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1 dicating HS Fe(II) in deoxy and LS Fe(II) in carboxy.
2  of nitroxide and reference hydroxylamine (3-carboxy-1-hydroxy-2,2,5,5-tetramethylpyrrolidine-1-oxyl-
3 hmdC), 5-formyl-2'-deoxycytidine (fdC) and 5-carboxy-2'-deoxycytidine (cadC) were recently discovered
4 margin; also 5-formyl-2'-deoxycytidine and 5-carboxy-2'-deoxycytidine were lower in colorectal carcin
5 -deoxycytidine, 5-formyl-2'-deoxycytidine, 5-carboxy-2'-deoxycytidine, 5-(hydroxymethyl)-2'-deoxyurid
6  (18)F-PSMA-1007 (((3S,10S,14S)-1-(4-(((S)-4-carboxy-2-((S)-4-carboxy-2-(6-(18)F-fluoronicotinamid o)
7 (((3S,10S,14S)-1-(4-(((S)-4-carboxy-2-((S)-4-carboxy-2-(6-(18)F-fluoronicotinamid o)butanamido)butana
8 in variants capable of providing access to 1-carboxy-2-aryl-cyclopropanes with high trans-(1R,2R) sel
9 action as a model system, we designed a 9-(2-carboxy-2-cyanovinyl) julolidine-based p53 peptide repor
10 hway ofPseudomonas putidaKT2440 requires a 4-carboxy-2-hydroxymuconate (CHM) hydratase (GalB), which
11 tion by identifying 5-carboxyvanillate and 4-carboxy-2-hydroxypenta-2,4-dienoate as the products and
12 l doubly caged GABA analog, termed bis-alpha-carboxy-2-nitrobenzyl-GABA (bis-CNB-GABA).
13 lcypromine 7, a known LSD1 inhibitor, with 4-carboxy-4'-carbomethoxy-2,2'-bipyridine 8 or 5-carboxy-8
14 llylamine hydrochloride and in poly-1-[p-(3'-carboxy-4'-hydroxyphenylazo) benzenesulfonamido]-1,2-eth
15 7 by the small molecule agonist MDL29,951 (2-carboxy-4,6-dichloro-1H-indole-3-propionic acid) decreas
16                                      Serum 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (CMPF) (P-in
17 osapentaenoic acid (fish) (P-raw = 0.041), 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid (CMPF) (
18 oxidized analogue of the natural substrate 6-carboxy-5,6,7,8-tetrahydropterin (CPH4), is shown to be
19 acterial enzyme catalyzes the formation of 6-carboxy-5,6,7,8-tetrahydropterin.
20     The PSMA-targeting Auger emitter 2-[3-[1-carboxy-5-(4-(125)I-iodo-benzoylamino)-pentyl]-ureido]-p
21                   PSMA-targeted (2S)-2-(3-(1-carboxy-5-(4-(211)At-astatobenzamido)pentyl)ureido)-pent
22  PET/CT tracers, first (18)F-DCFPyL (2-(3-{1-carboxy-5-[(6-(18)F-fluoro-pyridine-3-carbonyl)-amino]-p
23        Meanwhile, MIP-1404, PSMA-11, 2-(3-{1-carboxy-5-[(6-fluoro-pyridine-3-carbonyl)-amino]-pentyl}
24      The first series contains L-Ala and D-4-carboxy-5-methyl-oxazolidin-2-one (D-Oxd).
25 -based, 4-(5-(((4-acetoxybenzyl)oxy)amino)-2-carboxy-5-oxopentyl)benzoic acid, 12, provided 5-fold hi
26 nversion of the carboxylic acid containing 7-carboxy-7-deazaguanine (CDG) into its corresponding nitr
27                                            7-Carboxy-7-deazaguanine (CDG) synthase (QueE) catalyzes a
28 rboxy-4'-carbomethoxy-2,2'-bipyridine 8 or 5-carboxy-8-hydroxyquinoline 9, two 2-oxoglutarate competi
29 f 5-aminoimidazole ribonucleotide (AIR) to 4-carboxy-AIR (CAIR) represents an unusual divergence in p
30 ety in adducts can produce the corresponding carboxy, aldehyde, and ketone compounds under very mild
31                   In this study we show that carboxy(alkylpyrrole) protein adducts represent novel un
32                                            4-Carboxy-alpha-[3-(hydroxyamino)-3-oxopropyl]-benzeneprop
33  reactions for molecules containing methoxy, carboxy, amino, and sulfide substituents were carried ou
34  involve an acidic proton shared between the carboxy and amino function.
35 es C and pH 4 owing to the joint presence of carboxy and carboxylate groups.
36 OOH and -OH bonds leads to the wide range of carboxy and hydroxy functionalized alpha-amino esters (2
37 ructures of unligated (deoxy), CO-inhibited (carboxy), and O2-bound (oxy) hemes in myoglobin (MB) and
38 A general synthetic approach to vinylogous 4-carboxy- and 4-keto-2,3-dihydropyrroles is reported usin
39                             We find residual carboxy- and endo-peptidase gamma-secretase activities,
40 ing the amino groups of the dendrimer with 4-carboxy-benzenesulfonamide functionalities.
41 4-, 2,6-, 2,8-quinolinediols, and 1-methyl-3-carboxy-beta-carboline are described.
42 trained so as to juxtapose the amino (N) and carboxy (C) termini; several of these designed structure
43 expression, but not the expression of a CD81 carboxy (C)-terminal deletion mutant, increases cellular
44             In Saccharomyces cerevisiae, the carboxy (C)-terminal Q/N-rich domain of the Lsm4 subunit
45                                          The carboxy (C)-terminal section of the polypeptide loop is
46                       We find that the Brca1 carboxy (C)-terminal tandem BRCT repeat and regions of B
47                    p63 also encodes multiple carboxy (C)-terminal variants.
48  signalling molecules bind to NRPs through a carboxy (C)-terminal, basic sequence motif (C-end Rule o
49                      5-Formyl-dC (fdC) and 5-carboxy-dC (cadC) are newly discovered bases in the mamm
50                           The liposomal 5(6)-carboxy-DCFH2 can be targeted to other tissues where oxi
51                      Liposome-delivered 5(6)-carboxy-DCFH2 enabled real-time visualization and measur
52 to deliver the carboxylated derivative, 5(6)-carboxy-DCFH2, to hepatocytes in vivo.
53 the main urinary metabolite of THC, 11-nor-9-carboxy-Delta(9)-tetrahydrocannabinol (THC-COOH) with ch
54 nabidiol (CBD), and the metabolites 11-nor-9-carboxy-Delta(9)-tetrahydrocannabinol (THC-COOH), 11-hyd
55 trahydrocannabinol (11-OH-THC), and 11-nor-9-carboxy-Delta(9)-tetrahydrocannabinol glucuronide (THC-C
56  Delta9-tetrahidrocannabinol (THC), 11-nor-9-carboxy-Delta(9)-THC (THC-COOH) and 11-hidroxy-Delta(9)-
57 h abstinence before study; positive 11-nor-9-carboxy-delta-9-tetrahydrocannabinol urine levels) and c
58 rofiles of benzoylecgonine (BE) and 11-nor-9-carboxy-Delta9-tetrahydrocannabinol (THC-COOH) were show
59 ess to Nazarov cyclization precursors, alpha-carboxy divinyl ketones C.
60 on antigenic regions, we first expressed the carboxy domain of the hMPV N protein that was the most h
61 ly 20 degrees rotation between the amino and carboxy domains, which opens up a cleft in arrestin to a
62 rder to selectively capture HbA1c in sample, carboxy-EG6-undecanethiol was self-assembled on a gold t
63 ins in regulating legumain proteases via its carboxy-extended domain and papain-like proteases by its
64 led legumain (C13) protease inhibition via a carboxy-extended phytocystatin.
65  study reinforce the bifunctional ability of carboxy-extended phytocystatins in regulating legumain p
66 do derivative of the 5-carboxyl group from 5-carboxy-fluorescein diacetate or from Oregon green diace
67 spectively, cultured cells were stained with carboxy-fluorescein diacetate succinimidyl ester (CFDA S
68 lonRIalpha were measured as proliferation by carboxy-fluorescein diacetate succinimidyl ester dye dil
69 ed 2 independent assays (CD154 detection and carboxy-fluorescein succinimidyl ester dilution assays)
70    The reaction proceeded selectively at the carboxy function site to exclusively give the correspond
71 crylamide) (pCBAA), and a standard OEG-based carboxy-functional alkanethiolate self-assembled monolay
72 involved in functionalization of low-fouling carboxy-functional coatings have on the BRE capacity and
73 ith superior fouling resistance over various carboxy-functional low-fouling coatings including homopo
74 en compared with the widely used low-fouling carboxy-functional oligo(ethylene glycol) (OEG)-based al
75 oly(2-hydroxyethyl methacrylate) (pHEMA) and carboxy-functional poly(carboxybetaine acrylamide) (pCBA
76 (2-hydroxypropyl) methacrylamide (HPMAA) and carboxy-functional zwitterionic carboxybetaine methacryl
77                                              Carboxy-functionalised SWCNTs were covalently tethered o
78 d-supported synthetic approach using a novel carboxy-functionalized building block which bears a func
79             Lake water was dosed with AgNPs (carboxy-functionalized capping agent; approximately 10-n
80 annose and biotin ligands coupled to aqueous carboxy-functionalized gold nanoparticles through a spin
81 a and that binding did not require the gamma-carboxy glutamic acid domain.
82                     The hydrogen of the free carboxy group derived from the catalyst interacts with t
83 ocenter at C2 (allylic methine, alpha to the carboxy group) and the protecting groups at C17-OH and C
84     It is revealed that, in contrast to free carboxy-group-terminated OEG-SAMs, only a partial deacti
85 IV-1 proteinase, function with two aspartate carboxy groups at the active site.
86 activation of EDC/NHS-activated zwitterionic carboxy groups by spontaneous hydrolysis is possible in
87 e) even after covalent attachment of BREs to carboxy groups of CBMAA.
88 id deactivation agents to residual activated carboxy groups of pCB.
89 specific mechanisms of EDC/NHS activation of carboxy groups, BRE attachment, and deactivation of resi
90  arrangement of oppositely charged amino and carboxy groups.
91 ise unactivated amide positioned between two carboxy groups.
92 ed from CORM-3 by following the formation of carboxy-Hmp in respiring cells.
93 ar compounds is demonstrated by formation of carboxy-Hmp.
94 ant tissues: hydroxy-IBP, 1,2-dihydroxy-IBP, carboxy-IBP and glucopyranosyloxy-hydroxy-IBP.
95 nvolving amino acid unsymmetrical urea A and carboxy-imidazolyl-dipeptide ester B intermediates.
96 direct decarboxylative arylation of 1- and 3-carboxy isoquinaldic acid N-oxides with aryl iodides is
97 out with a conjugated push-pull system and a carboxy linker for a conceivable coupling with biomolecu
98 evented by disrupting the interaction of the carboxy-lobe of calmodulin with a calmodulin-binding dom
99 e also proposed for future investigation: 4'-carboxy-mephedrone, 4'-carboxy-normephedrone, 1-dihydro-
100               Xanthan, locust bean, guar and carboxy methyl cellulose significantly enhanced Bostwick
101        Different ingredients (guar, xanthan, carboxy methyl cellulose, locust bean gums, potato fiber
102 cytochrome c by replacing tyrosine 48 with p-carboxy-methyl-l-phenylalanine (pCMF).
103 trations of the NOC-specific DNA adduct O(6)-carboxy-methylguanine when pork underwent a more intense
104 ure investigation: 4'-carboxy-mephedrone, 4'-carboxy-normephedrone, 1-dihydro-mephedrone, 1-dihydro-n
105 a nucleoside monophosphonate scaffold, alpha-carboxy nucleoside phosphonate (alpha-CNP), was designed
106 reverse transcriptase (RT) inhibitors, alpha-carboxy nucleoside phosphonates (alpha-CNPs).
107  unrecognized aminopeptidase activity but no carboxy- or endopeptidase activity.
108  combining alpha-amylase, protease and gamma-carboxy peptidase allowing complete sample preparation w
109                For example, for mono(2-ethyl-carboxy-propyl) phthalate (MECPP), a metabolite of di(2-
110  functions as a soluble glycoprotein via its carboxy-proximal Fas1 domain and its normal cellular tra
111 ntly by molecular interactions involving its carboxy-proximal fasciclin 1 domain and that its amino-p
112                     The drug (R)-1-[6-[(R)-2-carboxy-pyrrolidin-1-yl]-6-oxo-hexanoyl]pyrrolidine-2-ca
113           DFT calculations show that (amino)(carboxy) radicals evolve from C-centered radical to ambi
114                A series of monomeric (amino)(carboxy) radicals featuring carbonyl substituents with i
115                             Although (amino)(carboxy) radicals had been previously considered as high
116 enzyme that recognizes the unique metabolite carboxy-S-adenosine-L-methionine (Cx-SAM) and catalyzes
117 in of MccB and the MccS enzyme that produces carboxy-SAM, which serves as a donor of the carboxymethy
118 ) or pH (pH(i)) were measured with Indo-1 or Carboxy-SNARF, respectively.
119 firmed by using the ratiometric pH indicator carboxy-SNARF-1.
120 targeted to the Z ring through the conserved carboxy tail of FtsZ leading to breakage of FtsZ filamen
121 a2+ regulation, and transplanting the NaV1.4 carboxy tail onto Ca2+ channels recapitulates Ca2+ regul
122  distinct ion channel superfamilies, yet the carboxy tails of these channels exhibit high homology, h
123 ing from neutral and deprotonated forms of 4-carboxy-TEMPO have been measured in solution (acetonitri
124 s to protein storage vacuoles is mediated by carboxy terminal and internal sorting determinants (ISDs
125  residues for DNA binding in cGAS as well as carboxy terminal tail domain for transducing signals in
126                   SPAK possesses a conserved carboxy-terminal (CCT) domain, which recognises RFXV/I m
127                         Here we identify the carboxy-terminal acidic tail of the yeast lipin Pah1p as
128 tment and the tagging of nascent chains with carboxy-terminal Ala and Thr extensions ("CAT tails").
129 -dependent ubiquitination and Rqc2p-mediated Carboxy-terminal Alanine and Threonine (CAT) tail elonga
130 from classical IgE by the replacement of two carboxy-terminal amino acids with eight novel residues t
131 s a metalloproteinase catalytic domain and a carboxy-terminal ancillary domain, the latter determinin
132  hotspots, requiring the repair functions of carboxy-terminal binding protein (CtBP)-interacting prot
133                                          The carboxy-terminal binding protein (CtBP)-interacting prot
134 S effector TRP120 is conjugated to SUMO at a carboxy-terminal canonical consensus SUMO conjugation mo
135 an amino-terminal alpha-helical region and a carboxy-terminal caspase-like catalytic domain.
136 pha), and bone metabolism (osteocalcin [OC], carboxy-terminal collagen crosslinks [CTX], and N-termin
137 ) RNA requires additional phosphorylation of carboxy-terminal Dicer residues (S1728 and S1852).
138 n and processing, and the role of the Pol II carboxy-terminal domain (CTD) in regulating these proces
139 man immunodeficiency virus type 1 (HIV-1) CA carboxy-terminal domain (CTD) is essential for CA-CA int
140                              In mammals, the carboxy-terminal domain (CTD) of RNA polymerase (Pol) II
141 i-subunit complex stably associated with the carboxy-terminal domain (CTD) of RNA polymerase II (RNAP
142 2)-Pro(3)-Thr(4)-Ser(5)-Pro(6)-Ser(7) in the carboxy-terminal domain (CTD) of the largest RNA polymer
143                                          The carboxy-terminal domain (CTD) of the RNA polymerase II (
144 inase 9 (CDK9) recruitment and phospho-Ser 2 carboxy-terminal domain (CTD) RNA polymerase (Pol) II fo
145 its, a core that binds UPF1 and a protruding carboxy-terminal domain (CTD) that binds the SMG1 kinase
146 n of the amino-terminal domain (NTD) and the carboxy-terminal domain (CTD) was found to be essential
147 s Pol II around the Rpb4-Rpb7 stalk near the carboxy-terminal domain (CTD).
148 is its long C-terminal extension, called the carboxy-terminal domain (CTD).
149                  We recently showed that the carboxy-terminal domain (Cterm) of human mt-leucyl tRNA
150 using a recombinant OcXII harboring only the carboxy-terminal domain and this part did not exhibit an
151                                     The Elp1 carboxy-terminal domain contains a highly conserved argi
152  and involving a region of the middle domain/carboxy-terminal domain interface previously suggested t
153 utionarily restrictive catalytic core domain-carboxy-terminal domain linker regions.
154                                          The carboxy-terminal domain of DNTTIP1 has a structure relat
155 between FMRP and Ca(V)2.2 occurs between the carboxy-terminal domain of FMRP and domains of Ca(V)2.2
156   We determined the crystal structure of the carboxy-terminal domain of human SRAP and found that it
157                    Our results show that the carboxy-terminal domain of N protein, N3, is necessary a
158 is model suggested that POA binds within the carboxy-terminal domain of ribosomal protein S1 (RpsA) a
159 gulates transcription by phosphorylating the carboxy-terminal domain of RNA polymerase II.
160 t the Na(+)-K(+)-ATPase, upon binding to the carboxy-terminal domain of the alpha subunit of the chan
161                        The RVA PDE forms the carboxy-terminal domain of the minor core protein VP3 (V
162                                          The carboxy-terminal domain of the receptor shows an extensi
163 binding motifs and instead is similar to the carboxy-terminal domain of the yeast spliceosome protein
164 tion results in premature termination of the carboxy-terminal domain of VIR, resembling McClintock's
165                                          The carboxy-terminal domain of YTHDF2 selectively binds to m
166  novel interaction between tRNA and the Elp1 carboxy-terminal domain.
167 s secreted by T9SSs typically have conserved carboxy-terminal domains (CTDs) belonging to the TIGRFAM
168 cretion of numerous other proteins that have carboxy-terminal domains associated with targeting to th
169  catalytic core domain flanked by amino- and carboxy-terminal domains essential for the concerted int
170                                              Carboxy-terminal domains line the central ion pore, and
171 arged regions conserved in the J-domains and carboxy-terminal domains of each J-protein class, and ar
172 d amino-terminal and the leucine-rich repeat carboxy-terminal domains of Tmod.
173     These include rotation of the amino- and carboxy-terminal domains relative to each other, and a m
174 of phosphorylation in the amino-terminal and carboxy-terminal domains that are positioned to alloster
175 l as alpharetroviruses by providing critical carboxy-terminal domains to the intasome core that canno
176 and STING interacted directly, through their carboxy-terminal domains, to promote STING dimerization,
177 ngage the core structure via their integrase carboxy-terminal domains.
178 on coded a truncated protein that lacked the carboxy-terminal end of the VWF protein.
179  amino-terminal end and hexahistidine at the carboxy-terminal end to generate CPD-MAGE-A3 in a pQE-70
180 -381 and serine-382, located in the C-linker carboxy-terminal end, which prevent KAT2 surface express
181  Similar acidic sequences are present in the carboxy-terminal ends of all yeast lipin orthologues.
182 robably impacts Cre activity in strains with carboxy-terminal Ert2 fusion.
183 rice, OcXII is the only gene possessing this carboxy-terminal extension.
184 aused by elevated levels of the beta-cleaved carboxy-terminal fragment of APP (betaCTF).
185            We identify higher molecular mass carboxy-terminal fragments (CTFs) of APP, termed CTF-eta
186           Its catalytic domain comprises the carboxy-terminal half (containing TM6-10) and envelops t
187 the lamin-A binding domain was mapped to the carboxy-terminal half of matrin-3.
188 on depends on a beta-propeller domain in the carboxy-terminal half of the protein, which is fused to
189  Three layers of hydrophobic residues on the carboxy-terminal half of the TM1 helices form a bottlene
190 ostly rigid body movements of the amino- and carboxy-terminal halves of SecY.
191                We therefore propose that the carboxy-terminal helicase module of Brr2p acquired a reg
192 proaches, we investigated interaction of the carboxy-terminal helicase module, in particular the carb
193 -binding domains remain in contact via their carboxy-terminal helices.
194       Deleterious mutations of the ubiquitin carboxy-terminal hydrolase BAP1 found in cancers are pre
195 mposed of a four-helix bundle connected to a carboxy-terminal immunoglobulin (Ig)-like domain through
196 s N-SH2 domain and a previously unrecognized carboxy-terminal immunoreceptor tyrosine-based activatio
197 ese SARD (UT-69 and UT-155) also binding the carboxy-terminal ligand binding domain.
198                                            A carboxy-terminal linker connecting S6 and the cyclic-nuc
199 o acids between the leucine-rich repeats and carboxy-terminal low-complexity acidic region domains.
200                              We identified a carboxy-terminal modification that is sufficient to conf
201 stinct from SGR in genomic location, encoded carboxy-terminal motif, and expression through plant and
202 l transfer protein (PITP) domain linked to a carboxy-terminal nodulin domain.
203 ng motifs, and the catalytic function of the carboxy-terminal PARP domain.
204 hat target the degradation of p53 and have a carboxy-terminal PDZ ligand that is required for stable
205               Finally, we found that the DAT carboxy-terminal PDZ-binding motif was required for DAT
206 al sequence, the protein was identified as a carboxy-terminal peptide of the acute phase protein seru
207 tsZ, referred to here as the CCTP (conserved carboxy-terminal peptide), is required for the interacti
208                            Our work uncovers carboxy-terminal phosphorylation-independent noncanonica
209       In the structure of the complex of the carboxy-terminal portion of Na(v)1.5 (CTNa(v)1.5) with c
210                                     Next the carboxy-terminal portion of Ssp2 forms a complex with Sm
211 e range of potential substrates that undergo carboxy-terminal processing.
212                                          The carboxy-terminal proline-rich domain of DAZAP1 interacts
213 e tissue growth factor (CTGF), procollagen I carboxy-terminal propeptide (PICP), amino-telopeptide of
214 he characterization of two novel enzymes for carboxy-terminal protein modification provides novel ins
215 ralizing epitopes have been found within the carboxy-terminal receptor binding domains (RBDs) of TcdA
216 cleolar (NoLS) localization signals near the carboxy-terminal region of AAP2 (amino acid positions 14
217 inus, or deletion of regions in the internal carboxy-terminal region of E protein, led to virus atten
218                            The intracellular carboxy-terminal region of each subunit contains several
219 an E3 ligase substrate adaptor DCAF1 and the carboxy-terminal region of human SAMHD1.
220  an extended alpha-helix from the disordered carboxy-terminal region of nucleoprotein-core links nucl
221                                    While the carboxy-terminal region of S-layer glycoproteins, consis
222 ns or deletions in the amino-terminal or the carboxy-terminal regions of the E protein were generated
223 chromes consist of a photosensory core and a carboxy-terminal regulatory domain.
224                           (iii) However, the carboxy-terminal repeat in the VEEV HVD is indispensable
225  acid composition and charge at the six most carboxy-terminal residues.
226 fs in Slx5 to aid in substrate targeting and carboxy-terminal RING domains in both Slx5 and Slx8 for
227 -terminal helicase module, in particular the carboxy-terminal Sec63-2 domain, with the splicing RNA h
228 d with Bacillus subtilis spores expressing a carboxy-terminal segment (TcdA26-39) of C. difficile tox
229 e amino acid sequence DDDDK identical to the carboxy-terminal sequence of the FLAG epitope.
230      Cellular alpha-tubulin can bear various carboxy-terminal sequences: full-length tubulin arising
231 m substrates have been proposed to contain a carboxy-terminal signal sequence that is necessary and s
232      Several PPR proteins in plants harbor a carboxy-terminal small-MutS-related (SMR) domain, but th
233         Pre-fusion gp41 encircles amino- and carboxy-terminal strands of gp120 with four helices that
234   Here we investigate the negatively charged carboxy-terminal tail domains (CTTs) of alpha- and beta-
235 P4, has previously been shown to bind to the carboxy-terminal tail of MTA1.
236                                          The carboxy-terminal tail of TFAM is essential for activatio
237 dentify serine residue 1166 (Ser1166) in the carboxy-terminal tail of the NMDAR subunit GluN2B to be
238 his activation requires histidine 711 in the carboxy-terminal tail of TRPV5.
239 oth alpha- and beta-tubulin proteins possess carboxy-terminal tail regions (CTTs) that are negatively
240 with the extracellular face, rather than the carboxy-terminal tail, of the receptors.
241        The posttranslational modification of carboxy-terminal tails of tubulin plays an important rol
242 investigate the inhibition effect of tubulin carboxy-terminal tails using peptide sequences of alpha-
243  the tubulin and specifically depends on the carboxy-terminal tails.
244   Uric acid, C-reactive protein, galectin-3, carboxy-terminal telopeptide of collagen type I, and end
245 l products expressed through the cytoplasmic carboxy-terminal Toll/IL-1 domain.
246                        Before insertion, the carboxy-terminal transmembrane domains of tail-anchored
247 ease domain of P3 and the domains within the carboxy-terminal two-thirds of PB2 are completely rearra
248 ith STAT3 and p300 to transactivate, whereas carboxy-terminal unphosphorylated Smad3 interacts with S
249  describe a new recombinant PRV expressing a carboxy-terminal VP26-mCherry fusion.
250 plex interacts with tubulin monomers via the carboxy-terminal winged-helix domain of Ska1, providing
251 ure with an amino-terminal coiled-coil and a carboxy-terminal zinc binuclear cluster.
252 ditionally, Rqc2 modifies stalled NCs with a carboxy-terminal, Ala- and Thr-containing extension-the
253                   Furthermore, expression of carboxy-terminal-truncated VE-cadherin increases the num
254 protection was successful, and the resulting carboxy-terminated dendrimers were analyzed by NMR and D
255 olymer brushes (pCB) as well as conventional carboxy-terminated oligo(ethylene glycol)-based alkaneth
256 ly related ryanodine receptor, the cytosolic carboxy termini are uniquely arranged in a left-handed a
257 t-handed super-helical coiled-coil and their carboxy termini arrayed in a left-handed super-helical c
258 changes, with direct binding mediated by the carboxy termini of Dam1p and Duo1p.
259                     While the YopD amino and carboxy termini participate in pore formation, the role
260 able region 2 (VR2) and two cysteines at the carboxy terminus (CT) as S-acylation sites.
261                              For F, only the carboxy terminus (Fstem) was required, and addition of f
262 ed amphiphilic repression (EAR) motif at the carboxy terminus abolishes BZR1's abilities to regulate
263 ugh an isopeptide bond between the ubiquitin carboxy terminus and a substrate lysyl amino group.
264 Together, the data show that P, M, and the F carboxy terminus are sufficient for robust viral protein
265            The binding of receptors or their carboxy terminus as well as certain truncations induce a
266 rylation of S477 and T479 at the Akt extreme carboxy terminus by cyclin-dependent kinase 2 (Cdk2)/cyc
267 on between its HECT (homologous to the E6-AP carboxy terminus domain) and two central WW domains.
268 apsids via their amino terminus, whereas the carboxy terminus is unstructured and therefore may bette
269 dentify clusters of basic amino acids in the carboxy terminus of AAP from AAV serotype 2 (AAV2) that
270                                The cytosolic carboxy terminus of AQP1 has two acidic motifs homologou
271 script stability and by restoring the native carboxy terminus of Cre, resulting in a five- to tenfold
272       A short conserved motif located at the carboxy terminus of FtsZ, referred to here as the CCTP (
273 Vpx binding domain of SAMHD1 is fused to the carboxy terminus of green fluorescent protein (GFP) and
274 dence that mapped interactions with N to the carboxy terminus of M, it was not possible to define a s
275 re mediated by a conserved region within the carboxy terminus of perilipin 1 that binds and stabilize
276    Chimeric proteins generated by fusing the carboxy terminus of perilipin 1 to the amino terminus of
277 the Tyr208Asn amino acid substitution in the carboxy terminus of SHP-1 (referred to as Ptpn6(spin) mi
278  of the NS2B/3 protease cleavage site at the carboxy terminus of the C protein.
279 tion is enhanced by a positive charge at the carboxy terminus of the peptide, which triggers an inwar
280 of interactions, one with the phosphorylated carboxy terminus of the receptor and the other with its
281 and E3 three-enzyme cascade, which links the carboxy terminus of ubiquitin to the epsilon-amino group
282 ins a tethered cluster-binding domain at its carboxy terminus that moves in and out of the active sit
283               Residues 582 to 596 in the DAT carboxy terminus were identified as the primary binding
284 between the 20 kDa amino terminus and 65 kDa carboxy terminus, after proteolytic processing.
285 tional crosstalk between the pore region and carboxy terminus, involved in Ca(2+)-calmodulin-mediated
286 IK (AAP2BR5), from the amino terminus to the carboxy terminus.
287  coding region at C329, Q330, or Y331 in the carboxy terminus.
288 lexed alone with an IQ domain on the channel carboxy terminus.
289 el CLH-3b is reduced by phosphorylation of a carboxy-terminus "activation domain," which disrupts its
290 terozygous frameshift mutation affecting the carboxy-terminus (439fs) of perilipin 1 in two unrelated
291 elices designated "A-R" and an intracellular carboxy-terminus containing two cystathionine-beta-synth
292 rylated (hp) Tau and to E3 ubiquitin ligase, carboxy-terminus of heat shock-70 interacting protein.
293 n binding (Fab) (scFab) format, in which the carboxy-terminus of the light chain is linked to the ami
294 ropose that alteration and elongation of the carboxy-terminus of the protein has a dominant-negative
295 eas deletion of the S. Typhimurium flagellin carboxy-terminus prevented caspase-1 maturation only.
296                       Addition of Q17 at its carboxy-terminus reduces the extent of the main basin to
297 hanism for all domains except for the distal carboxy-terminus.
298 , and two major metabolites of THC, 11-nor-9-carboxy-THC and 11-hydroxy-THC, in active users and part
299                                    The alpha-carboxy-tropone substructure is ideal for this purpose a
300 ng cerebrovascular perfusion with ROX, SE (5-Carboxy-X-Rhodamine, Succinimidyl Ester), a fluorescent

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