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1 ate compounds containing galactofuranose and galactopyranose.
2 lly substituted by 2-acetamido-2-deoxy-alpha-galactopyranose (13%) and 2-acetamido-2-deoxy-alpha-gluc
5 mimetics (d-glycero-d-talo- and d-glycero-d-galactopyranose analogues), a subset of the recently pub
6 dues and lesser content of 1,3-linked beta-D-galactopyranose and 1,5-linked alpha-L-arabinofuranose r
9 y glycosyl cations in the d-glucopyranose, d-galactopyranose, and l-arabinofuranose series using low-
10 strate for galactan synthesis and UDP-[(14)C]galactopyranose as the immediate precursor of UDP-[(14)C
12 dvanced 2-acetamido-4-amino-2,4,6-trideoxy-d-galactopyranose building block, was achieved on the 30 g
14 o transfer of IAA occurs with myo-inositol-d-galactopyranose, cyclohexanol, mannitol, or glycerol as
15 al is found to stabilize the alpha-anomer of galactopyranose derivatives relative to monocyclic analo
16 out a 6-homologation on the less flexible d-galactopyranose, followed by a very successful conversio
17 tuted with 2-O-arabinopyranose (Arap) or 2-O-galactopyranose (Gal) residues in some plant species, bu
19 10-24) of 2-acetamido-2-deoxy-1-thio-alpha-D-galactopyranose have been prepared in good yields and wi
21 binding site overlaps that of the substrate galactopyranose moiety, and thus NADPH and substrate bin
25 luster of three K. kingae genes encoding UDP-galactopyranose mutase (ugm) and two putative galactofur
27 the galactofuranose biosynthetic enzyme UDP-galactopyranose mutase (UGM) from T. cruzi, which are th
33 to-3,6-dideoxygalactose synthase (YerE), UDP-galactopyranose mutase (UGM), and type II isopentenyl di
37 nd in humans supports the development of UDP-galactopyranose mutase and galactofuranosyl transferase
39 n addition, an HPLC assay for the enzyme UDP-galactopyranose mutase is presented that requires 0.5 mi
42 neered a C. neoformans strain that lacks UDP-galactopyranose mutase; this enzyme forms UDP-Galf, the
43 furanoic form of d-galactose produced by UDP-galactopyranose mutases (UGMs), is present in surface gl
44 eta1,2-linked to an unusual tetrasubstituted galactopyranose of the glucuronoxylomannogalactan (GXMGa
45 ed region contained mainly 1,4-linked beta-D-galactopyranose residues and lesser content of 1,3-linke
46 ed region contained mainly 1,4-linked beta-d-galactopyranose residues and, to a lesser extent, 1,5-li
47 e presence of galactans, 3,6-anhydro-alpha-L-galactopyranose, sulphated galactose and the gelling age
48 l assignment of 1 to 3, a change of an alpha-galactopyranose to an alpha-galactofuranose headgroup.
49 ormed in nature by a ring contraction of UDP-galactopyranose to UDP-galactofuranose catalyzed by the
50 oenzyme that catalyzes the conversion of UDP-galactopyranose to UDP-galactofuranose, which is a centr
53 ion of UDP-galactofuranose (UDP-Galf) to UDP-galactopyranose (UDP-Galp) and is an important virulence
54 talyze the reversible interconversion of UDP-galactopyranose (UDP-Galp) and UDP-galactofuranose (UDP-
55 aining glycoconjugates, is produced from UDP-galactopyranose (UDP-Galp) by the flavoenzyme UDP-galact
57 t catalyzes the reversible conversion of UDP-galactopyranose (UDP-Galp) to UDP-galactofuranose (UDP-G
58 t catalyzes the reversible conversion of UDP-galactopyranose (UDP-Galp) to UDP-galactofuranose (UDP-G
59 ents of microorganisms is derived from UDP-D-galactopyranose (UDP-Galp) via a unique ring contraction