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寡糖基转移酶活性位点与内质网内膜之间距离的测定

Determination of the distance between the oligosaccharyltransferase active site and the endoplasmic reticulum membrane.

作者信息

Nilsson I M, von Heijne G

机构信息

Department of Molecular Biology, Karolinska Institute Center for Structural Biochemistry, NOVUM, Huddinge, Sweden.

出版信息

J Biol Chem. 1993 Mar 15;268(8):5798-801.

PMID:8449946
Abstract

By in vitro transcription/translation of model proteins in the presence of dog pancreas microsomes, we have measured the minimum distance of an acceptor site from the lumenal end of a transmembrane segment required for N-linked glycosylation, both when the acceptor site is placed N- and C-terminally to the membrane anchor. We observe a sharp threshold at a distance of 12-14 residues, suggesting that the oligosaccharyltransferase active site is 30-40 A above the membrane and is oriented roughly parallel to the membrane surface.

摘要

通过在犬胰腺微粒体存在的情况下对模型蛋白进行体外转录/翻译,我们测量了N-连接糖基化所需的受体位点与跨膜片段腔端的最小距离,受体位点分别位于膜锚定的N端和C端。我们观察到在12 - 14个残基的距离处有一个明显的阈值,这表明寡糖基转移酶活性位点在膜上方30 - 40埃处,且大致平行于膜表面定向。

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