ライフサイエンスコーパス: carbohydrate chain

1 IR), the signature Cys-loop and the N-linked carbohydrate chain.

2 th sialic acids on both branches of the GT1b carbohydrate chain.

3 atic properties and type of activity against carbohydrate chains.

4 lecular mass (Mr)=45,000 containing N-linked carbohydrate chains.

5 aride subunits of peptidoglycan to form long carbohydrate chains.

6 d viral entry, and cleaving sialic acid from carbohydrate chains.

7 vivo degradation of sphingolipids with short carbohydrate chains.

8 beta3 is a glycoprotein containing N-linked carbohydrate chains.

9 ed neuraminidase sensitive, complex N-linked carbohydrate chains.

10 n as well as the characterization of various carbohydrate chains.

11 pparent loss of sugar residues from within a carbohydrate chain and can produce ambiguous results dur

12 ion site (Ser126) had an additional O-linked carbohydrate chain and not an additional N-linked carboh

13 al function, the biosynthetic pathway of the carbohydrate chain and particularly the elongation steps

14 an HSPG, such as long heparitinase-sensitive carbohydrate chains and a highly negative net charge.

15 sylated form, the complex without one of the carbohydrate chains, and the deglycosylated proteins-are

16 HS carbohydrate chains are complex and can contain rare str

17 ies suggest some degree of compaction of the carbohydrate chains around the protein.

18 ugh a precipitation method by using the free carbohydrate chains as phase tags.

19 obule that has three disulfide bridges and a carbohydrate chain at each pole.

20 in E is a glycoprotein, carrying an N-linked carbohydrate chain at position 108.

21 n F is a glycoprotein, carrying two N-linked carbohydrate chains at positions 36 and 88.

22 Golgi mannosidase inhibition to prevent carbohydrate chain branching and elongation resulted in

23 Using this method, the primary sequences of carbohydrate chains can be determined in a relatively sh

24 Keratan sulfate carbohydrate chains consist of repeating N-acetyllactosa

25 embranes and are comprised of ceramides with carbohydrate chains containing 5-25 carbohydrates, all c

26 at the nascent apoE is heavily modified with carbohydrate chains containing sialic acid.

27 ffect the addition of O-fucose but do impair carbohydrate chain elongation by Fringe.

28 t aldehyde functionality present in reducing carbohydrate chain ends.

29 l that, at physiological ionic strength, the carbohydrate chains extend beyond the range of the unmod

30 glycosylation, we have compared the O-linked carbohydrate chains from MUC-1 immunoprecipitated from [

31 ent in humans, comprises part of the core of carbohydrate chain in A and B antigens.

32 as used under mild conditions to oxidize the carbohydrate chains in AGP for attachment to a hydrazide

33 owed recognition and binding of the branched carbohydrate chain inhibited spread in the mouse, though

34 alogues (1-6) the first (inner) sugar in the carbohydrate chain is a 3-azido-2,3,6-trideoxy-L-lyxo-al

35 udies we demonstrated that the Pg 2 O-linked carbohydrate chain is essential for its binding to CD26

36 e are also accessible to antibodies when the carbohydrate chain is fully extended.

37 x) oligosaccharide structure found in PSGL-1 carbohydrate chains is reported.

38 affinity for carbohydrate ligands depends on carbohydrate chain length, supporting a binding model in

39 y to a specific LPS variant, by altering the carbohydrate chain length.

40 en combined with modifications of Asn-linked carbohydrate chains near the heparin-binding site, also

41 to wild-type LPS which has a fully extended carbohydrate chain of immunotype L3,7, as well as to the

42 lucifer yellow (LY) covalently linked to the carbohydrate chains of beta have demonstrated that the b

43 ctosamine (Gal(beta)1-4GlcNAc-R) on N-linked carbohydrate chains of glycoproteins and glycolipids.

44 Heparan sulfates, the carbohydrate chains of heparan sulfate proteoglycans, pl

45 ycosylases), which catalyze formation of the carbohydrate chains of peptidoglycan from disaccharide s

46 lambda-lysozyme, an enzyme that degrades the carbohydrate chains of peptidoglycan.

47 Synthesis of alpha-Gal epitopes on carbohydrate chains of PR8 virus (PR8(alpha gal)) was ca

48 ype Chinese hamster ovary cells the N-linked carbohydrate chains of SCAP were mostly in the endoglyco

49 Carbohydrate chains on alpha 1-acid glycoprotein were co

50 ites to determine the effect of the putative carbohydrate chains on the activities of the receptor.

51 The glycan shield comprised of multiple carbohydrate chains on the human immunodeficiency virus

52 method is based on enzymatic engineering of carbohydrate chains on virus envelope hemagglutinin to c

53 and the spatially restricted modification of carbohydrate chains play pivotal roles in the mechanisms

54 ttachment of poly(ribosyl-ribitol phosphate) carbohydrate chains results in a still 'more open' state

55 hydrate chain and not an additional N-linked carbohydrate chain suggesting that structural requiremen

56 ycosylation sites bear N-linked mannose-rich carbohydrate chains, suggesting an important structural

57 rase (alpha1,3GT) is an enzyme that produces carbohydrate chains termed alphaGal epitopes found in mo

58 A virus with their common ligand/substrate: carbohydrate chains terminating in sialic acid.

59 e data suggest that the third sugar from the carbohydrate chain terminus is important for virus bindi

60 st cancer cell lines has simpler, and fewer, carbohydrate chains than MUC-1 from normal breast epithe

61 pecies revealed a very flexible, amphiphilic carbohydrate chain that has frequent dynamic interaction

62 DC-SIGN contains a single N-linked carbohydrate chain that is important for efficient cell

63 The carbohydrate chains that form the backbone of peptidogly

64 spicule, SM 30, has been shown to contain a carbohydrate chain (the 1223 epitope) that has been impl

65 ues is to provide tunnel shape and guide the carbohydrate chain to the active site.

66 of linear and conformational structures and carbohydrate chains to B cell epitopes.

67 meric intermediates, the reducing end of the carbohydrate chain was converted to the semicarbazone.

68 replaced Ser34, Arg37, or Leu39, this second carbohydrate chain was not added.

69 nzymatic replacement of sialic acid on these carbohydrate chains with Galalpha1-3Galbeta1-4GlcNAc-R (