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鉴定新型蛋白质Yip4p和Yip5p为Rab GTP酶相互作用因子。

Identification of the novel proteins Yip4p and Yip5p as Rab GTPase interacting factors.

作者信息

Calero Monica, Winand Nena J, Collins Ruth N

机构信息

Department of Molecular Medicine, Cornell University, Ithaca, NY 14853-6401, USA.

出版信息

FEBS Lett. 2002 Mar 27;515(1-3):89-98. doi: 10.1016/s0014-5793(02)02442-0.

Abstract

The Rab GTPases are key regulators of membrane traffic. Yip1p is a membrane protein of unknown function that has been reported to interact with the Rabs Ypt1p and Ypt31p. In this study we identify Yif1p, and two unknown open reading frames, Ygl198p and Ygl161p, which we term Yip4p and Yip5p, as Yip1p-related sequences. We demonstrate that the Yip1p-related proteins possess several features: (i) they have a common overall domain topology, (ii) they are capable of biochemical interaction with a variety of Rab proteins in a manner dependent on C-terminal prenylation, and (iii) they share an ability to physically associate with other members of the YIP1 family.

摘要

Rab GTP酶是膜泡运输的关键调节因子。Yip1p是一种功能未知的膜蛋白,据报道它可与Rabs Ypt1p和Ypt31p相互作用。在本研究中,我们鉴定出Yif1p以及两个未知的开放阅读框Ygl198p和Ygl161p(我们将其命名为Yip4p和Yip5p)为与Yip1p相关的序列。我们证明,与Yip1p相关的蛋白质具有以下几个特征:(i)它们具有共同的整体结构域拓扑结构;(ii)它们能够以依赖于C末端异戊二烯化的方式与多种Rab蛋白进行生化相互作用;(iii)它们具有与YIP1家族其他成员进行物理缔合的能力。

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