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呈现多种拓扑取向的膜蛋白。

Membrane proteins which exhibit multiple topological orientations.

作者信息

Levy D

机构信息

University of Southern California, School of Medicine, Department of Biochemistry and Molecular Biology, Los Angeles 90033, USA.

出版信息

Essays Biochem. 1996;31:49-60.

PMID:9078457
Abstract

Membrane protein folding patterns can be divided into several classes based on their orientation and the topogenic sequences that regulate their insertion into the ER membrane. The orientation of membrane proteins is regulated by charge distribution in the polypeptide chain as well folding characteristics of the N-terminal domain. Protein targeting characteristic are determined by several sequence motifs found in the C- and N-terminal domains as well as by oligomerization. Several proteins, such as Pgp, ductin, CP450s and mEH, have been shown to exhibit more than one topological orientation in the ER which can result in protein targeting to more than one cell compartment as well as the expression of multiple biological functions.

摘要

膜蛋白折叠模式可根据其方向以及调节其插入内质网(ER)膜的拓扑序列分为几类。膜蛋白的方向由多肽链中的电荷分布以及N端结构域的折叠特性调节。蛋白质靶向特性由C端和N端结构域中发现的几个序列基序以及寡聚化决定。已显示几种蛋白质,如Pgp、导管蛋白、细胞色素P450s和微粒体环氧水解酶(mEH),在内质网中表现出不止一种拓扑方向,这可能导致蛋白质靶向不止一个细胞区室以及多种生物学功能的表达。

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