Literature DB >> 15078142

High-throughput structural biology in drug discovery: protein kinases.

T J Stout1, P G Foster, D J Matthews.   

Abstract

Structural biology is an invaluable tool in modern drug discovery, providing key insights into the interactions of small-molecule drugs with their protein targets. As in many aspects of the drug discovery process, significant synergies can be realized in structural biology by the contemporaneous pursuit of many target proteins from a single structural and functional class. We will review some of those synergies here using the example of the protein kinases--an important class of drug targets that has recently been the subject of intensive study. We conclude by discussing some of the technical advances in X-ray crystallography that have enabled implementation of high-throughput structural biology as applied to drug lead optimization.

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Year:  2004        PMID: 15078142     DOI: 10.2174/1381612043452695

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


  16 in total

Review 1.  Recent advances in the treatment of systemic sclerosis.

Authors:  Vasiliki Kalliopi K Bournia; Panayiotis G Vlachoyiannopoulos; Carlo Selmi; Haralampos M Moutsopoulos; M Eric Gershwin
Journal:  Clin Rev Allergy Immunol       Date:  2009-06       Impact factor: 8.667

2.  Enzymatic and functional analysis of a protein phosphatase, Pph3, from Myxococcus xanthus.

Authors:  Yoshio Kimura; Yumi Mori; Youhei Ina; Kaoru Takegawa
Journal:  J Bacteriol       Date:  2011-03-11       Impact factor: 3.490

Review 3.  Manipulation of Focal Adhesion Signaling by Pathogenic Microbes.

Authors:  Korinn N Murphy; Amanda J Brinkworth
Journal:  Int J Mol Sci       Date:  2021-01-29       Impact factor: 5.923

Review 4.  Mechanosensitivity and compositional dynamics of cell-matrix adhesions.

Authors:  Herbert B Schiller; Reinhard Fässler
Journal:  EMBO Rep       Date:  2013-05-17       Impact factor: 8.807

5.  Building a human kinase gene repository: bioinformatics, molecular cloning, and functional validation.

Authors:  Jaehong Park; Yanhui Hu; T V S Murthy; Fredrik Vannberg; Binghua Shen; Andreas Rolfs; Jessica E Hutti; Lewis C Cantley; Joshua Labaer; Ed Harlow; Leonardo Brizuela
Journal:  Proc Natl Acad Sci U S A       Date:  2005-05-31       Impact factor: 11.205

6.  Comparative analysis of the human and zebrafish kinomes: focus on the development of kinase inhibitors.

Authors:  Nathan Wlodarchak; Rehan Tariq; Rob Striker
Journal:  Trends Cell Mol Biol       Date:  2015

7.  Comprehensive structural and functional characterization of the human kinome by protein structure modeling and ligand virtual screening.

Authors:  Michal Brylinski; Jeffrey Skolnick
Journal:  J Chem Inf Model       Date:  2010-10-25       Impact factor: 4.956

8.  Cross-reactivity virtual profiling of the human kinome by X-react(KIN): a chemical systems biology approach.

Authors:  Michal Brylinski; Jeffrey Skolnick
Journal:  Mol Pharm       Date:  2010-11-08       Impact factor: 4.939

9.  In vitro selection of a DNA-templated small-molecule library reveals a class of macrocyclic kinase inhibitors.

Authors:  Ralph E Kleiner; Christoph E Dumelin; Gerald C Tiu; Kaori Sakurai; David R Liu
Journal:  J Am Chem Soc       Date:  2010-08-25       Impact factor: 15.419

10.  Structural features of human inositol phosphate multikinase rationalize its inositol phosphate kinase and phosphoinositide 3-kinase activities.

Authors:  Huanchen Wang; Stephen B Shears
Journal:  J Biol Chem       Date:  2017-09-07       Impact factor: 5.157

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