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1 denotes arginine or lysine and X denotes non-acidic amino acids).
2 ominantly heptameric pore with a basic or an acidic amino acid.
3 mutagenesis approach that targets conserved acidic amino acids.
4 r k(cat)/K(m) when substrates contain nearby acidic amino acids.
5 ovel NLS identified in this study is rich in acidic amino acids.
6 ested that the active site contains reactive acidic amino acids.
7 y N terminal to the acidic box, a stretch of acidic amino acids.
8 E. coli sequence by inspection of conserved acidic amino acids.
9 intra- and intermolecular repulsions between acidic amino acids.
10 re it is coordinated by both MHC and peptide acidic amino acids.
11 divalent metal actually interacts with these acidic amino acids.
12 c surface with a pK value similar to that of acidic amino acids.
13 halophilic archaeal proteins are enriched in acidic amino acids.
14 may be due to strong binding of water by the acidic amino acids.
15 whether their activity is enhanced by nearby acidic amino acids.
16 a novel high-affinity system for neutral and acidic amino acids.
17 latory phosphorylation sites were changed to acidic amino acids.
18 ectus strains contained large proportions of acidic amino acids (13 to 27%) and that >34% of the amin
20 tes the matrix protein is relatively high in acidic amino acids, a feature consistent with its solubi
21 cytosolic domain of gB contains a cluster of acidic amino acids, a motif that plays a pivotal role in
22 monstrated that the deletion of a cluster of acidic amino acids (aa 44 to 59) prevented wild-type tra
24 ficiency studies reveal that two clusters of acidic amino acids (ACs) within the PC6B-cd contain diff
29 replacing the lysines that flank VQDLL with acidic amino acids also reduced inhibitory activity, sug
31 th appreciable activities for cleavage after acidic amino acids and a broadened activity for cleavage
33 ch as a BRCA1 C-terminal domain, clusters of acidic amino acids and consensus motifs for post-transla
34 DLL motif, which has a unique arrangement of acidic amino acids and hydrophobic leucines, functions a
35 M for the neutral amino acids and 500 nM for acidic amino acids and were used to analyze samples coll
36 eplaced with alanine, glycine, valine, or an acidic amino acid, and the activities of the mutated pro
37 His-2 zinc fingers, an N-terminal stretch of acidic amino acids, and a C-terminal leucine zipper-like
38 pecific sequence motif, in which one or more acidic amino acids are found at the carboxy end interact
42 -GlcNAcylation sites, several motifs with an acidic amino acid around the sites were identified, whic
44 e exposed to the cytoplasm, we identify four acidic amino acids as putative calcium-binding residues.
46 flavodoxin mutants were studied in which 10 acidic amino acids--Asp62, Asp63, Glu66, Asp69, Asp70, A
47 smaller Pf% was due to protonation of three acidic amino acids (Asp646, Glu648, and Glu651) that are
48 tional activity; mutation of the sites to an acidic amino acid, aspartic acid, stimulates constitutiv
49 cleavage sites are frequently observed when acidic amino acids, aspartic and glutamic acids, are pre
50 critical determinant for this effect was an acidic amino acid at position 13 in the CCR5 N terminus,
52 and full phosphorylation at P2 required the acidic amino acids at A1 or their neutral counterparts.
53 Q386E impaired the ability of ASCT1 to bind acidic amino acids at pH 5.5; however, this was reversed
54 he SMT active center is composed of a set of acidic amino acids at positions 125, 152, 195, and 276,
56 e are caused by differences in the number of acidic amino acids at the C terminus, so each protein is
58 The present study investigated the role of acidic amino acids between P1 and P2 in regulating recep
63 so less active than phosphorylated wt, i.e., acidic amino acids cannot substitute for phospho-Ser-627
64 for the full activation of arrestin and that acidic amino acids (carboxyl and sulfonic) do not mimic
66 that neutralizing or reversing the charge of acidic amino acid clusters stalled translocation in the
67 -terminal region of the heavy chain contains acidic amino acid clusters that are important for cofact
68 in the KRYK (VI) or KYEK (VII) sequences to acidic amino acids create mutants that bind F-actin with
69 a subunit by mutating three highly conserved acidic amino acids, D211V, E212L, and E226L, resulted in
70 C-terminal tail of PKAc within a cluster of acidic amino acids (DDYEEEE), which is a characteristic
71 uch as nucleoside phosphates or oligomers of acidic amino acids disaggregate actin bundles into singl
72 de of the anion conductance activated by the acidic amino acids does not correlate with rates of tran
73 o constructed a mutant in which a cluster of acidic amino acids (EDDDDAE) in the sensor domain is rep
75 binding site, only conversion of Val68 to an acidic amino acid facilitates ternary complex assembly w
77 hift to pAP* was mimicked by substituting an acidic amino acid for either Thr231 or Ser235, but the s
79 removal of covalently associated, inhibitory acidic amino acids from proximity with the Crp4 componen
81 moving the fixed negative charge of a single acidic amino acid (Glu(51)) in the lateral entrance to t
82 groups prompted evaluation of four invariant acidic amino acids (Glu-19, Glu-193, Asp-204, and Glu-29
83 tive site comprises the side-chains of three acidic amino acids (Glu20, Asp55 and Glu65) together wit
84 mains included a high proportion of strongly acidic amino acids (glutamate and aspartate), and these
85 urine, a gamma-aminobutyric acid (GABA)-like acidic amino acid, has previously been shown to be promi
87 ase Sa) (pI=3.5) and a variant in which five acidic amino acids have been changed to lysine (5K) (pI=
88 tagenesis study of this protein, whereby all acidic amino acids have been individually replaced by ot
89 ast to other enzymes in this class, in which acidic amino acids have been shown to be essential for g
90 F from sugars accelerated in the presence of acidic amino acids (i.e. glutamic and aspartic acids).
94 ion as alphaA-wt, whereas the mutant with an acidic amino acid in this position, R116D, showed drasti
95 ized by a cytosolic YXXL downstream of three acidic amino acids in a sequence known as a hemITAM (hem
97 es required for toxin binding, extracellular acidic amino acids in domains I and IV of the type IIa N
98 sis and to also test whether other conserved acidic amino acids in Drosophila Rhodopsin 1 (Rh1) may s
101 , MPZ-1 also interacts with other GPCRs with acidic amino acids in the -3 position of their PDZ bindi
106 tro binding assays, we identified a group of acidic amino acids in the N-terminal leucine zipper dime
107 prin beta subunit has a clear preference for acidic amino acids in the P1 and P1' sites of substrates
108 structural changes caused by substitution of acidic amino acids in the Q(B) binding pocket of the bac
110 factor (FGF) receptors contain a cluster of acidic amino acids in their extracellular domains that i
114 he wild-type lysine with either a neutral or acidic amino acid inhibited E5-induced receptor activati
116 a critical function in import of neutral and acidic amino acids into the tapetum cells for synthesis
117 phorylation of Ser-1106, which is flanked by acidic amino acids, is regulated in vivo by casein kinas
120 region at the COOH-end, and regions rich in acidic amino acids, leads to the hypothesis that the Pra
124 ikely form ionic interactions with conserved acidic amino acids on E7 since a stable pRB/E7 interacti
128 ow a differential effect of mutations to two acidic amino acids potentially involved in cation bindin
130 ts of the study suggested the presence of an acidic amino acid residue at the S(1)'-subsite of calpai
131 sults are consistent with the presence of an acidic amino acid residue at the S(1)'-subsite of calpai
134 tion with earlier studies which implicate an acidic amino acid residue, suggest that a crucial intera
135 ted that segments of ICP0R that were rich in acidic amino acid residues (amino acids 9 to 76 and 233
136 ffective method for profiling and localizing acidic amino acid residues (D/E), amide-containing resid
137 ve identified two homologous creatine kinase acidic amino acid residues (Glu232 and Asp326), and thes
138 ne residues are embedded within a cluster of acidic amino acid residues and account for nearly 90% of
139 n the protonated dimethylamino group and the acidic amino acid residues Asp(50), Glu(85), and Glu(94)
140 , at most contributing equivalently with the acidic amino acid residues clustered around the flavin t
142 ectoenzyme that catalyzes the hydrolysis of acidic amino acid residues from the amino termini of reg
144 SH3 domain-binding surface and a cluster of acidic amino acid residues in Nef, both of which are als
146 )(2+), we individually mutated each of these acidic amino acid residues in topoisomerase IIalpha to e
147 of these studies, we conclude that the four acidic amino acid residues interact with metal ions in t
148 ctions through the neutralization of certain acidic amino acid residues leading to faster overall obs
150 cting programs, TopPred II and MEMSAT, eight acidic amino acid residues located near or within transm
151 alysis of the pKa values of ion-coordinating acidic amino acid residues suggested that the face-speci
153 y neutralized by the substitution of the six acidic amino acid residues with their amide equivalents.
154 omain of Akt and a "pseudoligand" containing acidic amino acid residues, between cyan and yellow muta
155 ion 659-663, which contains five consecutive acidic amino acid residues, by site-directed mutagenesis
157 nopropyl)carbodiimide (EDAC), which modifies acidic amino acid residues, resulted in a time- and conc
158 pha-lactalbumin, which displays a cluster of acidic amino acid residues, showed enhanced adsorption a
163 k output genes (the PAR [rich in proline and acidic amino acid residues] transcription factors dbp, h
164 mutagenesis of VH1-46 Abs demonstrates that acidic amino-acid residues introduced by somatic mutatio
166 a factor (HLF), a member of the proline- and acidic amino acid-rich (PAR) subfamily of bZIP transcrip
167 namely the period genes and the proline- and acidic amino acid-rich basic leucine zipper (PAR-bZip) c
168 A targeting sequence (AYRV) and a second, acidic amino acid-rich region of the gpI cytosolic domai
171 uclear localization signal, and a stretch of acidic amino acids similar to the activation domains of
172 a PB1 sequence that contains three essential acidic amino acids, similar to the active sites of other
174 tidine (basic amino acid) for aspartic acid (acidic amino acid) substitution in the encoded protein d
175 ivo activity of a form of ANTP that contains acidic amino acid substitutions at its CKII target sites
177 onsistent with phosphorylation of S338-S339, acidic amino acid substitutions of these residues partia
179 ivation domain and alteration of most single acidic amino acids, suggesting that a previously postula
180 al catalytic core domain includes a triad of acidic amino acids that bind Mn2+ or Mg2+, the metal cof
181 e(44) in mouse pro-Crp4-(20-92) removes nine acidic amino acids that collectively block the membrane-
182 nal tails, specifically by the last 8 highly acidic amino acids that comprise the binding site for it
184 which is homologous to the highly conserved acidic amino acids that link protonation to activation o
185 codes a protein rich in glycine, serine, and acidic amino acids that shows no significant similarity
186 sess a stretch of 10-15 residues enriched in acidic amino acids, the acidic domain (AD), in the flexi
187 closely with hydroxyapatite, positioning the acidic amino acids to aid in controlling crystal growth.
189 ilies possess a protein domain containing an acidic amino acid triad (DDE or DDD) that catalyzes the
190 a consensus motif for a calcium-coordinated acidic amino acid triad cluster as originally identified
191 d by the Y subunit, that cleaves bonds after acidic amino acids was designated as peptidylglutamyl-pe
193 is of the sequence identity of SS, conserved acidic amino acids were mutagenized to identify the spec
194 ved surface residues, including a cluster of acidic amino acids, were found to be located on a single
196 ctivating cleavages after branched chain and acidic amino acids while inhibiting cleavage of peptidyl
202 nine may be substituted for the aromatic and acidic amino acids without destroying transcriptional ac
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