<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Honglin Wang</submitter><species>Mus Musculus</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0018390000</full_dataset_link><submitter_email>Honglin.wang@sjtu.edu.cn</submitter_email><submitter_affiliation>Shanghai Jiao Tong University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>HSD17B4 interactome in mouse keratinocytes reveals association with splicing factors and RNA processing</name><description>This project aims to elucidate the molecular mechanism by which HSD17B4 regulates CYP7B1 expression in mouse keratinocytes (mKCs). To identify proteins that interact with HSD17B4, we performed co-immunoprecipitation (Co-IP) using an HSD17B4-specific antibody, followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. The raw mass spectrometry data were acquired and processed to identify HSD17B4-interacting proteins. Subsequent Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses of the HSD17B4 interactome revealed a significant overrepresentation of proteins involved in RNA splicing and RNA processing. These findings suggest that HSD17B4 may regulate CYP7B1 expression through interactions with splicing factors, pointing to a previously unrecognized nuclear function of HSD17B4 beyond its enzymatic activity. This project contains the MS data for the interacting protein of HSD17B4 we identified.</description><dates><publication>Thu Jul 16 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD081170</accession><cross_references><TAXONOMY>10090</TAXONOMY></cross_references></HashMap>