{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Gomes FC"],"funding":["Medical Research Council"],"pagination":["89-96"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2857504"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["171(2)"],"pubmed_abstract":["The activity of cyclin-dependent kinases (CDKs), which are key regulators of the eukaryotic cell cycle, is regulated through post-translational mechanisms, including binding of a cyclin and phosphorylation. Previously studies have shown that Leishmania mexicana CRK3 is an essential CDK that is a functional homologue of human CDK1. In this study, recombinant histidine tagged L. mexicana CRK3 and the cyclin CYCA were combined in vitro to produce an active histone H1 kinase that was inhibited by the CDK inhibitors, flavopiridol and indirubin-3'-monoxime. Protein kinase activity was observed in the absence of phosphorylation of the T-loop residue Thr178, but increased 5-fold upon phosphorylation by the CDK activating kinase Civ1 of Saccharomyces cerevisiae. Seven recombinant L. major CRKs (1, "],"journal":["Molecular and biochemical parasitology"],"pubmed_title":["Recombinant Leishmania mexicana CRK3:CYCA has protein kinase activity in the absence of phosphorylation on the T-loop residue Thr178."],"pmcid":["PMC2857504"],"funding_grant_id":["G0400028(69107)","G0400028","G9722968"],"pubmed_authors":["Gomes FC","Walker RG","Mottram JC","Grant KM","Brown E","Ali NO"],"additional_accession":[]},"is_claimable":false,"name":"Recombinant Leishmania mexicana CRK3:CYCA has protein kinase activity in the absence of phosphorylation on the T-loop residue Thr178.","description":"The activity of cyclin-dependent kinases (CDKs), which are key regulators of the eukaryotic cell cycle, is regulated through post-translational mechanisms, including binding of a cyclin and phosphorylation. Previously studies have shown that Leishmania mexicana CRK3 is an essential CDK that is a functional homologue of human CDK1. In this study, recombinant histidine tagged L. mexicana CRK3 and the cyclin CYCA were combined in vitro to produce an active histone H1 kinase that was inhibited by the CDK inhibitors, flavopiridol and indirubin-3'-monoxime. Protein kinase activity was observed in the absence of phosphorylation of the T-loop residue Thr178, but increased 5-fold upon phosphorylation by the CDK activating kinase Civ1 of Saccharomyces cerevisiae. Seven recombinant L. major CRKs (1, ","dates":{"release":"2010-01-01T00:00:00Z","publication":"2010 Jun","modification":"2025-04-04T13:38:41.003Z","creation":"2019-03-27T00:30:15Z"},"accession":"S-EPMC2857504","cross_references":{"pubmed":["20338198"],"doi":["10.1016/j.molbiopara.2010.03.002"]}}