The 1.9 A structure of alpha-N-acetylgalactosaminidase: molecular basis of glycosidase deficiency diseases (Q27638971)

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Linda Hannick

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Alex Zhu

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David N Garboczi

Murine alpha-N-acetylgalactosaminidase: isolation and expression of a full-length cDNA and genomic organization: further evidence of an alpha-galactosidase gene family

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language of work or name

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March 2002

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published in

Structure

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volume

10

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issue

3

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page(s)

425-34

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cites work

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Schindler disease: the molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes an infantile neuroaxonal dystrophy

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Enzymatic Defect in Fabry's Disease

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Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease

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Enzyme replacement therapy in Fabry disease: a randomized controlled trial

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Preselective gene therapy for Fabry disease

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Group B erythrocytes enzymatically converted to group O survive normally in A, B, and O individuals

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Further evidence for the presence of A antigen on group B erythrocytes through the use of specific exoglycosidases

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Crystallization and preliminary X-ray analysis of human alpha-galactosidase A complex

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Mechanisms of enzymatic glycoside hydrolysis

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Glycosidase mechanisms

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Crystal structure of Thermoactinomyces vulgaris R-47 alpha-amylase II (TVAII) hydrolyzing cyclodextrins and pullulan at 2.6 A resolution

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Alpha-N-acetylgalactosaminidase: Isolation, properties and distribution of the human enzyme

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Sequence differences between glycosylated and non-glycosylated Asn-X-Thr/Ser acceptor sites: implications for protein engineering

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7 January 2021

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