Literature DB >> 7476156

Pro-sequence-assisted protein folding.

J Eder1, A R Fersht.   

Abstract

Many proteins, including proteases and growth factors, are synthesized as precursors in the form of pre-pro-proteins. Whereas the pre-sequences usually act as signal peptides for transport, the pro-sequences of an increasing number of these proteins have been found to be essential for the correct folding of their associated proteins. In contrast to the action of molecular chaperones, pro-sequences appear to catalyse the protein-folding reaction directly. The similarity between the pro-sequence-assisted folding mechanisms of different proteases supports the hypothesis that a common folding mechanism has developed through convergent evolution. Further, the frequent requirement of the pro-sequences for both folding and intracellular transport or secretion suggests that these two functionalities are intimately related.

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Year:  1995        PMID: 7476156     DOI: 10.1111/j.1365-2958.1995.tb02423.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  44 in total

1.  PapD-like chaperones provide the missing information for folding of pilin proteins.

Authors:  M M Barnhart; J S Pinkner; G E Soto; F G Sauer; S Langermann; G Waksman; C Frieden; S J Hultgren
Journal:  Proc Natl Acad Sci U S A       Date:  2000-07-05       Impact factor: 11.205

2.  The Kex2p proregion is essential for the biosynthesis of an active enzyme and requires a C-terminal basic residue for its function.

Authors:  G Lesage; A Prat; J Lacombe; D Y Thomas; N G Seidah; G Boileau
Journal:  Mol Biol Cell       Date:  2000-06       Impact factor: 4.138

3.  Crystal structure of the precursor of galactose oxidase: an unusual self-processing enzyme.

Authors:  S J Firbank; M S Rogers; C M Wilmot; D M Dooley; M A Halcrow; P F Knowles; M J McPherson; S E Phillips
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-06       Impact factor: 11.205

4.  The protein encoded at the 3' end of the serine protease gene of Aeromonas sobria functions as a chaperone in the production of the protease.

Authors:  Tomohiko Nomura; Yoshio Fujii; Hiroyasu Yamanaka; Hidetomo Kobayashi; Keinosuke Okamoto
Journal:  J Bacteriol       Date:  2002-12       Impact factor: 3.490

5.  Structural dissection of alkaline-denatured pepsin.

Authors:  Yuji O Kamatari; Christopher M Dobson; Takashi Konno
Journal:  Protein Sci       Date:  2003-04       Impact factor: 6.725

6.  Dynamics of thermodynamically stable, kinetically trapped, and inhibitor-bound states of pepsin.

Authors:  Derek R Dee; Brenna Myers; Rickey Y Yada
Journal:  Biophys J       Date:  2011-10-05       Impact factor: 4.033

7.  The prodomain of Ssy5 protease controls receptor-activated proteolysis of transcription factor Stp1.

Authors:  Thorsten Pfirrmann; Stijn Heessen; Deike J Omnus; Claes Andréasson; Per O Ljungdahl
Journal:  Mol Cell Biol       Date:  2010-04-26       Impact factor: 4.272

8.  Understanding the mechanism of prosegment-catalyzed folding by solution NMR spectroscopy.

Authors:  Shenlin Wang; Yasumi Horimoto; Derek R Dee; Rickey Y Yada
Journal:  J Biol Chem       Date:  2013-11-21       Impact factor: 5.157

9.  Differences in the autocatalytic cleavage of pro-PC2 and pro-PC3 can be attributed to sequences within the propeptide and Asp310 of pro-PC2.

Authors:  K Scougall; N A Taylor; J L Jermany; K Docherty; K I Shennan
Journal:  Biochem J       Date:  1998-09-15       Impact factor: 3.857

10.  The CXC motif: a functional mimic of protein disulfide isomerase.

Authors:  Kenneth J Woycechowsky; Ronald T Raines
Journal:  Biochemistry       Date:  2003-05-13       Impact factor: 3.162

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