1 Phosphoamino acid analyses indicated that all three prot
2 d be due to tyrosine phosphorylation of NR2,
phosphoamino acid analyses of NR2 were performed.
3 Phosphopeptide mapping and
phosphoamino acid analyses of Plk labeled in vivo and ph
4 Phosphoamino acid analyses of the ROMK phosphoproteins r
5 Phosphopeptide mapping and
phosphoamino acid analyses showed that CTP synthetase 1
6 licing the gel into approximately 60 slices,
phosphoamino acid analyses were carried out on the prote
7 Phosphoamino acid analysis also revealed that Stat5a/b p
8 EC) using 32P metabolic labeling followed by
phosphoamino acid analysis and by phosphotyrosine specif
9 osphopeptides were purified and subjected to
phosphoamino acid analysis and Edman degradation.
10 Phosphoamino acid analysis and manual Edman degradation
11 tibodies and immunoprecipitation followed by
phosphoamino acid analysis and phosphopeptide mapping sh
12 Phosphoamino acid analysis and phosphopeptide mapping st
13 Phosphopeptide mapping,
phosphoamino acid analysis and radiosequence analysis of
14 Phosphoamino acid analysis and Western blot analysis wit
15 Phosphoamino acid analysis by thin-layer chromatography
16 hosphorylation with several PKC isozymes and
phosphoamino acid analysis confirmed that TEF-1 is a pot
17 ing with anti-phosphotyrosine antibodies and
phosphoamino acid analysis demonstrated that the Gq/G11
18 Phosphoamino acid analysis demonstrates that the pp75/85
19 Phosphoamino acid analysis establishes that insulin rece
20 onally, orthophosphate labeling coupled with
phosphoamino acid analysis identified Phb1 to be serine
21 Phosphoamino acid analysis identified serine as the majo
22 hosphorylated in response to insulin whereas
phosphoamino acid analysis indicated that this phosphory
23 h phosphorylation/dephosphorylation of mOAT;
phosphoamino acid analysis indicated this phosphorylatio
24 paxillin phosphorylation by two-dimensional
phosphoamino acid analysis indicates that paxillin is 99
25 Phosphoamino acid analysis indicates that this phosphory
26 Phosphoamino acid analysis of 32P-labeled native NETs fr
27 Two-dimensional
phosphoamino acid analysis of ACF immunopurified from he
28 Phosphoamino acid analysis of eNOS from bovine aortic en
29 Phosphoamino acid analysis of I was performed using eith
30 sphatase PTP1B to dephosphorylate it, and by
phosphoamino acid analysis of IkappaBalpha immunoprecipi
31 Two-dimensional
phosphoamino acid analysis of in vitro phosphorylated PL
32 Phosphorylation and
phosphoamino acid analysis of insulin proreceptors revea
33 Phosphoamino acid analysis of Kv2.1 expressed in transfe
34 Phosphoamino acid analysis of metabolically labeled LRP
35 Phosphoamino acid analysis of NS5A from the 1a isolate i
36 In vivo 32P-labeling and subsequent
phosphoamino acid analysis of p66shc indicated that both
37 Phosphoamino acid analysis of phosphorylated PI3K alpha
38 Phosphoamino acid analysis of pp65a and pp65b detected p
39 Phosphoamino acid analysis of radiolabeled Ets2 revealed
40 Phosphoamino acid analysis of Rin cell 7B2 indicated the
41 Phosphoamino acid analysis of Stat 5 showed S179D PRL to
42 A two-dimensional
phosphoamino acid analysis of Stk1 revealed strong phosp
43 Phosphoamino acid analysis of the cotransport protein in
44 Phosphoamino acid analysis of the glutathione S-transfer
45 nly a single phosphopeptide; two-dimensional
phosphoamino acid analysis of the phosphopeptide reveale
46 Phosphoamino acid analysis of the phosphorylated recepto
47 Phosphoamino acid analysis of the radiolabeled NSF indic
48 Phosphoamino acid analysis of the tryptic product establ
49 parated phosphopeptides, taken together with
phosphoamino acid analysis of the tryptic product, revea
50 Phosphoamino acid analysis of UBF immunoprecipitated fro
51 Phosphoamino acid analysis revealed phosphorylation of c
52 Phosphoamino acid analysis revealed phosphorylation on s
53 Phosphoamino acid analysis revealed phosphoserine to be
54 Phosphoamino acid analysis revealed that all phosphoryla
55 Phosphoamino acid analysis revealed that basal and stimu
56 Phosphoamino acid analysis revealed that both the 30 KDa
57 Interestingly,
phosphoamino acid analysis revealed that Fsk-treated cel
58 Phosphoamino acid analysis revealed that growth factor-i
59 Phosphoamino acid analysis revealed that ICAM-3 from act
60 The
phosphoamino acid analysis revealed that myosin III is a
61 Phosphatase digestion and
phosphoamino acid analysis revealed that p65e3B1 is a ph
62 Phosphoamino acid analysis revealed that phosphorylation
63 In the present study,
phosphoamino acid analysis revealed that the increased p
64 Phosphoamino acid analysis revealed that the phosphoryla
65 Phosphoamino acid analysis revealed that the tyrosine an
66 Subsequent
phosphoamino acid analysis revealed that UDG1A is phosph
67 l phosphopeptide mapping in combination with
phosphoamino acid analysis reveals that JNK does not pho
68 ed phosphorylation of the beta3 subunit, and
phosphoamino acid analysis reveals that only threonine r
69 Phosphoamino acid analysis showed 32P labeling of serine
70 Under all these conditions,
phosphoamino acid analysis showed that NHE3V was phospho
71 Phosphoamino acid analysis showed that serine and tyrosi
72 Phosphoamino acid analysis showed that serine is the onl
73 Phosphoamino acid analysis showed the presence of phosph
74 Phosphoamino acid analysis shows that TRAP is histidine-
75 bined with the results from mutant subunits,
phosphoamino acid analysis suggests that the enzyme is s
76 desensitize the PDGFRbeta, we first found by
phosphoamino acid analysis that cells expressing GRK2 co
77 rylation of exogenous substrate was shown by
phosphoamino acid analysis to occur not only on serine a
78 By using
phosphoamino acid analysis we found that Ser residues of
79 Using metabolic labeling,
phosphoamino acid analysis, and mutagenesis studies, we
80 or phosphorylation sites, using mutagenesis,
phosphoamino acid analysis, and site-specific anti-Stat5
81 Analysis of charge shifts,
phosphoamino acid analysis, and stoichiometry was consis
82 Site-directed mutagenesis,
phosphoamino acid analysis, and use of synthetic peptide
83 transfected COS-1 cells, in conjunction with
phosphoamino acid analysis, Edman degradation, and phosp
84 (3)PO(4), modified manual Edman degradation,
phosphoamino acid analysis, endoproteinase digestion, an
85 In vivo and in situ phosphorylation,
phosphoamino acid analysis, immunoprecipitation, 2-dimen
86 Using
phosphoamino acid analysis, JAK3 and STAT5 were determin
87 tides from the in vitro maps were eluted and
phosphoamino acid analysis, manual sequencing, strong ca
88 ing, high performance liquid chromatography,
phosphoamino acid analysis, matrix-assisted laser desorp
89 As determined by
phosphoamino acid analysis, the phosphorylation of Gsalp
90 By
phosphoamino acid analysis, Thr233 was determined to be
91 ction in HUVEC of a tail-less E-selectin and
phosphoamino acid analysis, we documented phosphorylatio
92 ted mutagenesis, phosphopeptide mapping, and
phosphoamino acid analysis, we identified that >90% of i
93 Using (32)Pi labeling and
phosphoamino acid analysis, we show that yeast MIPS is a
94 olysis, two-dimensional peptide mapping, and
phosphoamino acid analysis.
95 Ser(176), is the IL4-regulated site based on
phosphoamino acid analysis.
96 entified using site-directed mutagenesis and
phosphoamino acid analysis.
97 tibodies, labelling with [gamma-32P]ATP, and
phosphoamino acid analysis.
98 om calmodulin phosphorylated in vitro and by
phosphoamino acid analysis.
99 Phosphoamino-acid analysis and site-directed mutagenesis
100 Phosphoamino-acid analysis and Western blot analysis by
101 sitol 3-kinase (wortmannin) as determined by
phosphoamino acid and DNA binding analysis, thus suggest
102 Phosphoamino acid and phosphopeptide mapping analyses of
103 y laser mass spectrometry, identification of
phosphoamino acid,
and phosphorylation of mutant forms o
104 sphatase inhibitors is readily recognized by
phosphoamino acid antibodies.
105 very gel slice, with two major peaks of this
phosphoamino acid around M(r)'s of 59 and 36 kilodaltons
106 ng of fusions of cyan fluorescent protein, a
phosphoamino acid binding domain (14-3-3tau), a consensu
107 resis sample buffer and samples analyzed for
phosphoamino acids by Western blotting.
108 Although studies with NPE-caged
phosphoamino acids have provided valuable information, t
109 The context of these
phosphoamino acids implicates glycogen synthase kinase 3
110 O-Phosphoserine (Sep), the most abundant
phosphoamino acid in the eukaryotic phosphoproteome, is
111 rhodopsin were identified using proteolytic,
phosphoamino acid,
mass spectrometric, and peptide seque
112 This
phosphoamino acid residue was efficiently phosphorylated
113 nsional gel analysis, Western analysis using
phosphoamino acid-
specific antiserum, and in vivo 32P la
114 This
phosphoamino acid was phosphorylated in vitro by protein
115 Previous Pin1 inhibitors contained
phosphoamino acids,
which are metabolically unstable and