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Bromoacetate histidine residues

The presence of imidazole groups in the active site region of human carbonic anhydrase B has, in fact, been demonstrated by chemical modification. Thus, bromoacetate reacts specifically with the 3 -N of a histidine residue to give a partially active monocarboxymethyl enzyme (65). The reaction depends on the initial combination of the bromoacetate ion with the anion binding site (65,83). In a detailed study, Bradbury (83) has shown that the irreversible reaction at saturation with iodoacetate... [Pg.177]

Reactions of C enriched reactants with biologically interesting molecules have also been monitored by C NMR. Nigen et al. (184) carboxymethylat-ed harbor seal and sperm whale cyanoferrimyoglobin with enriched [2-i C] bromoacetate. Adducts of the NHg terminal residues of histidine and lysine were observed in the > C spectra. In denatured cyanoferrimyoglobins all histidine residues were converted to the dicarboxymethyl derivative. [Pg.414]


See other pages where Bromoacetate histidine residues is mentioned: [Pg.686]    [Pg.188]    [Pg.117]    [Pg.550]    [Pg.109]    [Pg.118]    [Pg.261]    [Pg.292]    [Pg.98]   
See also in sourсe #XX -- [ Pg.686 , Pg.688 ]




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