A study of structural properties on profiles HMMs
Juliana S Bernardes, Alberto Davila, Vitor Santos Costa, Gerson, Zaverucha

TL;DR
This paper introduces HMMER-STRUCT, a novel method that enhances profile HMMs for protein family detection by incorporating structural information during training, resulting in improved sensitivity and performance.
Contribution
The paper presents a new algorithm that weights residues in pHMMs based on structural properties, and demonstrates its effectiveness through experiments on the SCOP database.
Findings
Structurally weighted pHMMs outperform standard models.
Voting-based model combination improves sensitivity.
Significant performance gains confirmed by statistical tests.
Abstract
Motivation: Profile hidden Markov Models (pHMMs) are a popular and very useful tool in the detection of the remote homologue protein families. Unfortunately, their performance is not always satisfactory when proteins are in the 'twilight zone'. We present HMMER-STRUCT, a model construction algorithm and tool that tries to improve pHMM performance by using structural information while training pHMMs. As a first step, HMMER-STRUCT constructs a set of pHMMs. Each pHMM is constructed by weighting each residue in an aligned protein according to a specific structural property of the residue. Properties used were primary, secondary and tertiary structures, accessibility and packing. HMMER-STRUCT then prioritizes the results by voting. Results: We used the SCOP database to perform our experiments. Throughout, we apply leave-one-family-out cross-validation over protein superfamilies. First, we…
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Taxonomy
TopicsMachine Learning in Bioinformatics · Protein Structure and Dynamics · Genomics and Phylogenetic Studies
