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Src酪氨酸激酶通过SH3结构域与一种人类钾通道的关联。

Association of Src tyrosine kinase with a human potassium channel mediated by SH3 domain.

作者信息

Holmes T C, Fadool D A, Ren R, Levitan I B

机构信息

Department of Biochemistry and Volen Center for Complex Systems, Brandeis University, Waltham, MA 02254, USA.

出版信息

Science. 1996 Dec 20;274(5295):2089-91. doi: 10.1126/science.274.5295.2089.

Abstract

The human Kv1.5 potassium channel (hKv1.5) contains proline-rich sequences identical to those that bind to Src homology 3 (SH3) domains. Direct association of the Src tyrosine kinase with cloned hKv1.5 and native hKv1.5 in human myocardium was observed. This interaction was mediated by the proline-rich motif of hKv1.5 and the SH3 domain of Src. Furthermore, hKv1.5 was tyrosine phosphorylated, and the channel current was suppressed, in cells coexpressing v-Src. These results provide direct biochemical evidence for a signaling complex composed of a potassium channel and a protein tyrosine kinase.

摘要

人类Kv1.5钾通道(hKv1.5)含有与那些结合至Src同源3(SH3)结构域的序列相同的富含脯氨酸的序列。观察到Src酪氨酸激酶与克隆的hKv1.5以及人心肌中的天然hKv1.5直接缔合。这种相互作用是由hKv1.5的富含脯氨酸基序和Src的SH3结构域介导的。此外,在共表达v-Src的细胞中,hKv1.5发生酪氨酸磷酸化,并且通道电流受到抑制。这些结果为一种由钾通道和蛋白酪氨酸激酶组成的信号复合物提供了直接的生化证据。

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