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On the reliability and the limits of inference of amino acid sequence alignments

MOTIVATION: Alignments are correspondences between sequences. How reliable are alignments of amino acid sequences of proteins, and what inferences about protein relationships can be drawn? Using techniques not previously applied to these questions, by weighting every possible sequence alignment by i...

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Detalles Bibliográficos
Autores principales: Rajapaksa, Sandun, Sumanaweera, Dinithi, Lesk, Arthur M, Allison, Lloyd, Stuckey, Peter J, Garcia de la Banda, Maria, Abramson, David, Konagurthu, Arun S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235515/
https://www.ncbi.nlm.nih.gov/pubmed/35758808
http://dx.doi.org/10.1093/bioinformatics/btac247
Descripción
Sumario:MOTIVATION: Alignments are correspondences between sequences. How reliable are alignments of amino acid sequences of proteins, and what inferences about protein relationships can be drawn? Using techniques not previously applied to these questions, by weighting every possible sequence alignment by its posterior probability we derive a formal mathematical expectation, and develop an efficient algorithm for computation of the distance between alternative alignments allowing quantitative comparisons of sequence-based alignments with corresponding reference structure alignments. RESULTS: By analyzing the sequences and structures of 1 million protein domain pairs, we report the variation of the expected distance between sequence-based and structure-based alignments, as a function of (Markov time of) sequence divergence. Our results clearly demarcate the ‘daylight’, ‘twilight’ and ‘midnight’ zones for interpreting residue–residue correspondences from sequence information alone. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.