<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Huang Y</submitter><funding>Guangdong Basic and Applied Basic Research Foundation</funding><pagination>742</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12292072</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(7)</volume><pubmed_abstract>The TRIM CIV subfamily, distinguished by its C-terminal PRY-SPRY domains, constitutes nearly half of the human TRIM family and plays pivotal roles in cancer progression through ubiquitination. Identifying TRIM CIV substrates and interactors has emerged as a critical approach for elucidating tumorigenesis. Current protein-protein interaction (PPI) prediction models face challenges, including an inherent deficiency of negative datasets, biased feature integration, and the absence of a cancer-specific interaction context. To achieve the precise identification of TRIMCIV targets, we developed TRIMCIVtargeter with predictive models that systematically integrates multi-dimensional PPI features-expression differences and correlations in specific cancer, comparable protein-docking scores, and canc</pubmed_abstract><journal>Biology</journal><pubmed_title>A TRIM Family-Based Strategy for TRIMCIV Target Prediction in a Pan-Cancer Context with Multi-Omics Data and Protein Docking Integration.</pubmed_title><pmcid>PMC12292072</pmcid><funding_grant_id>2023A1515011221</funding_grant_id><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Liang J</pubmed_authors><pubmed_authors>Luo Y</pubmed_authors><pubmed_authors>Gao X</pubmed_authors><pubmed_authors>Xuan J</pubmed_authors><pubmed_authors>Liu W</pubmed_authors></additional><is_claimable>false</is_claimable><name>A TRIM Family-Based Strategy for TRIMCIV Target Prediction in a Pan-Cancer Context with Multi-Omics Data and Protein Docking Integration.</name><description>The TRIM CIV subfamily, distinguished by its C-terminal PRY-SPRY domains, constitutes nearly half of the human TRIM family and plays pivotal roles in cancer progression through ubiquitination. Identifying TRIM CIV substrates and interactors has emerged as a critical approach for elucidating tumorigenesis. Current protein-protein interaction (PPI) prediction models face challenges, including an inherent deficiency of negative datasets, biased feature integration, and the absence of a cancer-specific interaction context. To achieve the precise identification of TRIMCIV targets, we developed TRIMCIVtargeter with predictive models that systematically integrates multi-dimensional PPI features-expression differences and correlations in specific cancer, comparable protein-docking scores, and canc</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jun</publication><modification>2026-07-04T03:17:53.493Z</modification><creation>2025-08-28T03:09:19.858Z</creation></dates><accession>S-EPMC12292072</accession><cross_references><pubmed>40723303</pubmed><doi>10.3390/biology14070742</doi></cross_references></HashMap>