ライフサイエンスコーパス: arabinogalactan protein

1 O-glycan epitopes previously associated with arabinogalactan proteins.

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

3 of Arabidopsis cell-wall polysaccharides and arabinogalactan proteins.

4 ferase likely involved in galactosylation of arabinogalactan proteins.

5 taining pectic cell wall polysaccharides and 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 evealed a distinct spatiotemporal pattern of arabinogalactan protein (AGP) deposition and significant

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

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

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

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

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

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

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

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

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

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

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

21 Plant arabinogalactan proteins (AGPs) are a diverse group of c

22 Arabinogalactan proteins (AGPs) are a family of extracel

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

24 Arabinogalactan proteins (AGPs) are abundant plant prote

25 Arabinogalactan proteins (AGPs) are complex, hyperglycos

26 s Ara or gum arabic, a commercial product of arabinogalactan proteins (AGPs) from Acacia senegal.

27 Arabinogalactan proteins (AGPs) represent a major class

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

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

30 Arabinogalactan proteins (AGPs), a family of hydroxyprol

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

32 Arabinogalactan proteins (AGPs), a superfamily of plant

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

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

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

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

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

38 Arabinogalactan-proteins (AGPs) are cell wall proteoglyc

39 Arabinogalactan-proteins (AGPs) are extracellular proteo

40 Arabinogalactan-proteins (AGPs) are glycoproteins that i

41 Arabinogalactan-proteins (AGPs) are highly glycosylated

42 Arabinogalactan-proteins (AGPs) are hydroxyproline-rich

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

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

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

46 The non-enzyme wines had elevated levels of arabinogalactan protein and pectin epitopes (notably bio

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

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

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

50 bidopsis (Arabidopsis thaliana), showed that arabinogalactan-proteins and arabinans represent substan

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

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

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

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

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

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

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

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

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

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

61 Arabinogalactan proteins constitute a class of plant cel

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

63 ylation of xyloglucan, N-linked glycans, and arabinogalactan proteins did not explain the aberrant wa

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

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

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

67 Arabinogalactan-protein, for example, shows an increased

68 However, the arabinogalactan protein fraction from pea attracts zoosp

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

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

71 , including pectins, xyloglucans (XyGs), and arabinogalactan proteins in isolated vesicles.

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

73 Arabinogalactan proteins increased up to 8 DAG and showe

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

75 loglucan (LM25), heteroxylan (LM11/LM27) and arabinogalactan-protein (LM2) epitopes, and sandwich-ELI

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

77 es from the neutral sugar side chains (e.g., arabinogalactan protein) of soluble pectic polysaccharid

78 perones (Ca(2+) , Pb(2+) , polyhistidine, or arabinogalactan-protein oligopeptides).

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

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

81 Classical arabinogalactan proteins partially defined by type II O-

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

83 20K, and NaPELPIII, these latter three being arabinogalactan proteins previously shown to interact di

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

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

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