optional: If True, will continue to penalize gaps even after one sequence has been aligned through its end. This behavior is true Needleman-Wunsch alignment, but results in (biologically irrelevant) artifacts when the sequences being aligned are of different length. This is False by default, which is very likely to be the behavior you want in all or nearly all cases.

Returns:

tuple: TabularMSA object containing the aligned sequences, alignment score (float), and start/end positions of each input sequence (iterable of two-item tuples). Note that start/end positions are indexes into the unaligned sequences.