Protein stability changes of the novel p.Arg180Cys mutant A glycosyltransferase resulted in a weak A phenotype

Authors
Lee, H. -S.Choi, K. -M.Won, E. J.Phan, M. -T. ThiLee, S. Y.Shin, D. -J.Chun, S.Park, G.Kim, S. -K.Lee, K. -B.Lee, H. -J.Cho, D.
Issue Date
2016-11
Publisher
WILEY-BLACKWELL
Citation
VOX SANGUINIS, v.111, no.4, pp.441 - 444
Abstract
A novel A subgroup allele (c.538C>T p.Arg180Cys) showing weak A phenotype was found in a 30-year-old Korean woman with ABO discrepancy. Using 3D structural analysis, protein stability prediction and flow cytometric analysis of ABO antigen expression on HeLa cells transfected with plasmids containing the p.Arg180Cys mutant, we found that the Arg180 residue in the loop region of the A glycosyltransferases (GTA) structure plays significant role in stabilizing its closed conformation, which is required for substrate binding and catalysis study.
Keywords
GROUP-B-GLYCOSYLTRANSFERASE; ALLELE; SUBSTITUTION; GROUP-B-GLYCOSYLTRANSFERASE; ALLELE; SUBSTITUTION; blood groups; genetics; genotyping; immunogenetics; RBC antigens and antibodies
ISSN
0042-9007
URI
https://pubs.kist.re.kr/handle/201004/123525
DOI
10.1111/vox.12440
Appears in Collections:
KIST Article > 2016
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