Human non-histone lysine crotonylation plays crucial roles in biological activities.However,traditional wet-lab experiments are time-consuming and labor-intensive,making computational prediction methods increasingly popular in recent years.Despite the biological importance of lysine crotonylation,there are relatively few studies on human non-histone proteins.In this study,we developed an ensemble deep learning predictor named iHNHC-RsFPN by constructing a Residual Pyramid Network(RsFPN).First,three feature extraction methods were employed to encode sequence samples.Next,weak classifi-ers based on RsFPN were individually trained for different feature types.Finally,these weak classifiers were integrated to build a robust final predictor.Independent test results demonstrated that iHNHC-RsF-PN achieved outstanding performance across four key metrics:sensitivity(Sn=0.8580),specificity(Sp=0.7463),accuracy(Acc=0.7798),and Matthews correlation coefficient(MCC=0.5586).Comparative experiments revealed that iHNHC-RsFPN significantly improved prediction accuracy for hu-man non-histone crotonylation sites over existing methods.Additionally,we established a user-friendly web server(http://www.lzzzlab.top/ihnc/)that provides straightforward prediction services without complex calculations,facilitating further research for experts in related fields.

Human non-histone lysine crotonylation plays crucial roles in biological activities.However,traditional wet-lab experiments are time-consuming and labor-intensive,making computational prediction methods increasingly popular in recent years.Despite the biological importance of lysine crotonylation,there are relatively few studies on human non-histone proteins.In this study,we developed an ensemble deep learning predictor named iHNHC-RsFPN by constructing a Residual Pyramid Network(RsFPN).First,three feature extraction methods were employed to encode sequence samples.Next,weak classifi-ers based on RsFPN were individually trained for different feature types.Finally,these weak classifiers were integrated to build a robust final predictor.Independent test results demonstrated that iHNHC-RsF-PN achieved outstanding performance across four key metrics:sensitivity(Sn=0.8580),specificity(Sp=0.7463),accuracy(Acc=0.7798),and Matthews correlation coefficient(MCC=0.5586).Comparative experiments revealed that iHNHC-RsFPN significantly improved prediction accuracy for hu-man non-histone crotonylation sites over existing methods.Additionally,we established a user-friendly web server(http://www.lzzzlab.top/ihnc/)that provides straightforward prediction services without complex calculations,facilitating further research for experts in related fields.