BetAware-Deep: An Accurate Web Server for Discrimination and Topology Prediction of Prokaryotic Transmembrane beta-barrel Proteins

摘要

TransMembrane beta-Barrel (TMBB) proteins located in the outer membranes of Gram-negative bacteria are crucial for many important biological processes and primary candidates as drug targets. Structure determination of TMBB proteins is challenging and hence computational methods devised for the analysis of TMBB proteins are important for complementing experimental approaches. Here, we present a novel web server called BetAware-Deep that is able to accurately identify the topology of TMBB proteins (i.e. the number and orientation of membrane-spanning segments along the protein sequence) and to discriminate them from other protein types. The method in BetAware-Deep defines new features by exploiting a non-canonical computation of the hydrophobic moment and by adopting sequence-profile weighting of the White&Wimley hydrophobicity scale. These features are processed using a two-step approach based on deep learning and probabilistic graphical models. BetAware-Deep has been trained on a dataset comprising 58 TMBBs and benchmarked on a novel set of 15 TMBB proteins. Results showed that BetAware-Deep outperforms two recently released state-of-the-art methods for topology prediction, predicting correct topologies of 10 out of 15 proteins. TMBB detection was also assessed on a larger dataset comprising 1009 TMBB proteins and 7571 non-TMBB proteins. Even in this benchmark, BetAware-Deep scored at the level of top-performing methods. A web server has been developed allowing users to analyze input protein sequences and providing topology prediction together with a rich set of information including a graphical representation of the residue-level annotations and prediction probabilities. (C) 2020 The Authors. Published by Elsevier Ltd.