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Biosynthesis of heparin. Availability of glucosaminyl 3-O-sulfation sites.
Kusche M, Torri G, Casu B, Lindahl U. Kusche M, et al. Among authors: lindahl u. J Biol Chem. 1990 May 5;265(13):7292-300. J Biol Chem. 1990. PMID: 2332430 Free article.
The two tetrasaccharide sequences, -IdoA-GlcNAc(6-OSO3)-GlcA-GlcNSO3- and -IdoA-GlcNAc(6-OSO3)-GlcA-GlcNSO3(6-OSO3)- , recently implicated as part of the acceptor site for glucosaminyl 3-O-sulfate groups (Kusche, M., Backstrom, G., Riesenfeld, J., Petitou, M., Choay, J., and L …
The two tetrasaccharide sequences, -IdoA-GlcNAc(6-OSO3)-GlcA-GlcNSO3- and -IdoA-GlcNAc(6-OSO3)-GlcA-GlcNSO3(6-OSO3)- , recently implicated a …
Biosynthesis of heparin. Enzymatic sulfation of pentasaccharides.
Kusche M, Oscarsson LG, Reynertson R, Rodén L, Lindahl U. Kusche M, et al. Among authors: lindahl u. J Biol Chem. 1991 Apr 25;266(12):7400-9. J Biol Chem. 1991. PMID: 1902219 Free article.
The antithrombin-binding region, essential for the blood anticoagulant activity of heparin, has been identified as a pentasaccharide sequence with the predominant structure GlcNR(6-OSO3)-GlcA-GlcNSO3(3,6-di-OSO3)-++ +IdoA(2-OSO3)-GlcNSO3(6-OSO3) (where R represents either a sulfa …
The antithrombin-binding region, essential for the blood anticoagulant activity of heparin, has been identified as a pentasaccharide sequenc …
Biosynthesis of heparin and heparan sulfate.
Lindahl U, Kusche M, Lidholt K, Oscarsson LG. Lindahl U, et al. Ann N Y Acad Sci. 1989;556:36-50. doi: 10.1111/j.1749-6632.1989.tb22488.x. Ann N Y Acad Sci. 1989. PMID: 2525361 Review. No abstract available.
268 results