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1 s to show how Coulombic interactions between ionizable 2,3-diaminopropionic acid (Dap) side chains ca
2 ent triplex stability uniquely observed with ionizable 4-amino substituent on proline enables one to
4 be generated through a single hydrophobic-to-ionizable amino acid replacement that generates a partia
7 proposed that involve distinct and conserved ionizable amino acid residues, one a glutamate, and the
8 als of mean force (PMF) between all possible ionizable amino acid side chain pairs in various protona
10 acid residues 18-25 of Ost4p were mutated to ionizable amino acids and defects were observed in the i
15 bout local and nonlocal interactions between ionizable and nonionizable residues in the growing famil
17 gram revealed the importance of two negative ionizable and one positive charge feature for both aryl-
21 inated diamond surfaces contain few, if any, ionizable carbon-oxygen functionalities (e.g., carboxyli
25 ters and the subsequent performance of those ionizable cationic lipids in in vivo studies would be be
26 hobic regions, H-bond acceptor sites, and an ionizable (cationic) feature as key determinants for lig
27 We prepared formulations of lipoplexes with ionizable, cationic or zwitterionic lipids, externally c
29 les typically contain an abundance of easily ionizable chemical groups, there is a gap in understandi
30 ng approach for characterizing the uptake of ionizable chemicals from water and sediments into aquati
34 response factor values indicated that highly ionizable components of aquatic DOM mixtures are more hy
45 rin (LMWH) as a model for highly soluble and ionizable drugs and a 3 x 3 full factorial design to pre
46 ndem approach can likely be extended to more ionizable drugs and may eventually be utilized in view o
47 e preferred method for optimizing loading of ionizable drugs in liposomes as measured by drug-to-lipi
51 hin-films can be directly immersed in highly ionizable environments and used as flow-through heating
52 ating element can prevent CNT degradation in ionizable environments such as high-salinity brines.
53 lternate enzyme pathways that utilize either ionizable enzyme residues (self-rescue) and/or exogenous
55 dels indicate the importance of two negative ionizable features, one hydrophobic feature, and one hal
57 252C, D275C, and D279C enzymes depend on the ionizable form of the same group as in wild-type enzyme
58 date, potent FXR agonists share a negatively ionizable function that might compromise their pharmacok
60 chains extend along the surface and the two ionizable functionalities (a phosphate and an amine) sit
61 with full shielding of the analytes from the ionizable functionalities and excellent chromatographic
66 0.5) obtained for tPA revealed an additional ionizable group (pKa, 6.0-6.2) affecting the reaction.
67 on of Lys-443 identified this residue as the ionizable group at pKa approximately 8.1 apparent in the
69 The rational regulation of the pK(a) of an ionizable group in a synthetic device could be achieved
72 arby base, we conclude that L-proline is the ionizable group in the ES complex and that amino acids a
75 teady-state kinetic studies indicate that an ionizable group on the enzyme with a pK of 6.4 must be u
77 e that Glu-19 comes in close contact with an ionizable group that has a pK(a) of approximately 6.7 wh
78 We also demonstrated that PikDH2 has a key ionizable group with a pK(a) of 7.0 and can be irreversi
79 on of ACL with [gamma-(33)P]-ATP revealed an ionizable group with a pK(a) value of ~7.5, which must b
80 se kinetic data are consistent with a single ionizable group with a pKa near 9.5 promoting the Lys 73
81 tified at least one catalytically important, ionizable group with an apparent pKa of 7.5, which corre
82 his class of sigma(1) ligands are a positive ionizable group, a H-bond acceptor group, two hydrophobi
83 ith a neutral residue does not eliminate the ionizable group, although the observed pK(a) is 1 or 2 p
84 structures, where at least one metal ion, an ionizable group, and the conformation of the phosphate b
85 e pH versus k(cat)(DHS) profile revealed two ionizable groups (pK(a1) = 7.9 +/- 0.1, and pK(a2) = 9.3
87 n be applied to systems of a large number of ionizable groups and the computational cost scales linea
88 s with implicit sites produced pKas of all 9 ionizable groups and the results agree qualitatively wit
90 lectric constants reported by these internal ionizable groups are high because they reflect conformat
92 ble groups are shifted; many of the internal ionizable groups are probably neutral at physiological p
94 hat the pK(a) values of most of the internal ionizable groups are shifted; many of the internal ioniz
96 om accumulation of mutations that introduced ionizable groups at internal positions, followed by evol
99 the flavin couples suggests the presence of ionizable groups coupled to the flavin redox/protonation
100 enzymes and other proteins that use internal ionizable groups for functional purposes could have evol
102 lectrostatics method are not useful to treat ionizable groups in cases where pK(a) values are governe
103 Estimation of the pKa values of all the ionizable groups in GLP-1 suggest it is the protonation/
104 rness the free energy of folding to position ionizable groups in highly specific environments that st
105 mists are interested in the pK values of the ionizable groups in proteins and how these pK values dep
107 iew what has been learned about pK values of ionizable groups in proteins from experimental studies a
112 and have been shown to be important whenever ionizable groups interact with hydrophobic environments.
113 agnetic probes based on the incorporation of ionizable groups into the structure of persistent triary
116 ble to those of naturally occurring internal ionizable groups involved in catalysis and biological H(
118 icate that protonation of ligand and protein ionizable groups is coupled to the complex formation bet
119 tionally intensive, solvent accessibility of ionizable groups is displayed, from which the user can i
121 y decreasing the pH (protonation of multiple ionizable groups is required) or by addition of volume e
122 the ability of proteins to tolerate internal ionizable groups might be a property common to many prot
123 ictated in part by the protonation states of ionizable groups on PLP and the reacting substrates and
124 nated surfaces as surrogates for charged and ionizable groups on silica-mineralizing organic matrices
125 w a detailed model of protonation states for ionizable groups on the cofactor, substrates, and nearby
126 e explored several strategies of introducing ionizable groups on the lipopeptide, as well as the syst
127 is124 are embedded in a network of polar and ionizable groups on the surface of staphylococcal nuclea
128 oatings with a high surface concentration of ionizable groups onto the surface of the paper fibers in
129 fication of the BODIPY fluorophore core with ionizable groups or substitution at the boron center.
130 in-label was found to be unaffected by other ionizable groups present in side chains of unstructured
131 rstanding how to control the charge state of ionizable groups represents a powerful yet straightforwa
133 of the marked shifts in the pK(a) values of ionizable groups that can occur in an enzyme active site
134 al structural adaptations are not needed for ionizable groups to exist stably in the hydrophobic inte
135 CD), a beta-cyclodextrin derivative carrying ionizable groups to render propofol amenable to iontopho
136 ergy landscape of proteins by using internal ionizable groups to stabilize partially unfolded states.
137 o examine the unusual properties of internal ionizable groups we measured the pK(a) of glutamic acid
138 se and of 10 variants with internal polar or ionizable groups were performed to investigate systemati
139 stent with the pK(a) of the highest of three ionizable groups which modulate formation of the histidi
141 ed, depending on the ionization state of two ionizable groups with apparent pK values of 6.2 and 8.3.
142 how that nucleotidyl transfer depends on two ionizable groups with pK(a) values of 7.0 or 8.2 and 10.
143 ce of the fast phase kinetic data shows that ionizable groups with pKa values near 6.8 and 9 modulate
144 PS inhibition both consisted of two negative ionizable groups, a positive charge feature and an endoc
145 approximately 6.6 and has unmasked two other ionizable groups, besides the ligand replacing Met 80, t
146 an-field approach to quantify the density of ionizable groups, GAG concentration, and cross-linking d
148 work affects the electrostatic properties of ionizable groups, the tautomeric state and the pK(a) val
157 loyed to fine tune the hydrophobicity of the ionizable hydrophobic block, which led to a desired tran
158 bond acceptor, hydrogen bond donor, positive ionizable, hydrophobic) of these femtomolar-acting compo
163 e high-pH form occurs by deprotonation of an ionizable ligand bound to Mn3+, implicated to be a water
164 A new series of alkenyl amino alcohol (AAA) ionizable lipid nanoparticles (LNPs) capable of deliveri
166 Special (lipid) delivery: The role of the ionizable lipid pK(a) in the in vivo delivery of siRNA b
167 ere, we developed a combinatorial library of ionizable lipid-like materials to identify mRNA delivery
172 ll-established sets of both nonionizable and ionizable low molecular weight probe solutes to demonstr
176 the regiochemistry of benzannulation and the ionizable moieties afford (iv) tunable deep-red to NIR e
182 icle, we report a novel method to screen for ionizable molecules with high HSA binding affinity based
183 ay play a critical role in the permeation of ionizable molecules, including pharmaceuticals and drug-
184 d with an "interior" layer consisting of the ionizable monomer, 2-acrylamido-2-methyl-1-propanesulfon
185 ive holographic sensors were fabricated from ionizable monomers incorporated into thin, polymeric, hy
186 made of sequence-controlled hydrophobic and ionizable monomers on the inner surface of solid-state n
187 rporated into "smart" hydrogel films bearing ionizable monomers, were used to monitor the pH change r
188 marked differences in the removal of polar, ionizable MPs at different operational pHs during activa
190 tic structural optimization of uncharged but ionizable N-substituted 2-hydroxyiminoacetamido alkylami
192 PR probe (IMTSL-PTE) containing a reversibly ionizable nitroxide tag attached to the lipids' polar he
193 ubstrates (e.g. colchicine or paclitaxel) or ionizable non-Pgp substrates (e.g. cisplatin or carbopla
195 used to generate end-functionalized acetoxy ionizable oligomers for the structural deciphering of di
200 ter knowledge of biotransformation rates for ionizable organic compounds (IOCs) in fish is required t
201 minants of emerging concern are polar and/or ionizable organic compounds, whose removal from engineer
202 ffects in studying accumulation of polar and ionizable organic contaminants and their metabolites.
204 also capable of the detection of most major ionizable organic molecules in typical aquatic mixtures,
205 conclude that pH-dependent removal of polar, ionizable organic MPs in activated sludge systems is les
209 umnavigation expedition, and analyzed for 14 ionizable PFASs, including perfluorooctanoate (PFOA), pe
210 iated mechanism of MDR was not found for non-ionizable Pgp substrates (e.g. colchicine or paclitaxel)
211 dels to predict the pH-dependent toxicity of ionizable pharmaceuticals in embryos of the zebrafish Da
213 dine, fluoxetine, and gemfibrozil, and other ionizable PPCPs, to confirm the utility of both models.
215 tudies provide insight into the roles of the ionizable propionate side chains in substrate discrimina
217 yrins, which are neutral macrocycles without ionizable protons, also showed interesting coordination
219 ts, although specific contacts through gamma-ionizable residue side chains are not essential for esta
220 eic acid complexes there exists at least one ionizable residue that changes its charge state upon lig
222 d species and apparent pK(a) values for each ionizable residue, we show that C3d-CR2(SCR1-2) recognit
224 he pH midpoints (pH(m)) of the amides in the ionizable residues (Asp or Glu) and, consequently, the s
225 sample side-chain protonation states of five ionizable residues (Asp, Glu, His, Tyr, Lys) on-the-fly
228 thways for proton transfer between conserved ionizable residues along the center of the membrane doma
229 ococcal nuclease (SNase) mutants with buried ionizable residues and probed their dynamics in differen
235 irus family reveals evolutionarily conserved ionizable residues at all regions along the chain and su
238 (CpHMD(MSlambdaD)) to investigate the buried ionizable residues comprehensively and to elucidate thei
241 region, where approximately one out of five ionizable residues experiences substantial pK change reg
242 ade with this method concerning the roles of ionizable residues for allosteric communication can then
243 Although membrane proteins often rely on ionizable residues for structure and function, their ion
244 elix interface among the TM domains involved ionizable residues from all three chains, the TM arginin
245 t remains open up to pH 9.0 by replacing key ionizable residues from the N and C termini of KcsA with
247 nges upon ligand binding for a total of 5899 ionizable residues in 20 protein-protein, 20 protein-sma
249 inding is appreciable: on average, 6% of all ionizable residues in protein-small molecule complexes,
250 mine required for catalysis and the roles of ionizable residues in the active site in amine oxidation
251 There are a number of conserved hydrophilic, ionizable residues in the active site, all of which must
252 us propose that the overall configuration of ionizable residues in the channel that may orient water
253 exogenous buffer and assuming no additional ionizable residues in the PT pathway, indicates the like
254 has been what the protonation states of the ionizable residues in the substrate-binding active-site
255 s separation arises from the distribution of ionizable residues of MscS and suggests a specific, yet
256 otein design in elucidating the influence of ionizable residues on a particular redox system, an impo
257 ansport intermediary from the active site to ionizable residues on the rim of the active site, reveal
258 approach that monitors the pKa variations of ionizable residues over the course of molecular dynamics
264 ally relevant pH range of 4-8, the number of ionizable residues that experience substantial pK change
268 philic active site of the B-isozyme with two ionizable residues, C280 and D281, replacing the neutral
269 three BR acids, D85 in a central cluster of ionizable residues, D96, nearer the intracellular, and E
270 e element is coupled to proton uptake by two ionizable residues, H196 and E203, located at the protei
271 rization of the chromophore is controlled by ionizable residues, primarily the Schiff base and Asp97.
272 lying the VMMS method to a heptapeptide of 3 ionizable residues, we calculated the pKas of those resi
273 l microenvironment on the proton affinity of ionizable residues, we have engineered individual lysine
276 (1) containing a dansyl group in the proton-ionizable side arm has been employed in selective sensin
277 table conformations) and mutations involving ionizable side chains (which could have affected proton-
278 t or slightly higher for proteins containing ionizable side chains deeply buried in the core and expe
281 0.6 unit for proteins containing few buried ionizable side chains to 1.0 unit or slightly higher for
282 utagenic screen of all amino acids harboring ionizable side chains within this domain to investigate
283 to estimate the protonation state of native ionizable side chains, that anion-selective-type sequenc
286 nuclease variants I92E and I92K, in which an ionizable side-chain is placed in the hydrophobic core o
287 ible, replacing buried, non-hydrogen bonded, ionizable side-chains with non-polar side-chains is an e
289 ependent segment with the highest density of ionizable sites in the disordered ensembles of fragments
290 to the detection of particulates composed of ionizable species (organic or inorganic) in gaseous envi
292 ting that complex formation stabilizes their ionizable states, whereas the histidines are predicted t
293 he most potent of which mimic the acidic and ionizable structure of the enzyme's natural substrate, a
295 rporate into phospholipid bilayers, with the ionizable sulfonamide exposed to the aqueous interface a
298 e vicinity of the retinal Schiff base is not ionizable, the yield of 9-cis species at low pH shows a
299 pped-flow methods to probe the nature of the ionizable "trigger" group for this conformational change