The Relative Distance Prediction of Transmembrane Protein Surface Residue Based on Improved Residual Networks

Abstract

(1) Background: Transmembrane proteins (TMPs) act as gateways connecting the intra- and extra-biomembrane environments, exchanging material and signals crossing the biofilm. Relevant evidence shows that corresponding interactions mostly happen on the TMPs’ surface. Therefore, knowledge of the relative distance among surface residues is critically helpful in discovering the potential local structural characters and setting the foundation for the protein’s interaction with other molecules. However, the prediction of fine-grained distances among residues with sequences remains challenging; (2) Methods: In this study, we proposed a deep-learning method called TMP-SurResD, which capitalized on the combination of the Residual Block (RB) and Squeeze-and-Excitation (SE) for simultaneously predicting the relative distance of functional surface residues based on sequences’ information; (3) Results: The comprehensive evaluation demonstrated that TMP-SurResD could successfully capture the relative distance between residues, with a Pearson Correlation Coefficient (PCC) of 0.7105 and 0.6999 on the validation and independent sets, respectively. In addition, TMP-SurResD outperformed other methods when applied to TMPs surface residue contact prediction, and the maximum Matthews Correlation Coefficient (MCC) reached 0.602 by setting a threshold to the predicted distance of 10; (4) Conclusions: TMP-SurResD can serve as a useful tool in supporting a sequence-based local structural feature construction and exploring the function and biological mechanisms of structure determination in TMPs, which can thus significantly facilitate the research direction of molecular drug action, target design, and disease treatment.

Keywords

• transmembrane protein
• distances among residues
• co-evolution
• residual network