Identifying molecular recognition features in intrinsically disordered regions of proteins by transfer learning

Author:

Hanson Jack1ORCID,Litfin Thomas2,Paliwal Kuldip1,Zhou Yaoqi2ORCID

Affiliation:

1. Signal Processing Laboratory, Griffith University, Brisbane, QLD 4122, Australia

2. Institute for Glycomics, School of Information and Communication Technology, Griffith University, Southport, QLD 4222, Australia

Abstract

Abstract Motivation Protein intrinsic disorder describes the tendency of sequence residues to not fold into a rigid three-dimensional shape by themselves. However, some of these disordered regions can transition from disorder to order when interacting with another molecule in segments known as molecular recognition features (MoRFs). Previous analysis has shown that these MoRF regions are indirectly encoded within the prediction of residue disorder as low-confidence predictions [i.e. in a semi-disordered state P(D)≈0.5]. Thus, what has been learned for disorder prediction may be transferable to MoRF prediction. Transferring the internal characterization of protein disorder for the prediction of MoRF residues would allow us to take advantage of the large training set available for disorder prediction, enabling the training of larger analytical models than is currently feasible on the small number of currently available annotated MoRF proteins. In this paper, we propose a new method for MoRF prediction by transfer learning from the SPOT-Disorder2 ensemble models built for disorder prediction. Results We confirm that directly training on the MoRF set with a randomly initialized model yields substantially poorer performance on independent test sets than by using the transfer-learning-based method SPOT-MoRF, for both deep and simple networks. Its comparison to current state-of-the-art techniques reveals its superior performance in identifying MoRF binding regions in proteins across two independent testing sets, including our new dataset of >800 protein chains. These test chains share <30% sequence similarity to all training and validation proteins used in SPOT-Disorder2 and SPOT-MoRF, and provide a much-needed large-scale update on the performance of current MoRF predictors. The method is expected to be useful in locating functional disordered regions in proteins. Availability and implementation SPOT-MoRF and its data are available as a web server and as a standalone program at: http://sparks-lab.org/jack/server/SPOT-MoRF/index.php. Contact jack.s.hanson93@gmail.com or yaoqi.zhou@griffith.edu.au Supplementary information Supplementary data are available at Bioinformatics online.

Funder

Australian Research Council

National Health and Medical Research Council

Queensland Cyber Infrastructure Foundation

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Reference62 articles.

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2. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs;Altschul;Nucleic Acids Res,1997

3. Sequence-based prediction of molecular recognition features in disordered proteins;Chun;J. Med. Bioeng,2013

4. MoRFpred, a computational tool for sequence-based prediction and characterization of short disorder-to-order transitioning binding regions in proteins;Disfani;Bioinformatics,2012

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