ライフサイエンスコーパス: arabinogalactan protein

1 ferase likely involved in galactosylation of arabinogalactan proteins.

2 abinose and galactose, two major residues of arabinogalactan proteins.

3 of Arabidopsis cell-wall polysaccharides and arabinogalactan proteins.

4 taining pectic cell wall polysaccharides and arabinogalactan proteins.

5 O-glycan epitopes previously associated with arabinogalactan proteins.

6 heteropolysaccharides that characterize the arabinogalactan-proteins.

7 Here, we show that the classical arabinogalactan protein 18 (AGP18) exerts an active regu

8 ed an atypical Hyp-rich glycoprotein, AGP31 (arabinogalactan protein 31), which displays a multidomai

9 isoforms of a purified Arabidopsis thaliana arabinogalactan protein (AGP) encoded by hydroxyproline-

10 have shown that a stylar transmitting tissue arabinogalactan protein (AGP) from Nicotiana tabacum (to

11 thaliana), we have identified a nonclassical arabinogalactan protein (AGP) gene, AGP31, and show that

12 Arabidopsis thaliana, consisting of a short arabinogalactan protein (AGP) motif, a His stretch, a Pr

13 e core protein of an immunoaffinity-purified arabinogalactan protein (AGP) secreted aucus carota (car

14 In contrast, the application of the arabinogalactan-protein (AGP) binding beta-glucosyl Yari

15 glycosylphosphatidylinositol (GPI)-anchored arabinogalactan-protein (AGP) in tomato (Lycopersicon es

16 This gene encodes an arabinogalactan-protein (AGP) that is known to play a ro

17 The high molecular weight component in arabinogalactan-proteins (AGP/GP), and more "branched" c

18 HRGPs such as arabinogalactan proteins (AGPs) and extensios play signi

19 ined whether immunostimulatory plant-derived arabinogalactan proteins (AGPs) and the honeybee-derived

20 Arabinogalactan proteins (AGPs) are a family of extracel

21 Arabinogalactan proteins (AGPs) are a family of highly g

22 Arabinogalactan proteins (AGPs) are abundant plant prote

23 Arabinogalactan proteins (AGPs) represent a major class

24 d 120-kDa glycoprotein (120K) are two pistil arabinogalactan proteins (AGPs) that share a conserved C

25 s of biosynthetic mutants, water-extractable arabinogalactan proteins (AGPs) were isolated from the l

26 Arabinogalactan proteins (AGPs), a family of hydroxyprol

27 nanoparticles are predominantly composed of arabinogalactan proteins (AGPs), a superfamily of hydrox

28 Arabinogalactan proteins (AGPs), a superfamily of plant

29 -> 3)-d-galactans, structures found in plant arabinogalactan proteins (AGPs), is described.

30 consists of three members: hyperglycosylated arabinogalactan proteins (AGPs), moderately glycosylated

31 though plants contain substantial amounts of arabinogalactan proteins (AGPs), the enzymes responsible

32 enzymes responsible for the glycosylation of arabinogalactan proteins (AGPs).

33 Arabinogalactan-proteins (AGPs) are a family of hydroxy-

34 Arabinogalactan-proteins (AGPs) are cell wall proteoglyc

35 Arabinogalactan-proteins (AGPs) are extracellular proteo

36 Arabinogalactan-proteins (AGPs) are highly glycosylated

37 Since arabinogalactan-proteins (AGPs) are known to play a role

38 Functional analysis of the hyperglycosylated arabinogalactan-proteins (AGPs) attempts to relate biolo

39 l glycoside that interacts specifically with arabinogalactan-proteins (AGPs), a class of plant cell s

40 ifferences between B. napus and pea root cap arabinogalactan proteins and (2) a cross-link between th

41 the extractability of arabinans, galactans, arabinogalactan proteins and mannans.

42 biosynthesis, localization, and function of arabinogalactan proteins and toward stimulating other st

43 organization and biogenesis (e.g., tubulins, arabinogalactan proteins) and DNA or RNA metabolism (e.g

44 coproteins, changes in the types of secreted arabinogalactan proteins, and an increase in the amounts

45 timulatory components, including apalbumins, arabinogalactan proteins, and apisimin, whose levels did

46 This suggests that root arabinogalactan proteins are involved in the control of

47 ilage hydrocolloid was primarily composed of arabinogalactan protein-associated pectin whereas pulp h

48 h both phosphatidylinositol 3-phosphate- and arabinogalactan protein-binding domains.

49 Plasma membrane vesicles readily shed arabinogalactan proteins by an inherent mechanism that a

50 structural analysis now show that some rose arabinogalactan proteins carry a ceramide class glycosyl

51 oteic fraction is probably represented by an arabinogalactan-protein complex that binds poorly with b

52 onstituted by four fractions, one of them an arabinogalactan-protein complex.

53 Arabinogalactan proteins constitute a class of plant cel

54 n upex1, suggesting that primexine-localized arabinogalactan proteins could play roles in sporopollen

55 We confirm the presence of arabinogalactan protein epitopes on root cap cell walls

56 Commonly divided into the arabinogalactan proteins, extensins, and proline-rich pr

57 Fasciclin-like arabinogalactan proteins (FLAs) are involved in numerous

58 Arabinogalactan-protein, for example, shows an increased

59 However, the arabinogalactan protein fraction from pea attracts zoosp

60 e structural similarity between some soluble arabinogalactan proteins from the cell wall space and so

61 The Hyp-AGs were isolated from two different arabinogalactan protein fusion glycoproteins expressed i

62 Our results suggest an evolutionary role for arabinogalactan proteins in the acquisition of monospory

63 quence for plasma membrane localization, two arabinogalactan protein-like domains, two fasciclin-like

64 We find that although the arabinogalactan proteins of both species induce encystme

65 Finally, we assessed the impact of root cap arabinogalactan proteins on the behavior of zoospores of

66 s thetaiotaomicron that were up-regulated by arabinogalactan proteins or AGPs.

67 Classical arabinogalactan proteins partially defined by type II O-

68 xyproline-rich glycoproteins (extensins) and arabinogalactan proteins, peroxidases, receptor-like kin

69 20K, and NaPELPIII, these latter three being arabinogalactan proteins previously shown to interact di

70 CELLULOSE SYNTHASE5 (CESA5) and the arabinogalactan protein SALT-OVERLY SENSITIVE5 (SOS5) ar

71 ta 120-kD glycoprotein (120K) is an abundant arabinogalactan protein that is taken up from the ECM; i

72 ll space and some plasma membrane-associated arabinogalactan proteins, thus inspiring the present inv