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首页> 外文期刊>DNA research: an international journal for rapid publication of reports on genes and genomes >Biochemical examination of the potential eukaryotic-type protein kinase genes in the complete genome of the unicellular Cyanobacterium synechocystis sp. PCC 6803.
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Biochemical examination of the potential eukaryotic-type protein kinase genes in the complete genome of the unicellular Cyanobacterium synechocystis sp. PCC 6803.

机译:生化检查潜在的真核生物型蛋白激酶基因在单细胞蓝藻的完整基因组中。 PCC 6803。

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摘要

The complete genome of the unicellular motile cyanobacterium Synechocystis sp. PCC 6803 harbors seven putative genes for a subfamily Pkn2 of the eukaryotic-type (or "Hanks-type") protein kinase. Previously, SpkA and SpkB were shown to have protein kinase activity and to be required for cell motility. Here, the other five genes were examined. These genes, except for spkG (slr0152), were successfully expressed in Escherichia coli. Eukaryotic-type protein kinase activity of the expressed SpkC (Slr0599), SpkD (S110776) and SpkF (Slr1225) was demonstrated as autophosphorylation and phosphorylation of the general substrate proteins. SpkE (Slr1443) did not show any activity, a finding consistent with its lack of several key amino acid residues in its kinase motif. Gene-disrupted mutants showed no discernible defect in phenotype except that spkD was apparently essential for survival.
机译:单细胞运动蓝藻Synechocystis sp。的完整基因组。 PCC 6803为真核型(或“汉克斯型”)蛋白激酶的一个亚家族Pkn2保留了七个推定基因。以前,SpkA和SpkB被证明具有蛋白激酶活性,是细胞运动所必需的。在这里,检查了其他五个基因。除spkG(slr0152)外,这些基因已在大肠杆菌中成功表达。表达的SpkC(Slr0599),SpkD(S110776)和SpkF(Slr1225)的真核型蛋白激酶活性被证明是一般底物蛋白的自磷酸化和磷酸化。 SpkE(Slr1443)没有显示任何活性,这一发现与其激酶基序中缺少几个关键氨基酸残基相符。基因破坏的突变体没有明显的表型缺陷,只是spkD显然是生存所必需的。

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