Site-directed Mutagenesis of Essential Residues Involved in the Mechanism of Bacterial Glycosylasparaginase
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference36 articles.
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2. Aspartylglycosaminuria: protein chemistry and molecular biology of the most common lysosomal storage disorder of glycoprotein degradation
3. The Metabolic Basis of Inherited Disease;Beaudet,1989
4. Enzymatic cleavage of glycopeptides
5. Substrate specificity and reaction mechanism of human glycoasparaginase. The N-glycosidic linkage of various glycoasparagines is cleaved through a reaction mechanism similar to L-asparaginase.
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2. Structural and biophysical studies of new L-asparaginase variants: lessons from random mutagenesis of the prototypic Escherichia coli Ntn-amidohydrolase;Acta Crystallographica Section D Structural Biology;2022-06-28
3. The Human Ntn-Hydrolase Superfamily: Structure, Functions and Perspectives;Cells;2022-05-10
4. The T99K variant of glycosylasparaginase shows a new structural mechanism of the genetic disease aspartylglucosaminuria;Protein Science;2019-04-09
5. Biochemical and structural insights into an allelic variant causing the lysosomal storage disorder – aspartylglucosaminuria;FEBS Letters;2018-07-23
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