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PMID: 3196333 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Human glucosamine-6-sulfatase cDNA reveals homology with steroid sulfatase.

Biochemical and biophysical research communications ·Vol. 157 ·No. 1 ·1988-11-30 ·Pages 218-24

Robertson DA, Freeman C, Nelson PV, Morris CP, Hopwood JJ

Abstract

Glucosamine-6-sulfatase is a lysosomal enzyme which degrades glycosaminoglycans and is deficient in mucopolysaccharidosis type IIID. Human liver contains two major active forms of glucosamine-6-sulfatase, form A which has a single 78 kDa polypeptide and form B which has two polypeptides of 48 kDa and 32 kDa. A 1761 base pair cDNA clone encoding the complete 48 kDa polypeptide of form B was isolated. Form A is shown to be processed to form B with the 48 kDa polypeptide C-terminal to the 32 kDa polypeptide, and it is shown that C-terminal processing is limited to a region of thirty amino acids. The glucosamine-6-sulfatase sequence reveals homology with steroid sulfatase, a microsomal enzyme.

MeSH Terms
Amino Acid Sequence Arylsulfatases/genetics Base Sequence Cloning, Molecular DNA/genetics Humans Molecular Sequence Data Molecular Weight Steryl-Sulfatase Sulfatases/genetics
Chemicals
DNA Sulfatases Arylsulfatases N-acetylglucosamine-6-sulfatase Steryl-Sulfatase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Robertson D A
Department of Chemical Pathology, Adelaide Children's Hospital, South Australia.
Freeman C
Nelson P V
Morris C P
Hopwood J J
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1988-11-30
Pages
218-24
Language
English
Region
United States
NLM ID
0372516
Subset
IM
Databases
GENBANK
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