| http://purl.uniprot.org/citations/23795888 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/23795888 | http://www.w3.org/2000/01/rdf-schema#comment | "S-acylation of eukaryotic proteins is the reversible attachment of palmitic or stearic acid to cysteine residues, catalysed by protein S-acyl transferases that share an Asp-His-His-Cys (DHHC) motif. Previous evidence suggests that in Arabidopsis S-acylation is involved in the control of cell size, polarity and the growth of pollen tubes and root hairs. Using a combination of yeast genetics, biochemistry, cell biology and loss of function genetics the roles of a member of the protein S-acyl transferase PAT family, AtPAT10 (At3g51390), have been explored. In keeping with its role as a PAT, AtPAT10 auto-S-acylates, and partially complements the yeast akr1 PAT mutant, and this requires Cys(192) of the DHHC motif. In Arabidopsis AtPAT10 is localized in the Golgi stack, trans-Golgi network/early endosome and tonoplast. Loss-of-function mutants have a pleiotropic phenotype involving cell expansion and division, vascular patterning, and fertility that is rescued by wild-type AtPAT10 but not by catalytically inactive AtPAT10C(192) A. This supports the hypothesis that AtPAT10 is functionally independent of the other Arabidopsis PATs. Our findings demonstrate a growing importance of protein S-acylation in plants, and reveal a Golgi and tonoplast located S-acylation mechanism that affects a range of events during growth and development in Arabidopsis."xsd:string |
| http://purl.uniprot.org/citations/23795888 | http://purl.org/dc/terms/identifier | "doi:10.1111/nph.12385"xsd:string |
| http://purl.uniprot.org/citations/23795888 | http://purl.uniprot.org/core/author | "Hooley R."xsd:string |
| http://purl.uniprot.org/citations/23795888 | http://purl.uniprot.org/core/author | "Qi B."xsd:string |
| http://purl.uniprot.org/citations/23795888 | http://purl.uniprot.org/core/author | "Doughty J."xsd:string |
| http://purl.uniprot.org/citations/23795888 | http://purl.uniprot.org/core/date | "2013"xsd:gYear |
| http://purl.uniprot.org/citations/23795888 | http://purl.uniprot.org/core/name | "New Phytol"xsd:string |
| http://purl.uniprot.org/citations/23795888 | http://purl.uniprot.org/core/pages | "444-456"xsd:string |
| http://purl.uniprot.org/citations/23795888 | http://purl.uniprot.org/core/title | "A Golgi and tonoplast localized S-acyl transferase is involved in cell expansion, cell division, vascular patterning and fertility in Arabidopsis."xsd:string |
| http://purl.uniprot.org/citations/23795888 | http://purl.uniprot.org/core/volume | "200"xsd:string |
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| http://purl.uniprot.org/uniprot/A0A178VFJ8 | http://purl.uniprot.org/core/mappedCitation | http://purl.uniprot.org/citations/23795888 |
| http://purl.uniprot.org/uniprot/Q7XA86 | http://purl.uniprot.org/core/mappedCitation | http://purl.uniprot.org/citations/23795888 |
| http://purl.uniprot.org/uniprot/A0A1I9LQT3 | http://purl.uniprot.org/core/mappedCitation | http://purl.uniprot.org/citations/23795888 |