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Boryeu Mao

Publications and source records attributed to Boryeu Mao.

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Toward the regularization of E value from BLAST similarity search into a dissimilarity measure as distance function, and the metrication of protein sequence space

Sequence matching algorithms such as BLAST and FASTA have been widely used in searching for evolutionary origin and biological functions of newly discovered nucleic acid and protein sequences. As parts of these search tools, alignment scores and E values are useful indicators of the quality of search results (and the relevance of the matches) from querying a database of annotated sequences, whereby a high alignment score (and inversely a low E value) reflects significant similarity between the query and the subject (target) sequences. For cross-comparison of results from sufficiently different queries however, the interpretation of alignment score as a similarity measure and E value a dissimilarity measure becomes somewhat nuanced, and prompts herein a judicious distinction of different types of similarity. Via a simulated formulation, we show that an adjustment of E value to account for self-matching of query and subject sequences corrects for certain ostensibly anomalous similarity comparisons, resulting in 'regularized' dissimilarity and similarity measures that would be more appropriate for cross-comparisons, as well as database applications, such as all-on-all sequence alignment or selection of diverse subsets. In actual practice, the 'regularization' of E value dissimilarity improves clustering and subset selection. While both E value and the 'regularized' E value share two of the four axiomatic properties of a metric space, positivity and symmetry, the latter E value further becomes reflexive and meets the condition of triangle inequality, the remaining two axioms, thus itself an appropriate distance function for metricating protein sequence space.

q-bio.BM

Protein folding classes -- High-dimensional geometry of amino acid composition space revisited

In this study, the distributions of protein structure classes (or folding types) of experimentally determined structures from a legacy dataset and a comprehensive database (SCOP) are modeled precisely with geometric constructs such as convex polytopes in high-dimensional amino acid composition space. This is a follow-up of a previous non-statistical, geometry-motivated modeling of protein classes with ellipsoidal models, which is superseded presently in three important respects: (1) as a paradigm shift a descriptive 'distribution model' of experimental data is de-coupled from, and serves as the basis for, a possible future predictive 'domain model' generalizable to proteins in the same class for which 3D structures have yet to be determined experimentally, (2) the geometric and analytic characteristics of class distributions are obtained via exact computational geometry calculations, and (3) the full data from a comprehensive database are included in such calculations, eschewing training set selection and biases. In contrast to statistical and machine-learning approaches, the analytical, non-statistical geometry models of protein class distributions demonstrated in this study furnish complete and precise information on their size and relative disposition in the high-dimensional space (vis-\`a-vis any overlaps leading to ambiguity and classification limits). Intended primarily as an accurate and summary description of the complex relationships between amino acid composition and protein classes, and suitably as a basis for predictive modeling where possible, the results suggest that pen-ultimately they may be useful adjuncts for validating sequence-based protein structure predictions and contribute to theoretical and fundamental understanding of secondary structure formation and protein folding, demonstrating the role of high dimensional amino acid composition space in protein studies.

q-bio.BM