Abstract
Sorting of transmembrane proteins to various intracellular compartments depends on specific signals present within their cytosolic domains. Among these sorting signals, the tyrosine-based motif (YXX) is one of the best characterized and is recognized by -subunits of the four clathrin-associated adaptor complexes (AP-1 to AP-4). Despite their overlap in specificity, each -subunit has a distinct sequence preference dependent on the nature of the X-residues. Moreover, combinations of these residues exert cooperative or inhibitory effects towards interaction with the various APs. This complexity makes it impossible to predict a priori, the specificity of a given tyrosine-signal for a particular -subunit. Here, we describe the results obtained with a computational approach based on the Artificial Neural Network (ANN) paradigm that addresses the issue of tyrosine-signal specificity, enabling the prediction of YXX- interactions with accuracies over 90. Therefore, this approach constitutes a powerful tool to help predict mechanisms of intracellular protein sorting. Copyright © 2012 Debarati Mukherjee et al.
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CITATION STYLE
Mukherjee, D., Hanna, C. B., & Aguilar, R. C. (2012). Artificial neural network for the prediction of tyrosine-based sorting signal recognition by adaptor complexes. Journal of Biomedicine and Biotechnology, 2012. https://doi.org/10.1155/2012/498031
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