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is a critical post-translational modification involved in the regulation of almost all cellular processes. However, less than 5% of thousands of recently discovered phosphorylation sites have a known function. Here, we devised a chemical genetic approach to study the functional relevance of phosphorylation in S. cerevisiae. We generated 474 phospho-deficient mutants that, along with the gene deletion library, were screened for fitness in 102 conditions.</long_description><repository>ENA</repository><description_synonyms>Saccharomyces oviformis, Sccharomyces cerevisiae, Yeast, Candida robusta, lager beer yeast., Saccharomyces capensis, yeast, Saccharomyes cerevisiae, baker's yeast, brewer's yeast, Saccharomyces uvarum var. melibiosus, Saccharomyces italicus, Saccaromyces cerevisiae</description_synonyms><name_synonyms>Saccharomyces oviformis, Sccharomyces cerevisiae, Yeast, Candida robusta, lager beer yeast., Saccharomyces capensis, yeast, Saccharomyes cerevisiae, baker's yeast, brewer's yeast, Saccharomyces uvarum var. melibiosus, Saccharomyces italicus, Saccaromyces cerevisiae</name_synonyms></additional><is_claimable>false</is_claimable><name>Sequencing of yeast phosphomutants</name><description>Sequencing of yeast phosphomutants</description><dates><last_updated>2020-06-04</last_updated><first_public>2020-06-08</first_public></dates><accession>PRJEB38714</accession><cross_references/></HashMap>