{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Mitchem MM"],"funding":["National Institutes of Health","National Science Foundation"],"pagination":["110672"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12506479"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["301(10)"],"pubmed_abstract":["Cell division cycle 37 (Cdc37) is a kinase-specific cochaperone that scaffolds protein kinase clients to the heat shock 90 (Hsp90) chaperone system. Although phosphorylation at residues S14 and S17 is known to regulate Cdc37 function, the broader role of phosphorylation across the protein remains unclear. To systematically investigate this, we created a \"Cdc37 code collection,\" a set of 46 yeast strains expressing single phosphosite mutants of Cdc37, and performed phenotypic profiling across a wide panel of environmental and chemical stressors. While canonical sites like S14 and S17 were essential for stress tolerance, 34 additional phosphomutants exhibited distinct phenotypes, often in a stress-specific manner. Notably, the mutations displayed little overlap in their stress responses, sug"],"journal":["The Journal of biological chemistry"],"pubmed_title":["Dissecting the Cdc37 cochaperone code: Functional roles in chaperone-mediated stress adaptation."],"pmcid":["PMC12506479"],"funding_grant_id":["R01GM149639","R01GM139885"],"pubmed_authors":["Choi A","Mitchem MM","Mirikar DA","Deb R","Truman AW"],"additional_accession":[]},"is_claimable":false,"name":"Dissecting the Cdc37 cochaperone code: Functional roles in chaperone-mediated stress adaptation.","description":"Cell division cycle 37 (Cdc37) is a kinase-specific cochaperone that scaffolds protein kinase clients to the heat shock 90 (Hsp90) chaperone system. Although phosphorylation at residues S14 and S17 is known to regulate Cdc37 function, the broader role of phosphorylation across the protein remains unclear. To systematically investigate this, we created a \"Cdc37 code collection,\" a set of 46 yeast strains expressing single phosphosite mutants of Cdc37, and performed phenotypic profiling across a wide panel of environmental and chemical stressors. While canonical sites like S14 and S17 were essential for stress tolerance, 34 additional phosphomutants exhibited distinct phenotypes, often in a stress-specific manner. Notably, the mutations displayed little overlap in their stress responses, sug","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Sep","modification":"2026-06-04T07:39:13.801Z","creation":"2026-06-01T03:05:54.746Z"},"accession":"S-EPMC12506479","cross_references":{"pubmed":["40902971"],"doi":["10.1016/j.jbc.2025.110672"]}}