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混合谱系激酶LZK中功能结构域的鉴定与表征

Identification and characterization of functional domains in a mixed lineage kinase LZK.

作者信息

Ikeda A, Masaki M, Kozutsumi Y, Oka S, Kawasaki T

机构信息

Department of Biological Chemistry and CREST (Core Research for Educational Science and Technology) Project, Japan Science and Technology Corporation, Graduate School of Pharmaceutical Sciences, Kyoto University, 606-8501, Kyoto, Japan.

出版信息

FEBS Lett. 2001 Jan 19;488(3):190-5. doi: 10.1016/s0014-5793(00)02432-7.

Abstract

The mixed lineage kinase (MLK) family is a recently described protein kinase family. The MLKs contain a kinase domain followed by a dual leucine zipper-like motif. We previously reported the molecular cloning of LZK (leucine zipper-bearing kinase), a novel MLK, and that LZK activated the c-Jun NH2 terminal kinase (JNK)/stress-activated protein kinase (SAPK) pathway through MKK7 in cells. Here, we reveal that LZK forms dimers/oligomers through its dual leucine zipper-like motif, and that this is necessary for activation of the JNK/SAPK pathway. We also identify the C-terminal functional region of LZK, which is indispensable for the activation of SEK1, but not that of MKK7.

摘要

混合谱系激酶(MLK)家族是最近被描述的一个蛋白激酶家族。MLK包含一个激酶结构域,其后是一个双亮氨酸拉链样基序。我们之前报道了新型MLK——含亮氨酸拉链激酶(LZK)的分子克隆,并且LZK在细胞中通过MKK7激活c-Jun氨基末端激酶(JNK)/应激激活蛋白激酶(SAPK)途径。在此,我们揭示LZK通过其双亮氨酸拉链样基序形成二聚体/寡聚体,并且这对于JNK/SAPK途径的激活是必需的。我们还鉴定了LZK的C末端功能区域,其对于SEK1的激活是不可或缺的,但对于MKK7的激活并非如此。

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