Literature DB >> 10847611

High-throughput screening of enzyme inhibitors: automatic determination of tight-binding inhibition constants.

P Kuzmic1, S Sideris, L M Cregar, K C Elrod, K D Rice, J W Janc.   

Abstract

Determination of tight-binding inhibition constants by nonlinear least-squares regression requires sufficiently good initial estimates of the best-fit values. Normally an initial estimate of the inhibition constant must be provided by the investigator. This paper describes an automatic procedure for the estimation of tight-binding inhibition constants directly from dose-response data. Because the procedure does not require human intervention, it was incorporated into an algorithm for high-throughput screening of enzyme inhibitors. A suitable computer program is available electronically (http://www.biokin.com). Representative experimental data are shown for the inhibition of human mast-cell tryptase.

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Year:  2000        PMID: 10847611     DOI: 10.1006/abio.2000.4501

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  7 in total

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2.  Adenosine analogue-oligo-arginine conjugates (ARCs) serve as high-affinity inhibitors and fluorescence probes of type I cGMP-dependent protein kinase (PKGIalpha).

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Journal:  Biochim Biophys Acta       Date:  2010-04-18

3.  Potent macrocycle inhibitors of the human SAGA deubiquitinating module.

Authors:  Michael Morgan; Tatsuya Ikenoue; Hiroaki Suga; Cynthia Wolberger
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4.  Quantitative characterization of the activation steps of mannan-binding lectin (MBL)-associated serine proteases (MASPs) points to the central role of MASP-1 in the initiation of the complement lectin pathway.

Authors:  Márton Megyeri; Veronika Harmat; Balázs Major; Ádám Végh; Júlia Balczer; Dávid Héja; Katalin Szilágyi; Dániel Datz; Gábor Pál; Péter Závodszky; Péter Gál; József Dobó
Journal:  J Biol Chem       Date:  2013-02-05       Impact factor: 5.157

5.  Highly potent inhibitors of cathepsin K with a differently positioned cyanohydrazide warhead: structural analysis of binding mode to mature and zymogen-like enzymes.

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Journal:  J Enzyme Inhib Med Chem       Date:  2022-12       Impact factor: 5.051

6.  Development and validation of a cytochrome c-coupled assay for pteridine reductase 1 and dihydrofolate reductase.

Authors:  Emma J Shanks; Han B Ong; David A Robinson; Stephen Thompson; Natasha Sienkiewicz; Alan H Fairlamb; Julie A Frearson
Journal:  Anal Biochem       Date:  2009-09-11       Impact factor: 3.365

7.  One scaffold, three binding modes: novel and selective pteridine reductase 1 inhibitors derived from fragment hits discovered by virtual screening.

Authors:  Chidochangu P Mpamhanga; Daniel Spinks; Lindsay B Tulloch; Emma J Shanks; David A Robinson; Iain T Collie; Alan H Fairlamb; Paul G Wyatt; Julie A Frearson; William N Hunter; Ian H Gilbert; Ruth Brenk
Journal:  J Med Chem       Date:  2009-07-23       Impact factor: 7.446

  7 in total

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