Literature DB >> 15197470

Protein N-terminal methionine excision.

C Giglione1, A Boularot, T Meinnel.   

Abstract

N-terminal methionine excision (NME) is the major proteolytic pathway responsible for the diversity of N-terminal amino acids in proteins. Dedicated NME components have been identified in all organisms, in all compartments in which protein synthesis occurs: cytoplasm, plastids and mitochondria. Recent studies have revealed that NME is regulated at various levels and plays an important role in controlling protein turnover. NME is essential in Eubacteria and lower eukaryotes and is the target of many natural and synthetic inhibitors. Such inhibitors have considerable potential for use in the treatment of various human diseases, from cancer to bacterial and parasitic infections.

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Year:  2004        PMID: 15197470     DOI: 10.1007/s00018-004-3466-8

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  110 in total

1.  Protein N-terminal processing: substrate specificity of Escherichia coli and human methionine aminopeptidases.

Authors:  Qing Xiao; Feiran Zhang; Benjamin A Nacev; Jun O Liu; Dehua Pei
Journal:  Biochemistry       Date:  2010-07-06       Impact factor: 3.162

2.  Omics Assisted N-terminal Proteoform and Protein Expression Profiling On Methionine Aminopeptidase 1 (MetAP1) Deletion.

Authors:  Veronique Jonckheere; Daria Fijałkowska; Petra Van Damme
Journal:  Mol Cell Proteomics       Date:  2018-01-09       Impact factor: 5.911

3.  Synthesis and biological evaluation of salicylate-based compounds as a novel class of methionine aminopeptidase inhibitors.

Authors:  Wen-Long Wang; Sergio C Chai; Qi-Zhuang Ye
Journal:  Bioorg Med Chem Lett       Date:  2011-09-24       Impact factor: 2.823

4.  Large scale comparative proteomics of a chloroplast Clp protease mutant reveals folding stress, altered protein homeostasis, and feedback regulation of metabolism.

Authors:  Boris Zybailov; Giulia Friso; Jitae Kim; Andrea Rudella; Verenice Ramírez Rodríguez; Yukari Asakura; Qi Sun; Klaas J van Wijk
Journal:  Mol Cell Proteomics       Date:  2009-08       Impact factor: 5.911

Review 5.  The ribosome as a platform for co-translational processing, folding and targeting of newly synthesized proteins.

Authors:  Günter Kramer; Daniel Boehringer; Nenad Ban; Bernd Bukau
Journal:  Nat Struct Mol Biol       Date:  2009-06       Impact factor: 15.369

6.  Interplay between N-terminal methionine excision and FtsH protease is essential for normal chloroplast development and function in Arabidopsis.

Authors:  Zach Adam; Frédéric Frottin; Christelle Espagne; Thierry Meinnel; Carmela Giglione
Journal:  Plant Cell       Date:  2011-10-18       Impact factor: 11.277

7.  An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase.

Authors:  Reetta Hinttala; Florin Sasarman; Tamiko Nishimura; Hana Antonicka; Catherine Brunel-Guitton; Jeremy Schwartzentruber; Somayyeh Fahiminiya; Jacek Majewski; Denis Faubert; Elsebet Ostergaard; Jan A Smeitink; Eric A Shoubridge
Journal:  Hum Mol Genet       Date:  2015-04-24       Impact factor: 6.150

8.  Characterization of the Ovarian Tumor Peptidome.

Authors:  Tao Liu; Karin D Rodland; Richard D Smith
Journal:  Vitam Horm       Date:  2018-02-22       Impact factor: 3.421

9.  FE(II) is the native cofactor for Escherichia coli methionine aminopeptidase.

Authors:  Sergio C Chai; Wen-Long Wang; Qi-Zhuang Ye
Journal:  J Biol Chem       Date:  2008-07-31       Impact factor: 5.157

Review 10.  Redox Signaling by Reactive Electrophiles and Oxidants.

Authors:  Saba Parvez; Marcus J C Long; Jesse R Poganik; Yimon Aye
Journal:  Chem Rev       Date:  2018-08-27       Impact factor: 60.622

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