GPCRTOP: A Novel G Protein-Coupled Receptor Topology Prediction Method Based on Hidden Markov Model Approach Using Viterbi Algorithm
Babak Sokouti, Farshad Rezvan, Guy Yachdav and Siavoush DastmalchiAffiliation:
School of Pharmacy and Biotechnology Research Center, Tabriz University of Medical Sciences, Daneshgah Street, Tabriz 51664, Iran.
Knowledge about the topology of G protein-coupled receptors (GPCRs) can be very useful in predicting diverse range of properties about these proteins, such as function, three dimensional structure, and ligand binding site. Considering that only few GPCRs have known structures, many computational efforts have been carried out to develop methods for predicting their topology.
A novel method to predict the location and the length of transmembrane helices in GPCRs was proposed. This method consists of a “one by one” amino acid feature extraction window which makes it possible for the method to learn the amino acid distribution in helical segments of GPCR proteins. It is based on hidden Markov model (HMM) with a specific architecture that takes advantage of Viterbi decoding algorithm and the observed frequency values for adjusting the transition probabilities.
The prediction capability of the method was evaluated for per-protein, per-segment and per-residue accuracies on two datasets consisting of 649 (at least one GPCR from each family) and 2898 (all GPCRs) sequences extracted from UniProt database and compared with other commonly used existing methods. It was found that in all three assessments, the prediction accuracies for the new method on the larger dataset, i.e., 2898 GPCRs, were higher than that obtained by other methods. The results showed that our method was able to predict the topology of GPCR proteins without any sequence length limitation with the accuracies of 88.9 % and 87.4% for the small (i.e., 649 GPCRs) and large (i.e., 2898 GPCRs) datasets, respectively. (Availability status: The source code is available upon request from the authors)
GPCRs, HMM, topology prediction, transmembrane proteins, viterbi algorithm.
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