<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Yi-Gang Li</submitter><species>Mus Musculus</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0015868000</full_dataset_link><submitter_email>liyigang@xinhuamed.com.cn</submitter_email><submitter_affiliation>Department of Cardiology, Xinhua Hospital affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Quantitative TMT phosphoproteomics in neonatal mouse ventricular myocytes (NMVMs) upon NUAK1 overexpression</name><description>This dataset contains TMT-based quantitative phosphoproteomics data generated from neonatal mouse ventricular myocytes (NMVMs) comparing control cells versus NUAK1 overexpression (three biological replicates per group; CTL_1–3 and OE_1–3). Samples were analyzed by LC–MS/MS with fractionated runs (raw fractions F1–F3). MS/MS spectra were searched using MaxQuant (v1.6.15.0) against the UniProt Mus musculus reference proteome (release 2024-06-04). Enzyme was set to Trypsin/P. Fixed modification: Carbamidomethyl (C). Variable modifications: Oxidation (M), Protein N-term acetylation, and Phospho (STY). Mass tolerances were set to 20 ppm (first search) and 5 ppm (main search) for precursor ions and 20 ppm for fragment ions. Protein and PSM FDR were controlled at 1%. The submission includes the raw files and identification/quantification summary tables used for downstream QC and differential phosphorylation analyses.</description><dates><publication>Wed Feb 25 00:00:00 GMT 2026</publication></dates><accession>PXD074878</accession><cross_references><TAXONOMY>10090</TAXONOMY></cross_references></HashMap>