Publications by authors named "Enfeng Qi"

Great efforts have been devoted to the development of novel and multifunctional wound dressing materials to meet the different needs of wound healing. Herein, we covalently grafted quaternary ammonium groups (QAGs) containing 12-carbon straight-chain alkanes to the dextran polymer skeleton. We then oxidized the resulting product into oxidized quaternized dextran (OQD).

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Article Synopsis
  • Recent advancements in long-read RNA sequencing are promising for analyzing transcriptomes, but current clustering algorithms demand significant computational resources.
  • A new algorithm called GeLuster has been developed, demonstrating exceptional speed (2.9-17.5 times faster) and lower memory usage compared to existing methods while maintaining higher clustering accuracy on long RNA-seq datasets.
  • GeLuster is publicly available for use, enhancing the potential for large-scale transcriptome studies in the future.
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Based on substrate sequences, we proposed a novel method for comparing sequence similarities among 68 proteases compiled from the MEROPS online database. The rank vector was defined based on the frequencies of amino acids at each site of the substrate, aiming to eliminate the different order variances of magnitude between proteases. Without any assumption on homology, a protease specificity tree is constructed with a striking clustering of proteases from different evolutionary origins and catalytic types.

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Proteases play critical roles in a wide variety of fundamental biological functions, and numerous protease inhibitors have been developed to treat various diseases including cancer. A wide range of experimental and computational methods have been developed to investigate the specificity and catalytic mechanisms of proteases. However, these methods only focused on the preferences of a single position around a cleavage site in a substrate, rarely on the compositionality of the subsites.

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Background: Protein feature extraction plays an important role in the areas of similarity analysis of protein sequences and prediction of protein structures, functions and interactions. The feature extraction based on graphical representation is one of the most effective and efficient ways. However, most existing methods suffer limitations from their method design.

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Background: The mechanism of action of proteases has been widely studied based on substrate specificity. Prior research has been focused on the amino acids at a single amino acid site, but rarely on combinations of amino acids around the cleavage bond.

Results: We propose a novel block-based approach to reveal the potential combinations of amino acids which may regulate the action of proteases.

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