nhKcr

nhKcr predicts lysine crotonylation (Kcr) sites on nonhistone proteins to enable computational identification of post-translational crotonylation events and to complement high-resolution mass spectrometry-based discovery.


Key Features:

  • Specialization: Predicts lysine crotonylation (Kcr) sites exclusively on nonhistone proteins.
  • Deep learning framework (CNNrgb): Implements the CNNrgb deep learning-based computational framework for site prediction.
  • Feature integration: Integrates diverse types of features for enhanced predictive accuracy.
  • Benchmarking: Performance was compared against random forest, logitboost, naïve Bayes, and logistic regression classifiers.
  • Validation: Evaluated using 10-fold cross-validation and independent testing.
  • Scalability: Demonstrated high computational efficiency on large datasets.
  • Method comparison foundation: Development was informed by a review of six existing crotonylation site prediction methods.

Scientific Applications:

  • Annotation of Kcr sites: Annotates lysine crotonylation sites on nonhistone proteins for downstream biological and pathophysiological studies.
  • Experimental prioritization: Prioritizes candidate Kcr sites for validation by high-resolution mass spectrometry.
  • Large-scale sequence analysis: Enables high-throughput analysis of large nonhistone protein sequence datasets to identify potential crotonylation sites.

Methodology:

Implements the CNNrgb deep learning framework integrating diverse feature types; development was informed by a review of six existing predictors and performance was benchmarked against random forest, logitboost, naïve Bayes, and logistic regression using 10-fold cross-validation and independent testing.

Topics

Details

Tool Type:
web application
Added:
10/25/2021
Last Updated:
11/24/2024

Operations

Publications

Chen Y, Wang Z, Wang Y, Ying G, Chen Z, Song J. nhKcr: a new bioinformatics tool for predicting crotonylation sites on human nonhistone proteins based on deep learning. Briefings in Bioinformatics. 2021;22(6). doi:10.1093/bib/bbab146. PMID:34002774. PMCID:PMC8768455.

PMID: 34002774
PMCID: PMC8768455
Funding: - National Natural Science Foundation of China: 81772843 - National Health and Medical Research Council: 1092262 - Australian Research Council: DP120104460, LP110200333 - National Institutes of Health: R01 AI111965

Documentation

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