Literature DB >> 12576022

Bioinformatic analysis of ClpS, a protein module involved in prokaryotic and eukaryotic protein degradation.

Andrei N Lupas1, Kristin K Koretke.   

Abstract

ClpS is a small protein, usually encoded immediately upstream of ClpA in the genomes of proteobacteria. Recent results show that it is a molecular adaptor for substrate recognition by ClpA in Escherichia coli. We analyzed ClpS by bioinformatic methods and found that ClpS homologs are also found in organisms that lack ClpA, such as actinobacteria, cyanobacteria, and plant chloroplasts. Furthermore, ClpS is homologous to a domain in the eukaryotic E3 ubiquitin ligase, N-recognin. This domain has previously been described as responsible for the recognition of type 2 N-end rule substrates. Despite very low levels of sequence similarity to proteins of known structure, there appears to be substantial structural similarity between ClpS and the C-terminal domain of ribosomal protein L7/12 (1CTF).

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Year:  2003        PMID: 12576022     DOI: 10.1016/s1047-8477(02)00582-8

Source DB:  PubMed          Journal:  J Struct Biol        ISSN: 1047-8477            Impact factor:   2.867


  28 in total

1.  Crystal structures of leucyl/phenylalanyl-tRNA-protein transferase and its complex with an aminoacyl-tRNA analog.

Authors:  Kyoko Suto; Yoshihiro Shimizu; Kazunori Watanabe; Takuya Ueda; Shuya Fukai; Osamu Nureki; Kozo Tomita
Journal:  EMBO J       Date:  2006-11-16       Impact factor: 11.598

2.  Aminoacyl-transferases and the N-end rule pathway of prokaryotic/eukaryotic specificity in a human pathogen.

Authors:  Emmanuelle Graciet; Rong-Gui Hu; Konstantin Piatkov; Joon Haeng Rhee; Erich M Schwarz; Alexander Varshavsky
Journal:  Proc Natl Acad Sci U S A       Date:  2006-02-21       Impact factor: 11.205

3.  Molecular basis of substrate selection by the N-end rule adaptor protein ClpS.

Authors:  Giselle Román-Hernández; Robert A Grant; Robert T Sauer; Tania A Baker
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-18       Impact factor: 11.205

4.  Structural basis of N-end rule substrate recognition in Escherichia coli by the ClpAP adaptor protein ClpS.

Authors:  Verena J Schuenemann; Stephanie M Kralik; Reinhard Albrecht; Sukhdeep K Spall; Kaye N Truscott; David A Dougan; Kornelius Zeth
Journal:  EMBO Rep       Date:  2009-04-17       Impact factor: 8.807

Review 5.  Adapting the machine: adaptor proteins for Hsp100/Clp and AAA+ proteases.

Authors:  Janine Kirstein; Noël Molière; David A Dougan; Kürşad Turgay
Journal:  Nat Rev Microbiol       Date:  2009-08       Impact factor: 60.633

Review 6.  The N-end rule pathway and regulation by proteolysis.

Authors:  Alexander Varshavsky
Journal:  Protein Sci       Date:  2011-08       Impact factor: 6.725

7.  The expanded specificity and physiological role of a widespread N-degron recognin.

Authors:  Xiaohui Gao; Jinki Yeom; Eduardo A Groisman
Journal:  Proc Natl Acad Sci U S A       Date:  2019-08-26       Impact factor: 11.205

8.  The molecular basis of N-end rule recognition.

Authors:  Kevin H Wang; Giselle Roman-Hernandez; Robert A Grant; Robert T Sauer; Tania A Baker
Journal:  Mol Cell       Date:  2008-11-07       Impact factor: 17.970

9.  Substrate-binding sites of UBR1, the ubiquitin ligase of the N-end rule pathway.

Authors:  Zanxian Xia; Ailsa Webster; Fangyong Du; Konstantin Piatkov; Michel Ghislain; Alexander Varshavsky
Journal:  J Biol Chem       Date:  2008-06-19       Impact factor: 5.157

10.  Modification of PATase by L/F-transferase generates a ClpS-dependent N-end rule substrate in Escherichia coli.

Authors:  Robert L Ninnis; Sukhdeep K Spall; Gert H Talbo; Kaye N Truscott; David A Dougan
Journal:  EMBO J       Date:  2009-05-14       Impact factor: 11.598

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