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ura7 (O42644) is the sole essential S. pombe CTP synthase (Cts1), catalyzing ATP-dependent amination of UTP to CTP using glutamine-derived ammonia, regulated by GTP activation and CTP feedback inhibition.
"is the sole essential CTPS enzyme catalyzing ATP-dependent UTP→CTP conversion, using glutamine-derived ammonia and regulated by GTP activation and CTP feedback inhibition"
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S. pombe carries a single CTPS gene at the cts1 locus, distinguishing it from organisms (human CTPS1/2; budding yeast URA7/URA8) with two paralogs. The "ura7" symbol is the PomBase standard name; the primary literature refers to the gene/protein as cts1/Cts1/CTPS.
"fission yeast as a model with **a single CTPS gene**, encoded at the **cts1** locus"
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CTPS is a two-domain class I glutamine amidotransferase: an N-terminal synthase (ammonia ligase) domain that binds ATP/UTP, and a C-terminal GATase domain that hydrolyzes glutamine, coupled by an intramolecular NH3 tunnel.
"an N-terminal **synthase (ammonia ligase) domain** that binds ATP/UTP and performs the phosphorylation/amination chemistry, and"
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In S. pombe, Cts1 forms cytoplasmic cytoophidia present in >90% of log-phase cells that disassemble in stationary phase, with CTPS protein (but not mRNA) declining in stationary phase, indicating regulation at the protein-stability level.
"cytoophidia that are **highly abundant during logarithmic growth** (reported **>90%** of cells) and largely **disappear in stationary phase**"
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Filament integrity is functionally coupled to cell-cycle control (G2 length), cell size, and gene expression (slm9), arguing cytoophidia are a regulated supramolecular state rather than a passive storage depot.
"Filament integrity is functionally linked to cell-cycle control (G2 length), cell size, and gene expression (slm9)"
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CTPS abundance/turnover in S. pombe is reported to involve ubiquitin binding and ubiquitin-mediated degradation, consistent with post-translational control of the enzyme and its filaments.
"post-translational regulation associated with **ubiquitin binding** and **ubiquitin-mediated degradation**"