The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I
Author:
Affiliation:
1. Department of Life Sciences and Reproduction, Section of Biological Chemistry, University of Verona, Strada Le Grazie 8 37134 Verona, Italy
2. Siena Biotech S.p.A., Strada del Petriccio e Belriguardo, 35 53100 Siena, Italy
Funder
Fondazione Telethon
Publisher
American Chemical Society (ACS)
Subject
Molecular Medicine,General Medicine,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acschembio.5b00480
Reference45 articles.
1. Molecular aetiology of primary hyperoxaluria and its implications for clinical management
2. Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I
3. Oxalate Dynamics in Chronic Renal Failure
4. Crystal Structure of Alanine:Glyoxylate Aminotransferase and the Relationship Between Genotype and Enzymatic Phenotype in Primary Hyperoxaluria Type 1
5. Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implications
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3. Identification of Human Alanine–Glyoxylate Aminotransferase Ligands as Pharmacological Chaperones for Variants Associated with Primary Hyperoxaluria Type 1;Journal of Medicinal Chemistry;2022-07-13
4. Role of misfolding in rare enzymatic deficits and use of pharmacological chaperones as therapeutic approach;Frontiers in Bioscience-Landmark;2021-12-30
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