CaLMPhosKAN: prediction of general phosphorylation sites in proteins via fusion of codon aware embeddings with amino acid aware embeddings and wavelet-based Kolmogorov-Arnold network.

Pawel Pratyush, Callen Carrier, Suresh Pokharel, Hamid D Ismail, Meenal Chaudhari, Dukka B Kc
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Abstract

Motivation: The mapping from codon to amino acid is surjective due to codon degeneracy, suggesting that codon space might harbor higher information content. Embeddings from the codon language model have recently demonstrated success in various protein downstream tasks. However, predictive models for residue-level tasks such as phosphorylation sites, arguably the most studied Post-Translational Modification (PTM), and PTM sites prediction in general, have predominantly relied on representations in amino acid space.

Results: We introduce a novel approach for predicting phosphorylation sites by utilizing codon-level information through embeddings from the codon adaptation language model (CaLM), trained on protein-coding DNA sequences. Protein sequences are first reverse-translated into reliable coding sequences by mapping UniProt sequences to their corresponding NCBI reference sequences and extracting the exact coding sequences from their GenBank format using a dynamic programming-based global pairwise alignment. The resulting coding sequences are encoded using the CaLM encoder to generate codon-aware embeddings, which are subsequently integrated with amino acid-aware embeddings obtained from a protein language model, through an early fusion strategy. Next, a window-level representation of the site of interest, retaining the full sequence context, is constructed from the fused embeddings. A ConvBiGRU network extracts feature maps that capture spatiotemporal correlations between proximal residues within the window. This is followed by a prediction head based on a Kolmogorov-Arnold network (KAN) using the derivative of gaussian wavelet transform to generate the inference for the site. The overall model, dubbed CaLMPhosKAN, performs better than the existing approaches across multiple datasets.

Availability and implementation: CaLMPhosKAN is publicly available at https://github.com/KCLabMTU/CaLMPhosKAN.

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callphoskan:通过密码子感知嵌入与氨基酸感知嵌入融合和基于小波的Kolmogorov-Arnold网络预测蛋白质的一般磷酸化位点。
动机:由于密码子简并,密码子到氨基酸的映射是满射的,说明密码子空间可能蕴藏着更高的信息量。密码子语言模型的嵌入最近在各种蛋白质下游任务中取得了成功。然而,残基水平任务的预测模型,如磷酸化位点,可以说是研究最多的翻译后修饰(PTM),以及一般的PTM位点预测,主要依赖于氨基酸空间的表示。结果:我们引入了一种新的方法,通过嵌入密码子适应语言模型(CaLM),利用密码子水平的信息预测磷酸化位点,该模型是在蛋白质编码DNA序列上训练的。首先,通过将UniProt序列映射到相应的NCBI参考序列,并使用基于动态规划的全局两两比对从GenBank格式中提取准确的编码序列,将蛋白质序列反向翻译成可靠的编码序列。所得到的编码序列使用CaLM编码器编码,生成密码子感知嵌入,随后通过早期融合策略将其与从蛋白质语言模型获得的氨基酸感知嵌入整合。接下来,从融合嵌入中构建感兴趣的位置的窗口级表示,保留完整的序列上下文。ConvBiGRU网络提取特征图,捕获窗口内近端残基之间的时空相关性。其次是基于Kolmogorov-Arnold网络(KAN)的预测头,该预测头采用高斯小波变换的导数来生成站点的推断。整个模型被称为CaLMPhosKAN,在多个数据集上比现有的方法表现得更好。可用性和实施:CaLMPhosKAN可在https://github.com/KCLabMTU/CaLMPhosKAN.Supplementary上公开获取:补充数据可在Bioinformatics在线获得。
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