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1                          In addition, beta,D-galactopyranosyl 1-thio-beta,D-galactopyranoside induces
2 e (NEM) in the presence or absence of beta-D-galactopyranosyl 1-thio-beta-D-galactopyranoside (TDG) o
3 hange significantly after addition of beta-d-galactopyranosyl 1-thio-beta-d-galactopyranoside (TDG),
4 easured in the absence or presence of beta-D-galactopyranosyl 1-thio-beta-D-galactopyranoside (TDG),
5 48 exhibit K(D) values for lactose or beta-d-galactopyranosyl 1-thio-beta-d-galactopyranoside of appr
6 eincubation with the substrate analog beta-D-galactopyranosyl 1-thio-beta-D-galactopyranoside protect
7 uring the catabolism of raffinose (O-alpha-D-galactopyranosyl-1, 6-alpha-D-glucopyranosyl-beta-D-fruc
8  mM for lactose and 15-20 microM for beta, D-galactopyranosyl-1-thio-beta,D-galactopyranoside (TDG).
9 ructure with a bound lactose homolog, beta-D-galactopyranosyl-1-thio-beta-D-galactopyranoside, reveal
10 ulations of 20-25 ns each with beta(alpha)-d-galactopyranosyl-(1,1)-beta-d-galactopyranoside (betabet
11  with kaempferol-3-O-[glucopyranosyl-(1-->2)-galactopyranosyl-(1-->2)-glucopyranoside, identified as
12 lo-hexopyranosyl-(1-->4)-[3-O-benzyl-beta-D -galactopyranosyl-(1-->3)]-6-O-benzyl-2-deoxy-2-trichloro
13 5-N-acetyl-alpha-d-neuraminyl-(2-->3)-beta-d-galactopyranosyl-(1-->4)-1-thio-beta -d-glucopyranoside;
14 rimethylsilyl)ethyl 3-O-carboxymethyl-beta-D-galactopyranosyl-(1-->4)-[alpha-L-fucosyl-(1-->6) ]-beta
15 onization due to specific binding to alpha-D-galactopyranosyl-(1-4)-beta-D-galactopyranoside receptor
16  with full-length Val331Cys permease, beta-D-galactopyranosyl 10thio-beta-D-galactopyranoside quenche
17 l-2-deoxy-3-O-(2,3,4,6-tetra-O-acetyl-beta-D-galactopyranosyl)-2-trichlo roacetamido-beta-D-glucopyra
18 (1-->3)-beta-d-glucopyranosyl (1-->2)-beta-d-galactopyranosyl 26-O-alpha-l-rhamnopyranosyl (1-->2)-be
19 (1-->3)-beta-d-glucopyranosyl (1-->2)-beta-d-galactopyranosyl 26-O-beta-d-glucopyranoside (4a,4b), (2
20 Its structure is 4-O-(2-amino-2-deoxy-beta-D-galactopyranosyl)-3-O-methyl-D-chiro-inositol 1 (INS-2,
21 xo-28-(phenylmethoxy)oleanan-3-yl 2-O-beta-d-galactopyranosyl-3-O-(phenylmethyl)-, butyl ester beta-d
22 he activity of 3,alpha4,alpha5-tri-O-(beta-D-galactopyranosyl)-6-fluoropyridoxol 4, 3-O-(beta-D-galac
23 yl-1-beta-D-glucurano-pyranoside (4) alpha-D-galactopyranosyl-(6 --> 1')-alpha-D-galactopyranosyl-(6'
24  alpha-D-galactopyranosyl-(6 --> 1')-alpha-D-galactopyranosyl-(6' --> 1'')-alpha-D-galactopyranosyl-(
25 lpha-D-galactopyranosyl-(6' --> 1'')-alpha-D-galactopyranosyl-(6'' --> 1''')-alpha-d-galactopyranosid
26 o-nitrophenyl-2-acetamido-2-deoxy-3-O-beta-D-galactopyranosyl-alpha- D-galactopyranosides, were found
27 osyl)-6 -fluoropyridoxol 12, and 3-O-(beta-D-galactopyranosyl)-alpha4,alpha5-di-O-(alpha-D-mannopyran
28 opyranosyl)-6-fluoropyridoxol 4, 3-O-(beta-D-galactopyranosyl)-alpha4,alpha5-di-O-(beta-D-glucopyrano
29 to a direct stacking interaction between the galactopyranosyl and indole rings.
30  kcat/Km for catalysis of cleavage of beta-D-galactopyranosyl azide, which is the microscopic reverse
31 -nitrophenyl-2-acetamido-2-deoxy-3-O-beta -D-galactopyranosyl-beta-D-galactopyranoside, which is a co
32 h 3,4,6-tri-O-acetyl-2-O-bromoacetyl-alpha-d-galactopyranosyl bromide afforded the beta-linked disacc
33 d with 3,4,6-tri-O-acetyl-2-O-benzyl-alpha-D-galactopyranosyl chloride to give the 1,2-cis alpha-link
34                               9-(5-O-alpha-D-galactopyranosyl)-D-arabinityl-1,3,7-trihydropurine-2,6,
35 lactopyranosyl-D-mannopyranoside, 3-O-beta-D-galactopyranosyl-D-arabinose, 2'-O-methyllactose, lacto-
36 methyl beta-lactoside, lactulose, 4-O-beta-D-galactopyranosyl-D-mannopyranoside, 3-O-beta-D-galactopy
37 461Q enzyme give both the corresponding beta-galactopyranosyl derivatives and D-galactose, and the fo
38 a-selectivity of 4,6-O-benzylidene-protected galactopyranosyl donors bearing neighboring group-active
39 ilibrium constant for transfer of the beta-D-galactopyranosyl group from beta-galactosidase to azide
40 er rate constants for transfer of the beta-D-galactopyranosyl group from the galactosyl-enzyme interm
41  for enzyme-catalyzed transfer of the beta-d-galactopyranosyl group from the substrate to form a cova
42  determine the role of Glu-461 in the beta-D-galactopyranosyl group transfer reaction catalyzed by be
43 ilization of the transition state for beta-d-galactopyranosyl group transfer to water by interactions
44                 The example reaction of beta-galactopyranosyl isonitrile (7) with a protected asparti
45  to date, and S-(2-acetamido-2-deoxy-alpha-D-galactopyranosyl)-L-cysteine, which could be considered
46 e H-bond with the C-4 and C-3 O atoms of the galactopyranosyl moiety and an H-bond with Glu-269 (heli
47  in 30 min stereoselectively leads to a beta-galactopyranosyl-N-formyl-asparagine (9).
48  transformations readily convert 9 into beta-galactopyranosyl-N-methyl-asparagine (11).
49 er series it is elongated by the activity of galactopyranosyl or galactofuranosyl transferases giving
50 it is suggested that the C-3 OH group of the galactopyranosyl ring may play an important role in spec
51 -272 (helix VIII) interact directly with the galactopyranosyl ring of alpha-NPG to provide specificit
52 ortant role in hydrophobic stacking with the galactopyranosyl ring of substrate and that Glu-269 (hel
53 ich include hydrophobic stacking between the galactopyranosyl ring of substrate and the indole side c
54  of the binding site, probably orienting the galactopyranosyl ring so that important H-bond interacti
55 clude interaction of a hydroxyl group in the galactopyranosyl ring with Glu269.
56 d solely by side-chain interactions with the galactopyranosyl ring, whereas affinity is increased by
57 nding probably by aromatic stacking with the galactopyranosyl ring.
58 id 1, BbGL-I), and 1,2-di-O-acyl-3-O-alpha-d-galactopyranosyl-sn-glycerol (BbGL-II).
59 3-azi-1-[([6-3H]2-acetamido-2-deoxy-1-beta-D-galactopyranosyl)thio ]-b utane, was used to identify th
60 at stabilize the transition state for beta-d-galactopyranosyl transfer only develop upon moving from
61  (replacement of Lys(1265) with Hyl(O-beta-d-galactopyranosyl)) versus non-glycosylated ligand.

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