Literature DB >> 12515557

A Cys3His zinc-binding domain from Nup475/tristetraprolin: a novel fold with a disklike structure.

Barbara T Amann1, Mark T Worthington, Jeremy M Berg.   

Abstract

Nup475 (also known as tristetraprolin and TIS11) includes two zinc-binding domains of the form Cys-X8-Cys-X5-Cys-X3-His. These domains are required for rapid degradation of tumor necrosis factor (TNF) and other mRNAs through the interaction with AU-rich elements in their 3'-untranslated regions. The three-dimensional solution structure of the first domain was determined by multidimensional nuclear magnetic resonance spectroscopy, revealing a novel fold around a central zinc ion. The core structure is disk-like with a diameter of approximately 25 A and a width of approximately 12 A. This structure provides a basis for evaluating the role of individual residues for structural stability and for nucleic acid binding.

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Year:  2003        PMID: 12515557     DOI: 10.1021/bi026988m

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  19 in total

1.  Predicting 13Calpha chemical shifts for validation of protein structures.

Authors:  Jorge A Vila; Myriam E Villegas; Hector A Baldoni; Harold A Scheraga
Journal:  J Biomol NMR       Date:  2007-06-09       Impact factor: 2.835

2.  Probing the structural and dynamical effects of the charged residues of the TZF domain of TIS11d.

Authors:  Brittany R Morgan; Laura M Deveau; Francesca Massi
Journal:  Biophys J       Date:  2015-03-24       Impact factor: 4.033

3.  Crystal structure of the essential transcription antiterminator M2-1 protein of human respiratory syncytial virus and implications of its phosphorylation.

Authors:  Sian J Tanner; Antonio Ariza; Charles-Adrien Richard; Hannah F Kyle; Rachel L Dods; Marie-Lise Blondot; Weining Wu; José Trincão; Chi H Trinh; Julian A Hiscox; Miles W Carroll; Nigel J Silman; Jean-François Eléouët; Thomas A Edwards; John N Barr
Journal:  Proc Natl Acad Sci U S A       Date:  2014-01-13       Impact factor: 11.205

4.  Cu(I) Disrupts the Structure and Function of the Nonclassical Zinc Finger Protein Tristetraprolin (TTP).

Authors:  Geoffrey D Shimberg; Kiwon Ok; Heather M Neu; Kathryn E Splan; Sarah L J Michel
Journal:  Inorg Chem       Date:  2017-05-30       Impact factor: 5.165

5.  Expression, purification, and biochemical characterization of the antiinflammatory tristetraprolin: a zinc-dependent mRNA binding protein affected by posttranslational modifications.

Authors:  Heping Cao
Journal:  Biochemistry       Date:  2004-11-02       Impact factor: 3.162

Review 6.  The emerging role of RNA-binding proteins in the life cycle of Trypanosoma brucei.

Authors:  Nikolay G Kolev; Elisabetta Ullu; Christian Tschudi
Journal:  Cell Microbiol       Date:  2014-02-16       Impact factor: 3.715

Review 7.  Multiple functions of tristetraprolin/TIS11 RNA-binding proteins in the regulation of mRNA biogenesis and degradation.

Authors:  Delphine Ciais; Nadia Cherradi; Jean-Jacques Feige
Journal:  Cell Mol Life Sci       Date:  2012-09-12       Impact factor: 9.261

8.  Inhibition of tristetraprolin deadenylation by poly(A) binding protein.

Authors:  Robert M Rowlett; Carol A Chrestensen; Melanie J Schroeder; Mary G Harp; Jared W Pelo; Jeffery Shabanowitz; Robert DeRose; Donald F Hunt; Thomas W Sturgill; Mark T Worthington
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2008-05-08       Impact factor: 4.052

Review 9.  TIS11 family proteins and their roles in posttranscriptional gene regulation.

Authors:  Maria Baou; Andrew Jewell; John J Murphy
Journal:  J Biomed Biotechnol       Date:  2009-08-06

10.  Inactivation of respiratory syncytial virus by zinc finger reactive compounds.

Authors:  Marina S Boukhvalova; Gregory A Prince; Jorge C G Blanco
Journal:  Virol J       Date:  2010-01-26       Impact factor: 4.099

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