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c-Abl对布鲁顿酪氨酸激酶的磷酸化作用。

Phosphorylation of Bruton's tyrosine kinase by c-Abl.

作者信息

Bäckesjö Carl Magnus, Vargas Leonardo, Superti-Furga Giulio, Smith C I

机构信息

Clinical Research Center, Karolinska Institutet, Huddinge University Hospital, Huddinge, Sweden.

出版信息

Biochem Biophys Res Commun. 2002 Dec 6;299(3):510-5. doi: 10.1016/s0006-291x(02)02643-8.

Abstract

Bruton's tyrosine kinase (Btk) is necessary for B-lymphocyte development. Mutation in the gene coding for Btk causes X-linked agammaglobulinemia (XLA) in humans. Similar to Btk, c-Abl is a tyrosine kinase shuttling between the cytoplasm and the nucleus where it is involved in different functions depending on the localization. In this report we describe for the first time that c-Abl and Btk physically interact and that c-Abl can phosphorylate tyrosine 223 in the SH3 domain of Btk. Interestingly, the Btk sequence matched a v-Abl substrate [correction] identified from a randomized peptide library and was also highly related to a number of previously found c-Abl substrates.

摘要

布鲁顿酪氨酸激酶(Btk)对B淋巴细胞发育至关重要。编码Btk的基因突变会导致人类X连锁无丙种球蛋白血症(XLA)。与Btk相似,c-Abl是一种穿梭于细胞质和细胞核之间的酪氨酸激酶,根据其定位参与不同功能。在本报告中,我们首次描述了c-Abl与Btk存在物理相互作用,并且c-Abl可以磷酸化Btk的SH3结构域中的酪氨酸223。有趣的是,Btk序列与从随机肽库中鉴定出的一种v-Abl底物[校正]相匹配,并且也与许多先前发现的c-Abl底物高度相关。

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