Hata S
National Institute of Agrobiological Resources, Ibaraki, Japan.
FEBS Lett. 1991 Feb 11;279(1):149-52. doi: 10.1016/0014-5793(91)80271-4.
A cDNA clone, named R2, has been isolated by screening a rice cell cDNA library with a redundant oligonucleotide probe derived from the conserved ATP binding site of cdc2+/CDC28 protein kinases. The cDNA contained the entire coding sequence for a 424 amino acid polypeptide with a molecular mass of 47.6 kDa. The R2 mRNA, 2.1 kb in size, was expressed in both cultured rice cells and rice seedlings at similar levels. The predicted R2 protein has canonical motifs for ATP binding and catalysis, and is significantly homologous (up to 47%) to members of the cdc2+/CDC28 subfamily of serine/threonine protein kinase. The R2 protein is a novel member of the subfamily.
通过用源自cdc2+/CDC28蛋白激酶保守ATP结合位点的冗余寡核苷酸探针筛选水稻细胞cDNA文库,分离出一个名为R2的cDNA克隆。该cDNA包含一个424个氨基酸多肽的完整编码序列,分子量为47.6 kDa。大小为2.1 kb的R2 mRNA在培养的水稻细胞和水稻幼苗中均以相似水平表达。预测的R2蛋白具有ATP结合和催化的典型基序,并且与丝氨酸/苏氨酸蛋白激酶的cdc2+/CDC28亚家族成员具有显著同源性(高达47%)。R2蛋白是该亚家族的一个新成员。