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1 6.0473 Da, attributed to the neutral loss of deoxyribose.
2 ts this enzyme to distinguish ribose from 2'-deoxyribose.
3 n species (ROS) damage to membrane lipids or deoxyribose.
4 precursor with a dihydrofuran derivative of deoxyribose.
5 o increased by thymidine phosphorylase and 2-deoxyribose.
6 se and subsequent extracellular release of 2-deoxyribose.
7 ce that effectively replaces the ribose with deoxyribose.
8 A and causes sequence-selective oxidation of deoxyribose.
9 lecule for nucleophilic attack at C1' of the deoxyribose.
10 ns whereupon it was partially converted to 2-deoxyribose.
11 e synthesis resin in which Cy3B is linked to deoxyribose.
12 tic patch that appears selective for binding deoxyriboses.
14 rsenate with thymidine to form thymine and 2-deoxyribose 1-arsenate, which rapidly decomposes to 2-de
19 dine were duplicated by the TP metabolite, 2-deoxyribose-1-phosphate (dR-1-P), and 10-fold more poten
20 ow that cleavage of thymidine to thymine and deoxyribose-1-phosphate by the host thymidine phosphoryl
21 ernative yjjG (dUMP phosphatase) pathway for deoxyribose-1-phosphate generation greatly exacerbated t
22 s suggest that the dgt-dependent pathway for deoxyribose-1-phosphate generation may operate under var
23 adily converted by the DeoD phosphorylase to deoxyribose-1-phosphate, the critical intermediate that
28 patches (1-5 nt) in damaged DNA and removing deoxyribose 5'-phosphate from the 5'-side of damaged DNA
31 s) of backbone motion to the DNA binding and deoxyribose 5'-phosphate lyase function of this domain.
32 five-carbon phosphorylated monosaccharide, 2-deoxyribose 5-phosphate (2dR5P), as an alternate substra
36 er binding affinity of 5-phenyl-1-indolyl-2'-deoxyribose-5'-triphosphate and suggests that the polyme
37 ously demonstrated that 5-nitro-1-indolyl-2'-deoxyribose-5'-triphosphate, a nonnatural nucleobase pos
38 -terminal abasic sites are excised by the 5'-deoxyribose-5-phosphate (5'-dRP) lyase activity of DNA p
39 ution structures of wild-type and mutant d-2-deoxyribose-5-phosphate (DRP) aldolase complexes with DR
40 yed an average seven-fold acceleration, with deoxyribose-5-phosphate aldolase (DERA) achieving an ave
41 f the bacterial (Escherichia coli) class I 2-deoxyribose-5-phosphate aldolase (DERA) has been determi
42 one-pot tandem aldol reaction catalyzed by a deoxyribose-5-phosphate aldolase (DERA) to form a 6-carb
44 (BER) process requires removal of an abasic deoxyribose-5-phosphate group, a catalytic activity that
45 moiety of the downstream strand by the 5'-2-deoxyribose-5-phosphate lyase activity of either DNA pol
50 demonstrate that although this 5'-terminal 2-deoxyribose-5-phosphate mimic does not affect the fideli
51 a 1,2-dideoxyribose-5-phosphate moiety, a 2-deoxyribose-5-phosphate mimic, we measured the incorpora
52 sion repair, the excision of a 5'-terminal 2-deoxyribose-5-phosphate moiety of the downstream strand
54 cent 3' base pair and to be inhibited when 2-deoxyribose-5-phosphate, rather than phosphate, constitu
55 ta-pol was covalently cross-linked to a 5'-2-deoxyribose-5-phosphate-containing DNA substrate by sodi
56 pairs, puckering differences between A and T deoxyriboses, a narrow minor groove, and a stable water
58 tative cross-link remnant 9b composed of a 2-deoxyribose adduct attached to the exocyclic N(2)-amino
59 The transition state model predicts that deoxyribose adopts a mild 3'-endo conformation during nu
62 ay, using magnetic particles bearing 21-mer, deoxyribose analogues of the complement to microRNA-143
63 eavage of the glycosidic bond between the 2'-deoxyribose and base, corresponding to B[a]PDE adducts o
65 dyad related molecules form four consecutive deoxyribose and ribose zipper hydrogen bonds in the mino
66 isotope analogs of dGuo revealed the loss of deoxyribose and secondarily the loss of a series of stab
67 ides, containing a covalent bond between the deoxyribose and the purine base, represent an important
68 muM), which contain one or two 2'-fluoro-2'-deoxyriboses and/or bis-phosphorothioate linkages, are m
69 Variations in the sugar component (ribose or deoxyribose) and the nature of the phosphodiester linkag
70 was constructed by reattaching uracil to the deoxyribose, and both complexes were studied by molecula
71 cai (Euterpe oleracea) genotypes using ABTS, deoxyribose, and glutathione oxidation assays, as well a
72 ses A, G, C, T, and U, the sugars ribose and deoxyribose, and the phosphate backbone were determined
80 sembly, because an siRNA strand bearing a 2'-deoxyribose at this position can inhibit the cognate str
81 s are a DNA/RNA mimic in which the phosphate deoxyribose backbone has been replaced by uncharged link
82 structures suggested that the DNA phosphate-deoxyribose backbone is recognized by RAGE through well-
83 ic bleomycin causes two major lesions in the deoxyribose backbone of DNA: formation of 4'-keto abasic
84 s in the nucleotide bases and phosphodiester-deoxyribose backbone, as reflected in a substantial (34%
89 mation of a Schiff base adduct of the abasic deoxyribose C-1' with a lysine residue (K312 in the case
92 radical attack on the C1', C3' and C4' of 2-deoxyribose can give rise to epimeric 2-deoxyribose lesi
93 study shows that structural features of the deoxyribose carbons reporting on the sugar pucker are st
96 that an anti glycosidic torsion with C1'-exo deoxyribose conformation allows AAF-dG to be Watson-Cric
98 ' and C5', considered to be key reporters of deoxyribose conformation, fall near or beyond the edges
99 anded helix with all nucleotides in anti, 2'-deoxyribose conformations within the C2'-endo/C1'-exo ra
100 s been crystallized with a cationic 1-aza-2'-deoxyribose-containing DNA that mimics the ultimate tran
101 However, the complexity of nucleobase and 2-deoxyribose damage caused by strong oxidants such as ion
103 except hexane, were effective in preventing deoxyribose degradation, and the inhibition was increase
104 orted here by using three different methods: deoxyribose degradation, hydroxylation of benzoate and h
105 nd 2-methyltetrahydrofuran, simple models of deoxyribose, do not reflect differences in reaction exot
106 on the metabolism of [U-(13)C(6)]glucose to deoxyribose (DR) and then incorporation of [U-(13)C(5)]D
108 ed on the incorporation of (2)H(2)O into the deoxyribose (dR) moiety of purine deoxyribonucleotides i
109 for measuring DNA synthesis by labeling the deoxyribose (dR) moiety of purine deoxyribonucleotides t
116 ee radical attack on the C1' position of DNA deoxyribose generates the oxidized abasic (AP) site 2-de
117 conformational exchange of the phosphate and deoxyribose groups of the DNA oligomers d(GCGTACGC)(2) a
119 aluating D4GTP (the planar 2',3'-unsaturated deoxyribose guanosine analogue that is complementary to
120 s between the 1,N(2)-epsilondG imidazole and deoxyribose H1' protons and between the 1,N(2)-epsilondG
123 oligonucleotide containing a cationic 1-aza-deoxyribose (I) oxacarbenium ion mimic is a potent inhib
124 nucleotide (AIA) containing a cationic 1-aza-deoxyribose (I) residue designed to be a stable mimic of
126 both lipid peroxidation and 4'-oxidation of deoxyribose in DNA, and with base propenals also derived
127 minant of hydroxyl radical reactivity with 2-deoxyribose in DNA, but the large differences between ga
128 sphate residues arising from 5'-oxidation of deoxyribose in DNA, caused by the enediyne neocarzinosta
129 f UDG enforces distortions of the uracil and deoxyribose in the flipped-out nucleotide substrate that
130 o DNA, followed by abstraction of C4'-H from deoxyribose in the rate-limiting step for DNA degradatio
132 3',5'-cyclic phosphoester ring derived from deoxyribose indicated strain energies at least 5.4 kcal/
134 Pentoses, such as arabinose, ribose, and deoxyribose, inhibit the interaction between SP-D and ma
136 helical and well-stacked and the abasic site deoxyribose is predominantly extrahelical, consistent wi
138 present mechanistic studies revealing the 2'-deoxyribose isomerization and subsequent deglycosylation
139 raniloyl modification at the 3'-OH of the 2'-deoxyribose leads to ligands (mant-deoxy-ATP [dATP], man
141 ctive oxygen species produce oxidized bases, deoxyribose lesions and DNA strand breaks in mammalian c
142 of 2-deoxyribose can give rise to epimeric 2-deoxyribose lesions, for which the in vivo occurrence an
144 xyguanosine, pyrimido[1,2-a]purin-10(3H)-one deoxyribose (M(1)dG), and 1,N(2)-propanodeoxyguanosine i
147 from entering holo-RISC; in contrast, the 2'-deoxyribose-modified strand has enhanced activity in the
148 erturbation of specific vibrational modes of deoxyribose moieties and presumably reflect desolvation
150 a the abstraction of H1' and/or H5' from the deoxyribose moiety and by base modification, resulting i
151 s located close to the 2'-carbon atom of the deoxyribose moiety and is proposed to act as the selecti
152 cling of 5'-deoxyadenosine, whereupon the 5'-deoxyribose moiety of 5'-deoxyinosine is further metabol
153 based on incorporation of (2)H(2)O into the deoxyribose moiety of deoxyribonucleotides in dividing c
154 entified a series of modifications of the 2'-deoxyribose moiety of DNA arising from the exposure of i
155 y for 84 days, and 2H incorporation into the deoxyribose moiety of DNA of newly divided B-CLL cells w
156 ((2)H) from heavy water ((2)H(2)O) into the deoxyribose moiety of purine deoxyribonucleotides in DNA
157 ((2)H) from heavy water ((2)H(2)O) into the deoxyribose moiety of purine deoxyribonucleotides in DNA
159 e primer terminus and the ring oxygen of the deoxyribose moiety of the incoming dNTP to align the 3'-
160 riginal methodology's neutral loss of the 2'-deoxyribose moiety to allow for the detection of all DNA
161 e activities that nick the DNA strand at the deoxyribose moiety via a beta- or beta,delta-elimination
162 alog of dUTP in which the ring oxygen of the deoxyribose moiety was replaced by a methylene group.
163 sidic orientation, an S conformation for the deoxyribose moiety, and quite close shape mimicry of gua
166 DNA polymerase yeast pol eta inserts pyrene deoxyribose monophosphate (dPMP) in preference to A oppo
167 resulting in the formation of normal product deoxyribose monophosphate (dR5P) or methoylated-dR5P.
169 ee energy perturbation simulations of ribose-deoxyribose mutations in a single-strand dodecamer and i
170 n phosphate B(I) and B(II) conformations and deoxyribose N and S conformations was expressed as perce
171 e calculate binding free energies for a free deoxyribose nucleotide triphosphate, dATP or dGTP, to Po
173 o transfer damage from the nucleobase to the deoxyribose of an adjacent nucleotide in DNA under hypox
174 upling constants for adjacent protons of the deoxyribose of both the alpha and beta anomers of the ab
175 e native C2'-endo/C3'-exo form of B-DNA, the deoxyribose of the 5'-nucleoside always adopts the C2'-e
177 mical-specific cleavage at the C-4' H of the deoxyribose of the pyrimidine has remained controversial
179 rect effect of thymidine phosphorylase and 2-deoxyribose on signaling pathways associated with endoth
182 ed previously, using 2'-OH (ribose) to 2'-H (deoxyribose) or 2'-O-methyl substitutions in the stem 2
184 ted to 40% and 35%, respectively, of total 2-deoxyribose oxidation as measured by a plasmid nicking a
187 reaction of aldehyde- and ketone-containing deoxyribose oxidation products and abasic sites with [(1
188 ensitive method to quantify abasic sites and deoxyribose oxidation products arising in damaged DNA.
190 r the rigorous quantification of two major 2-deoxyribose oxidation products: the 2-deoxyribonolactone
191 -deoxyribonolactone at 7% and 24% of total 2-deoxyribose oxidation, respectively, with frequencies of
194 /pi interactions between AlkD and the lesion deoxyribose participate in catalysis of glycosidic bond
195 ver, the O4'-exo pseudorotation of the S-cdG deoxyribose perturbed the helical twist and base pair st
197 iates containing the 5'-AMP or 5'-adenylated-deoxyribose phosphate (5'-AMP-dRP) lesions may accumulat
199 ere, we show that Pol theta has intrinsic 5'-deoxyribose phosphate (5'-dRP) lyase activity that is in
200 ovalent Schiff base intermediate with the 5'-deoxyribose phosphate (5'-dRP) residue that results from
201 l gamma acts to catalyze the removal of a 5'-deoxyribose phosphate (dRP) group in addition to playing
202 lso has a dRP lyase activity that cleaves 5'-deoxyribose phosphate (dRP) groups from DNA, thus contri
205 We found earlier that human pol iota has deoxyribose phosphate (dRP) lyase activity and unusual s
207 filling DNA synthesis and removal of the 5'-deoxyribose phosphate (dRP) of the abasic site, whereas
211 y the abstraction of hydrogen atoms from the deoxyribose phosphate backbone of duplex DNA, but exact
213 w that the excision of the characteristic 5'-deoxyribose phosphate containing oligonucleotide (dRP-ol
217 hat LCA suppresses the DNA polymerase and 5'-deoxyribose phosphate lyase activities of DNA pol beta b
218 helix-4, which provides the DNA binding and deoxyribose phosphate lyase activities of the enzyme.
219 er Pol beta gap-filling and much stronger 5'-deoxyribose phosphate lyase activities than was observed
220 (UL30) exhibits apurinic/apyrimidinic and 5'-deoxyribose phosphate lyase activities that are integral
223 cterized and found to be an inhibitor of the deoxyribose phosphate lyase and DNA polymerase activitie
225 mbinantly, are active as DNA polymerases and deoxyribose phosphate lyases, but their polymerase activ
227 ding to [(B[a]Ptriol+phosphate)-H]- and [(2'-deoxyribose+phosphate+B[a]Ptriol)-H]-, respectively.
229 the apparent equilibrium constant K' for the deoxyribose-phosphate aldolase reaction makes it possibl
231 Consistent with the important role that deoxyribose plays in strand exchange, oligonucleotides w
234 single-strand breaks (SSBs) with 5'-blocking deoxyribose products generated directly or as repair int
236 n-Drew dodecamer was used to re-evaluate the deoxyribose pseudorotation profile and the Lennard-Jones
237 umes a very steep distance-dependent form, a deoxyribose pseudorotation profile with reduced energy b
239 /6.682(2)/36.02(2) A, Z = 4) shows C2'- endo deoxyribose puckering, and the base is found in the anti
243 to creation of an abasic (AP) site leaving a deoxyribose residue in the strand, is a frequent lesion
244 articipates in a tight interaction with a 2'-deoxyribose residue of the 5'-terminal G of a neighborin
245 nant 6 in which the anomeric carbon of the 2-deoxyribose residue was connected to the exocyclic N(6)-
246 eters indicate that the conformations of the deoxyribose residues of each strand are dynamically coup
248 tion, these crosspeak resonances and several deoxyribose resonances are multiply split, presumably th
249 s showed that substitution of ribose -5 with deoxyribose resulted in a 24-fold decrease in binding af
250 e radicals also abstract hydrogen atoms from deoxyribose, resulting in the formation of apurinic/apyr
253 y associated with the conformation of the 2'-deoxyribose ring is the value of the C-N torsion angle c
256 atom abstraction from the 4'-position of the deoxyribose ring rather than redox-induced base oxidatio
258 2',3'-unsaturation in its planar carbocyclic deoxyribose ring that acts on HIV-1 reverse transcriptas
260 ydrogen atom abstraction from the respective deoxyribose ring, and that 2-deoxyribonolactone formatio
266 ing a benzyl group at the 2' position of the deoxyribose rings in the backbone, we observed that the
267 show that both thymidine phosphorylase and 2-deoxyribose stimulated the formation of focal adhesions
271 the magnitude of the free energy change for deoxyribose substitutions is determined to a larger exte
273 ine of its N-terminal proline) on C1' of the deoxyribose sugar at a damaged base, which results in th
276 ne radical cations results in high yields of deoxyribose sugar radicals in DNA, guanine deoxyribonucl
277 '-deoxyribonucleotides leads to formation of deoxyribose sugar radicals in remarkably high yields.
279 These analogs contain substitutions on the deoxyribose sugar ring at the 4' carbon (4'C-methyl dT a
280 e nucleophile to attack C1' on the ring-open deoxyribose sugar to form a transient peptide-DNA imino
285 modification preorganizes the ribose and 2'-deoxyribose sugars for a C3'-endo conformation, and stab
289 than that in bulk water and that attached to deoxyribose, suggesting a unique role for the dynamics o
291 e AlkD active site interacts with the lesion deoxyribose through a series of C-H/pi interactions.
292 -glycosylic bond between the uracil base and deoxyribose to initiate the uracil-DNA base excision rep
293 phosphoramidite monomers with Cy3B linked to deoxyribose, to the 5-position of thymine, and to a hexy
294 precedented activity was further extended to deoxyribose triphosphate, and in vitro biosyntheses coul
295 ss tC on the template strand and incorporate deoxyribose-triphosphate-tC into the growing primer term
296 zing several unique 5-substituted indolyl 2'-deoxyribose triphosphates and defining their kinetic par
298 e 2-chloro pharmacophore, rather than the 2'-deoxyribose was responsible for the reduced 2CdA uptake
299 BCNA) 6-pentylphenylfuro[2,3-d]pyrimidine-2'-deoxyribose was synthesized using carbocyclic 2'-deoxyur
300 etermine the properties of combinations of 2-deoxyribose with each of the isolated DNA bases for both
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