ライフサイエンスコーパス: acceptor site

1 on site in K(2P)3.1 and K(2P)9.1 is a glycan acceptor site.

2 Rac1 was identified as a polyubiquitination acceptor site.

3 ecific toward hydrophobic amino acids at the acceptor site.

4 Lys-13 in Sestrin-2 is a putative ubiquitin acceptor site.

5 nucleotides upstream of the canonical splice acceptor site.

6 erminal) position relative to the Ser or Thr acceptor site.

7 n addition, Asn replaces Asp at the expected acceptor site.

8 O-1 attachment to Nkx2.5 on the primary SUMO acceptor site.

9 ryptic promoter activity or a cryptic splice acceptor site.

10 wo new cis-acting sequences, which flank the acceptor site.

11 ces of a polyadenylation signal and a splice acceptor site.

12 that cysteine 224 is a major S-nitrosylation acceptor site.

13 bases form a consensus sequence for a splice acceptor site.

14 lized the 3' end in the vicinity of a splice acceptor site.

15 codons and one allele changes a splice site acceptor site.

16 The other two alleles change a splice site acceptor site.

17 hrough its impact on the conformation of the acceptor site.

18 otif where lysine can serve as an ADP-ribose acceptor site.

19 rosylcysteine at Cys-145, which is the alkyl acceptor site.

20 six changes is likely to create a new splice acceptor site.

21 -708,906 derivative binds selectively to the acceptor site.

22 (-2)--> G substitution at the exon 14 splice acceptor site.

23 mutation in intron 6, upstream of the exon 7 acceptor site.

24 t in vitro substrate by exposing its phospho-acceptor site.

25 at is generated by the use of an alternative acceptor site.

26 5 and Lys 29 on ubiquitin is the major ISG15 acceptor site.

27 in NZB mice, which generates a novel splice acceptor site.

28 ion and mutating the COOLAIR proximal splice acceptor site.

29 a previously unreported mutation in a splice acceptor site.

30 es, with its evolutionary origin as a splice acceptor site.

31 dification at a single functionally critical acceptor site.

32 k1 as the evolutionarily conserved ubiquitin acceptor site.

33 ates, both in the acyl donor and in the acyl acceptor sites.

34 -proximal lysine 273 as one of the potential acceptor sites.

35 role of the protein milieu between donor and acceptor sites.

36 e among the residues identified as ubiquitin acceptor sites.

37 s ensured by the presence of rigid donor and acceptor sites.

38 for MS analysis and for mapping of ubiquitin acceptor sites.

39 n, and alternative usage of splice donor and acceptor sites.

40 to identify point mutations in splice donor/acceptor sites.

41 dentified T24 and S29 as the primary phospho-acceptor sites.

42 contain numerous functional splice donor and acceptor sites.

43 ts that PmHAS contains at least two distinct acceptor sites.

44 80 to 120 bases away from the ends of splice acceptor sites.

45 also enriched in introns with weak donor or acceptor sites.

46 eporter proteins that contain closely spaced acceptor sites.

47 ree minor, Gln105, Gln783, and Gln830, amine acceptor sites.

48 the hydrophobicity at the EF helix beta6 Val acceptor sites.

49 ons to multiple alternative splice donor and acceptor sites.

50 found to be strongly favored as integration acceptor sites.

51 orylation of NCAM1 on a cluster of cytosolic acceptor sites.

52 nd Lys-91 within survivin serve as ubiquitin acceptor sites.

53 y transfer for an electron between donor and acceptor sites.

54 achieve N-glycosylation of cysteine proximal acceptor sites.

55 hyperglycosylated on cryptic N-linked glycan acceptor sites.

56 to facilitate access of STT3B to unmodified acceptor sites.

57 A cryptic acceptor site -100 nucleotide within intron 13 is used i

58 There are alternative splice acceptor sites, 3 base pairs apart, which account for th

59 ide polymorphism in the XPC intron 11 splice acceptor site (58% C in 97 normals) decreased its inform

60 rmality leading to the use of an alternative acceptor site 8 bp downstream of the normal site, result

61 n of 16S ribosomal RNA in the aminoacyl tRNA acceptor site (A-site).

62 affect key protein regions, including a SUMO acceptor site, a central disordered alanine-rich motif,

63 The activity of the 3' acceptor site A7 is tightly regulated through a complex

64 markedly reduced whereas that of alternative acceptor sites (AA) is significantly increased post-fert

65 ion results in the loss of the exon 2 splice acceptor site, absence of exon 2 from the CP49 mRNA, and

66 o identify the splice donor sites and splice acceptor sites accurately and quickly, a deep sparse aut

67 ealed that serine serves as a new ADP-ribose acceptor site across the proteome.

68 e-leaving group of lipid II, and E100 in the acceptor site acts as general base for the 4-OH of GlcNA

69 fficient cotranslational glycosylation of an acceptor site adjacent to the N-terminal signal sequence

70 axation times at the favored carbonyl oxygen acceptor sites also have the largest order in the upper

71 These products are derived from alternative acceptor sites, alternative donor sites, and retained in

72 e env-like ORF begins with a putative splice acceptor site and encodes a protein with a predicted cen

73 r elevated temperature but alternative donor/acceptor site and exon skipping are mainly induced, indi

74 and Ser-259 serve as a PKC-specific phospho-acceptor site and that phosphorylation of this motif is

75 omplex with ACV at the nucleoside phosphoryl acceptor site and UDP at the phosphoryl donor site.

76 c domain alone, and concerted recognition of acceptor sites and adjacent GalNAc-glycosylated sites by

77 and Lys-19 in hsTAF12 as the primary SUMO-1 acceptor sites and show that SUMO conjugation has no det

78 osin binding protein-C (1 nonsense, 1 splice acceptor site, and 3 missense), cardiac troponin I (2 mi

79 allele (SNP rs12252-C) that alters a splice acceptor site, and functional assays show the minor CC g

80 These structures reveal the location of the acceptor site, and the molecular determinants of substra

81 uired mutations at or adjacent to the splice acceptor site, and three others had acquired dual mutati

82 that identified hydrophobic regions, H-bond acceptor sites, and an ionizable (cationic) feature as k

83 and GUK domains contained the main ubiquitin acceptor sites, and deletion of a Hook domain (an import

84 solvent competition for hydrogen bond donor/acceptor sites, and simplicity of structure.

85 ne residues in Tat can function as ubiquitin acceptor sites, and variable combinations of these lysin

86 cal trans-acting factors and Gap1p ubiquitin acceptor sites are involved in both processes, we define

87 with protein O-fucosyltransferase 2 (POFUT2) acceptor sites are modified by a dHexHex disaccharide, w

88 ibit increased reactivity when the donor and acceptor sites are perfectly aligned.

89 l domain of the IL-22R serves as a ubiquitin acceptor site as disruption of this site by deletion or

90 he rate of heat exchange among the donor and acceptor sites as functions of the temperature differenc

91 mplementarity between the RNA primer and the acceptor site at DR2 in HBV.

92 ssive points within intron 1 well before the acceptor site at exon 2 is made.

93 a 52 bp exon with a non-canonical 3' splice acceptor site at its 5' end and an internal 3' splice ac

94 onor site at nucleotide (nt) 226, the splice acceptor site at nt 409, or a TATAA box at nt 7890.

95 or region near the 5' end of the pgRNA to an acceptor site at or near the P AUG, and the shunt accept

96 tide repeat (TPR) domains that bind a common acceptor site at the carboxyl terminus of Hsp90.

97 G1 and is located between alternative splice acceptor sites at the 5' end of exon 2; its inclusion or

98 There are no splicing acceptor sites at the PTP-oc transcription site.

99 sequences, named omega and located 3' of the acceptor site, base pairs with phi to contribute to the

100 ggested to function as a potential ubiquitin acceptor site based on the fact that previous studies ha

101 the hydrophobicity of the EF helix beta6 Val acceptor sites (beta73 Leu).

102 By changing the donor sequence, acceptor sites between genomic nt 33 and 97 (identical b

103 nism by which the lectin domain enables free acceptor sites binding of glycopeptides into the catalyt

104 albeit not due to c.594-2A > C impairing the acceptor site but rather by c.641A > G modifying exon 10

105 all localization scores for ADP-ribosylation acceptor sites but also boosts ADP-ribosylated peptide i

106 fied the possible lysine donor and glutamine acceptor sites but have failed to define the respective

107 hment of ESEs is associated with weak splice acceptor sites but not weak donor sites.

108 the hydrophobicity of the EF helix beta6 Val acceptor sites by the beta73 Asp to Leu or Asn changes d

109 amino acid residues surrounding the phospho-acceptor site can effect the specific activity of the ki

110 study, providing evidence that U12-dependent acceptor sites can also be recognized by the U2-type spl

111 dependent glycosylation of cysteine-proximal acceptor sites can be reduced by eliminating cysteine re

112 h to last cysteine, the putative S-acylation acceptor site, causes a dramatic change in AGG2 but not

113 allele enhances the use of a cryptic splice acceptor site, causing the introduction of a premature t

114 site at its 5' end and an internal 3' splice acceptor site consensus 45 bp downstream.

115 arginine residues N-terminal to the phospho-acceptor site, creating a better DAPK-1 peptide consensu

116 ted in alkyl transfer including the cysteine acceptor site (Cys145), the O6-alkylguanine binding pock

117 activity and mutation of the phosphorylation-acceptor sites deregulates p53 Ser46 phosphorylation and

118 ely 3' to the predicted FMO6 intron 8 splice acceptor site, diminishing the efficiency of this site.

119 silicate chains which serve as hydrogen-bond acceptor sites, directionally orienting the hydrogen ato

120 polyUb of A3F and A3G can occur at multiple acceptor sites dispersed along predicted lysine-enriched

121 ansfer of the primer generated at DR1 to the acceptor site (DR2) near the opposite end of the minus-s

122 to arginine mutations of the identified SUMO acceptor sites drastically inhibited LEDGF SUMOylation,

123 ition to observe differential effects at the acceptor site due to the nature of the nucleotide at the

124 n the splice donor site (E6SD) or the splice acceptor site (E6SA), a deletion of the intron (E6ID), o

125 enting Drp1 SUMOylation by mutating the SUMO acceptor sites enhances binding to Mff.

126 Fet3-Ftr1 lacking cytosolic lysyl ubiquitin acceptor sites, Fet3-Ftr1 is constitutively sorted into

127 cine (G) at position 2, which is a potential acceptor site for a myristoyl moiety.

128 ous mutation (G>T) in intron 3 at the splice acceptor site for exon 4, leading to a frameshift with p

129 ng epithelial cells through lysine 183 as an acceptor site for K48 polyubiquitination.

130 where the inhibitor moenomycin binds) and an acceptor site for lipid II substrate.

131 he catalytic site for O2 reduction or to the acceptor site for pumped protons.

132 55 in PIPKIgamma acts as the major ubiquitin acceptor site for Smurf1.

133 of the NY-ESO-1 cancer/testis antigen as the acceptor site for the formation of canonical Lys-48-link

134 Furthermore, the connector domain as an acceptor site for the P protein represents a new underst

135 translocation, and subsequently acts as the acceptor site for the second template switch, termed cir

136 of the protein also served as a major amine acceptor site for transglutaminase and mediated self-ass

137 These results show that crossover acceptor sites for discontinuous transcription (i) need

138 ing requirements distinct from the donor and acceptor sites for human hepatitis B virus (HBV) was lac

139 The NDV-BC F protein contains six potential acceptor sites for N-linked glycosylation at residues 85

140 tide sequences around the splicing donor and acceptor sites for PB2-S1 were highly conserved among pr

141 al carbons, C-3 and C-22/C-20, as the atomic acceptor sites for the methyl additions to squalene and

142 Mutagenesis of potential acceptor sites for ubiquitination in the cytosolic domai

143 utility of this HAC, which has a unique gene acceptor site, for delivery of full-length genes and cor

144 icing that are subsequent to terminal splice acceptor site function, but before catalysis, have littl

145 ad been previously structurally defined, the acceptor site had not.

146 Most alternative splice donor and acceptor sites had a relatively high information content

147 in BCR variable regions, of N-glycosylation acceptor sites harboring unusual high-mannose oligosacch

148 es and pyridine ligands equipped with H-bond acceptor sites have allowed systematic quantification of

149 These isoforms differ in their splice acceptor sites; human MPI is translated into a polygluta

150 ence of an additional hydrogen bond donor or acceptor site (i.e., the presence of a heteroatom-hydrog

151 ddition to SUMO conjugation activity, a SUMO acceptor site in COP1 and the SUMO E3 ligase SAP and Miz

152 1A) splices exclusively to a weaker internal acceptor site in exon 2, skipping a fragment designated

153 rnative use of 5' splice sites with the same acceptor site in intron 3.

154 is associated with a mutation at the splice acceptor site in intron 4.

155 tructural similarity to IscU, and the sulfur-acceptor site in SufE coincides with the location of the

156 n phosphorylate TRF2 in vitro at a consensus acceptor site in the amino-terminal basic domain of TRF2

157 POMGnT1 is dependent on the location of the acceptor site in the context of the underlying polypepti

158 -II, which has a single, conserved ubiquitin acceptor site in the cytosolic domain, we found that mul

159 We demonstrate that the major ISG15 acceptor site in the NS1A protein in infected cells is a

160 plore the role of Thr(95), another phosphate acceptor site in the PDZ I domain, on hormone-mediated r

161 lavin hydride donor site and quinone hydride acceptor site in the QPAs, an observation that is in agr

162 e promoter system linked to intron donor and acceptor sites in a new binary vector configuration.

163 te that internal lysines are the dominant Ub acceptor sites in both A3F and A3G.

164 to involve a docking of the metal donor and acceptor sites in close proximity to one another.

165 acks MagT1, allows efficient modification of acceptor sites in cysteine-rich protein domains before d

166 ompletely abolished when all three phosphate acceptor sites in domain I or both sites in domain II we

167 The use of cryptic acceptor sites in exon 5 occurred in transcripts in whic

168 Our data therefore reveal ubiquitin acceptor sites in FLNa and establish that ASB2alpha-medi

169 nisms revealed a lower density of C-terminal acceptor sites in glycoproteins because of reduced posit

170 In addition, like HDAC1, the phospho-acceptor sites in HDAC2 are located in the C-terminal po

171 nd/or the use of alternative splice donor or acceptor sites in introns 3, 4, 6, and 8, resulting in n

172 the presence of nonequivalent hydrogen bond acceptor sites in molecular structures are addressed by

173 tive of the presence or absence of ubiquitin acceptor sites in PFV Gag.

174 cm sumoylation because mutations in the SUMO acceptor sites in Scm enhance its recruitment to the PRE

175 Mutation of these SUMO acceptor sites in Sharp-1 does not impact its subcellula

176 lylation and serve as better recognition and acceptor sites in the polysialylation process than those

177 ferential p65 phosphorylation on four serine acceptor sites in the Rel homology domain for the expres

178 re to compare glycosylation of roughly 1,000 acceptor sites in wild type and mutant cells.

179 ferases, each containing a donor site and an acceptor site, in one polypeptide.

180 equired for glycosylation of STT3B-dependent acceptor sites including those that are closely brackete

181 losed several new classes of STT3A-dependent acceptor sites including those with suboptimal flanking

182 tion of multiple carboxyl-terminal phosphate acceptor sites, including threonine 370, serine 375, and

183 changes to consensus UL37x1 donor and UL37x2 acceptor sites increased the efficiency of UL37x1-UL37x2

184 r(47) within histone H4 serves as a putative acceptor site, indicative of Lpcat1-mediated O-palmitoyl

185 el pathway by which glycosylation of cryptic acceptor sites influences the function and fate of an ER

186 We demonstrate that a terminal splice acceptor site is essential to establish coupling with th

187 UHRF1, but not by UHRF1 in which the phospho-acceptor site is mutated, demonstrating that UHRF1 phosp

188 phosphate and the local architecture of the acceptor site is perturbed.

189 The phospho-acceptor site is very highly conserved across multiple p

190 as shown to be L-selective at both donor and acceptor sites ((L)C(L)) by site-directed mutagenesis st

191 n of a novel intra-exonic pre-mRNA 3' splice acceptor site leading to in-frame loss of 27 nucleotides

192 Acceptor sites located in short loops of multi-spanning

193 a frameshift, and one had a canonical splice acceptor site loss.

194 face region of ubiquitin in proximity to the acceptor site Lys-48.

195 beta-TrCP ubiquitinates LPCAT1 at an acceptor site (Lys(221)), as substitution of Lys(221) wi

196 damage, the Rad6-Rad18 complex, the putative acceptor site (lysine 197), and loading of the complex o

197 raint, the sequence context of the potential acceptor site may have an important role in 3' splice si

198 n insertion, while CHG methylation at splice acceptor sites may inhibit RNA splicing.

199 We also found that the SUMO acceptor site mutant PIF3(K13R) binds more strongly to t

200 e-exome capture revealed a homozygous splice acceptor site mutation (c.698G>T) in the renal Mg(2+) tr

201 tem and we have characterized a novel splice-acceptor site mutation in patched2 that results in enhan

202 describe a new mouse model carrying a splice acceptor site mutation in Rpgrip1, herein referred to as

203 sulfides can interfere with glycosylation of acceptor sites (NXT/S) in nascent polypeptides.

204 nor site within the first exon to the splice acceptor site of exon 2.

205 contribute to splicing, was low only for the acceptor site of exon II, which is preceded by a region

206 -3Galbeta-O-naphthalenemethanol binds to the acceptor site of human beta1-4-galactosyltransferase muc

207 The mutation appeared at the splice-acceptor site of intron 12, resulted in the skipping of

208 on of the A in the AG dinucleotide of the 3' acceptor site of intron 9.

209 OP-Puro enters the acceptor site of ribosomes and incorporates into nascent

210 of cured cells and that the major phosphate acceptor site of subtype 1b NS5A is not essential for HC

211 with modified sequences containing the SUMO-acceptor site of target proteins.

212 nic mutation, g.31701T>A, in the last splice acceptor site of the adenosine deaminase (ADA) gene.

213 ocated 80 nucleotides upstream of the splice acceptor site of the downstream exon E10) is composed of

214 ariant (c.3383-1G>A) in the canonical splice acceptor site of the final exon.

215 identifies a catalytic histidine and how the acceptor site of UGT76G1 achieves regioselectivity for b

216 f surface water and the excess hydrogen-bond acceptor sites of 1-butanol.

217 ition, mutation of all the known sumoylation acceptor sites of AR does not affect the transrepression

218 Mutation of the phospho-acceptor sites of both HPV-16 and BPV-1 L2 resulted in t

219 tensive consensus sequences at the donor and acceptor sites of longer introns.

220 lybasic motif proximal to the palmitoylation acceptor sites of R7BP mediates nuclear localization, pa

221 that can discriminate between the donor and acceptor sites of the PGTs.

222 assess the contribution of splice donor and acceptor sites of transposon sequences, we inserted a Ds

223 en, we identified a highly conserved phospho-acceptor site on the HPV-16 and bovine papillomavirus 1

224 PNP indicate that nearly every H-bond donor/acceptor site on the inhibitor is fully engaged in favor

225 s of YdiB, in close proximity to the hydride acceptor site on the nicotinamide ring.

226 ratricopeptide repeat (TPR) domains to a TPR acceptor site on the ubiquitous and essential protein ch

227 find that the I kappa B kinase (IKK) phospho-acceptor sites on I kappa B alpha, core components of th

228 neered neutralizing mutations of PKA phospho-acceptor sites on MEF2D (S121/190A).

229 identification of well defined hydrogen bond acceptor sites on the anions by a combination of experim

230 The electron acceptor sites on the montmorillonite are postulated to

231 ey affect splicing by creating cryptic donor-acceptor sites or by disturbing exonic splicing enhancer

232 oding variation, variants in splice donor or acceptor sites, or copy number variation events were obs

233 Removal of the N-terminal myristate acceptor site partially reduced McCPK1 plasma membrane (

234 reased utilization of an alternate 3' splice acceptor site, perturbing normal alpha-spectrin mRNA spl

235 amino acid long insertion caused by a splice acceptor site polymorphism.

236 Here, we investigated the acceptor-site preferences for 23 homologs with natural s

237 owed unique, as yet unknown, rules governing acceptor-site preferences.

238 ce donor site in conjunction with the splice acceptor site present between intron 8 and exon 9 result

239 inoacyl donor site) adjacent to an aminoacyl acceptor site provided by a covalently tethered amino ac

240 uinones in the primary and secondary quinone acceptor sites, Q(A) and Q(B), which exhibit very differ

241 ce between the branch site adenosine and the acceptor site ranges from 10 to 39 nt, significantly lon

242 The mutation creates a new splice acceptor site resulting in aberrant OPA1 transcripts wit

243 terminal exon by selection of an alternative acceptor site, resulting in an isoform, FE65a2, with an

244 B and 1C always splice to the stronger first acceptor site, retaining exon 2'.

245 eless, accurate assignment of the ADP-ribose acceptor site(s) within the modified proteins identified

246 We identified 5' splice-acceptor sites (SAS) and polyadenylation sites (PAS) for

247 However, a better understanding of acceptor site selection could help to predict ubiquitina

248 ecular interactions between H-bond donor and acceptor sites separated by a variable linker.

249 the information content of splice donor and acceptor site sequences, and discuss possible explanatio

250 y in which the sequence flanking the phospho-acceptor site (Ser.Pro.X.Arg/Lys) is recognized by CDK2,

251 two newly discovered serine phosphorylation acceptor sites, Ser106 and Ser110, effectively abolished

252 terized protein kinase (PK)A/PKC/PKG phospho-acceptor site Ser1928.

253 of bacterial OSTs follow their own rules for acceptor-site specificity, thereby expanding the glycoen

254 , unbiased proteomic approach to identify Ub acceptor sites targeted by Vif.

255 for retrovirus viability, such as a splicing acceptor site, TATA box and polyA addition signal sequen

256 ment for repeated sequences at the donor and acceptor sites, template switching requires at least thr

257 se promotes the isomerization by means of an acceptor site that binds glucose after its cleavage from

258 g and increased use of an alternative splice acceptor site that causes a partial intron retention eve

259 t is consistent with blocking the tryptophan acceptor site that is thought to be necessary for Dsg-me

260 as well-structured activation loop phosphate acceptor sites that are positioned next to the catalytic

261 ition, less is known about the downstream Ub acceptor sites that are targeted.

262 enhancers between polypyrimidine tracts and acceptor sites that bind nSR100 to potently activate exo

263 e antisense orientation, they provide splice acceptor sites that can result in incorporation of novel

264 t of the relationships between the donor and acceptor sites that could facilitate use of a cryptic do

265 transfer many diverse glycan structures, the acceptor sites that it recognizes are restricted predomi

266 Carboxylic acid dimers have exposed H-bond acceptor sites that solvate H-bond donor solutes with a

267 The alcohol aggregates have exposed H-bond acceptor sites that solvate H-bond donor solutes with si

268 sites (donor sites) and six 3' splice sites (acceptor sites) that are highly conserved in other papil

269 mers of mutants in the previously identified acceptor site, the donor site, or the catalytic site wer

270 moethane by reacting with it at its cysteine acceptor site to form a highly reactive half-mustard, wh

271 of a flexible helix that bridges the phospho-acceptor site to the rigid PNT domain.

272 nly essential near the chromophore donor and acceptor sites to ensure large NLO responses.

273 ' half of epsilon to juxtapose the donor and acceptor sites to facilitate the first-strand template s

274 llow sequential scanning of polypeptides for acceptor sites to insure the maximal efficiency of N-gly

275 ithin silicone oil and provide hydrogen bond acceptor sites to interact with acid functional drug mol

276 inhibitor scaffold can act as hydrogen bond acceptor sites to the serine hydroxyl.

277 enthusiasm for the amenability of APOBEC3 Ub acceptor sites to therapeutic intervention.

278 tyrosine phosphorylation on specific phospho-acceptor site (Tyr-438) within the plekstrin homology do

279 enesis was examined by eliminating potential acceptor sites using a reverse genetics system for the m

280 quent integration of BAC constructs into the acceptor sites, utilizing the loxP and lox511 sites pres

281 lecules that present hydrogen-bond donor and acceptor sites via a carboxamide group, and a DNA base,

282 A small ubiquitin-like modifier (SUMO) acceptor site was recently described in human RXRalpha,

283 relay inserted between the proton donor and acceptor sites was studied electrochemically.

284 s that could function as potential ubiquitin acceptor sites, we found that only three (Lys501, Lys525

285 mutants in which residues near the cysteine acceptor site were replaced by corresponding residues fr

286 env transcripts and various splice donor and acceptor sites were detected in breast cancers.

287 esent in the same subunit that contained the acceptor site, whereas the donor site had to be provided

288 The splice acceptor site which generates env mRNA has been mapped e

289 er, the amide aggregates have exposed H-bond acceptor sites, which solvate H-bond donor solutes with

290 ine, which indicates that OU749 occupies the acceptor site while binding to the gamma-glutamyl substr

291 The canyon is divided into donor and acceptor sites with the catalytic residues at their junc

292 n ISCU that likely strengthens a weak splice acceptor site, with consequent exon retention.

293 licing variant STAT3beta uses an alternative acceptor site within exon 23 that leads to a truncated i

294 ary USF2 transcript using a cryptic splicing acceptor site within exon 6.

295 s to the side chain contains a hydrogen bond acceptor site within the plane of the ring.

296 ne 151 residue was identified as a ubiquitin acceptor site within TTF1 in both cell types.

297 een different types and numbers of donor and acceptor sites within a given IL.

298 entation methods when determining ADP-ribose acceptor sites within complex cellular samples.

299 and an even smaller amount in which cryptic acceptor sites within exon 5 were used.

300 describe two previously non-reported phospho-acceptor sites within the p65 RHD.