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Comput Chem. 1999 Jun 15;23(3-4):341-64.

Two strategies for sequence comparison: profile-preprocessed and secondary structure-induced multiple alignment.

Author information

1
Division of Mathematical Biology, National Institute for Medical Research (NIMR), Mill Hill, London, UK. jhering@nimr.mrc.ac.uk

Abstract

Multiple sequence alignment remains one of the most powerful tools for assessing sequence relateness and the identification of structurally and functionally important protein regions. In this work, two new techniques are introduced to increase the sensitivity of dynamic programming and to enable checks for alignment consistency: Profile-preprocessed and secondary structure-induced alignments. Both strategies are based upon the hierarchical dynamic programming technique and can be applied separately or used in combination. Alignments resulting from the strategies are shown in comparison with the multiple alignment methods CLUSTALX and MULTAL for distant sequence sets of the flavoxin and cupredoxin protein families.

PMID:
10404624
[Indexed for MEDLINE]

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