Literature DB >> 4005264

Studies on the catalytic residues at the active site of human liver alpha-L-fucosidase.

W J White, K J Schray, J A Alhadeff.   

Abstract

Kinetic studies and chemical modifications were performed on purified human liver alpha-L-fucosidase (alpha-L-fucoside fucohydrolase, EC 3.2.1.51) in an attempt to identify the catalytic residues at the active site. Plots of log Vmax vs. pH (computer-fitted to a theoretical model) displayed two apparent pK values, of approx. 3.8 and 7.3. The temperature dependence of these pK values yielded heats of ionization of 3 and 0 kcal/mol from Van't Hoff plots for the lower and higher pK values, respectively. Reaction of alpha-L-fucosidase with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide and sodium p-(hydroxymercuri)benzoate resulted in complete inactivation of the enzyme. Other nonspecific inactivators had little or no effect on enzyme activity. These results suggest two carboxyl groups whose ionization state is important to activity, a non-active-site cysteine residue important to activity, and at least one active-site carboxyl group.

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Year:  1985        PMID: 4005264     DOI: 10.1016/0167-4838(85)90237-7

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


  3 in total

1.  Isolation and sequence analysis of a cDNA encoding rat liver alpha-L-fucosidase.

Authors:  K J Fisher; N N Aronson
Journal:  Biochem J       Date:  1989-12-15       Impact factor: 3.857

2.  Inhibition of alpha-L-fucosidase by derivatives of deoxyfuconojirimycin and deoxymannojirimycin.

Authors:  B Winchester; C Barker; S Baines; G S Jacob; S K Namgoong; G Fleet
Journal:  Biochem J       Date:  1990-01-01       Impact factor: 3.857

3.  Change in specificity of glycosidase inhibition by N-alkylation of amino sugars.

Authors:  S al Daher; G Fleet; S K Namgoong; B Winchester
Journal:  Biochem J       Date:  1989-03-01       Impact factor: 3.857

  3 in total

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