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1 thiols from either dithiothreitol or reduced ribonuclease A.
2 es was demonstrated with a tryptic digest of ribonuclease A.
3 process analogous to that used by the enzyme ribonuclease A.
4 -PLC) has been suggested to resemble that of ribonuclease A.
5 to the one observed earlier for valine 63 in ribonuclease A.
6 H dependence of the folding and unfolding of ribonuclease A.
7 e found in the active site of the prototype, ribonuclease A.
8 ical exchange is demonstrated on the protein ribonuclease A.
9 1 snRNP that was sensitive to treatment with ribonuclease A.
10 er similar to that of the catalytic triad of ribonuclease A.
11 mpounds were indeed selective for displacing ribonuclease A.
12 mo-trypsinogen A, it had no interaction with ribonuclease A.
13 reduced non-specific displacement by BSA and ribonuclease A.
14 lid heavy-chain antibody (VHH) that binds to ribonuclease A.
15 d model protein fragment, the C peptide from ribonuclease A.
16 e extensively studied case of reduced bovine ribonuclease A (13,689 Da), only Asn67 deamidation has b
17 Refolding intermediates of bovine pancreatic ribonuclease A, a model system for this study, are block
18 were conducted using the model protein pairs ribonuclease A/alpha-chymotrypsinogen A and cytochrome C
19 nts were conducted with a mixture containing ribonuclease A and alpha-chymo-trypsinogen A which exhib
20 two protein pairs, alpha-chymotrypsinogen A/ribonuclease A and cytochrome c/lysozyme, using batch an
21 the nonspecific binding of bovine pancreatic ribonuclease A and Escherichia coli lac repressor to dou
22 euterium exchange data from disulfide-intact ribonuclease A and from cytochrome c are discussed to ex
23 is of the [M + 12H]12+ to [M + 5H]5+ ions of ribonuclease A and its N-linked glycosylated analogue, r
24 nt reductive unfolding rates and pathways of ribonuclease A and its structural homologue onconase can
25 d lower than the maximum values exhibited by ribonuclease A and ONC, respectively, and there is littl
26 the cleavage reaction is similar to that of ribonuclease A and the arrangement of the active sites i
27 zing acetyl-PEO-biotin labeled peptides from ribonuclease A and the ICAT-labeled proteome of Deinococ
28 of the cspA mRNA was used as a substrate for ribonucleases A and T1, the addition of CspA significant
29 omplexes are treated with elevated levels of ribonucleases A and T1, the nascent transcript can be cl
30 cytochrome c, alpha-chymotrypsinogen A, and ribonuclease A) and six acidic proteins (myoglobin, deox
31 tryptic peptide from unfolded and deamidated ribonuclease A, and a tryptic peptide from calmodulin de
33 e I region of poly-l-lysine, concanavalin A, ribonuclease A, and lysozyme show cross-peaks between th
34 or four of the proteins (ubiquitin, eglin c, ribonuclease A, and lysozyme) appear to converge to a co
35 h three reduced secreted proteins (lysozyme, ribonuclease A, and riboflavin binding protein (RfBP)).
36 sozyme, bovine pancreatic trypsin inhibitor, ribonuclease A, and T4 lysozyme) were examined carefully
37 or L in the model protein, bovine pancreatic ribonuclease A, and through analysis of temperature fact
39 REACH lattice dynamics model of crystalline ribonuclease A are also in satisfactory agreement with t
40 peratures of both hen egg white lysozyme and ribonuclease A are sensitive to the PA of the PIL as muc
41 apparatus with both stationary phases using ribonuclease A as a model protein and applied potentials
44 dative folding pathways of bovine pancreatic ribonuclease A at pH 8.0 and 25 degrees C involve a pre-
45 ulation study of water hydrating the protein Ribonuclease A, at a series of temperatures in cluster,
46 validated under column conditions, with the ribonuclease A being displaced and the alpha-chymotrypsi
47 ll-characterized proteins (bovine pancreatic ribonuclease A, bovine pancreatic trypsin inhibitor, and
48 netics of disulfide-intact bovine pancreatic ribonuclease A by fluorescence-detected stopped-flow tec
49 tudies of the glycation of the model protein ribonuclease A by glucose and ribose leading to the form
50 sinogen A, while no binding was observed for ribonuclease A, confirming that protein-displacer bindin
54 Myoglobin, lysozyme, beta-lactoglobulin, ribonuclease A, E-cadherin 5, and concanavalin A were co
55 models of ribonuclease cleavage and for the ribonuclease A enzyme itself, based on our studies of th
56 s subdomains on the rate-determining step in ribonuclease A folding and on the physical structure-for
59 (Uvf) of disulfide-intact bovine pancreatic ribonuclease A has been monitored by circular dichroism
63 on model proteins, such as cytochrome c and ribonuclease A, identified a limited number of peptide c
64 e show that rabbit antibodies to MG-modified ribonuclease A identify proteins modified by the Maillar
65 able-pressure NMR data for bovine pancreatic ribonuclease A in 2H2O at pH 2.0 and 295 K yielded the f
66 egation line observed for both ovalbumin and ribonuclease A in ammonium sulfate, interpreted theoreti
67 pon unfolding of model proteins lysozyme and ribonuclease A, in solutions containing varying cosolute
68 state of disulfide-intact bovine pancreatic ribonuclease A is a heterogeneous mixture of unfolded sp
69 state of disulfide-intact bovine pancreatic ribonuclease A is a heterogeneous mixture of unfolded sp
71 a K(o)T indicates that the denatured form of ribonuclease A is more compressible than the native form
73 atalysis of RNA 2'-O-transphosphorylation by ribonuclease A is proposed to involve electrostatic stab
74 escence unfolding phase of bovine pancreatic ribonuclease A is studied by stopped-flow kinetics and s
75 olding of disulfide-intact bovine pancreatic ribonuclease A is used as an example to illustrate the k
76 studies of the homologous protein guinea pig ribonuclease A; it is proposed here that Lys113 in the l
77 so, it was also found that ligand binding to ribonuclease A led to changes in alpha, suggesting a bur
79 threitol (DTT)-dependent reduction of native ribonuclease A, microbial ribonuclease, and pancreatic t
80 olomyoglobin, as well as native lysozyme and ribonuclease A, nevertheless, TFE stabilizes native apom
81 The published data on kinetic effects with ribonuclease A of substituting thiophosphate groups for
82 est (by microinjection with ricin A chain or ribonuclease A) of the inducer or either of the fusion p
83 eight cysteine residues of reduced unfolded ribonuclease A or to site-specific locations using appro
87 nsions of a denatured protein, fully reduced ribonuclease A (r-RNase A), have been measured using syn
88 haracteristics of reduced and carboxamidated ribonuclease A (RCAM RNase) were determined for transfer
90 n a disulfide-bond-containing loop region of ribonuclease A results in the localized modulation of pr
92 oxidative folding of both bovine pancreatic ribonuclease A (RNase A) and a 58-72 fragment thereof fr
94 uantitative noncovalent interactions between ribonuclease A (RNase A) and cytidylic acid ligands (2'-
95 The interactions between bovine pancreatic ribonuclease A (RNase A) and its RNA substrate extend be
96 The interaction between bovine pancreatic ribonuclease A (RNase A) and its RNA substrate extends b
98 o the oxidative folding of bovine pancreatic ribonuclease A (RNase A) and show that des[40-95] and de
100 miting millisecond motions in wild-type (WT) Ribonuclease A (RNase A) are modulated by histidine 48.
104 es have shown that divalent anion binding to ribonuclease A (RNase A) contributes to RNase A folding
108 three-disulfide mutant of bovine pancreatic ribonuclease A (RNase A) from the fully reduced unfolded
110 During the regeneration of bovine pancreatic ribonuclease A (RNase A) from the reduced to the native
112 idative folding pathway of bovine pancreatic ribonuclease A (RNase A) has been examined at various pH
116 vated by two different schemes to immobilize ribonuclease A (RNase A) in either a preferred orientati
117 P93A, P114A, and P117A) of bovine pancreatic ribonuclease A (RNase A) in which each mutant has one of
120 The active-site cleft of bovine pancreatic ribonuclease A (RNase A) is lined with cationic residues
121 three-disulfide mutants of bovine pancreatic ribonuclease A (RNase A) missing the 65-72 disulfide bon
122 oxidative regeneration of bovine pancreatic ribonuclease A (RNase A) proceeds through des-[40-95] RN
123 Select members of the bovine pancreatic ribonuclease A (RNase A) superfamily are potent cytotoxi
125 in human angiogenin (hANG), a member of the ribonuclease A (RNase A) superfamily known to be involve
126 pread and functionally varied members of the ribonuclease A (RNase A) superfamily provide an excellen
127 an amphibian member of the bovine pancreatic ribonuclease A (RNase A) superfamily, is in phase III cl
128 neurotoxin (EDN), a protein belonging to the ribonuclease A (RNase A) superfamily, which has recently
129 f the polypeptide chain of bovine pancreatic ribonuclease A (RNase A) that are critical for stabilizi
132 ar dynamics simulations of bovine pancreatic ribonuclease A (RNase A) up to its melting temperature (
134 3'-phosphate (pTppAp) with bovine pancreatic ribonuclease A (RNase A) was characterized by calorimetr
135 n the dissociation of enzymatic product from ribonuclease A (RNase A) was investigated by creation of
138 s (space group P3(2)21) of bovine pancreatic ribonuclease A (RNase A) were prepared at a pH of 5.5 in
139 setrade mark, a homolog of bovine pancreatic ribonuclease A (RNase A) with high conformational stabil
141 rvested from wild-type mice generated CML on ribonuclease A (RNase A), a model protein, by a pathway
142 was compared with that of the parent enzyme ribonuclease A (RNase A), and a model was devised to ass
143 We now demonstrate that a model protein, ribonuclease A (RNase A), exposed to free L-serine and H
144 its structural homologue, bovine pancreatic ribonuclease A (RNase A), has been isolated and characte
145 enin (Ang), a homologue of bovine pancreatic ribonuclease A (RNase A), is a potent inducer of blood v
147 enin (ANG), a homologue of bovine pancreatic ribonuclease A (RNase A), promotes the growth of new blo
149 used to analyze salt effects on catalysis by ribonuclease A (RNase A), which is a cationic enzyme tha
159 nant HsQSOX1 is highly active toward reduced ribonuclease A (RNase) and dithiothreitol but shows a >1
160 e (LiP) was examined using bovine pancreatic ribonuclease A (RNase) as a polymeric lignin model subst
161 g an Amadori intermediate in the reaction of ribonuclease A (RNase) with ribose for rapid studies of
162 ffusivity of the positively charged protein, ribonuclease A (RNase), in solutions of dextrans of vari
164 e pairings in two unfolded reduced proteins: ribonuclease A (RNase, four disulfide bonds and 105 disu
165 rotein model mixture comprised of ubiquitin, ribonuclease A (RNaseA), cyclophilin A (CypA), and bovin
166 r model protein systems including ubiquitin, ribonuclease A (RNaseA), cyclophilin A (CypA), and bovin
167 kinetics, as demonstrated by the binding of ribonuclease A (RNaseA, 13.7 kDa) with cytidine nucleoti
170 sodium chloride for six proteins (ovalbumin, ribonuclease A, soybean trypsin inhibitor, lysozyme, and
172 eless as effective as 3-MHD in cross-linking ribonuclease A suggested that protein lysine condensatio
173 ibility of the region to ribonuclease V1 and ribonuclease A suggesting the geometry formed by the rep
174 tations in Angiogenin (ANG), a member of the Ribonuclease A superfamily (also known as RNase 5) are k
175 onuclease cluster, a group of eight distinct ribonuclease A superfamily genes that are more closely r
176 bonucleases (EARs), which are members of the ribonuclease A superfamily with known antipathogen activ
177 tations in angiogenin (ANG), a member of the ribonuclease A superfamily, are associated with amyotrop
178 Onconase (P-30 protein), an enzyme in the ribonuclease A superfamily, exerts cytostatic, cytotoxic
179 n dielectric constant; (4) the pKa shifts in ribonuclease A that result from phosphate binding are re
180 helix formation in the isolated C-peptide in ribonuclease A, there is growing evidence that a signifi
185 ermally induced unfolding of lysozyme and of ribonuclease A was determined by means of differential s
186 somerase IIalpha interaction is sensitive to ribonuclease A, we explored whether the RHA-topoisomeras
188 glyceraldehyde-3-phosphate dehydrogenase and ribonuclease A when the reaction was supplemented with B
190 w-folding and fast-folding forms of unfolded ribonuclease A, which led to the understanding that prol
192 lectivity, displacing essentially all of the ribonuclease A while displacing minimal alpha-chymotryps
193 etreatment of glyceraldehyde-3-phosphate and ribonuclease A with BOH increased their rate of degradat
194 n-6 with barium chloride, and the binding of ribonuclease A with cytidine 2'-monophosphate within rea
196 Three tyrosine-to-phenylalanine mutants of ribonuclease A (Y25F, Y92F, and Y97F) are investigated f
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