Literature DB >> 6236849

Precautions when determining kinetically the order of inactivation of enzymes by functionally irreversible inhibitors.

G M Carlson.   

Abstract

The number of molecules of an irreversible inhibitor that are responsible for inactivation of a catalytic site is often deduced from the slope of a plot of the log of the apparent rate of inactivation (k') at different concentrations of inhibitor versus the log of the inhibitor concentrations. The purpose of this note is to urge caution in experimental design and interpretation if one attempts to utilize this kinetic technique to characterize the order of inactivation brought about by functionally irreversible inhibitors that initially bind reversibly to an enzyme in the process of inactivation. Representative literature cases which have utilized plots of log k' versus log [I] for this type of inactivation are discussed.

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Year:  1984        PMID: 6236849     DOI: 10.1016/0167-4838(84)90191-2

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


  11 in total

1.  CrossSearch, a user-friendly search engine for detecting chemically cross-linked peptides in conjugated proteins.

Authors:  Owen W Nadeau; Gerald J Wyckoff; Justin E Paschall; Antonio Artigues; Jessica Sage; Maria T Villar; Gerald M Carlson
Journal:  Mol Cell Proteomics       Date:  2008-02-16       Impact factor: 5.911

2.  An essential arginyl residue in the tonoplast pyrophosphatase from etiolated mung bean seedlings.

Authors:  S Y Kuo; R L Pan
Journal:  Plant Physiol       Date:  1990-07       Impact factor: 8.340

3.  Inhibition of tonoplast ATPase by 2',3'-dialdehyde derivative of ATP.

Authors:  W M Chow; C M Tzeng; C S Chen; S Y Kuo; M Y Wang; R L Pan
Journal:  Plant Physiol       Date:  1992-01       Impact factor: 8.340

4.  Evidence for the location of the allosteric activation switch in the multisubunit phosphorylase kinase complex from mass spectrometric identification of chemically crosslinked peptides.

Authors:  Owen W Nadeau; David W Anderson; Qing Yang; Antonio Artigues; Justin E Paschall; Gerald J Wyckoff; Jennifer L McClintock; Gerald M Carlson
Journal:  J Mol Biol       Date:  2006-10-21       Impact factor: 5.469

5.  Evidence for essential arginine residues at the active sites of maize branching enzymes.

Authors:  H Cao; J Preiss
Journal:  J Protein Chem       Date:  1996-04

6.  Essential Arginyl Residue at the Active Site of Pyrophosphate:Fructose 6-Phosphate 1-Phosphotransferase from Potato (Solanum tuberosum) Tuber.

Authors:  P. Montavon; N. J. Kruger
Journal:  Plant Physiol       Date:  1993-03       Impact factor: 8.340

7.  Two interacting binding sites for quinacrine derivatives in the active site of trypanothione reductase: a template for drug design.

Authors:  Ahilan Saravanamuthu; Tim J Vickers; Charles S Bond; Mark R Peterson; William N Hunter; Alan H Fairlamb
Journal:  J Biol Chem       Date:  2004-04-21       Impact factor: 5.157

8.  Inhibition of tonoplast ATPase from etiolated mung bean seedlings by fluorescein 5'-isothiocyanate.

Authors:  C M Tzeng; L H Hsu; R L Pan
Journal:  Biochem J       Date:  1992-08-01       Impact factor: 3.857

9.  Drosophila melanogaster alcohol dehydrogenase. Biochemical properties of the NAD+-plus-acetone-induced isoenzyme conversion.

Authors:  J O Winberg; J S McKinley-McKee
Journal:  Biochem J       Date:  1988-04-01       Impact factor: 3.857

10.  Inactivation of the endogenous argininosuccinate lyase activity of duck delta-crystallin by modification of an essential histidine residue with diethyl pyrocarbonate.

Authors:  H J Lee; S H Chiou; G G Chang
Journal:  Biochem J       Date:  1993-07-15       Impact factor: 3.857

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