ライフサイエンスコーパス: galactopyranosyl

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します

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 pyranosyl-(1->3)-d-glucopyranoside or beta-d-galactopyranosyl-(1->3)-2-acetamido-2-deoxy-d-glucopyran

12 eoxy-d-glucose/glucosamine to lead to beta-d-galactopyranosyl-(1->3)-d-glucopyranoside or beta-d-gala

13 with kaempferol-3-O-[glucopyranosyl-(1-->2)-galactopyranosyl-(1-->2)-glucopyranoside, identified as

14 lo-hexopyranosyl-(1-->4)-[3-O-benzyl-beta-D -galactopyranosyl-(1-->3)]-6-O-benzyl-2-deoxy-2-trichloro

15 5-N-acetyl-alpha-d-neuraminyl-(2-->3)-beta-d-galactopyranosyl-(1-->4)-1-thio-beta -d-glucopyranoside;

16 rimethylsilyl)ethyl 3-O-carboxymethyl-beta-D-galactopyranosyl-(1-->4)-[alpha-L-fucosyl-(1-->6) ]-beta

17 onization due to specific binding to alpha-D-galactopyranosyl-(1-4)-beta-D-galactopyranoside receptor

18 with full-length Val331Cys permease, beta-D-galactopyranosyl 10thio-beta-D-galactopyranoside quenche

19 l-2-deoxy-3-O-(2,3,4,6-tetra-O-acetyl-beta-D-galactopyranosyl)-2-trichlo roacetamido-beta-D-glucopyra

20 hydroxy-2-oxoindolin-3-yl)acetic acid 3-O-6'-galactopyranosyl-2"-(2"oxoindolin-3"yl) acetate, giffoni

21 (1-->3)-beta-d-glucopyranosyl (1-->2)-beta-d-galactopyranosyl 26-O-alpha-l-rhamnopyranosyl (1-->2)-be

22 (1-->3)-beta-d-glucopyranosyl (1-->2)-beta-d-galactopyranosyl 26-O-beta-d-glucopyranoside (4a,4b), (2

23 Its structure is 4-O-(2-amino-2-deoxy-beta-D-galactopyranosyl)-3-O-methyl-D-chiro-inositol 1 (INS-2,

24 xo-28-(phenylmethoxy)oleanan-3-yl 2-O-beta-d-galactopyranosyl-3-O-(phenylmethyl)-, butyl ester beta-d

25 he activity of 3,alpha4,alpha5-tri-O-(beta-D-galactopyranosyl)-6-fluoropyridoxol 4, 3-O-(beta-D-galac

26 yl-1-beta-D-glucurano-pyranoside (4) alpha-D-galactopyranosyl-(6 --> 1')-alpha-D-galactopyranosyl-(6'

27 alpha-D-galactopyranosyl-(6 --> 1')-alpha-D-galactopyranosyl-(6' --> 1'')-alpha-D-galactopyranosyl-(

28 lpha-D-galactopyranosyl-(6' --> 1'')-alpha-D-galactopyranosyl-(6'' --> 1''')-alpha-d-galactopyranosid

29 o-nitrophenyl-2-acetamido-2-deoxy-3-O-beta-D-galactopyranosyl-alpha- D-galactopyranosides, were found

30 osyl)-6 -fluoropyridoxol 12, and 3-O-(beta-D-galactopyranosyl)-alpha4,alpha5-di-O-(alpha-D-mannopyran

31 opyranosyl)-6-fluoropyridoxol 4, 3-O-(beta-D-galactopyranosyl)-alpha4,alpha5-di-O-(beta-D-glucopyrano

32 to a direct stacking interaction between the galactopyranosyl and indole rings.

33 kcat/Km for catalysis of cleavage of beta-D-galactopyranosyl azide, which is the microscopic reverse

34 -nitrophenyl-2-acetamido-2-deoxy-3-O-beta -D-galactopyranosyl-beta-D-galactopyranoside, which is a co

35 h 3,4,6-tri-O-acetyl-2-O-bromoacetyl-alpha-d-galactopyranosyl bromide afforded the beta-linked disacc

36 d with 3,4,6-tri-O-acetyl-2-O-benzyl-alpha-D-galactopyranosyl chloride to give the 1,2-cis alpha-link

37 9-(5-O-alpha-D-galactopyranosyl)-D-arabinityl-1,3,7-trihydropurine-2,6,

38 lactopyranosyl-D-mannopyranoside, 3-O-beta-D-galactopyranosyl-D-arabinose, 2'-O-methyllactose, lacto-

39 methyl beta-lactoside, lactulose, 4-O-beta-D-galactopyranosyl-D-mannopyranoside, 3-O-beta-D-galactopy

40 461Q enzyme give both the corresponding beta-galactopyranosyl derivatives and D-galactose, and the fo

41 reoselectivity of the 4-O-benzoyl-4-C-methyl galactopyranosyl donor depends on reaction concentration

42 re NMR studies with a 4-C-methyl-4-O-benzoyl galactopyranosyl donor enable the observation and charac

43 ion of a 4-C-methyl group into a 4-O-benzoyl galactopyranosyl donor enables nuclear magnetic resonanc

44 a-selectivity of 4,6-O-benzylidene-protected galactopyranosyl donors bearing neighboring group-active

45 Migrating 3-beta-galactopyranosyl glucose (<=8.9 mg/kg) and 2,5-diketo-d-

46 ilibrium constant for transfer of the beta-D-galactopyranosyl group from beta-galactosidase to azide

47 er rate constants for transfer of the beta-D-galactopyranosyl group from the galactosyl-enzyme interm

48 for enzyme-catalyzed transfer of the beta-d-galactopyranosyl group from the substrate to form a cova

49 determine the role of Glu-461 in the beta-D-galactopyranosyl group transfer reaction catalyzed by be

50 ilization of the transition state for beta-d-galactopyranosyl group transfer to water by interactions

51 The example reaction of beta-galactopyranosyl isonitrile (7) with a protected asparti

52 to date, and S-(2-acetamido-2-deoxy-alpha-D-galactopyranosyl)-L-cysteine, which could be considered

53 e H-bond with the C-4 and C-3 O atoms of the galactopyranosyl moiety and an H-bond with Glu-269 (heli

54 ere treated with [(C2S, 3S, 4R)-1-O-(alpha-d-galactopyranosyl)-N-tetracosanoyl-2-amino-1,3,4-nonanetr

55 ce were treated with [(C2S, 3S, 4R)-1-O-(a-d-galactopyranosyl)-N-tetracosanoyl-2-amino-1,3,4-nonanetr

56 in 30 min stereoselectively leads to a beta-galactopyranosyl-N-formyl-asparagine (9).

57 transformations readily convert 9 into beta-galactopyranosyl-N-methyl-asparagine (11).

58 er series it is elongated by the activity of galactopyranosyl or galactofuranosyl transferases giving

59 it is suggested that the C-3 OH group of the galactopyranosyl ring may play an important role in spec

60 -272 (helix VIII) interact directly with the galactopyranosyl ring of alpha-NPG to provide specificit

61 ortant role in hydrophobic stacking with the galactopyranosyl ring of substrate and that Glu-269 (hel

62 ich include hydrophobic stacking between the galactopyranosyl ring of substrate and the indole side c

63 of the binding site, probably orienting the galactopyranosyl ring so that important H-bond interacti

64 clude interaction of a hydroxyl group in the galactopyranosyl ring with Glu269.

65 d solely by side-chain interactions with the galactopyranosyl ring, whereas affinity is increased by

66 nding probably by aromatic stacking with the galactopyranosyl ring.

67 id 1, BbGL-I), and 1,2-di-O-acyl-3-O-alpha-d-galactopyranosyl-sn-glycerol (BbGL-II).

68 3-azi-1-[([6-3H]2-acetamido-2-deoxy-1-beta-D-galactopyranosyl)thio ]-b utane, was used to identify th

69 at stabilize the transition state for beta-d-galactopyranosyl transfer only develop upon moving from

70 that fungal GH26 endomannanases accommodate galactopyranosyl units in the -3 and -2 subsites.

71 (replacement of Lys(1265) with Hyl(O-beta-d-galactopyranosyl)) versus non-glycosylated ligand.