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FIND: Identifying Functionally and Structurally Important Features in Protein Sequences with Deep Neural Networks

Ranjani Murali, James Hemp, Victoria Orphan, Yonatan Bisk
doi: https://doi.org/10.1101/592808
Ranjani Murali
1Division of Geological and Planetary Sciences, California Institute of Technology
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  • For correspondence: m.ranjani@gmail.com
James Hemp
2School of Medicine, University of Utah
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  • For correspondence: m.ranjani@gmail.com
Victoria Orphan
1Division of Geological and Planetary Sciences, California Institute of Technology
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Yonatan Bisk
3Paul G. Allen School of Computer Science & Engineering, University of Washington
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Abstract

The ability to correctly predict the functional role of proteins from their amino acid sequences would significantly advance biological studies at the molecular level by improving our ability to understand the biochemical capability of biological organisms from their genomic sequence. Existing methods that are geared towards protein function prediction or annotation mostly use alignment-based approaches and probabilistic models such as Hidden-Markov Models. In this work we introduce a deep learning architecture (Function Identification with Neural Descriptions or FIND) which performs protein annotation from primary sequence. The accuracy of our methods matches state of the art techniques, such as protein classifiers based on Hidden Markov Models. Further, our approach allows for model introspection via a neural attention mechanism, which weights parts of the amino acid sequence proportionally to their relevance for functional assignment. In this way, the attention weights automatically uncover structurally and functionally relevant features of the classified protein and find novel functional motifs in previously uncharacterized proteins. While this model is applicable to any database of proteins, we chose to apply this model to superfamilies of homologous proteins, with the aim of extracting features inherent to divergent protein families within a larger superfamily. This provided insight into the functional diversification of an enzyme superfamily and its adaptation to different physiological contexts. We tested our approach on three families (nitrogenases, cytochrome bd-type oxygen reductases and heme-copper oxygen reductases) and present a detailed analysis of the sequence characteristics identified in previously characterized proteins in the heme-copper oxygen reductase (HCO) superfamily. These are correlated with their catalytic relevance and evolutionary history. FIND was then applied to discover features in previously uncharacterized members of the HCO superfamily, providing insight into their unique sequence features. This modeling approach demonstrates the power of neural networks to recognize patterns in large datasets and can be utilized to discover biochemically and structurally important features in proteins from their amino acid sequences.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted March 30, 2019.
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FIND: Identifying Functionally and Structurally Important Features in Protein Sequences with Deep Neural Networks
Ranjani Murali, James Hemp, Victoria Orphan, Yonatan Bisk
bioRxiv 592808; doi: https://doi.org/10.1101/592808
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FIND: Identifying Functionally and Structurally Important Features in Protein Sequences with Deep Neural Networks
Ranjani Murali, James Hemp, Victoria Orphan, Yonatan Bisk
bioRxiv 592808; doi: https://doi.org/10.1101/592808

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