ライフサイエンスコーパス: carboxyl

1 5hmdC), 5-formy-2'deoxycytidine (5fdC) and 5-carboxyl-2'deoxycytidine (5cadC).

2 5-hydroxymethyl (5hmC), 5-formyl (5fC), or 5-carboxyl (5caC) forms.

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

4 eeded framework enabling this highly unusual carboxyl addition/elimination reaction.

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

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

7 a coated QDs (QD@SiO2), modified with amino, carboxyl and epoxy groups and stabilized with polyethyle

8 rieties of nanotubes, carrying predominantly carboxyl and hydroxyl functionalities, respectively, fac

9 3(+)) and directly compare it with a similar carboxyl and hydroxyl functionalized derivative.

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

11 ns the allowed distance between the backbone carboxyl and the amide carbon of any L-ASP substrate.

12 nt of an intramolecular reaction between the carboxyl and the amine termini of two fragments.

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

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

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

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

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

18 e BADC isoforms interact with the two biotin carboxyl carrier protein (BCCP) isoforms of A. thaliana

19 iotinylation reaction of the acceptor biotin carboxyl carrier protein (BCCP), through the expected bi

20 ene families, including P450 monooxygenases, carboxyl/cholinesterases, glutathione-S-transferases, an

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

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

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

24 s fluorescence enhancement upon binding with carboxyl-containing molecules.

25 tion over structural analogs and non-related carboxyl-containing molecules.

26 There was an increase in amylose content, carboxyl content and acidity with irradiation.

27 acid anion adsorption increased with surface carboxyl content, despite electrostatic repulsion from t

28 The percentage of carbonyl (CO) and carboxyl (COOH) groups in oxidized starches also increas

29 main (46-290) for memory suppression whereas carboxyl domain (598-854) and the amino-terminal residue

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

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

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

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

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

35 A new carboxyl esterase, AF-Est2, from the hyperthermophilic a

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

37 In addition, we have conjugated hydroxyl or carboxyl function groups on the ICG-NPs for future molec

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

39 , aliphatic C), a relative increase in amide/carboxyl functional groups and a significant increase in

40 For all cases, edge-based carboxyl functional groups are highly correlated to obse

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

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

43 ombined with iron oxide precipitation afford carboxyl functional groups suitable for immobilization o

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

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

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

47 Carboxyl-functionalization of graphene carbon can modula

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

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

50 Recently, carboxyl-functionalized synthetic polymers have been sho

51 d to acidification of both the amino and the carboxyl functions by approximately one unit.

52 least one of the essential membrane-embedded carboxyls, generates a binding site for reserpine.

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

54 additional polar functional group such as a carboxyl group (as in 3x) or a monosaccharide (as in 4x

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

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

57 Addition of a carboxyl group at the alpha position of carbocyclic nucl

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

59 GO chemical properties including C/O ratios, carboxyl group concentrations, and C-C fractions.

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

61 show that the ethylamido derivative of the 5-carboxyl group from 5-carboxy-fluorescein diacetate or f

62 y line the proton inlet path to an essential carboxyl group in the c-subunit in the proton uptake sit

63 nyl)ethoxy-1,3,2-dioxaphospholane, bearing a carboxyl group in the gamma-position with respect to the

64 A free carboxyl group in the product provides versatility for f

65 a K(+)-ionophore, provided that the glycine carboxyl group is appropriately masked.

66 s buried within the protein, and the exposed carboxyl group is bound by a Ser-93-fatty acid carboxyl-

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

68 ealing specific hydrogen bonds between the 5-carboxyl group of 5caC and the conserved epi-DNA recogni

69 These findings showed that loss of the carboxyl group of a C18 monounsaturated fatty acid lead

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

71 rived from the deprotonation of the terminal carboxyl group of MHA).

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

73 The carboxyl group of this segment was coupled to the N-term

74 the threonine and glycine residues, and the carboxyl group of threonine is amide-linked to the side

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

76 eractions between active site residues and a carboxyl group on the Pchlide molecule result in a polar

77 iate involves early proton transfer from the carboxyl group to water along with C-C bond cleavage, pr

78 luorescein diacetate, still possesses a free carboxyl group whose ionization constant is such that th

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

80 purpose as the proton can be carried on the carboxyl group, whereas the basicity of the tropylium io

81 Helix stabilization requires the protonated carboxyl group; unexpectedly, this stabilization could n

82 rmation from primary amines with hydroxyl or carboxyl groups (amino acids), but not from secondary am

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

84 d a fluorescent oxazole (5) having amine and carboxyl groups approximately the same distance apart as

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

86 e of hydrophobic acetyl groups, carbonyl and carboxyl groups caused a partial disorganization and dep

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

88 Acidic protons from carboxyl groups in both the lignite HA fraction and a sy

89 s of GAX, followed by more moderate PREs for carboxyl groups in homogalacturonan and rhamnogalacturon

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

91 -exchange kinetics for individual side-chain carboxyl groups in proteins has been achieved in only a

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

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

94 The carboxyl groups of PAA brushes can act as reducing moiet

95 tably trapped within the PAA brushes and the carboxyl groups of PAA can serve as internal proton sour

96 covalently conjugated ICG-NH2 to the pendant carboxyl groups of poly (ethylene glycol)-block-poly(2-m

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

98 To be specific, the richness of carboxyl groups of the CDs enabled strong adsorption of

99 n binding assays indicated that the retained carboxyl groups of the fatty acids helped maintain a tig

100 ment (coccolith vesicle) through the charged carboxyl groups of their uronic acid residues.

101 via diimide-activated amidation between the carboxyl groups on the CNT surface and amine groups on t

102 -1,2-ethandiyl (PCBS), resulting in terminal carboxyl groups on the LPG-ISAM.

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

104 ca-coated UCNPs (50 nm in diameter) exposing carboxyl groups on the surface were conjugated to a seco

105 latform for the DNA-c by the large number of carboxyl groups present on the functionalized gold nanop

106 lysis suggests that mechanisms involving two carboxyl groups result in the most stable bond to the mi

107 CNTs used in our studies were derivatized by carboxyl groups to facilitate their dispersion in water.

108 The terminal carboxyl groups were covalently conjugated to monoclonal

109 These carboxyl groups were utilized to achieve variable degree

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

111 Observations support the deprotonation of carboxyl groups with low acid dissociation constants (pK

112 Substrates having functionalities such as carboxyl groups, alcohols, or heterocycles in the vicini

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

114 and proton transfer involving the phenol and carboxyl groups.

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

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

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

118 turated acyl tail and the negatively charged carboxyl head group are required for PUFAs to open Kv7.1

119 s with ubiquitin involving (i) the ubiquitin carboxyl hydrolase catalytic domain of BAP1, which inter

120 fied to be amphiphilic by introducing either carboxyl, hydroxyl, or amine moieties.

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

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

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

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

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

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

127 Our findings demonstrate that carboxyl methylation of isoprenylated proteins is crucia

128 ggest that LCMT-1 coordinately regulates the carboxyl methylation of PP2A-related phosphatases and, c

129 Carboxyl methylation of the PP2A catalytic subunit (PP2A

130 Isoprenylcysteine carboxyl methyltransferase (ICMT) methylesterifies C-ter

131 ulated by the opposing activities of leucine carboxyl methyltransferase 1 (LCMT-1) and protein phosph

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

133 As encoding several S-adenosyl-Met-dependent carboxyl methyltransferase family members.

134 E-1), or the PP2A methyltransferase, leucine carboxyl methyltransferase-1 (LCMT-1), and examined the

135 odes a chloroplast-targeted putative leucine carboxyl methyltransferase.

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

140 solution is even more surprising because the carboxyl moiety is not a good electrophile due to the ne

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

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

143 in Acetobacteria: amidation at the alpha-(l)-carboxyl of meso-diaminopimelic acid and the presence of

144 ng (1)H and (13)C PREs were observed for the carboxyls of GAX, followed by more moderate PREs for car

145 tly lower, implicating distal effects of the carboxyl- on amino-terminal membrane binding.

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

147 n most cases, consists of negatively charged carboxyl or hydroxyl groups that limit attractive forces

148 functional groups (any one of primary amino, carboxyl, or primary hydroxyl) enables identification of

149 derived, and is most plausibly assigned as a carboxyl oxygen from E238.

150 The carboxyl oxygen of an adjacent peptide bond serves as th

151 In particular, the carboxyl oxygen of the alpha-CNP acts as the potential e

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

153 he development of a microarray platform with carboxyl-polyethylene glycol (PEG) as a functional layer

154 poly (ethylene glycol)-block-poly(2-methyl-2-carboxyl-propylene carbonate) (PEG-PCC) copolymer using

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

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

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

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

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

160 ort on the combination of poly [pyrrole-co-3-carboxyl-pyrrole] copolymer and aptamer for the developm

161 rinsic conjugation of the poly [pyrrole-co-3-carboxyl-pyrrole] copolymer and subsequently on its elec

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

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

164 on of carboxylates leads to the formation of carboxyl radicals, which upon rapid CO2-extrusion and F(

165 ccharide and their chemically desulfated and carboxyl-reduced derivatives revealed that the sulfate e

166 We then relocated this carboxyl residue to six positions on the surface of the

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

168 cationic substrates, LmrP contains catalytic carboxyl residues on the surface of a large interior cha

169 The results indicate that carboxyl-rich aromatic and N-containing aliphatic molecu

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

171 a new hypothesis that the substrate's alpha-carboxyl serves as a proton acceptor and activates one o

172 te constants (kon and koff, respectively) of carboxyl side chains, based on (13)C NMR relaxation meas

173 principally when a glycyl residue is at the carboxyl side of Asn and leads to formation of aspartyl

174 dergoes both amino terminal (N-terminal) and carboxyl terminal (C-terminal) proteolytic modifications

175 hiols with a length of 11 carbon atoms and a carboxyl terminal group can efficiently block the charge

176 on of surface electrostatic potential at the carboxyl terminal of the alpha1-helix of HLA class I all

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

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

179 hesis, isopropylmalate synthase, missing the carboxyl-terminal 160 amino acids.

180 ORF33-binding domain to the highly conserved carboxyl-terminal 19 amino acids (aa) of ORF45 and the U

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

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

183 vivin by interacting with Glu-126 within its carboxyl-terminal alpha helix.

184 4, (ii) the amino-terminal cysteine-rich and carboxyl-terminal basic domains of ORF31 mediate the ORF

185 s-associated speck-like protein containing a carboxyl-terminal caspase-recruitment domain, and caspas

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

187 such as addition of an isoprenyl lipid to a carboxyl-terminal cysteine in proteins that terminate wi

188 eceptor is unique in having an intracellular carboxyl-terminal cysteine-rich region (Ccys).

189 7A and that binding is mediated in part by a carboxyl-terminal di-leucine motif.

190 Mutational analyses have indicated that the carboxyl-terminal domain (CTD) of hepadnavirus core prot

191 Mutational analyses have suggested that the carboxyl-terminal domain (CTD) of hepadnavirus core prot

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

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

194 el-forming transmembrane domain (TMD), and a carboxyl-terminal domain (CTD).

195 gating process, channels lacking the distal carboxyl-terminal domain are no longer regulated by the

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

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

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

199 one H3 at Ser(10) In addition, targeting the carboxyl-terminal domain of CS-GRP78 with a mAb suppress

200 An antibody against the carboxyl-terminal domain of GRP78 may have important app

201 3-kinase, mTORC, or an antibody against the carboxyl-terminal domain of GRP78.

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

203 ical signals manifested by RNA polymerase II carboxyl-terminal domain phosphorylation status.

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

205 In this study, we identified carboxyl-terminal domain RNA polymerase II polypeptide A

206 ) and PHD (plant homeo domain) fingers and a carboxyl-terminal domain that directly binds the largest

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

208 SK-3 serine phosphorylation sites within the carboxyl-terminal domain.

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

210 TH directly binds the substrate binding and carboxyl-terminal domains of Hsc70.

211 When the carboxyl-terminal domains of TcdB012 and TcdB027 are swa

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

213 ic domain, but differ conspicuously in their carboxyl-terminal domains.

214 inantly labeling only single residues in the carboxyl-terminal end of ECL2 and the amino-terminal end

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

216 Purified full-length UL37 and its carboxyl-terminal fragment were sufficient to deamidate

217 g as well as generation of a cell-associated carboxyl-terminal fragment with potential oncogenic func

218 Cys(6)-sec labeling multiple residues in the carboxyl-terminal half of ECL2 and throughout ECL3, Cys(

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

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

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

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

223 of MUC16 are ascribed to the cell-associated carboxyl-terminal MUC16 (MUC16-Cter), the exact biochemi

224 Through binding of Erk2 to the second of its carboxyl-terminal NPXY motifs, LRP1 beta-chain positivel

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

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

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

228 ng proteins, including E2f, interact through carboxyl-terminal protein interaction domains, but genet

229 protein lacking N-terminal myristoylation, a carboxyl-terminal pX extension of VP1, VP2 late domains

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

231 of the peptide-binding domain located at the carboxyl-terminal region of the avian HSPA2.

232 ipitation studies showed the alpha-actinin-4 carboxyl-terminal region specifically interacted with th

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

234 c-Jun specifically at the chromatin via its carboxyl-terminal region.

235 Transient expression of a carboxyl-terminal reporter gene construct directed SaB4H

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

237 ons and that alterations affecting the ATP7A carboxyl-terminal tail induce release of the copper tran

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

239 ction with a beta2-adrenoceptor fused to the carboxyl-terminal tail of the vasopressin type 2 recepto

240 (362), Ser(363) and Thr(366) residues at the carboxyl-terminal tail were primarily responsible for ss

241 ared with AVR1, A-L is shorter and lacks the carboxyl-terminal tail, the T-region that is crucial for

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

243 cer of conformational flexibility within the carboxyl-terminal transmembrane region.

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

245 protein-SlGGB1 fusion protein as well as the carboxyl-terminal yellow fluorescent protein-SlGGB1/amin

246 ransition coupled the phosphorylation of the carboxyl-terminal-domain (CTD) of RNA polymerase II (RNA

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

248 Bare and carboxyl-terminated CNPs did present some toxicity at th

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

250 d two extracellular loops with the amino and carboxyl termini facing the cytoplasm.

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

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

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

254 y conserved among different Cxs, whereas the carboxyl termini, often called the cytoplasmic tails, ar

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

256 nders GBM cells resistant to TMZ through its carboxyl terminus (CT).

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

258 tion of a helix extending toward the peptide carboxyl terminus and docking within the receptor amino

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

260 d V166E rClC-K1 demonstrated that the distal carboxyl terminus is necessary for slow cooperative gati

261 type II membrane protein with its catalytic carboxyl terminus located in the Golgi lumen.

262 To describe how the carboxyl terminus modifies the regulation by barttin we

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

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

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

266 Our results demonstrate that the carboxyl terminus of hClC-Kb is not part of the binding

267 t result in truncations of the intracellular carboxyl terminus of hClC-Kb.

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

269 Furthermore, deletion of the conserved carboxyl terminus of ORF45 in the KSHV genome drasticall

270 The carboxyl terminus of p17 is necessary for interaction wi

271 luorescent protein (YFP) was tethered to the carboxyl terminus of the alpha2A adrenergic receptor (al

272 he tyrosine kinase c-Src associated with the carboxyl terminus of the beta3 cytosolic tail.

273 f Gbetagamma-specific scavengers-namely, the carboxyl terminus of the G protein-coupled receptor kina

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

275 h an unexpected epsilon-glycinylglycinyl-Lys carboxyl terminus when the site of linkage is Lys48.

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

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

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

279 ane helices followed by a long intracellular carboxyl terminus, and earlier work demonstrated that th

280 nsible for processing Atg8 proteins near the carboxyl terminus, exposing a conserved glycine.

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

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

283 s it has an exceptionally long intracellular carboxyl terminus, which is predicted to be mainly disor

284 sphorylation of AQP2 at various sites in its carboxyl terminus, with Ser-256 phosphorylation critical

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

286 the exposure of neutralizing epitopes in the carboxyl terminus.

287 nters on a single residue serine 829, in the carboxyl terminus.

288 main that precedes the proteasome-activating carboxyl terminus.

289 Interactions of the carboxyl-terminus (CT) and cytoplasmic loop (CL) domains

290 ing Cx43 with ACT1, a peptide mimetic of the carboxyl-terminus of Cx43, accelerates fibroblast migrat

291 somal activity, suggesting that the extended carboxyl-terminus of this cofactor confers suboptimal bi

292 Intriguingly, the truncation of the PafE carboxyl-terminus resulted in the robust binding of PafE

293 the first extracellular loop domain and its carboxyl-terminus.

294 rboxyl group is bound by a Ser-93-fatty acid carboxyl-Thr-61-His-266 hydrogen bond network.

295 terminal groups, an amino, a hydroxyl, and a carboxyl, were investigated using two different molecule

296 We find that side-chain carboxyls with extreme values of koff or kon are involve

297 Finally, carboxyl zinc-finger deletion of Gata6 reduces cell-cycl

298 hermore, myocardial-specific deletion of the carboxyl zinc-finger of Gata6 alters atrioventricular co

299 Myocardial-specific deletion of the carboxyl zinc-finger of Gata6 induces loss of hyperpolar

300 Myocardial-specific deletion of the carboxyl zinc-finger of Gata6 is also associated with do