ライフサイエンスコーパス: carboxyl

1 tures of human TDG bound to DNA with cadC (5-carboxyl-2'-deoxycytidine) flipped into its active site.

2 -hydroxymethyl (5hmC), 5-formyl (5fC), and 5-carboxyl (5caC) derivatives; thus, DNA elements with mul

3 -hydroxymethyl (5hmC), 5-formyl (5fC), and 5-carboxyl (5caC) forms.

4 5-hydroxymethyl (5hmC), 5-formyl (5fC), or 5-carboxyl (5caC) forms.

5 The inhibitory domain has been mapped to the carboxyl acidic domain of TSPX, truncation of which rend

6 ation molecular functional groups, including carboxyl, amine, isopropyl, phenethyl, and tert-butylphe

7 neous modification of carbon electrodes with carboxyl-amine functionalities offers protection against

8 NDs were functionalized with mixture of carboxyl and amine groups NDandante or amine NDamine, ca

9 It reveals the carboxyl and amine groups would heal charged defects via

10 s, functionalized with multiple paired alpha-carboxyl and amino groups that bind to the large neutral

11 l-2-oxazoline as precursor to produce amine, carboxyl and oxazoline functional group rich surfaces.

12 r binding properties may, in addition to the carboxyl and phenolic groups, be influenced by the molec

13 ination of the chemically orthogonal groups, carboxyl and triisopropylsilylethynyl.

14 five groups (i.e., amine, phenol, hydroxyl, carboxyl, and carbonyl) are found to be the dominant cla

15 Moreover, data on carboxyl- and amino-terminal interactions were not provi

16 Especially, the sequestration of OM (rich in carboxyl, aromatic, and/or carbonyl C) by Fe-rich minera

17 deposition had not altered the abundance of carboxyl, aryl, alkyl, or O/N-alkyl C in forest floor, b

18 deposition had not altered the abundance of carboxyl, aryl, alkyl, or O/N-alkyl C in forest floor, b

19 where hydroxyls (H), amines and phenols (A), carboxyls (C), and carbonyls or ketones/aldehydes (K) ar

20 ith increasing DOM aromatic-, carbonyl-, and carboxyl-C content.

21 The carboxyl, carbonyl, acetyl groups were determined in mod

22 constants (T(1) ) for the labeled acetyl and carboxyl carbonyls were approximately 30 seconds, suppor

23 se (BC), carboxyltransferase (CT) and biotin carboxyl carrier protein (BCCP) components.

24 tachment domain-containing (BADC) and biotin carboxyl carrier protein (BCCP) subunits from Arabidopsi

25 ltransferase (CT)-alpha, CT-beta, and biotin carboxyl carrier protein (BCCP1 or BCCP2).

26 id metabolite 17-hydroxy-3-oxo-4-pregnene-20-carboxyl-CoA (17-HOPC-CoA).

27 lved in the metabolism of cyclohex-1,5-diene carboxyl-CoA to acetyl-CoA were in high abundance in S.

28 The synthesis of alpha-amino carbonyl/carboxyl compounds is a contemporary challenge in organi

29 nd slower rates were observed with increased carboxyl concentration and oxygen, heteroaliphatic, and

30 een eight characteristics (molecular weight, carboxyl concentration, and carbon, oxygen, nitrogen, al

31 of MWs (25 000-50 000 vs <200 Da) as well as carboxyl content (polygalacturonic acid (PGA) > citric a

32 A five amino acid stretch located at the carboxyl cytosolic region is essential for fibre formati

33 inuclear zirconium vertices and two flexible carboxyl-decorated tetraphenylethylene (TPE) spacers.

34 study revealed that graphitic sulfoxide and carboxyl dopants of graphene were the efficient binding

35 Compared to carboxyl dopants, the sulfoxide dopants further improved

36 s directed at a FLAG epitope included at the carboxyl end of the scFv.

37 Collectively, carboxyl-enriched 300 degrees C biochar likely formed st

38 ble number of tandem repeat (VNTR) domain of carboxyl ester lipase (CEL) presents an opportunity to s

39 nes favoring the production of R-9-PAHSA and carboxyl ester lipase (CEL), a PAHSA degradative enzyme,

40 tic lipase-related protein 2 (PNLIPRP2), and carboxyl ester lipase (CEL), which may leak into the vis

41 n of the structure of AF-Est2 with the human carboxyl esterase 1, which has CoA thioesterase activity

42 rivative (DEAdcCE) for the protection of the carboxyl function at the side chain of the aspartic acid

43 tions of a basic residue near the propionate carboxyl function of protoporphyrin IX.

44 rated that Fe(II) was complexed primarily by carboxyl functional groups in reduced NOM.

45 latform, permitting 5-12 periodically spaced carboxyl functional groups on the polymer backbone.

46 nzoylglycine (H3L), which bears catechol and carboxyl functionalities in tandem, on to the surface of

47 on; thus, we propose that these nitrogen and carboxyl functionalities of aromatic compounds may also

48 tic approach, it is herein demonstrated that carboxyl functionalization of poly(lactic-co-glycolic ac

49 Carboxyl-functionalization of graphene carbon can modula

50 s with a core-shell structure and subsequent carboxyl functionalizations (CSD-PLNPs) were rationally

51 chemical sensor using polyaniline (PANi) and carboxyl functionalized multi-walled carbon nanotubes (f

52 Does EDC-NHS activation of carboxyl functionalized nanoparticles surface really lea

53 work demonstrates the excellent potential of carboxyl-functionalized graphene oxide (GO-COOH) composi

54 Recently, carboxyl-functionalized synthetic polymers have been sho

55 ives of amino acids with free or derivatized carboxyl functions.

56 Four of them contained a gamma-carboxyl glutamic acid (Gla) domain, a calcium-binding m

57 ethylaminophenyl (4), 4-nitrophenyl (5), and carboxyl group (6) as substituents at the exocyclic doub

58 ric replacement of the tetrazole ring with a carboxyl group (60, IC(50) = 68 nM) gave a promising new

59 celerated in parallel to the extent that the carboxyl group acquires a second proton (1H(+)).

60 ree arginines that accommodates the terminal carboxyl group and a dedicated cavity that facilitates b

61 involves 2-phenylisopropyl protection of the carboxyl group and does not require excesses of commerci

62 Finally, the carboxyl group at C10 is methylated by TcCCMT, a member

63 ly attached biotin as a vector to transfer a carboxyl group between donor and acceptor molecules duri

64 an electrophile in the P site other than the carboxyl group during elongation.

65 imethylamino)propyl)carbodiimide activates a carboxyl group followed by nucleophilic attack by benzhy

66 protein-binding sites, we implemented a new carboxyl group footprinter, benzhydrazide, and refined i

67 dation of proteins (FPOP), and site-specific carboxyl group footprinting to investigate the HOS of pr

68 ast photochemical oxidation of proteins, and carboxyl group footprinting with glycine ethyl ester, we

69 ecarboxylase that catalyzes the removal of a carboxyl group from a d-stereocenter.

70 tem, such as the biphenyl system, and a free carboxyl group leads to highly potent and selective GIVA

71 residue is enzymatically linked to the gamma-carboxyl group of a glutamate in the primary sequence of

72 on requires a direct interaction between the carboxyl group of allosteric effectors and Arg-120 of Ea

73 amino group of free glutamate and the gamma-carboxyl group of an active-site glutamate in SidE.

74 Carboxyl group of syn-isomers may also participate in th

75 The carboxyl group of the substrate was bound by Arg(265) an

76 Dtx3L/Parp9 ADP-ribosylates the carboxyl group of Ub Gly76.

77 sol side-chain cleavage by reducing the C-20 carboxyl group on cortisol, yielding 20beta-dihydrocorti

78 d symmetric, and asymmetric vibration of the carboxyl group present in the ciprofloxacin.

79 antiradical moieties (catechol, guaiacyl and carboxyl group) and molecular conformation in antioxidat

80 profloxacin had peaks related to the ionised carboxyl group, i.e., at 1576 and 1392 cm(-1), which wer

81 ce of a receptor to bind the C-terminal free carboxyl group, the C-terminal amidated group, or the N-

82 nors), followed by surface modification with carboxyl-group-rich polymers.

83 iwalled carbon nanotubes functionalized with carboxyl groups (MWCNTf) was developed to modify glassy

84 nalized polystyrene nanospheres with surface carboxyl groups (PPs and QPs, respectively) were fabrica

85 -1) corresponded to methyl esterified uronic carboxyl groups and confirmed the higher equivalent weig

86 bination of readily functionalized amine and carboxyl groups attached to a chiral central core along

87 ectroscopy (TRLFS) identified phosphoryl and carboxyl groups from bacterial envelopes, among other re

88 The contents of the carbonyl and carboxyl groups in a starch molecule therefore indicate

89 solubilize amino acid derivatives with free carboxyl groups in CDCl(3) and to mediate their interact

90 demonstrate location-dependent ionization of carboxyl groups in NF polyamide films.

91 fers functionalized products with acetyl and carboxyl groups in one step, in good yields, and with sh

92 ves as a "stinger" and penetrates a triad of carboxyl groups in the S3-S4 linker of the voltage senso

93 Specifically, only surface carboxyl groups ionize under neutral pH, whereas interio

94 The presence of three equally reactive carboxyl groups leads to FTR modifications through react

95 enefited from the reactive functional groups-carboxyl groups of Alb NPs, p19 protein, a viral protein

96 mutants revealed that catalysis requires the carboxyl groups of Glu362 and Asp426, and not of Asp383,

97 groups of N-terminal residues but also gamma-carboxyl groups of internal (non-N-terminal) Asp and Glu

98 cium-driven electrostatic interactions among carboxyl groups of the AGPs and the pectic acids give ri

99 Electrochemically formed carboxyl groups on the surface of the graphite were cros

100 In contrast, ligands containing carboxyl groups only, such as succinate and propionate,

101 of Asp383, confirming the enzyme employs two carboxyl groups to degrade lippopolysaccharide using an

102 These carboxyl groups were utilized to achieve variable degree

103 Cloaking its carboxyl groups with a hydrophobic moiety is shown to en

104 d range of substrates (e.g. metabolites with carboxyl groups) for various applications, including bio

105 on nanotubes (CNTs; with and without surface carboxyl groups) into polyacrylonitrile (PAN) and polyst

106 lectronic effects from the 2-thio- and the 6-carboxyl groups, a lability that could, in turn, be usef

107 yl-aliphatic ketones, aliphatic and aromatic carboxyl groups, phenol, and methoxy phenyl ethers.

108 h amide bonds at both their alpha- and gamma-carboxyl groups.

109 e first oxidized to carbonyl groups, then to carboxyl groups.

110 mework (COF), COF-616, bearing pre-installed carboxyl groups.

111 the like-charge ion pair and the C-terminal carboxyl groups.

112 and proton transfer involving the phenol and carboxyl groups.

113 identate-mononuclear U(IV/VI) complexes with carboxyl groups.

114 lic component, this latter incorporating two carboxyl groups.

115 egradation activities, while deletion of the carboxyl GT-1 domain that is unique to the plant RNAse J

116 imilar carbon chain structure while SA has a carboxyl head group and GMS has two free hydroxyl groups

117 ower activation energies in the formation of carboxyl intermediate, in line with their higher activit

118 e mechanism with the formation of formate or carboxyl intermediates.

119 y of nanoconfined water drives the anomalous carboxyl ionization behavior.

120 Furthermore, we report that interior carboxyl ionization could improve the water-salt permsel

121 ps ionize under neutral pH, whereas interior carboxyl ionization requires pH >9.

122 ster carbonyl hydration, suggesting that the carboxyl is linked to more extended H-bond clusters than

123 ylate coupled to general acid catalysis by a carboxyl is not operative.

124 amates are then sequentially added via alpha-carboxyl-linkages to the growing glutamate side chain.

125 tamates, CCP5 uniquely metabolizes the gamma-carboxyl linked, branch point glutamate.

126 CCP5, we confirmed that it metabolized gamma-carboxyl-linked glutamate of synthetic substrates and tu

127 ereas most CCPs catalyze hydrolysis of alpha-carboxyl-linked glutamates, CCP5 uniquely metabolizes th

128 nmethylated phosphatases to show that PP6 is carboxyl-methylated and that LCMT-1 is the major methylt

129 ions, including lipidation, proteolysis, and carboxyl methylation.

130 Isoprenylcysteine carboxyl methyltransferase (ICMT) methylesterifies C-ter

131 Isoprenyl cysteine carboxyl methyltransferase (ICMT) plays a key role in po

132 he results of in vitro characterization of a carboxyl methyltransferase encoded in the cluster, Her8,

133 terminal half of Opi3 and isoprenyl cysteine carboxyl methyltransferases with a solved crystal struct

134 0, which makes a direct interaction with the carboxyl modification and the phosphate backbone of the

135 However, to accommodate the carboxyl modification, the phosphate backbone on the tem

136 th environmentally-sensitive probes Laurdan, carboxyl-modified Laurdan (C-Laurdan), Di-4-ANEPPDHQ, an

137 (Ab1) was immobilized on the surface of the carboxyl-modified MNPs.

138 Concurrent losses of carboxyl moieties and shifts in chemical composition dur

139 on radical efficiently substitutes the three carboxyl moieties of Finland trityl with a high rate con

140 racterization, demonstrating the presence of carboxyl moieties.

141 the hydrophobic (phenyl) and electrostatic (carboxyl) moieties using fluorescence microscopy.

142 ditions where a ureido group is added to the carboxyl moiety to form a cyclic amide, regenerating SP

143 valuated the potential for poly(lactic acid)/carboxyl-multiwalled carbon nanotube (PLA/ f-MWCNT) comp

144 and amine groups NDandante or amine NDamine, carboxyl NDvox or hydroxyl groups NDH and drop-casted or

145 well as preferentially interacting with the carboxyl of BA.

146 onjugation of L-glutamate primarily to the 8-carboxyl of isochorismate and yields the key SA biosynth

147 O-methyltransferase that methylates the free carboxyl of malonyl-ACP.

148 ic functionalization of these materials with carboxyl or amino functional groups.

149 action because only compounds that contain a carboxyl or hydroxyl group and have moderate steric hind

150 ectra revealed Sb in untreated peat bound to carboxyl or phenol groups with average Sb-carbon distanc

151 well as the elongation of either the Mo-O5 (carboxyl) or Mo-O7 (hydroxyl) distance that switches the

152 e different atoms of hGGT1 interact with the carboxyl oxygen of the cysteine of GSH.

153 to the anti-fouling effect conferred by the carboxyl-PEG layer, we could directly detect as little a

154 nsformations were less inhibited than in the carboxyl poor Fh-GA, and a crystalline lepidocrocite "sh

155 common functional groups (phenolic hydroxyl/carboxyl/primary amine).

156 poly(ethylene glycol)-block-poly(2-methyl-2-carboxyl-propylene carbonate-graft-dodecanol) (mPEG-b-PC

157 poly(ethylene glycol)-block-poly(2-methyl-2-carboxyl-propylene carbonate-graft-dodecanol; PEG-PCD) t

158 oly (ethylene glycol)-block-poly (2-methyl-2-carboxyl-propylene carbonate-graft-SMART-graft-dodecanol

159 phenyl carbon and C-C cleavage in which the carboxyl proton is also transferred to water.

160 decarboxylation of 1: transfer of the second carboxyl proton to the adjacent phenyl carbon and C-C cl

161 ecies that can be avoided by transfer of the carboxyl proton to water in the same step.

162 Conformers of carboxyl radical (HOCO) have been studied by IR spectros

163 lution, and spectroscopic observation of the carboxyl radical confirm its formation as a reaction int

164 nd trans conformers are found for deuterated carboxyl radical DOCO.

165 the lifetime (520 +/- 120 ns) of a reactive carboxyl radical in solution, and spectroscopic observat

166 insights on how truncation of the amino and carboxyl regions of alphasyn may modulate the propensity

167 ndependent dye efflux by removing one of the carboxyl residues in Cluster 1.

168 the amide group is flanked by two catalytic carboxyls, reveals key mechanistic information: (a) Gene

169 tionated permafrost thaw DOM directly showed carboxyl-rich alicyclic molecules, while the same compon

170 For carboxyl-rich coprecipitates (Fh-PGA and Fh-CA), mineral

171 thetic polymers have been shown to mimic the carboxyl-rich surface motifs of non-collagenous proteins

172 ree-energy simulations, we observed that the carboxyl side chain of Glu89 (located along the arch mot

173 4d with a carboxyl sidechain demonstrated the highest incorporatio

174 rimethyloctadecylammonium bromide, CTAB) and carboxyl (stearic acid, SA) functional groups.

175 uction of a second IQ domain to the Ca(V)1.3 carboxyl tail switched the apparent functional stoichiom

176 gle CaM preassociated with the alpha-subunit carboxyl tail.

177 structure of the beta2AR in complex with the carboxyl terminal 14 amino acids from Galphas along with

178 tically, ARID1A interacted with EZH2 via its carboxyl terminal and antagonized EZH2-mediated IFN resp

179 ssociates with CPL2, a plant-specific Pol II carboxyl terminal domain (CTD) phosphatase, to form the

180 The RNA polymerase II carboxyl terminal domain (RNAPII CTD) kinase complex (CT

181 se 9 (CDK9)-that phosphorylates NELF and the carboxyl terminal domain of Pol II-and enrichment of the

182 ansmembrane domain M3, and the intracellular carboxyl terminal domain.

183 slational termination impairment and protein carboxyl terminal extension), which mechanistically link

184 d APPswe mutant variant upregulates APP, APP carboxyl terminal fragments, and Abeta levels.

185 ive EF-hand-like Ca(2+) binding motif in the carboxyl terminal region of BTV nonstructural phosphopro

186 5-associated seven transmembrane full-length carboxyl terminal variants, MOR-1B1, MOR-1B2, MOR-1B3, M

187 ys indicate that BKIP-1 interacts with SLO-2 carboxyl terminal.

188 aking place at the amino-terminal (FERM) and carboxyl-terminal (FAT) domains and that both domains ar

189 Deletion of the carboxyl-terminal 66 amino acids of BGLF2 reduced the ab

190 modifies the nascent polypeptide by adding a carboxyl-terminal alanine and threonine (CAT) tail throu

191 nnels are characterized by the presence of a carboxyl-terminal cyclic nucleotide-binding domain (CNBD

192 pendent kinase 12 (CDK12) phosphorylates the carboxyl-terminal domain (CTD) of RNA polymerase II (pol

193 In endoplasmic reticulum (ER) membranes, the carboxyl-terminal domain (CTD) of SREBPs binds to the CT

194 The carboxyl-terminal domain (CTD) of the largest subunit of

195 oes not absolutely require the non-conserved carboxyl-terminal domain (CTD), which is necessary for r

196 ivator with glutamic acid/aspartic acid-rich carboxyl-terminal domain 2 (CITED2) as a critical intrin

197 ding and catalytic motifs, the isolated TlyA carboxyl-terminal domain exhibits no detectable affinity

198 LANA with point mutations in the carboxyl-terminal domain identified an MCM6 binding doma

199 ally occurring DLX3 mutant that disrupts the carboxyl-terminal domain leading to tricho-dento-osseous

200 These results suggest that the carboxyl-terminal domain of Cav2.1 is not essential for

201 The carboxyl-terminal domain of STN1 interacts with CTC1 at

202 We show that the carboxyl-terminal domain of TaiP exposes a mimic of an e

203 ylates p53, or with an acetylation mimicking carboxyl-terminal domain p53 mutant.

204 ts revealed that the Ssu72 RNA polymerase II carboxyl-terminal domain phosphatase, a critical determi

205 IV-1 STC and a higher-order form that adopts carboxyl-terminal domain rearrangements.

206 me interface includes the RNAP subunit alpha carboxyl-terminal domain, which is required for RNAP-rib

207 eractions bridge to the acidic intracellular carboxyl-terminal domain.

208 ARRDC3 on a conserved tyrosine (Y382) in the carboxyl-terminal domain.

209 served common docking (CD) domain within the carboxyl-terminal domains of ERK3 and ERK4 and the conse

210 ain, while MCM6 bound to both the amino- and carboxyl-terminal domains of LANA.

211 that the HD together with the DLX3 amino- or carboxyl-terminal domains was required for maximal inhib

212 imerization is stimulated by the lysine-rich carboxyl-terminal extension of UBE2S that is also requir

213 It also disclosed a carboxyl-terminal extension that forms a helix-helix int

214 with Astn2 TM2 leads to the appearance of a carboxyl-terminal fragment consistent with intramembrane

215 that STAT3 interacts with a calpain-cleaved carboxyl-terminal fragment of FLNA.

216 al analysis, and CRISPR editing identified a carboxyl-terminal fragment of thrombospondin-1 as an une

217 ino-terminal domains of NLRP1B, liberating a carboxyl-terminal fragment that is a potent caspase-1 ac

218 ulting metabolites, both alpha- and beta-APP carboxyl-terminal fragments and APP intracellular domain

219 pensable for the interaction with P, and the carboxyl-terminal half of P is sufficient for the intera

220 HBeAg from different patients exhibits minor carboxyl-terminal heterogeneity.

221 immunosensors for the detection of Ubiquitin carboxyl-terminal hydrolase (UCHL-1) biomarker of brain

222 oleucine, l-valine, l-aspartic and ubiquitin carboxyl-terminal hydrolase involved in protein degradat

223 e the serum levels of tau protein, ubiquitin carboxyl-terminal hydrolase L1 (UCH-L1), neurofilament l

224 Here, we show that ubiquitin carboxyl-terminal hydrolase-L5 (UCHL5 or UCH37) de-ubiqu

225 Ubiquitin carboxyl-terminal hydrolases (UCHs) belong to an enzymat

226 r (CL-II) in the juxtamembrane region of Smo carboxyl-terminal intracellular tail (C-tail).

227 Type B Ggamma subunits, lacking a carboxyl-terminal isoprenylation motif, are found only i

228 e Golgi is the pH-dependent recognition of a carboxyl-terminal Lys-Asp-Glu-Leu (KDEL) signal by the K

229 ifference between the isoforms with the same carboxyl-terminal microtubule-binding domain repeats, is

230 Recent research indicates a role of carboxyl-terminal modulator protein (CTMP) in Akt-signal

231 In conclusion, our findings identify carboxyl-terminal multisite phosphorylation as key step

232 The carboxyl-terminal peptide of AtABP1 induced an auxin-lik

233 raction with beta-arrestins is controlled by carboxyl-terminal phosphorylation.

234 trates via phosphopeptide recognition by its carboxyl-terminal polo-box domain (PBD) is poorly unders

235 study, the data demonstrate that within the carboxyl-terminal portion of mouse TG, T3 is formed de n

236 Previous studies suggest that the carboxyl-terminal portion of the pUL56 subunit interacts

237 luding an extended transmembrane helix 5 and carboxyl-terminal receptor tail that interacts with G pr

238 We used a peptide of the carboxyl-terminal region of AtABP1 as a tool.

239 mong known TRP structures, together with the carboxyl-terminal region, forms a large two-layered cyto

240 uncations of the highly charged and flexible carboxyl-terminal region.

241 omain and to the mitochondrial membrane by a carboxyl-terminal sequence (CTS).

242 e of S generates a polybasic Arg-Arg-Ala-Arg carboxyl-terminal sequence on S1, which conforms to a C-

243 r phosphorylation occurred primarily at four carboxyl-terminal serine (Ser) and threonine (Thr) resid

244 NSs bound to the carboxyl-terminal SPRY subdomain of TRIM21, enhancing p6

245 enhanced the interaction of PTPN22 with the carboxyl-terminal Src kinase (CSK), an interaction that

246 he amino-terminal region of the protein, and carboxyl-terminal tail identity both contribute to MLO a

247 ein interaction interface in the cytoplasmic carboxyl-terminal tail of Gpr161.

248 todomain, a transmembrane helix, and a short carboxyl-terminal tail, or as a soluble ectodomain that

249 through palmitoylation of the GLP-1R at its carboxyl-terminal tail.

250 promised by genetic perturbations within the carboxyl-terminal tail.

251 % (95% CI: 0% to 6%; p = 0.04) and increased carboxyl-terminal telopeptide of collagen type I by 4% (

252 sue inhibitor of matrix metalloproteinase 1, carboxyl-terminal telopeptide of collagen type I, and so

253 Recent research has demonstrated that the carboxyl-terminal transmembrane domain (TMD) of some Bcl

254 In addition to binding to the carboxyl-terminal tripeptide of HCN channels, TRIP8b als

255 dulation and is required for the activity of carboxyl-terminally encoded peptides (CEPs).

256 oth hydroxyl-terminated 'neutral' (D-OH) and carboxyl-terminated 'anionic' (D-COOH) Polyamidoamine (P

257 groups and the relative concentration of the carboxyl-terminated alkanethiols in a binary self-assemb

258 t across self-assembled monolayers (SAMs) of carboxyl-terminated monoterpenoids (O(2) C(C(9) HX)) and

259 We found that use of carboxyl-terminated poly(lactic-co-glycolic acid) (PLGA)

260 tion when the attachment surface was instead carboxyl-terminated.

261 nine dimer spokes radiate, placing the Sas-6 carboxyl termini at the outer edge of the approximately

262 a decreased interaction between the amino to carboxyl termini in the functional tagged murine TRPC6 t

263 imately 4-5 nm, revealing that the amino and carboxyl termini of Ana2 are located in the outer cartwh

264 The results indicate that the amino and carboxyl termini of PHO1 are both oriented toward the cy

265 cted cells, we determined that the amino and carboxyl termini reside in the extracellular space and a

266 The amino and carboxyl termini, not resolved in the density map, appea

267 tion between Nedd4 (WW1-3 domains) and Cx43 (carboxyl terminus (CT)).

268 utionarily conserved serine residue near the carboxyl terminus (Ser-883 in Xenopus).

269 y receptor phosphorylation, primarily in the carboxyl terminus but also in the cytoplasmic loops, and

270 ocess is initiated by phosphorylation of its carboxyl terminus by G protein-coupled receptor kinase 1

271 We progressively deleted the distal carboxyl terminus domain (CTD) of the cold-activated mel

272 no terminus (NTD), catalytic core (CCD), and carboxyl terminus domains (CTD).

273 either as fused domains (IbetaH(Asp)) at the carboxyl terminus of a nonribosomal peptide synthetase (

274 een the proline and the phenylalanine at the carboxyl terminus of Ang II.

275 molecular interaction assay reveals that the carboxyl terminus of APC interacts with the matrix regio

276 in bacterial proteasomal ATPases, buries the carboxyl terminus of each protomer in the central channe

277 A weaker interaction site within the carboxyl terminus of gamma-ENaC (K(d) ~800 mum) was also

278 Carboxyl terminus of Hsc70-interacting protein (CHIP) is

279 Here, we show that CHIP (carboxyl terminus of Hsc70-interacting protein), a U-box

280 he tryptophan-rich lipid-binding loop in the carboxyl terminus of LPL prevents homodimer formation an

281 The carboxyl terminus of p17 is necessary for interaction wi

282 ction network crucial for recognition of the carboxyl terminus of the KDEL signal.

283 Amino acids are transferred to the carboxyl terminus of the peptide through adenosine triph

284 MD), which leads to partial unwinding of the carboxyl terminus of transmembrane helix 6 and induces a

285 on to substrates, ADP-ribosylation of the Ub carboxyl terminus precludes ubiquitylation.

286 h the exclusion of exon 3 generates a unique carboxyl terminus with specific anti-apoptotic functions

287 e identify the HECT (homologous to the E6-AP carboxyl terminus) family E3 ubiquitin ligase, UBR5, as

288 g new gene) and HECT (homologous to the E6AP carboxyl terminus) types shed light on their enzymatic a

289 Calmodulin directly binds the AQP4 carboxyl terminus, causing a specific conformational cha

290 ductase, which has a joint Trx domain at the carboxyl terminus, termed NTRC.

291 p53 is subject to lysine methylation at its carboxyl terminus, which has been shown to repress p53's

292 main that precedes the proteasome-activating carboxyl terminus.

293 binding site of the opposite protomer at its carboxyl terminus.

294 an unexpected sequence located near the Bim carboxyl-terminus (residues 181-192).

295 sackievirus-adenovirus receptor fused to the carboxyl-terminus of human IgG) efficiently neutralizes

296 a cyan fluorescent protein, as a tag at the carboxyl-terminus of the murine TRPC6 protein.

297 the amino-terminus in close proximity to the carboxyl-terminus produced similar FRET ratios.

298 nt that truncation of alphasyn, particularly carboxyl truncation that can be augmented by dysfunction

299 d proton delivery to the amide nitrogen by a carboxyl, while the other carboxylate engages in nucleop

300 2-phenylisopropyl group can be cleaved from carboxyl with 2-3% (v/v) of TFA in acetonitrile (0-10 de