ライフサイエンスコーパス: ribitol

1 lpNAc-(1-->5)-Rbo-1-P-->, respectively (Rbo, ribitol).

2 acetamido-2-deoxy-beta-glucopyranosyl)-1-->4-ribitol-1-OPO3-->.

3 terin-6-ylmethyl-l-(4-aminophenyl)-1-deoxy-D-ribitol 5'-phosphate (4') in a reaction stimulated by th

4 terin-6-ylmethyl-1-(4-aminophenyl)-1-deoxy-D-ribitol (5').

5 ose (1-->3) glucose (1-->3) rhamnose (1-->3) ribitol (5-->phosphate.

6 1 (1-->3) glucose 2 (1-->3) rhamnose (1-->3) ribitol (5-->phosphate.

7 indings identify linkages from alpha-Galp to ribitol-5-phosphate and from this residue to adjacent Ga

8 accharide capsule is a polymer of ribose and ribitol-5-phosphate and is a critical determinant of vir

9 lpha1-2 transfer of Gal pyranoside (Galp) to ribitol-5-phosphate in the synthesis of CPS10A, CPS47F,

10 d CPS34 but with alpha1-1 transfer of Gal to ribitol-5-phosphate in the synthesis of CPS39.

11 It has been proposed that FKRP, a ribitol-5-phosphate transferase, is a participant in alp

12 ical, except for the linkage between Gal and ribitol-5-phosphate, which is alpha1-2 in strain SK144 v

13 s identify genetic markers for the different ribitol-5-phosphate-containing types of RPS present in S

14 associated with alpha1-1 transfer of Galp to ribitol-5-phosphate.

15 -dependent alpha1-4 linkages between Gal and ribitol-5-phosphate.

16 -5-[1-alpha -D- ribofuranosyl 5-phosphate]-D-ribitol (9').

17 f other bacterial polysaccharides containing ribitol and glycerol phosphates, including H. influenzae

18 One group was negative for I-erythritol and ribitol and included all the isolates belonging to Nocar

19 D-glucitol, i-myo-inositol, D-mannitol, and ribitol and susceptibility to amoxicillin-clavulanic aci

20 ee groups were positive for I-erythritol and ribitol and were grouped within Nocardia transvalensis.

21 d urinary excretion of erythritol, arabitol, ribitol, and pent(ul)ose-5-phosphates was detected, as w

22 a polyhydroxy alkane, including glycerol and ribitol, and phosphoric acid, joined to form phosphodies

23 precursor to the 1-(4-aminophenyl)-1-deoxy-D-ribitol (APDR) moiety present in the C(1) carrier coenzy

24 col (SG or UG) in residues such as glycerol, ribitol, arabinitol, furanosyl galactose, and sialic aci

25 s [(1S)-substituted 1, 4-dideoxy-1,4-imino-D-ribitols] are powerful inhibitors for the nonspecific nu

26 (9-deazaadenin-9-yl)-1,4-dideoxy-1,4-imino-D-ribitol at the depurination site binds four times better

27 r RNA stem-loop with 1,4-dideoxy-1,4-imino-D-ribitol at the depurination site binds with a K(d) of 1.

28 Disparity in GlcNAc to ribitol connectivity, as well as variable O-acetylation

29 nt pyridine nucleotide reductase and glucose/ribitol dehydrogenase families, respectively.

30 o 7,8-didemethyl-8-hydroxy-5-deazariboflavin ribitol (Fo).

31 9-deazaguanin-9-yl)-1,4-dideoxy-1, 4-imino-D-ribitol (immucillin-G).

32 azahypoxanthin-9-yl)-1,4-dideoxy-1,4-imino-D-ribitol (immucillin-H) and (1S)-1-(9-deazaguanin-9-yl)-1

33 educed sugar nucleotide for the insertion of ribitol in a phosphodiester linkage to the glycoprotein.

34 Thus, we propose a novel structure-a ribitol in a phosphodiester linkage-for the moiety on wh

35 levated amounts of erythritol, arabitol, and ribitol in the plasma of affected individuals.

36 azahypoxanthin-9-yl)-1,4-dideoxy-1,4-imino-D-ribitol] is a 23 pM inhibitor of bovine purine nucleosid

37 cells, FGGY can additionally participate in ribitol metabolism.

38 or with a protonated 1,4-dideoxy-1,4-imino-D-ribitol moiety, a 4-azasugar mimic, at the depurination

39 glycosyltransferase that in vivo transfers a ribitol phosphate group from a CDP -ribitol present in m

40 eaves WTA synthesis intermediates, releasing ribitol phosphate into the medium and recycling bactopre

41 d polymers containing repeating polyglycerol/ribitol phosphate moieties.

42 , catalyzes both the addition of the priming ribitol phosphate onto the linkage unit and the subseque

43 Complementation studies show that a putative ribitol phosphate polymerase, TarL, catalyzes both the a

44 Deltalcp mutant synthesized WTA yet released ribitol phosphate polymers into the extracellular medium

45 so a bifunctional enzyme that catalyzes both ribitol phosphate priming and polymerization.

46 Two major structures, 1,5-poly(ribitol phosphate) and 1,3-poly(glycerol phosphate), wit

47 ria toxin and the attachment of poly(ribosyl-ribitol phosphate) carbohydrate chains results in a stil

48 revised assembly pathway for the late-stage ribitol phosphate-utilizing enzymes is proposed.

49 ib capsular polysaccharide IgG, poly-ribosyl-ribitol-phosphate (PRP), IgG subclass, and cellular immu

50 , the form of IgA in response to polyribosyl-ribitol-phosphate (PRP), the capsular polysaccharide of

51 nd tetrasaccharides and a negatively charged ribitol-phosphate construct to BSA.

52 stor of BL21(DE3) may have produced a ribose/ribitol-phosphate containing polysaccharide.

53 cetylmuramic acid with wall teichoic acid, a ribitol-phosphate polymer tethered to murein linkage uni

54 Lipoteichoic acid (LTA), a cell wall ribitol polymer from Gram-positive organisms, mediates i

55 nsfers a ribitol phosphate group from a CDP -ribitol present in muscles to alpha-DG, while in vitro i

56 It is known that the putative ribitol primase, TarK, is also a bifunctional enzyme tha

57 ISPD is a CDP-ribitol (ribose) pyrophosphorylase that generates the re

58 This functional glycan contains a novel ribitol structure that links a phosphotrisaccharide to x

59 Ribitol teichoic acid (RTA) (1 microg/ml) induced a twof

60 ut not by dextran, dextran sulfate, heparin, ribitol teichoic acid, or soluble low molecular weight P

61 cells, ribulose could only be detected when ribitol was added to the cultivation medium, and under t

62 After all, from studying such pentitols as ribitol with Professor Touster at Vanderbilt University

63 h of which starts with glucose and ends with ribitol, with the lipid anchor predicted to be Glc(beta1