Literature DB >> 15078146

Protein phosphatase inhibition: structure based design. Towards new therapeutic agents.

Jennette A Sakoff1, Adam McCluskey.   

Abstract

Cellular signalling processes are governed by a delicate balance of phosphatase and kinase activity. Over the past few years there has been considerable effort directed toward the development of kinase based therapeutic agents, whilst phosphatase based therapeutics have lagged. Herein we address key issues relating to selected therapeutic targets: malignancy, diabetes, immunosuppression, cystic fibrosis, asthma and cardiovascular disease. As part of ongoing studies we examine the recent developments in understanding the key interactions between the okadaic acid class of compounds and the serine/threonine protein phosphatases 1, 2A and 2B. Crystal structure and molecular modelling guided inhibitor development is also a key focus of this article.

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Year:  2004        PMID: 15078146     DOI: 10.2174/1381612043452686

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  14 in total

1.  Small-molecule inhibitors of ser/thr protein phosphatases: specificity, use and common forms of abuse.

Authors:  Mark Swingle; Li Ni; Richard E Honkanen
Journal:  Methods Mol Biol       Date:  2007

Review 2.  Targeting protein serine/threonine phosphatases for drug development.

Authors:  Jamie L McConnell; Brian E Wadzinski
Journal:  Mol Pharmacol       Date:  2009-03-19       Impact factor: 4.436

3.  Utilization of the methoxymalonyl-acyl carrier protein biosynthesis locus for cloning of the tautomycin biosynthetic gene cluster from Streptomyces spiroverticillatus.

Authors:  Wenli Li; Jianhua Ju; Hiroyuki Osada; Ben Shen
Journal:  J Bacteriol       Date:  2006-06       Impact factor: 3.490

4.  Regulation of glioma cell migration by serine-phosphorylated P311.

Authors:  Wendy S McDonough; Nhan L Tran; Michael E Berens
Journal:  Neoplasia       Date:  2005-09       Impact factor: 5.715

5.  Crystal structures of protein phosphatase-1 bound to nodularin-R and tautomycin: a novel scaffold for structure-based drug design of serine/threonine phosphatase inhibitors.

Authors:  Matthew S Kelker; Rebecca Page; Wolfgang Peti
Journal:  J Mol Biol       Date:  2008-11-01       Impact factor: 5.469

6.  Characterization of the tautomycin biosynthetic gene cluster from Streptomyces spiroverticillatus unveiling new insights into dialkylmaleic anhydride and polyketide biosynthesis.

Authors:  Wenli Li; Jianhua Ju; Scott R Rajski; Hiroyuki Osada; Ben Shen
Journal:  J Biol Chem       Date:  2008-08-15       Impact factor: 5.157

Review 7.  Interrogating Protein Phosphatases with Chemical Activity Probes.

Authors:  Garrett R Casey; Cliff I Stains
Journal:  Chemistry       Date:  2018-03-08       Impact factor: 5.236

8.  Characterization of the tautomycetin biosynthetic gene cluster from Streptomyces griseochromogenes provides new insight into dialkylmaleic anhydride biosynthesis.

Authors:  Wenli Li; Yinggang Luo; Jianhua Ju; Scott R Rajski; Hiroyuki Osada; Ben Shen
Journal:  J Nat Prod       Date:  2009-03-27       Impact factor: 4.050

9.  Determinants for Substrate Specificity of Protein Phosphatase 2A.

Authors:  Andrew M Slupe; Ronald A Merrill; Stefan Strack
Journal:  Enzyme Res       Date:  2011-07-02

Review 10.  Use of okadaic acid to identify relevant phosphoepitopes in pathology: a focus on neurodegeneration.

Authors:  Miguel Medina; Jesús Avila; Nieves Villanueva
Journal:  Mar Drugs       Date:  2013-05-21       Impact factor: 5.118

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