Literature DB >> 518556

The equilibrium assumption is valid for the kinetic treatment of most time-dependent protein-modification reactions.

K Brocklehurst.   

Abstract

To facilitate mechanistic interpretation of the kinetics of time-dependent inhibition of enzymes and of similar protein modification reactions, it is important to know when the equilibrium assumption may be applied to the model: formula: (see text). The conventional criterion of quasi-equilibrium, k + 2 less than k-1, is not always easy to assess, particularly when k + 2 cannot be separately determined. It is demonstrated that the condition k + 2 less than k-1 is necessarily true, however, when the value of the apparent second-order rate constant for the modification reaction is much smaller than the value of k + 1. Since k + 1 is commonly at least 10(7)M-1.S-1 for substrates, it is probable that the equilibrium assumption may be properly applied to most irreversible inhibitions and modification reactions.

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Year:  1979        PMID: 518556      PMCID: PMC1161220          DOI: 10.1042/bj1810775

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  20 in total

1.  The reactivity of SH groups with a fluorogenic reagent.

Authors:  D J. Birkett; N C. Price; G K. Radda; A G. Salmon
Journal:  FEBS Lett       Date:  1970-02-25       Impact factor: 4.124

2.  Participation of buffer in the catalytic mechanism of carbonic anhydrase.

Authors:  B H Jonsson; H Steiner; S Lindskog
Journal:  FEBS Lett       Date:  1976-05-01       Impact factor: 4.124

3.  PH-dependence of the steady-state rate of a two-step enzymic reaction.

Authors:  K Brocklehurst; H B Dixon
Journal:  Biochem J       Date:  1976-04-01       Impact factor: 3.857

4.  Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.

Authors:  R KITZ; I B WILSON
Journal:  J Biol Chem       Date:  1962-10       Impact factor: 5.157

5.  A Note on the Kinetics of Enzyme Action.

Authors:  G E Briggs; J B Haldane
Journal:  Biochem J       Date:  1925       Impact factor: 3.857

6.  The quantitative relations between diffusion-controlled reaction rate and characteristic parameters in enzyme-substrate reaction systems. I. Neutral substrates.

Authors:  T T Li; K C Chou
Journal:  Sci Sin       Date:  1976 Jan-Feb

7.  Benzofuroxan as a thiol-specific reactivity probe. Kinetics of its reactions with papain, ficin, bromelain and low-molecular-weight thiols.

Authors:  M Shipton; K Brocklehurst
Journal:  Biochem J       Date:  1977-12-01       Impact factor: 3.857

8.  Characterization of the papain active centre by using two-protonic-state electrophiles as reactivity probes. Evidence for nucleophilic reactivity in the un-interrupted cysteine-25-histidine-159 interactive system.

Authors:  M Shipton; K Brochlehurst
Journal:  Biochem J       Date:  1978-05-01       Impact factor: 3.857

9.  Specific covalent modification of thiols: applications in the study of enzymes and other biomolecules.

Authors:  K Brocklehurst
Journal:  Int J Biochem       Date:  1979

10.  Essential and nonessential thiols of yeast hexokinase. Reactions with iodoacetate and iodoacetamide.

Authors:  J G Jones; S Otieno; E A Barnard; A K Bhargava
Journal:  Biochemistry       Date:  1975-06-03       Impact factor: 3.162

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  29 in total

1.  Differences in the chemical and catalytic characteristics of two crystallographically 'identical' enzyme catalytic sites. Characterization of actinidin and papain by a combination of pH-dependent substrate catalysis kinetics and reactivity probe studies targeted on the catalytic-site thiol group and its immediate microenvironment.

Authors:  E Salih; J P Malthouse; D Kowlessur; M Jarvis; M O'Driscoll; K Brocklehurst
Journal:  Biochem J       Date:  1987-10-01       Impact factor: 3.857

2.  Appendix: Analysis of pH-dependent kinetics in up to four reactive hydronic states.

Authors:  S M Brocklehurst; K Brocklehurst
Journal:  Biochem J       Date:  1988-12-01       Impact factor: 3.857

3.  Variation in aspects of cysteine proteinase catalytic mechanism deduced by spectroscopic observation of dithioester intermediates, kinetic analysis and molecular dynamics simulations.

Authors:  J D Reid; S Hussain; S K Sreedharan; T S Bailey; S Pinitglang; E W Thomas; C S Verma; K Brocklehurst
Journal:  Biochem J       Date:  2001-07-15       Impact factor: 3.857

4.  Kinetic parameters of the acyl-enzyme mechanism and conditions for quasi-equilibrium and for optimal catalytic characteristics.

Authors:  K Brocklehurst; C M Topham
Journal:  Biochem J       Date:  1990-09-01       Impact factor: 3.857

5.  Kinetic analysis of regeneration by dilution of a covalently modified protein.

Authors:  E T Rakitzis
Journal:  Biochem J       Date:  1990-06-15       Impact factor: 3.857

6.  Identification of signalling and non-signalling binding contributions to enzyme reactivity. Alternative combinations of binding interactions provide for change in transition-state geometry in reactions of papain.

Authors:  D Kowlessur; C M Topham; E W Thomas; M O'Driscoll; W Templeton; K Brocklehurst
Journal:  Biochem J       Date:  1989-03-15       Impact factor: 3.857

7.  Computer simulations of the kinetics of irreversible enzyme inhibition by an unstable inhibitor.

Authors:  C M Topham
Journal:  Biochem J       Date:  1986-12-15       Impact factor: 3.857

8.  Variation in the pH-dependent pre-steady-state and steady-state kinetic characteristics of cysteine-proteinase mechanism: evidence for electrostatic modulation of catalytic-site function by the neighbouring carboxylate anion.

Authors:  Syeed Hussain; Surapong Pinitglang; Tamara S F Bailey; James D Reid; Michael A Noble; Marina Resmini; Emrys W Thomas; Richard B Greaves; Chandra S Verma; Keith Brocklehurst
Journal:  Biochem J       Date:  2003-06-15       Impact factor: 3.857

9.  Evidence for association-activation effects in reactions of papain from studies on its reactivity towards isomeric two-protonic-state reactivity probes.

Authors:  K Brocklehurst; J A Herbert; R Norris; H Suschitzky
Journal:  Biochem J       Date:  1979-11-01       Impact factor: 3.857

10.  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

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