Additional file 2 of Systematic analysis of the lysine malonylome in Sanghuangporus sanghuang

Additional file 2: Table S1. The identified malonylated sites in S. sanghuang. Table S2. Protein annotation analysis. Table S3. Analysis the sequence motifs of the malonylpeptides. Table S4. GO functional annotation of the malonylproteins. Table S5. The modified proteins based on KEGG pathway enrichment analysis. Table S6. The malonylated proteins based on domain enrichment analysis. Table S7. The proteins obtained from PPI network analysis. Table S8. The 26 enzymes associated with triterpene and polysaccharide biosynthesis were found to be malonylated. Table S9. BH correction (FDR) of the GO enrichment. Table S10. BH correction (FDR) of the KEGG enrichment. Table S11. BH correction (FDR) of the protein domain enrichment.附加文件2：表S1。桑黄（S. sanghuang）中鉴定得到的丙二酰化位点。表S2：蛋白质注释分析。表S3：丙二酰化肽的序列基序分析。表S4：丙二酰化蛋白质的基因本体（Gene Ontology，GO）功能注释。表S5：基于京都基因与基因组百科全书（Kyoto Encyclopedia of Genes and Genomes，KEGG）通路富集分析得到的修饰蛋白质。表S6：基于结构域富集分析得到的丙二酰化蛋白质。表S7：经蛋白质-蛋白质相互作用（Protein-Protein Interaction，PPI）网络分析得到的蛋白质。表S8：26种与三萜及多糖生物合成相关的酶被证实存在丙二酰化修饰。表S9：GO富集分析的Benjamini-Hochberg校正（假发现率，False Discovery Rate，FDR）结果。表S10：KEGG富集分析的Benjamini-Hochberg校正（假发现率，False Discovery Rate，FDR）结果。表S11：蛋白质结构域富集分析的Benjamini-Hochberg校正（假发现率，False Discovery Rate，FDR）结果。