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Updated: Aug 9, 2026

A Protocol for Computer-Based Protein Structure and Function Prediction
Published on: November 3, 2011
The use of functional domains to improve transmembrane protein topology prediction
Emily W Xu1, Paul Kearney, Daniel G Brown
1Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Calgary, HS-1150, 3330 Hospital Drive NW, Calgary, AB T2N 4N1, Canada. ewxu@ucalgary.ca
Abstract:
Transmembrane proteins affect vital cellular functions and pathogenesis, and are a focus of drug design. It is difficult to obtain diffraction quality crystals to study transmembrane protein structure. Computational tools for transmembrane protein topology prediction fill in the gap between the abundance of transmembrane proteins and the scarcity of known membrane protein structures. Their prediction accuracy is still inadequate: TMHMM, the current state-of-the-art method, has less than 52% accuracy in topology prediction on one set of transmembrane proteins of known topology. Based on the observation that there are functional domains that occur preferentially internal or external to the membrane, we have extended the model of TMHMM to incorporate functional domains, using a probabilistic approach originally developed for computational gene finding. Our extension is better than TMHMM in predicting the topology of transmembrane proteins. As prediction of functional domain improves, our system's prediction accuracy will likely improve as well.
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