Literature DB >> 942375

The unreliability of estimates of group dissociation constants.

H B Dixon.   

Abstract

If a molecule contains two groups that bind a common ligand, then to determine their group dissociation constants it is necessary (1) to assume that some property of the molecule is affected by the degree of ligation of only one of the groups, and (2) to determine how this property varies with the concentration of free ligand. When assignment of group dissociation constants made on this basis suggests that the degree of ligation of each group greatly affects the dissociation constant of the other, then the original assumption that the chosen property is completely unaffected by ligation of the second group is rendered doubtful. Dissociation constants of interacting groups can therefore not be reliably determined.

Mesh:

Year:  1976        PMID: 942375      PMCID: PMC1172631          DOI: 10.1042/bj1530627

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


  12 in total

1.  THE IONIZATION OF CYSTEINE AND THE POSSIBLE ROLE OF HYDROGEN BONDING BY THE THIOL GROUP.

Authors:  J T EDSALL
Journal:  Biochemistry       Date:  1965-01       Impact factor: 3.162

2.  The case for assigning a value of approximately 4 to pKa-i of the essential histidine-cysteine interactive systems of papain, bromelain and ficin.

Authors:  M Shipton; M P Kierstan; J P Malthouse; T Stuchbury; K Brocklehurst
Journal:  FEBS Lett       Date:  1975-02-15       Impact factor: 4.124

3.  Kinetic exclusion rules applied to the study of pH-dependent enzyme reactions: application of the diffusion-controlled limit.

Authors:  H B Dunford
Journal:  J Theor Biol       Date:  1974-08       Impact factor: 2.691

4.  Curves of ligand binding. The use of hyperbolic functions for expressing titration curves.

Authors:  H B Dixon
Journal:  Biochem J       Date:  1974-03       Impact factor: 3.857

5.  The advantages of transition state and group acid dissociation constants for pH-dependent enzyme kinetics.

Authors:  H B Dunford; J E Critchlow; R J Maguire; R Roman
Journal:  J Theor Biol       Date:  1974-12       Impact factor: 2.691

6.  Conformational equilibria and the salt bridge in chymotrypsin.

Authors:  A R Fersht
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1972

7.  Negatively co-operative ligand binding.

Authors:  H B Dixon; K F Tipton
Journal:  Biochem J       Date:  1973-08       Impact factor: 3.857

8.  [Dissociation equilibrium of glutathione. A Fourier transform-13C-NMR spectroscopic study of pH-dependence and of charge densities].

Authors:  G Jung; E Breitmaier; W Voelter
Journal:  Eur J Biochem       Date:  1972-01-21

9.  Theory and practice for studies for peptides by 15N nuclear magnetic resonance at natural abundance: gramicidin S.

Authors:  G E Hawkes; E W Randall; C H Bradley
Journal:  Nature       Date:  1975-10-30       Impact factor: 49.962

10.  Ion-pair formation as a source of enhanced reactivity of the essential thiol group of D-glyceraldehyde-3-phosphate dehydrogenase.

Authors:  L Polgár
Journal:  Eur J Biochem       Date:  1975-02-03
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  13 in total

1.  The origin of multiply sigmoid curves of pH-dependence. The partitioning of groups among titration pK values.

Authors:  H B Dixon; S D Clarke; G A Smith; T K Carne
Journal:  Biochem J       Date:  1991-08-15       Impact factor: 3.857

2.  Part of the phospho group of pyridoxal phosphate may titrate over the pH range 5-8 in aspartate aminotransferase.

Authors:  H B Dixon
Journal:  Biochem J       Date:  1991-12-15       Impact factor: 3.857

3.  pH-activity curves for enzyme-catalysed reactions in which the hydron is a product or reactant.

Authors:  H B Dixon; K Brocklehurst; K F Tipton
Journal:  Biochem J       Date:  1987-12-01       Impact factor: 3.857

4.  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

5.  The pH-dependence of second-order rate constants of enzyme modification may provide free-reactant pKa values.

Authors:  K Brocklehurst; H B Dixon
Journal:  Biochem J       Date:  1977-12-01       Impact factor: 3.857

6.  Enzyme-substrate and enzyme-inhibitor complexes of triose phosphate isomerase studied by 31P nuclear magnetic resonance.

Authors:  I D Campbell; R B Jones; P A Kiener; S G Waley
Journal:  Biochem J       Date:  1979-06-01       Impact factor: 3.857

7.  Spectrophotometric studies on the interaction between triose phosphate isomerase and inhibitors.

Authors:  R B Jones; S G Waley
Journal:  Biochem J       Date:  1979-06-01       Impact factor: 3.857

8.  Mechanism of the reaction of papain with substrate-derived diazomethyl ketones. Implications for the difference in site specificity of halomethyl ketones for serine proteinases and cysteine proteinases and for stereoelectronic requirements in the papain catalytic mechanism.

Authors:  K Brocklehurst; J P Malthouse
Journal:  Biochem J       Date:  1978-11-01       Impact factor: 3.857

9.  Relations between the dissociation constants of dibasic acids.

Authors:  H B Dixon
Journal:  Biochem J       Date:  1988-08-01       Impact factor: 3.857

10.  The effect of pH on the kinetics of arylsulphatases A and B.

Authors:  C O'Fagain; B M Butler; T J Mantle
Journal:  Biochem J       Date:  1983-09-01       Impact factor: 3.857

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