Amino-acid substitution in the disordered loop of blood group B-glycosyltransferase enzyme causes weak B phenotype
Author:
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1537-2995.2005.00170.x/fullpdf
Reference24 articles.
1. The structural basis for specificity in human ABO(H) blood group biosynthesis
2. Molecular genetic basis of the histo-blood group ABO system
3. Sugar-nucleotide donor specificity of histo-blood group A and B transferases is based on amino acid substitutions.
4. Glycosyltransferases
5. Bovine alpha1,3-galactosyltransferase catalytic domain structure and its relationship with ABO histo-blood group and glycosphingolipid glycosyltransferases
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2. Identification of a novel variant c.761C>T on ABO*B.01 gene in ABO glycosyltransferases associated with Bweak phenotype;Vox Sanguinis;2023-08-11
3. Mechanism evaluation for an amino acid substitution p.Y246C of B‐glycosyltransferase enzyme with Bweak phenotype;Vox Sanguinis;2020-12-16
4. An exonic missense mutation c.28G>A is associated with weak B blood group by affecting RNA splicing of the ABO gene;Transfusion;2017-06-26
5. Protein stability changes of the novel p.Arg180Cys mutant A glycosyltransferase resulted in a weak A phenotype;Vox Sanguinis;2016-08-18
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