Data underlying the publication: SCS causes global protein succinylation contributing to the aflatoxin biosynthesis and development through the STA and Ach1

<strong>Figure 4/Figure 7</strong>: IP enrichment result of sucB-HA;<strong>Figure 5-Figure 9：</strong>1.Up-/down-regulatin proteins in aflatoxin biosynthesis pathway (ΔsucB vs. WT; xylpstA-ΔsucB vs. ΔsucB).2.Untargeted metabolomics analysis involved in A. flavus development and sclerotial formation，and aflatoxin biosynthesis pathway in ΔsucB.<strong>Figure S4: </strong>the distribution of abundance values between samples and principal component analysis (PCA) in proteomics.<strong>Figure S5:</strong> Differential analysis results statistics, differential protein grouping Venn diagram and GO analysis of differential protiens in WT, Δ<em>sucB</em> and ^{<em>xylP</em>}<em>stA</em>-Δ<em>sucB</em>.

**图4/图7**：sucB-HA的免疫沉淀（immunoprecipitation, IP）富集结果；**图5至图9**：1. 黄曲霉毒素生物合成途径中的差异上调/下调蛋白（ΔsucB菌株 vs 野生型（wild type, WT）菌株；xylP-stA-ΔsucB菌株 vs ΔsucB菌株）；2. ΔsucB菌株中涉及黄曲霉（Aspergillus flavus, A. flavus）生长发育、菌核形成及黄曲霉毒素生物合成途径的非靶向代谢组学分析。**图S4**：蛋白质组学中样本间丰度值分布与主成分分析（principal component analysis, PCA）结果。**图S5**：野生型（WT）、ΔsucB菌株及^xylPstA-ΔsucB菌株的差异蛋白差异分析结果统计、差异蛋白分组韦恩图及GO分析（Gene Ontology analysis）。