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1 rturbation of this interface leads to higher phosphorylation activity.
2 modulates glucose metabolism mainly by AMPKa phosphorylation activity.
3 activator alone and engenders dominant mono-phosphorylation activity.
4 phosphorylation is necessary for JIL-1 H3S10 phosphorylation activity.
5 tly marked PC12 cells with sustained protein phosphorylation activity.
6 tly increases RICK/NOD1 association and RICK phosphorylation activity.
7 re, HSV1-tk(A168H) demonstrated no thymidine phosphorylation activity.
8 of activity and also retained some oxidative phosphorylation activity.
9 nces while TSPX represses the cyclin B1-CDK1 phosphorylation activity.
10 family PTKs were required for this tyrosine phosphorylation activity.
11 d M. tuberculosis PknD KD fusions stimulated phosphorylation activity.
12 letely absent from compartments with Ser-473 phosphorylation activity.
13 nnels, and Ca(2+)-independent, involving MLC phosphorylation activity.
14 modeled to accommodate a change in oxidative phosphorylation activity.
15 lation (<5%) but retained near-wild-type H2B phosphorylation activity.
16 finity for aspartate is linked to changes in phosphorylation activity.
17 on, implying diminished glucose transport or phosphorylation activity.
18 ng decreased muscle glucose transport and/or phosphorylation activity.
19 due to a defect in glucose transport and/or phosphorylation activity.
20 lls demonstrated a 20-30% decrease in DNA-PK phosphorylation activity.
21 with another PTK, ZAP70, and stimulates its phosphorylation activity.
22 tion to aspartic or glutamic acids abolished phosphorylation activity.
23 y 2-3-fold weaker protein kinase C substrate phosphorylation activity.
24 by sequentially regulating FAK and paxillin phosphorylation/activity.
25 hearts and was accompanied by increased Akt phosphorylation/activity.
26 autophosphorylation and Myelin Basis Protein phosphorylation activities.
27 otein kinase C (PKC), and constitutive MYPT1 phosphorylation activities.
28 hesis distinct from that regulating the MtrA phosphorylation activities.
29 o blockade of protein kinase Mzeta (PKMzeta) phosphorylation activity, a manipulation that reverses h
30 , inhibited selectively this surface protein phosphorylation activity and blocked the stabilization o
31 Hexokinase-Like1 (HKL1) lacks glucose (Glc) phosphorylation activity and has been shown to act as a
32 erms of both autophosphorylation and histone phosphorylation activity and induces the same in vivo ph
33 ted both phosphoenolpyruvate-dependent sugar phosphorylation activity and sugar phosphate-dependent s
34 l effects were associated with preserved Akt phosphorylation/activity and attenuation of DOX-induced
35 metastatic melanoma cells by inhibiting CREB phosphorylation, activity, and binding to the MUC18 prom
36 n-dependent decrease in constitutive ERK-1/2 phosphorylation, activity, and nuclear localization that
37 ation-dependent loss of constitutive Erk-1/2 phosphorylation, activity, and nuclear localization.
38 ns of PKC consensus sites reduced Pcyt2alpha phosphorylation, activity, and phosphatidylethanolamine
39 imer's disease is related to reduced glucose phosphorylation activity as well as diminished glucose t
40 40% reduction in mitochondrial oxidative and phosphorylation activity, as assessed by in vivo 13C/31P
42 y differences in other areas associated with phosphorylation activity between wild-type and mutant Ka
43 , which retains autophosphorylation and ResD phosphorylation activities but is defective in ResD deph
44 9 to Met or Leu resulted in mutants that had phosphorylation activity but displayed greatly decreased
45 e established that mutation in A368S reduces phosphorylation activity by 40%; A41E mutation completel
46 rted an important role of increased tyrosine phosphorylation activity by Src in the modulation of hyp
47 3 sustained altered glycolytic and oxidative phosphorylation activities characteristic of cancer cell
48 bular networks in vitro showed that tyrosine phosphorylation activity colocalized specifically within
49 out the NH2-terminal domain is without H3S10 phosphorylation activity despite the fact that it locali
50 g human thymidine kinase exhibited thymidine phosphorylation activity equivalent to approximately 5%
51 skeletal function, ERK2 signaling (e.g. ERK2 phosphorylation/activity, ERK2-mediated Elk-1/ER alpha p
52 Ysr39tk, which exhibits specificity and high phosphorylation activity for acycloguanosine derivatives
55 mics, test tube kinetic assays of downstream phosphorylation activity, high-throughput bacteriophage-
58 ciated reductions in mitochondrial oxidative phosphorylation activity in skeletal muscle as a predisp
59 gression and decreased whole-brain oxidative phosphorylation activity in the honey bee (Apis mellifer
60 CheY in the reverse direction by quantifying phosphorylation activity in the presence and absence of
61 rmore, we show that the continuous oxidative phosphorylation activity is important for viral propagat
62 l receptor for IgE, and colocalized tyrosine phosphorylation activity, Lyn kinase and other proteins
63 hromatin structure and where catalytic H3S10 phosphorylation activity mediated by the first kinase do
64 Using the streptavidin capture assay the phosphorylation activities of recombinant IKK-1 and -2 w
66 in a conserved lysine residue important for phosphorylation activity of kinases (K118E) failed to co
67 chemical depalmitoylation reduces the casein phosphorylation activity of the palmitoylated, but not p
68 We have applied our method to measuring the phosphorylation activity of the Wee1 and Myt1 kinases.
71 lt in stimulation of mitochondrial oxidative phosphorylation activity, restore physiologic mitochondr
72 eal a delicate balance of ubiquitination and phosphorylation activities that alter the gene regulator
73 ssociated MAPK operates through constitutive phosphorylation activity to regulate microtubule functio
74 in vitro and also by comparing the relative phosphorylation activity toward a panel of peptide subst
81 ll VZVTK mutants tested retained significant phosphorylation activity with dThd as substrate, apart f
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