Literature DB >> 21971548

Mnl2, a novel component of the ER associated protein degradation pathway.

Elena Martinez Benitez1, Alexandra Stolz, Alexander Becher, Dieter H Wolf.   

Abstract

In eukaryotes, membrane and soluble proteins of the secretory pathway enter the endoplasmic reticulum (ER) after synthesis in an unfolded state. Directly after entry, most proteins are modified with glycans at suitable glycosylation sites and start to fold. A protein that cannot fold properly will be degraded in a process called ER associated degradation (ERAD). Failures in ERAD, either by loss of function or by premature degradation of proteins, are a cause of severe diseases. Therefore, the search for novel ERAD components to gain better insight in this process is of high importance. Carbohydrate trimming is a relevant process in ER quality control. In this work a novel putative yeast mannosidase encoded by the open reading frame YLR057W was identified and named Mnl2. Deletion of MNL2 diminished the degradation efficiency of misfolded CPY(*) in the absence of the cognate mannosidase Mnl1, indicating a specific role in ERAD.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21971548     DOI: 10.1016/j.bbrc.2011.09.100

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  1 in total

1.  Phenotypic analysis of α1,2-mannosidase-like protein deletion mutants in Saccharomyces cerevisiae.

Authors:  Seita Nakamasu; Takashi Kikuma; Yuji Hashiguchi; Sato Tada; Kanae Sano; Yukishige Ito; Yoichi Takeda
Journal:  MicroPubl Biol       Date:  2022-09-23
  1 in total

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