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1 anslation initiation factor eIF2 (eukaryotic initiation factor 2).
2 es by phosphorylating eukaryotic translation initiation factor 2.
3 the alpha subunit of eukaryotic translation initiation factor 2.
4 orylation of the alpha subunit of eukaryotic initiation factor 2.
5 starved cells by phosphorylating translation initiation factor 2.
6 nding site overlaps with the binding site of initiation factor 2.
7 inding domain of the prokaryotic translation initiation factor 2.
8 phorylating the alpha-subunit of translation initiation factor 2.
9 r amino acids by phosphorylating translation initiation factor 2.
10 orylation of the alpha-subunit of eukaryotic initiation factor 2.
11 erine 51 on the alpha subunit of translation initiation factor 2.
12 n of PKR and the alpha subunit of eukaryotic initiation factor 2.
13 orylation of the alpha-subunit of eukaryotic initiation factor 2.
14 sphorylating the alpha subunit of eukaryotic initiation factor-2.
15 quitin-conjugating enzyme (15%); translation-initiation factor 2 (6%); and GTP-binding protein, Rab38
19 ic heme-regulated inhibitor (HRI)-eukaryotic initiation factor 2 alpha (eIF2 alpha) kinase is activat
20 tional control by the eukaryotic translation initiation factor 2 alpha (eIF2alpha) bidirectionally re
21 bitor kinase (HRI), a eukaryotic translation initiation factor 2 alpha (eIF2alpha) kinase, plays crit
22 llular stress by deactivating the eukaryotic initiation factor 2 alpha (eIF2alpha) or other signal tr
23 PKR's pro-apoptotic role through eukaryotic initiation factor 2 alpha (eIF2alpha) phosphorylation is
24 ating protein translation through eukaryotic initiation factor 2 alpha (eIF2alpha) phosphorylation.
25 hosphorylation of the eukaryotic translation initiation factor 2 alpha (eIF2alpha), an important comp
28 capsid-induced phosphorylation of eukaryotic initiation factor 2 alpha and with capsid-mediated inhib
29 (phosphorylation) of eukaryotic translation initiation factor 2 alpha kinase 3 (EIF2AK3, also called
30 cientists discovered mutations in eukaryotic initiation factor 2 alpha kinase 4 (EIF2AK4) that cause
31 elic mutations in the eukaryotic translation initiation factor 2 alpha kinase 4 gene (EIF2AK4) are de
32 polysomes likewise depends on the eukaryotic initiation factor 2 alpha kinase 4, which associates wit
33 ment protein C1qB and eukaryotic translation initiation factor 2 alpha kinase 4-an orchestrator of th
34 nd phosphorylates the eukaryotic translation initiation factor 2 alpha subunit (cIF-2 alpha) to inhib
35 ication of S. mansoni eukaryotic translation initiation factor 2 alpha subunit (eIF2 alpha), through
36 R, we observed a reduced level of eukaryotic initiation factor 2 alpha subunit (eIF2alpha) phosphoryl
37 ct characterized by deficiency of eukaryotic initiation factor 2 alpha subunit phosphorylation, delay
38 ation (phosphorylated eukaryotic translation initiation factor 2 alpha), and cell death [terminal deo
40 that UV light-induced eukaryotic translation initiation factor 2 alpha-subunit phosphorylation transl
41 n site, Ser-51 in the eukaryotic translation initiation factor 2 alpha-subunit, is replaced with a no
42 aspase-12, and phosphorylation of eukaryotic initiation factor-2 alpha in a human dopaminergic neuron
43 (PKR), which then phosphorylates translation initiation factor 2-alpha (eIF-2alpha), and inhibits tra
44 protein synthesis by inactivating eukaryotic initiation factor 2-alpha (eIF2-alpha), to examine the m
46 s demonstrated phosphorylation of eukaryotic initiation factor 2-alpha (eIF2alpha), a 'collapsed' pol
47 dependent on the presence of the eukaryotic initiation factor 2-alpha homology region, mapping to th
48 , small molecule inhibitor of the eukaryotic initiation factor 2-alpha kinase 3 (EIF2AK3) or PERK, on
49 ation of eIF2alpha (eukaryotic translational initiation factor 2-alpha) and ensuing activation of p38
50 orylation of the alpha subunit of eukaryotic initiation factor 2 and NF-kappaB activity at 72 h posti
51 epressible 2), phosphorylation of eukaryotic initiation factor 2, and increased synthesis of activati
54 at phosphorylation of eukaryotic translation initiation factor 2 at Ser-51 on the alpha subunit was n
56 orylation of the alpha subunit of eukaryotic initiation factor 2 causes translating mRNAs to accumula
57 ns, OmpA and OmpB, we identified translation initiation factor 2, cell division protein FtsZ, and cys
58 complex (30SIC(Cy3)) containing Cy3-labeled initiation factor 2 complexed with GTP leads to rapid de
59 nase)-eIF2alpha (alpha subunit of eukaryotic initiation factor 2)-dependent pathway by SubAB-mediated
60 the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2 alpha), the primary physiolog
61 the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2) and total shutoff of protein
65 hosphorylate the alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha) and inhibit translation
66 the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2alpha) and the induction of ap
67 alpha-subunit of the eukaryotic translation initiation factor 2 (eIF-2alpha) and to apoptotic cell d
68 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha) by activated PKR, and,
69 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha) is a well-characterized
70 ated increase in alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha) phosphorylation and ini
72 R and the alpha subunit of protein synthesis initiation factor 2 (eIF-2alpha) was elevated severalfol
73 the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2alpha) was enhanced approximat
74 the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2alpha), a process that prevent
75 e (PERK) and the alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha), as well as induce robu
76 rate of PKR, the alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha), was equally phosphoryl
82 orylation of the alpha subunit of eukaryotic initiation factor-2 (eIF-2) is a well characterized mech
85 orylation of the alpha subunit of eukaryotic initiation factor-2 (eIF-2alpha) and inhibition of prote
89 the translation initiation factor eukaryotic initiation factor 2 (eIF2) and thereby inhibits protein
92 e to phosphorylation of the alpha-subunit of initiation factor 2 (eIF2) by its specific kinase, GCN2,
94 During translation initiation the eukaryotic initiation factor 2 (eIF2) forms a ternary complex (TC)
95 hange factor that converts protein synthesis initiation factor 2 (eIF2) from a GDP-bound form to the
96 rotein kinases that phosphorylate eukaryotic initiation factor 2 (eIF2) in coordinating stress gene r
97 tRNA(Met) binding to eukaryotic translation initiation factor 2 (eIF2) in response to eIF2 phosphory
106 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2) is fundamental to the process
111 se R (PKR), which inactivates the eukaryotic initiation factor 2 (eIF2) translation initiation factor
112 er RNA induces phosphorylation of eukaryotic initiation factor 2 (eIF2) via the GC nonderepressing 2
113 that can regulate the activity of eukaryotic initiation factor 2 (eIF2), a critical translation initi
114 Activated GCN2 phosphorylates eukaryotic initiation factor 2 (eIF2), altering gene-specific trans
116 al complexes on the IRES requires eukaryotic initiation factor 2 (eIF2), eIF3, eIF4A, and the central
117 rly initiation complex containing eukaryotic initiation factor 2 (eIF2), GTP, and methionine-charged
118 he translation initiation complex eukaryotic initiation factor 2 (eIF2), have a profound impact on is
120 specific ternary complex between eukaryotic initiation factor 2 (eIF2), the initiator methionyl-tRNA
121 osphorylates the alpha subunit of eukaryotic initiation factor 2 (eIF2), thus rendering eIF2 inactive
122 Recruitment of the eukaryotic translation initiation factor 2 (eIF2)-GTP-Met-tRNAiMet ternary comp
123 ly GTPase, has been implicated in eukaryotic initiation factor 2 (eIF2)-mediated translational contro
128 1A stimulates 40S-binding of the eukaryotic initiation factor 2 (eIF2)/GTP/Met-tRNA(iMet) ternary co
129 s regulated by phosphorylation of eukaryotic initiation factor 2 (eIF2-P) that causes decreased globa
130 activate Gcn2p phosphorylation of eukaryotic initiation factor-2 (eIF2) and the general amino acid co
132 ular stresses, phosphorylation of eukaryotic initiation factor-2 (eIF2) elicits gene expression desig
133 in kinases that phosphorylate the eukaryotic initiation factor-2 (eIF2) function in translational con
135 ntal stresses, phosphorylation of eukaryotic initiation factor-2 (eIF2) rapidly reduces protein synth
137 sphorylation of the alpha-subunit eukaryotic initiation factor-2 (eIF2), and its attendant regulation
140 ation of the alpha subunit of the eukaryotic initiation factor 2 (eIF2alpha) and inhibits global prot
141 orylates the alpha-subunit of the eukaryotic initiation factor 2 (eIF2alpha) and inhibits translation
142 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) and the consequent shuto
143 hosphorylate the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) are activated in stresse
145 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) by the endoplasmic retic
146 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) by the interferon-induce
148 tion of the alpha subunit of the translation initiation factor 2 (eIF2alpha) in an AR-dependent manne
149 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) in MEFs in an IFN-depend
150 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) in response to different
152 lation through phosphorylation of eukaryotic initiation factor 2 (eIF2alpha) is essential to preserve
153 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) is known to be an import
154 nitiation factor alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) is known to occur in res
156 tivation of the alpha subunit of translation initiation factor 2 (eIF2alpha) kinase GCN2 and conseque
157 fically phosphorylate eukaryotic translation initiation factor 2 (eIF2alpha) on Ser51 to regulate glo
158 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) on serine 51 integrates
159 iver, including alpha subunit of translation initiation factor 2 (eIF2alpha) phosphorylation, activat
160 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) protein via phosphorylat
161 rylation of the alpha-subunit of translation initiation factor 2 (eIF2alpha) represses translation an
162 rylation of the alpha-subunit of translation initiation factor 2 (eIF2alpha) represses translation in
163 es phosphorylation of eukaryotic translation initiation factor 2 (eIF2alpha) resulting in inhibition
165 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) to activate the integrat
166 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) translation initiation f
167 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha), attenuating translation
168 osphorylates the alpha-subunit of eukaryotic initiation factor 2 (eIF2alpha), inhibiting the function
169 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha), is an important protect
170 -subunit of wild-type eukaryotic translation initiation factor 2 (eIF2alpha), one of the known substr
171 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha), resulting in decreased
172 the alpha-subunit of eukaryotic translation initiation factor 2 (eIF2alpha), resulting in inhibition
173 the alpha-subunit of eukaryotic translation initiation factor 2 (eIF2alpha), resulting in the inhibi
174 ation of the alpha subunit of the eukaryotic initiation factor 2 (eIF2alpha), the cellular substrate
175 osphorylate the alpha subunit of translation initiation factor 2 (eIF2alpha), thus attenuating mRNA t
189 ated alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha-P), a regulator of genera
190 the alpha-subunit of eukaryotic translation initiation factor-2 (eIF2alpha) leading to inhibition of
191 e the beta subunit of eukaryotic translation initiation factor 2 (eIF2beta) and the N-terminal domain
192 eukaryotic translation initiation factor 5B/initiation factor 2 (eIF5B/IF2) impair yeast cell growth
194 ed" translation despite inhibited eukaryotic initiation factor 2-guanosine triphosphate-initiator met
195 ed kinase of the alpha subunit of eukaryotic initiation factor 2 (HRI) is activated in rabbit reticul
196 ationships among the components of bacterial initiation factor 2 (IF-2) and eukaryotic IF-2 (eIF-2)/e
199 S ribosomes in the presence of mitochondrial initiation factor 2 (IF2(mt)), [(35)S]fMet-tRNA, and eit
201 lation factors in prokaryotes and eukaryotes-initiation factor 2 (IF2) and eukaryotic initiation fact
202 The initiation of protein synthesis uses initiation factor 2 (IF2) in prokaryotes and a related p
203 ecycling factor (RRF) activity or increasing initiation factor 2 (IF2) levels enhanced initiation wit
205 ukaryotic initiation and elongation factors, initiation factor 2 (IF2), eukaryotic initiation factor
208 sence of the full-length form of Translation Initiation Factor 2 (IF2-1) or deficiency in helicase ac
209 cule tracking, the timing of initiator tRNA, initiation factor 2 (IF2; encoded by infB) and 50S subun
210 ent increased phosphorylation of translation initiation factor 2, IkappaBalpha, and JNK, indicating i
211 nase, and its downstream effector eukaryotic initiation factor 2 in human leukemia (HL60) and ovarian
213 n of PKR and the alpha subunit of eukaryotic initiation factor 2, indicating that K1L and C7L functio
214 the eIF-2alpha (alpha subunit of eukaryotic initiation factor 2) kinase PERK to transiently arrest p
215 The ZPR1 domain consists of an elongation initiation factor 2-like zinc finger and a double-strand
216 ifm1 mutants, lacking the mitochondrial initiation factor 2 (mIF2), are unable to respire, indic
217 in kinase R, which phosphorylates eukaryotic initiation factor 2, nor oligoadenylate synthetase, whic
218 orylation of the alpha subunit of eukaryotic initiation factor 2 on serine 51 was not detectably incr
219 es phosphorylation of eukaryotic translation initiation factor 2 on the alpha-subunit (eIF2alpha) and
220 f both protein kinase R (PKR) and eukaryotic initiation factor 2 on the alpha-subunit in skeletal mus
222 (AADR) such as phosphorylation of eukaryotic initiation factor 2 (p-eIF2) leading to increased mRNA l
223 orylation of the alpha subunit of eukaryotic initiation factor 2, requiring PKR-like endoplasmic reti
224 dent of source of infection, with eukaryotic initiation factor 2 signaling being the most enriched ca
225 impaired autophosphorylation and eukaryotic initiation factor 2 subunit alpha (eIF2alpha) phosphoryl
227 hosphorylation of the eukaryotic translation initiation factor 2 subunit alpha (EIF2S1 or EIF2A), whi
228 nae, increased phosphorylation of eukaryotic initiation factor 2 subunit alpha (P-eIF2alpha), reduced
230 osphorylates the alpha subunit of eukaryotic initiation factor 2, thereby inhibiting protein synthesi
231 osphorylates the alpha-subunit of eukaryotic initiation factor 2, thereby inhibiting protein synthesi
232 ate group on the alpha subunit of elongation initiation factor 2, thereby reversing the shutoff of pr
233 the alpha subunit of eukaryotic translation initiation factor 2 was defective after virus infection
234 ion of the alpha-subunit of eIF2 (eukaryotic initiation factor 2), which inhibits its guanine nucleot
235 al control via phosphorylation of eukaryotic initiation factor 2, which is implicated in learning and
236 ange factor (GEF) for eukaryotic translation initiation factor 2, which stimulates formation of the e
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