<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Meng Zhao</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0018744000</full_dataset_link><submitter_email>zhaomeng@tmu.edu.cn</submitter_email><submitter_affiliation>Tianjin Medical University Cancer Institute &amp;amp; Hospital</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Mass spectrometry-based identification of E3 ubiquitin ligases mediating MCT1 ubiquitination</name><description>This project aims to identify potential E3 ubiquitin ligases regulating MCT1 (monocarboxylate transporter 1) in human cells. We performed immunoprecipitation of MCT1 followed by LC-MS/MS analysis using a Q-Exactive HF X mass spectrometer. Samples included control (con) and MCT1-pulldown (MCT1) groups, each with 7 biological replicates. Proteins were identified via Mascot search against the human SwissProt database (20,324 sequences) with FDR &lt;1% at PSM level. A total of 398–1,201 proteins were identified per sample. The results will be used to screen for candidate E3 ligases interacting with MCT1.</description><dates><publication>Mon Aug 03 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD082071</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>