Literature DB >> 7646486

A 200-amino acid ATPase module in search of a basic function.

F Confalonieri1, M Duguet.   

Abstract

A fast growing family of ATPases has recently been highlighted. It was named the AAA family, for ATPases Associated to a variety of cellular Activities. The key feature of the family is a highly conserved module of 230 amino acids present in one or two copies in each protein. Despite extensive sequence conservation, the members of the family fulfil a large diversity of cellular functions: cell cycle regulation, gene expression in yeast and HIV, vesicle-mediated transport, peroxisome assembly, 26S protease function etc. In addition, several members of this family can be found in the same organism (up to 17 in S. cerevisiae). The contrast between functional diversity and structural conservation of the module, from archaebacteria to mammals, suggests that it plays an essential, but as yet unknown, role at key points of the cellular machinery. Two (non-exclusive) such possibilities are: (1) ATP-dependent proteasome function and (2) ATP-dependent anchorage of proteins. Finally, the basic biochemical activity of the AAA module is still a matter of speculation, and we propose that it acts as an ATP-dependent protein clamp.

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Year:  1995        PMID: 7646486     DOI: 10.1002/bies.950170710

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  82 in total

Review 1.  Assembly of the regulatory complex of the 26S proteasome.

Authors:  C Gorbea; D Taillandier; M Rechsteiner
Journal:  Mol Biol Rep       Date:  1999-04       Impact factor: 2.316

2.  Identification of TER94, an AAA ATPase protein, as a Bam-dependent component of the Drosophila fusome.

Authors:  A León; D McKearin
Journal:  Mol Biol Cell       Date:  1999-11       Impact factor: 4.138

Review 3.  Chaperone rings in protein folding and degradation.

Authors:  A L Horwich; E U Weber-Ban; D Finley
Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-28       Impact factor: 11.205

Review 4.  Hereditary spastic paraparesis: a review of new developments.

Authors:  C McDermott; K White; K Bushby; P Shaw
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-08       Impact factor: 10.154

5.  The McrBC restriction endonuclease assembles into a ring structure in the presence of G nucleotides.

Authors:  D Panne; S A Müller; S Wirtz; A Engel; T A Bickle
Journal:  EMBO J       Date:  2001-06-15       Impact factor: 11.598

6.  A nonproteolytic function of the proteasome is required for the dissociation of Cdc2 and cyclin B at the end of M phase.

Authors:  A Nishiyama; K Tachibana; Y Igarashi; H Yasuda; N Tanahashi; K Tanaka; K Ohsumi; T Kishimoto
Journal:  Genes Dev       Date:  2000-09-15       Impact factor: 11.361

7.  Dislocation of membrane proteins in FtsH-mediated proteolysis.

Authors:  A Kihara; Y Akiyama; K Ito
Journal:  EMBO J       Date:  1999-06-01       Impact factor: 11.598

8.  ATP-binding sites in brain p97/VCP (valosin-containing protein), a multifunctional AAA ATPase.

Authors:  Ran Zalk; Varda Shoshan-Barmatz
Journal:  Biochem J       Date:  2003-09-01       Impact factor: 3.857

9.  The absence of FtsH metalloprotease activity causes overexpression of the sigmaW-controlled pbpE gene, resulting in filamentous growth of Bacillus subtilis.

Authors:  Stephan Zellmeier; Ulrich Zuber; Wolfgang Schumann; Thomas Wiegert
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

10.  Dynamic flexibility of the ATPase p97 is important for its interprotomer motion transmission.

Authors:  Chengdong Huang; Guangtao Li; William J Lennarz
Journal:  Proc Natl Acad Sci U S A       Date:  2012-06-06       Impact factor: 11.205

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