Literature DB >> 16182621

Peptide inhibitors of protein kinases-discovery, characterisation and use.

Marie A Bogoyevitch1, Renae K Barr, Albert J Ketterman.   

Abstract

Protein kinases are now the second largest group of drug targets, and most protein kinase inhibitors in clinical development are directed towards the ATP-binding site. However, these inhibitors must compete with high intracellular ATP concentrations and they must discriminate between the ATP-binding sites of all protein kinases as well the other proteins that also utilise ATP. It would therefore be beneficial to target sites on protein kinases other than the ATP-binding site. This review describes the discovery, characterisation and use of peptide inhibitors of protein kinases. In many cases, the development of these peptides has resulted from an understanding of the specific protein-binding partners for a particular protein kinase. In addition, novel peptide sequences have been discovered in library screening approaches and have provided new leads in the discovery and/or design of peptide inhibitors of protein kinases. These approaches are therefore providing exciting new opportunities in the development of ATP non-competitive inhibitors of protein kinases.

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Year:  2005        PMID: 16182621     DOI: 10.1016/j.bbapap.2005.07.025

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  16 in total

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Journal:  J Biol Chem       Date:  2014-02-19       Impact factor: 5.157

Review 4.  Aspects of eukaryotic-like signaling in Gram-positive cocci: a focus on virulence.

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6.  A novel binding pocket of cyclin-dependent kinase 2.

Authors:  Hao Chen; Rachel Van Duyne; Naigong Zhang; Fatah Kashanchi; Chen Zeng
Journal:  Proteins       Date:  2009-01

7.  Selective enhancement of the uptake and bioactivity of a TAT-conjugated peptide inhibitor of glycogen synthase kinase-3.

Authors:  Aziza P Manceur; Brandon D Driscoll; Wei Sun; Julie Audet
Journal:  Mol Ther       Date:  2008-12-23       Impact factor: 11.454

Review 8.  Leucine-rich repeat kinase 2 (LRRK2) as a potential therapeutic target in Parkinson's disease.

Authors:  Byoung Dae Lee; Valina L Dawson; Ted M Dawson
Journal:  Trends Pharmacol Sci       Date:  2012-05-09       Impact factor: 14.819

9.  Conservation, variability and the modeling of active protein kinases.

Authors:  James D R Knight; Bin Qian; David Baker; Rashmi Kothary
Journal:  PLoS One       Date:  2007-10-03       Impact factor: 3.240

10.  Deregulations in the cyclin-dependent kinase-9-related pathway in cancer: implications for drug discovery and development.

Authors:  Gaetano Romano
Journal:  ISRN Oncol       Date:  2013-06-06
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