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1 ted binding specificity for myo-inositol and D-ribose.
2 s were accomplished in 24 steps from 2-deoxy-D-ribose.
3 nate, N-acetyl-D-glucosamine, D-mannose, and D-ribose.
4 ere both stereospecifically synthesized from D-ribose.
5 nthesized starting from tribenzoyl protected d-ribose.
6 rise from D-GlcNAc and 1 from uridine and/or D-ribose.
7 ized on EAH-Sepharose gel and glycated using d-ribose.
8 clic phosphate that might be found on a beta-D-ribose.
9 hieved by modifying reported procedures from D-(-)-ribose.
10 Instead, MTA is converted to 5-methylthio-d-ribose 1-phosphate (MTR 1-P) and adenine; MTR 1-P is i
12 ized forms is expected to apply to D-ribose, D-ribose 1-phosphate, ribonucleosides, and ribonucleotid
14 in a radical-based reaction producing alpha-D-ribose-1,2-cyclic-phosphate-5-phosphate and methane in
15 phoryl-5-phosphoribose via a 5-phospho-alpha-d-ribose-1-diphosphate:decaprenyl-phosphate 5-phospho-ri
16 The Rv3806c gene encoding 5-phospho-alpha-d-ribose-1-diphosphate:decaprenyl-phosphate 5-phosphorib
18 lphosphonate reacts with MgATP to form alpha-D-ribose-1-methylphosphonate-5-triphosphate (RPnTP) and
19 ase; (iii) LipM, a UTP:5-amino-5-deoxy-alpha-D-ribose-1-phosphate uridylyltransferase; and (iv) LipN,
21 ed pathway for RuBP synthesis from 5-phospho-D-ribose-1-pyrophosphate (PRPP) in M. jannaschii and oth
22 cide inhibition of decaprenylphosphoryl-beta-D-ribose 2' oxidase (DprE1), which is responsible for ce
23 st AQs, identified decaprenylphosphoryl-beta-d-ribose 2'-epimerase (DprE1) as the primary target resp
24 to 14 by mutating decaprenylphosphoryl-beta-d-ribose 2-oxidase (DprE1), an essential enzyme in arabi
29 (2dR5P), as an alternate substrate, but not D-ribose 5-phosphate (R5P) nor the four carbon analogue
30 superfamily members that interconvert alpha-D-ribose 5-phosphate (ribose 5-phosphate) and alpha-D-ri
33 y is derived from D-fructose 6-phosphate and D-ribose 5-phosphate via a transaldol reaction catalyzed
34 This shows that Delta(f)G degrees (2'-deoxy-D-ribose 5-phosphate(2)(-)) - Delta(f)G degrees (D-ribos
35 bose 5-phosphate(2)(-)) - Delta(f)G degrees (D-ribose 5-phosphate(2)(-)) = 147.86 kJ mol(-1) at 298.1
36 7-phosphate) and nucleotide metabolism (via D-ribose 5-phosphate) was associated with perturbations
37 ccharide analogues, D-arabinose 5-phosphate, D-ribose 5-phosphate, and 2-deoxy-D-ribose 5-phosphate,
38 phosphate, D-ribose 5-phosphate, and 2-deoxy-D-ribose 5-phosphate, were separately condensed with (Z)
41 mples of an alternate substrate derived from d-ribose (5-OH group instead of the 5-methylthio group i
43 The crystal structure of the complex with D-ribose-5-phosphate indicated that the phosphosugar is
45 osynthase, which catalyzes the attachment of D-ribose-5-phosphate to prealnumycin by formation of the
46 ity of 6-PG for oxidative decarboxylation to D-ribose-5-phosphate, which is essential for the utiliza
49 x 10(-2) M, as indicated by the Ki values of D-ribose and 1-methyl-D-ribofuranoside as competitive in
50 G degrees values for the species of 2'-deoxy-D-ribose and its derivatives makes it possible to calcul
52 aw heat capacity measurements on crystals of d-ribose and other calorimetric measurements make it pos
54 r pattern of endothelial plasticity: 2-deoxy-d-ribose and VEGFA produce transcriptional programs enco
55 d Q building blocks 9 (obtained from 2-deoxy-D-ribose) and 10 (obtained from D-ribose) followed by ri
56 o produce acid from carbohydrates other than D-ribose, and were biochemically and enzymatically fairl
57 ding allele affected C. crescentus growth on D-ribose as a carbon source, providing evidence that the
58 ficient to increase the affinity of IbpA for D-ribose by 10-fold while completely abolishing binding
59 owed that L-fucose stimulated utilization of D-ribose by the E. coli MG1655 DeltafucAO mutant but not
60 e populations of Escherichia coli B all lost D-ribose catabolic function during 2,000 generations of
61 al cells, VEGFA and the TYMP product 2-deoxy-d-ribose cooperatively repress tight junction proteins,
62 d and oxidized forms is expected to apply to D-ribose, D-ribose 1-phosphate, ribonucleosides, and rib
63 de novo preparation of L-ribulose, L-lyxose, D-ribose, D-tagatose, 1-amino-1-deoxy-D-lyxitol, and oth
64 nines or an N(2)-alkyl-6-chloroguanine and a D-ribose derivative containing a 2-ethyltetrazolyl moiet
65 ppropriate 5-O-alkyl-1,2,3-tri-O-acetyl-beta-D-ribose derivatives with 2,5,6-trichlorobenzimidazole f
67 from 2-deoxy-D-ribose) and 10 (obtained from D-ribose) followed by ring-closing metathesis to afford
69 ns it could have been formed from homochiral D ribose from the hydrolysis of amplified adenosine or c
70 rmediate 11b was synthesized in 4 steps from d-ribose in 41% overall yield via an efficient intramole
72 flavour enhancer solution (FES) (d-glucose, d-ribose, l-cysteine and thiamin) and of sous-vide cooki
73 when it was exposed to D-mannose, D-fucose, D-ribose, L-glucose, or L-galactose, but it changed mark
74 h the alternative substrates D-erythrose and D-ribose, making SalM the first reported stereospecific
75 ionine salvage pathway in which 5-methylthio-d-ribose (MTR) derived from 5'-methylthioadenosine is co
77 the geometry of sugars referred to D, as in D-ribose or D-glucose, is not an independent mystery.
80 was predetermined by the prior evolution of D-ribose RNA and probably was chirally directed by the o
82 visualize the oxidation of 5-chloro-5-deoxy-D-ribose to 5-chloro-5-deoxy-D-ribono-gamma-lactone in a
85 tricyclic core is derived from d-glucose and d-ribose, whereas the tiglyl moiety is derived from an i
86 olved reactions of d-xylose, d-arabinose and d-ribose with glycine, alpha-l- or beta-alanine and l-va
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