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 Phosphoamino acid analysis and phosphopeptide mapping re
12 tibodies and immunoprecipitation followed by
phosphoamino acid analysis and phosphopeptide mapping sh
13 Phosphoamino acid analysis and phosphopeptide mapping st
14 Phosphopeptide mapping,
phosphoamino acid analysis and radiosequence analysis of
15 Phosphoamino acid analysis and Western blot analysis wit
16 Phosphoamino acid analysis by thin-layer chromatography
17 hosphorylation with several PKC isozymes and
phosphoamino acid analysis confirmed that TEF-1 is a pot
18 Phosphoamino acid analysis coupled with phosphopeptide m
19 ing with anti-phosphotyrosine antibodies and
phosphoamino acid analysis demonstrated that the Gq/G11
20 Phosphoamino acid analysis demonstrates that the pp75/85
21 Phosphoamino acid analysis establishes that insulin rece
22 onally, orthophosphate labeling coupled with
phosphoamino acid analysis identified Phb1 to be serine
23 Phosphoamino acid analysis identified serine as the majo
24 hosphorylated in response to insulin whereas
phosphoamino acid analysis indicated that this phosphory
25 h phosphorylation/dephosphorylation of mOAT;
phosphoamino acid analysis indicated this phosphorylatio
26 paxillin phosphorylation by two-dimensional
phosphoamino acid analysis indicates that paxillin is 99
27 Phosphoamino acid analysis indicates that this phosphory
28 Phosphoamino acid analysis of 32P-labeled native NETs fr
29 Two-dimensional
phosphoamino acid analysis of ACF immunopurified from he
30 Phosphoamino acid analysis of eNOS from bovine aortic en
31 Phosphoamino acid analysis of I was performed using eith
32 sphatase PTP1B to dephosphorylate it, and by
phosphoamino acid analysis of IkappaBalpha immunoprecipi
33 Two-dimensional
phosphoamino acid analysis of in vitro phosphorylated PL
34 Phosphorylation and
phosphoamino acid analysis of insulin proreceptors revea
35 Phosphoamino acid analysis of Kv2.1 expressed in transfe
36 Phosphoamino acid analysis of metabolically labeled LRP
37 Phosphoamino acid analysis of NS5A from the 1a isolate i
38 In vivo 32P-labeling and subsequent
phosphoamino acid analysis of p66shc indicated that both
39 Phosphoamino acid analysis of phosphorylated PI3K alpha
40 Phosphoamino acid analysis of pp65a and pp65b detected p
41 Phosphoamino acid analysis of radiolabeled Ets2 revealed
42 Phosphoamino acid analysis of Rin cell 7B2 indicated the
43 Phosphoamino acid analysis of Stat 5 showed S179D PRL to
44 A two-dimensional
phosphoamino acid analysis of Stk1 revealed strong phosp
45 Phosphoamino acid analysis of the cotransport protein in
46 Phosphoamino acid analysis of the glutathione S-transfer
47 nly a single phosphopeptide; two-dimensional
phosphoamino acid analysis of the phosphopeptide reveale
48 Phosphoamino acid analysis of the phosphorylated recepto
49 Phosphoamino acid analysis of the radiolabeled NSF indic
50 Phosphoamino acid analysis of the tryptic product establ
51 parated phosphopeptides, taken together with
phosphoamino acid analysis of the tryptic product, revea
52 Phosphoamino acid analysis of UBF immunoprecipitated fro
53 Phosphoamino acid analysis revealed concurrent serine ph
54 Phosphoamino acid analysis revealed phosphorylation of c
55 Phosphoamino acid analysis revealed phosphorylation on s
56 Phosphoamino acid analysis revealed phosphoserine to be
57 Phosphoamino acid analysis revealed that all phosphoryla
58 Phosphoamino acid analysis revealed that basal and stimu
59 Phosphoamino acid analysis revealed that both the 30 KDa
60 Interestingly,
phosphoamino acid analysis revealed that Fsk-treated cel
61 Phosphoamino acid analysis revealed that growth factor-i
62 Phosphoamino acid analysis revealed that ICAM-3 from act
63 The
phosphoamino acid analysis revealed that myosin III is a
64 Phosphatase digestion and
phosphoamino acid analysis revealed that p65e3B1 is a ph
65 Phosphoamino acid analysis revealed that phosphorylation
66 In the present study,
phosphoamino acid analysis revealed that the increased p
67 Phosphoamino acid analysis revealed that the phosphoryla
68 Phosphoamino acid analysis revealed that the tyrosine an
69 Subsequent
phosphoamino acid analysis revealed that UDG1A is phosph
70 l phosphopeptide mapping in combination with
phosphoamino acid analysis reveals that JNK does not pho
71 ed phosphorylation of the beta3 subunit, and
phosphoamino acid analysis reveals that only threonine r
72 Phosphoamino acid analysis showed 32P labeling of serine
73 Under all these conditions,
phosphoamino acid analysis showed that NHE3V was phospho
74 Phosphoamino acid analysis showed that serine and tyrosi
75 Phosphoamino acid analysis showed that serine is the onl
76 Phosphoamino acid analysis showed the presence of phosph
77 Phosphoamino acid analysis shows that TRAP is histidine-
78 bined with the results from mutant subunits,
phosphoamino acid analysis suggests that the enzyme is s
79 desensitize the PDGFRbeta, we first found by
phosphoamino acid analysis that cells expressing GRK2 co
80 rylation of exogenous substrate was shown by
phosphoamino acid analysis to occur not only on serine a
81 By using
phosphoamino acid analysis we found that Ser residues of
82 Using metabolic labeling,
phosphoamino acid analysis, and mutagenesis studies, we
83 or phosphorylation sites, using mutagenesis,
phosphoamino acid analysis, and site-specific anti-Stat5
84 Analysis of charge shifts,
phosphoamino acid analysis, and stoichiometry was consis
85 Site-directed mutagenesis,
phosphoamino acid analysis, and use of synthetic peptide
86 transfected COS-1 cells, in conjunction with
phosphoamino acid analysis, Edman degradation, and phosp
87 (3)PO(4), modified manual Edman degradation,
phosphoamino acid analysis, endoproteinase digestion, an
88 In vivo and in situ phosphorylation,
phosphoamino acid analysis, immunoprecipitation, 2-dimen
89 Using
phosphoamino acid analysis, JAK3 and STAT5 were determin
90 tides from the in vitro maps were eluted and
phosphoamino acid analysis, manual sequencing, strong ca
91 ing, high performance liquid chromatography,
phosphoamino acid analysis, matrix-assisted laser desorp
92 As determined by
phosphoamino acid analysis, the phosphorylation of Gsalp
93 By
phosphoamino acid analysis, Thr233 was determined to be
94 ction in HUVEC of a tail-less E-selectin and
phosphoamino acid analysis, we documented phosphorylatio
95 ted mutagenesis, phosphopeptide mapping, and
phosphoamino acid analysis, we identified that >90% of i
96 Using (32)Pi labeling and
phosphoamino acid analysis, we show that yeast MIPS is a
97 olysis, two-dimensional peptide mapping, and
phosphoamino acid analysis.
98 Ser(176), is the IL4-regulated site based on
phosphoamino acid analysis.
99 entified using site-directed mutagenesis and
phosphoamino acid analysis.
100 tibodies, labelling with [gamma-32P]ATP, and
phosphoamino acid analysis.
101 om calmodulin phosphorylated in vitro and by
phosphoamino acid analysis.
102 Phosphoamino-acid analysis and site-directed mutagenesis
103 Phosphoamino-acid analysis and Western blot analysis by
104 sitol 3-kinase (wortmannin) as determined by
phosphoamino acid and DNA binding analysis, thus suggest
105 Phosphoamino acid and phosphopeptide mapping analyses of
106 y laser mass spectrometry, identification of
phosphoamino acid,
and phosphorylation of mutant forms o
107 sphatase inhibitors is readily recognized by
phosphoamino acid antibodies.
108 very gel slice, with two major peaks of this
phosphoamino acid around M(r)'s of 59 and 36 kilodaltons
109 ng of fusions of cyan fluorescent protein, a
phosphoamino acid binding domain (14-3-3tau), a consensu
110 ring precludes recognition of pTyr and other
phosphoamino acids by these mAbs.
111 resis sample buffer and samples analyzed for
phosphoamino acids by Western blotting.
112 Although studies with NPE-caged
phosphoamino acids have provided valuable information, t
113 The context of these
phosphoamino acids implicates glycogen synthase kinase 3
114 O-Phosphoserine (Sep), the most abundant
phosphoamino acid in the eukaryotic phosphoproteome, is
115 challenge, allowing direct incorporation of
phosphoamino acids into proteins during translation in r
116 rhodopsin were identified using proteolytic,
phosphoamino acid,
mass spectrometric, and peptide seque
117 rate homogeneous proteins with site-specific
phosphoamino acids or with functional mimics that are re
118 This
phosphoamino acid residue was efficiently phosphorylated
119 SAB1 physically interacts with ABI5 at
phosphoamino acid Ser-145, and reduces the phosphorylati
120 nsional gel analysis, Western analysis using
phosphoamino acid-
specific antiserum, and in vivo 32P la
121 This
phosphoamino acid was phosphorylated in vitro by protein
122 Previous Pin1 inhibitors contained
phosphoamino acids,
which are metabolically unstable and