Literature DB >> 2685324

A method for multiple sequence alignment with gaps.

S Subbiah1, S C Harrison.   

Abstract

A method that performs multiple sequence alignment by cyclical use of the standard pairwise Needleman-Wunsch algorithm is presented. The required central processor unit time is of the same order of magnitude as the standard Needleman-Wunsch pairwise implementation. Comparison with the one known case where the optimal multiple sequence alignment has been rigorously determined shows that in practice the proposed method finds the mathematically optimal solution. The more interesting question of the biological usefulness of such multiple sequence alignment over pairwise approaches is assessed using protein families whose X-ray structures are known. The two such cases studied, the subdomains of the ricin B-chain and the S-domains of virus coat proteins, have low pairwise similarity and thus fail to align correctly under standard pairwise sequence comparison. In both cases the multiple sequence alignment produced by the proposed technique, apart from minor deviations at loop regions, correctly predicts the true structural alignment. Thus, given many sequences of low pairwise similarity, the proposed multiple sequence method, can extract any familial similarity and so produce a sequence alignment consistent with the underlying structural homology.

Mesh:

Substances:

Year:  1989        PMID: 2685324     DOI: 10.1016/0022-2836(89)90592-5

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  17 in total

1.  Genetic and physical analysis of the nodD3 region of Rhizobium meliloti.

Authors:  B G Rushing; M M Yelton; S R Long
Journal:  Nucleic Acids Res       Date:  1991-02-25       Impact factor: 16.971

2.  A survey of multiple sequence comparison methods.

Authors:  S C Chan; A K Wong; D K Chiu
Journal:  Bull Math Biol       Date:  1992-07       Impact factor: 1.758

3.  The T-cell-receptor repertoire in the synovial fluid of a patient with rheumatoid arthritis is polyclonal.

Authors:  Y Uematsu; H Wege; A Straus; M Ott; W Bannwarth; J Lanchbury; G Panayi; M Steinmetz
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

4.  RNA-binding domain of the A protein component of the U1 small nuclear ribonucleoprotein analyzed by NMR spectroscopy is structurally similar to ribosomal proteins.

Authors:  D W Hoffman; C C Query; B L Golden; S W White; J D Keene
Journal:  Proc Natl Acad Sci U S A       Date:  1991-03-15       Impact factor: 11.205

5.  A multiple sequence comparison method.

Authors:  A K Wong; S C Chan; D K Chiu
Journal:  Bull Math Biol       Date:  1993-03       Impact factor: 1.758

Review 6.  De novo and inverse folding predictions of protein structure and dynamics.

Authors:  A Godzik; A Kolinski; J Skolnick
Journal:  J Comput Aided Mol Des       Date:  1993-08       Impact factor: 3.686

7.  Identification of glutamate-169 as the third zinc-binding residue in proteinase III, a member of the family of insulin-degrading enzymes.

Authors:  A B Becker; R A Roth
Journal:  Biochem J       Date:  1993-05-15       Impact factor: 3.857

8.  Rhizobium meliloti NodP and NodQ form a multifunctional sulfate-activating complex requiring GTP for activity.

Authors:  J S Schwedock; C Liu; T S Leyh; S R Long
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

9.  DNA sequence and translational product of a new nodulation-regulatory locus: syrM has sequence similarity to NodD proteins.

Authors:  M J Barnett; S R Long
Journal:  J Bacteriol       Date:  1990-07       Impact factor: 3.490

10.  Cloning and characterization of a Rhizobium meliloti homolog of the Escherichia coli cell division gene ftsZ.

Authors:  W Margolin; J C Corbo; S R Long
Journal:  J Bacteriol       Date:  1991-09       Impact factor: 3.490

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