-
1
-
-
0018071189
-
Evidence that the transforming gene of avian sarcoma virus encodes a protein kinase associated with a phosphor-protein
-
Levinsor AD, Oppermann H, Levintow L, Varmus HE, Bishop JM: Evidence that the transforming gene of avian sarcoma virus encodes a protein kinase associated with a phosphor-protein. Cell 1978;15:561-572.
-
(1978)
Cell
, vol.15
, pp. 561-572
-
-
Levinsor, A.D.1
Oppermann, H.2
Levintow, L.3
Varmus, H.E.4
Bishop, J.M.5
-
2
-
-
0018580807
-
An activity phosphorylating tyrosine in polyoma T antigen immunoprecipitates
-
Eckhart W, Hutchinson MA, Hunter T: An activity phosphorylating tyrosine in polyoma T antigen immunoprecipitates. Cell 1979;18:925-933.
-
(1979)
Cell
, vol.18
, pp. 925-933
-
-
Eckhart, W.1
Hutchinson, M.A.2
Hunter, T.3
-
4
-
-
13344261467
-
High throughput screening: Searching for higher productivity
-
Fox S, Farr-Jones S, Sopchak L, Boggs A, Comley J: High throughput screening: searching for higher productivity. J Biomol Screen 2004;9:354-358.
-
(2004)
J Biomol Screen
, vol.9
, pp. 354-358
-
-
Fox, S.1
Farr-Jones, S.2
Sopchak, L.3
Boggs, A.4
Comley, J.5
-
5
-
-
0032563807
-
Nuclear export of the stress-activated protein kinase p38 mediated by its substrate MAPKAP kinase-2
-
Ben-Levy R, Hooper S, Wilson R, Paterson HF, Marshall CJ: Nuclear export of the stress-activated protein kinase p38 mediated by its substrate MAPKAP kinase-2. Curr Biol 1998;8:1049-1057.
-
(1998)
Curr Biol
, vol.8
, pp. 1049-1057
-
-
Ben-Levy, R.1
Hooper, S.2
Wilson, R.3
Paterson, H.F.4
Marshall, C.J.5
-
6
-
-
0032526988
-
Leptomycine B-sensitive nuclear export of MAPKAP kinase 2 is regulated by phosphorylation
-
Engel K, Kotlyarov A, Gaestel M: Leptomycine B-sensitive nuclear export of MAPKAP kinase 2 is regulated by phosphorylation. EMBO J 1998;17:3363-3371.
-
(1998)
EMBO J
, vol.17
, pp. 3363-3371
-
-
Engel, K.1
Kotlyarov, A.2
Gaestel, M.3
-
7
-
-
0029993727
-
Active and inactive protein kinases: Structural basis for regulation
-
Johnson LN, Noble MEM, Owen DJ: Active and inactive protein kinases: structural basis for regulation. Cell 1996; 85:149-158.
-
(1996)
Cell
, vol.85
, pp. 149-158
-
-
Johnson, L.N.1
Noble, M.E.M.2
Owen, D.J.3
-
8
-
-
0037013143
-
The conformational plasticity of protein kinases
-
Huse M, Kuriyan J: The conformational plasticity of protein kinases. Cell 2002;109:275-282.
-
(2002)
Cell
, vol.109
, pp. 275-282
-
-
Huse, M.1
Kuriyan, J.2
-
9
-
-
0030766163
-
Crystal structure of the activated insulin receptor tyrosine kinase in complex with peptide substrate and ATP analog
-
Hubbard SR: Crystal structure of the activated insulin receptor tyrosine kinase in complex with peptide substrate and ATP analog. EMBO J 1997; 16:5572-5581.
-
(1997)
EMBO J
, vol.16
, pp. 5572-5581
-
-
Hubbard, S.R.1
-
10
-
-
0034665713
-
Structural mechanism for STI-571 inhibition of Abelson tyrosine kinase
-
Schindler T, Bornmann W, Pellicena P, Miller WT, Clarkson B, Kuriyan J: Structural mechanism for STI-571 inhibition of Abelson tyrosine kinase. Science 2000;289: 1938-1942.
-
(2000)
Science
, vol.289
, pp. 1938-1942
-
-
Schindler, T.1
Bornmann, W.2
Pellicena, P.3
Miller, W.T.4
Clarkson, B.5
Kuriyan, J.6
-
11
-
-
12144289677
-
Mechanism of activation of the RAFERK signalling pathway by oncogenic mutations of BRAF
-
Wan PTC, Garnett MJ, Roe SM, Lee S, Niculescu-Duvaz D, Good VM, et al.: Mechanism of activation of the RAFERK signalling pathway by oncogenic mutations of BRAF. Cell 2004; 116:855-867.
-
(2004)
Cell
, vol.116
, pp. 855-867
-
-
Wan, P.T.C.1
Garnett, M.J.2
Roe, S.M.3
Lee, S.4
Niculescu-Duvaz, D.5
Good, V.M.6
-
14
-
-
2142653053
-
A homogeneous fluorescence polarization assay adaptable for a range of protein serine/threonine and tyrosine kinases
-
Gaudet EA, Huang K-S, Zhang Y, Huang W, Mark D, Sportsman JR: A homogeneous fluorescence polarization assay adaptable for a range of protein serine/threonine and tyrosine kinases. J Biomol Screen 2003;8:164-175.
-
(2003)
J Biomol Screen
, vol.8
, pp. 164-175
-
-
Gaudet, E.A.1
Huang, K.-S.2
Zhang, Y.3
Huang, W.4
Mark, D.5
Sportsman, J.R.6
-
15
-
-
2442583662
-
High-throughput screening with immobilized metal ion affinity-based fluorescence polarization detection, a homogeneous assay for protein kinases
-
Loomans EEMG, van Doornmalen AM, Wat JWY, Zaman GJR: High-throughput screening with immobilized metal ion affinity-based fluorescence polarization detection, a homogeneous assay for protein kinases. Assay Drug Dev Technol 2003; 1:445-453.
-
(2003)
Assay Drug Dev Technol
, vol.1
, pp. 445-453
-
-
Loomans, E.E.M.G.1
van Doornmalen, A.M.2
Wat, J.W.Y.3
Zaman, G.J.R.4
-
17
-
-
24944497371
-
Features of selective kinase inhibitors
-
Knight ZA, Shokat KM: Features of selective kinase inhibitors. Chem Biol 2005; 12:621-637.
-
(2005)
Chem Biol
, vol.12
, pp. 621-637
-
-
Knight, Z.A.1
Shokat, K.M.2
-
18
-
-
0015861774
-
Relationship between the inhibition constant (KI) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
-
Cheng Y, Prusoff WH: Relationship between the inhibition constant (KI) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction. Biochem Pharmacol 1973;22:3099-3108.
-
(1973)
Biochem Pharmacol
, vol.22
, pp. 3099-3108
-
-
Cheng, Y.1
Prusoff, W.H.2
-
21
-
-
18344395134
-
Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site
-
Pargellis C, Tong L, Churchill L, Cirillo PF, Gilmore T, Graham AG, et al.: Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site. Nat Struct Biol 2002;9:268-272.
-
(2002)
Nat Struct Biol
, vol.9
, pp. 268-272
-
-
Pargellis, C.1
Tong, L.2
Churchill, L.3
Cirillo, P.F.4
Gilmore, T.5
Graham, A.G.6
-
22
-
-
27944490693
-
The identification of potent and selective imidazole-based inhibitors of B-Raf kinase
-
Takle AK, Brown MJB, Davies S, Dean DK, Francis G, Gaiba A, et al.: The identification of potent and selective imidazole-based inhibitors of B-Raf kinase. Bioorg Med Chem Lett 2006;16:378-381.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 378-381
-
-
Takle, A.K.1
Brown, M.J.B.2
Davies, S.3
Dean, D.K.4
Francis, G.5
Gaiba, A.6
-
23
-
-
0035171919
-
Kinetics of small molecule inhibitor binding to p38 kinase
-
Thurmond RL, Wadsworth SA, Schafer PH, Zivin RA, Siekierka JJ: Kinetics of small molecule inhibitor binding to p38 kinase. Eur J Biochem 2001;268:5747-5754.
-
(2001)
Eur J Biochem
, vol.268
, pp. 5747-5754
-
-
Thurmond, R.L.1
Wadsworth, S.A.2
Schafer, P.H.3
Zivin, R.A.4
Siekierka, J.J.5
-
24
-
-
0347359115
-
A Biacore biosensor method for detailed kinetic binding analysis of small molecule inhibitors of p38α mitogen-activated protein kinase
-
Casper D, Bukhityarova M, Springman EB: A Biacore biosensor method for detailed kinetic binding analysis of small molecule inhibitors of p38α mitogen-activated protein kinase. Anal Biochem 2004; 325:126-136.
-
(2004)
Anal Biochem
, vol.325
, pp. 126-136
-
-
Casper, D.1
Bukhityarova, M.2
Springman, E.B.3
-
25
-
-
0030924833
-
Pyridinyl imidazole inhibitors of p38 mitogen-activated protein kinase bind in the ATP site
-
Young PR, McLaughlin MM, Kumar S, Kassis S, Doyle ML, McNulty D, et al.: Pyridinyl imidazole inhibitors of p38 mitogen-activated protein kinase bind in the ATP site. J Biol Chem 1997;272:12116-12121.
-
(1997)
J Biol Chem
, vol.272
, pp. 12116-12121
-
-
Young, P.R.1
McLaughlin, M.M.2
Kumar, S.3
Kassis, S.4
Doyle, M.L.5
McNulty, D.6
-
26
-
-
0141768651
-
A high throughput, non-isotopic, competitive binding assay for kinases using Non-Selective Inhibitor Probes (Ed-NSIP™)
-
Vainstein I, Silveria S, Kaul P, Rouhani R, Eglen RM, Wang J: A high throughput, non-isotopic, competitive binding assay for kinases using Non-Selective Inhibitor Probes (Ed-NSIP™). J Biomol Screen 2002;7:507-514.
-
(2002)
J Biomol Screen
, vol.7
, pp. 507-514
-
-
Vainstein, I.1
Silveria, S.2
Kaul, P.3
Rouhani, R.4
Eglen, R.M.5
Wang, J.6
-
27
-
-
0141985986
-
Enzyme fragment complementation: A flexible high throughput screening assay technology
-
Eglen R: Enzyme fragment complementation: a flexible high throughput screening assay technology. Assay Drug Dev Technol 2002;1:97-104.
-
(2002)
Assay Drug Dev Technol
, vol.1
, pp. 97-104
-
-
Eglen, R.1
-
28
-
-
0142026209
-
p38 MAP kinases: Key signalling molecules as therapeutic targets for inflammatory diseases
-
Kumar S, Boehm J, Lee JC: p38 MAP kinases: key signalling molecules as therapeutic targets for inflammatory diseases. Nat Rev Drug Discov 2003;2:717-726.
-
(2003)
Nat Rev Drug Discov
, vol.2
, pp. 717-726
-
-
Kumar, S.1
Boehm, J.2
Lee, J.C.3
-
29
-
-
0030954172
-
A highly specific inhibitor of human p38 MAP kinase binds in the ATP pocket
-
Tong L, Pav S, White DM, Rogers S, Crane KM, Cywin CL, et al.: A highly specific inhibitor of human p38 MAP kinase binds in the ATP pocket. Nat Struct Biol 1997;4:311-316.
-
(1997)
Nat Struct Biol
, vol.4
, pp. 311-316
-
-
Tong, L.1
Pav, S.2
White, D.M.3
Rogers, S.4
Crane, K.M.5
Cywin, C.L.6
-
30
-
-
0032578559
-
The activation state of p38 mitogen-activated protein kinase determines the efficiency of ATP competition for pyridinylimidazole inhibitor binding
-
Frantz B, Klatt T, Pang M, Parsons J, Rolando A, Williams H, et al.: The activation state of p38 mitogen-activated protein kinase determines the efficiency of ATP competition for pyridinylimidazole inhibitor binding. Biochemistry 1998;37:13846-13853.
-
(1998)
Biochemistry
, vol.37
, pp. 13846-13853
-
-
Frantz, B.1
Klatt, T.2
Pang, M.3
Parsons, J.4
Rolando, A.5
Williams, H.6
-
31
-
-
17644437502
-
Regulation of stress-induced cytokine production by pyridinylimidazoles; inhibition of CSBP kinase
-
Gallagher T, Seibel GL, Kassis S, Laydon JT, Blumenthal MJ, Lee JC, et al.: Regulation of stress-induced cytokine production by pyridinylimidazoles; inhibition of CSBP kinase. Bioorg Med Chem 1997;5:49-64.
-
(1997)
Bioorg Med Chem
, vol.5
, pp. 49-64
-
-
Gallagher, T.1
Seibel, G.L.2
Kassis, S.3
Laydon, J.T.4
Blumenthal, M.J.5
Lee, J.C.6
-
32
-
-
0037019275
-
Pyrazole urea-based inhibitors of p38 MAP kinase: From lead compound to clinical candidate
-
Regan J, Breitfelder S, Cirillo P, Gilmore T, Graham AG, Hickey E, et al.: Pyrazole urea-based inhibitors of p38 MAP kinase: from lead compound to clinical candidate. J Med Chem 2002;45:2994-3008.
-
(2002)
J Med Chem
, vol.45
, pp. 2994-3008
-
-
Regan, J.1
Breitfelder, S.2
Cirillo, P.3
Gilmore, T.4
Graham, A.G.5
Hickey, E.6
-
33
-
-
19744365702
-
A small molecule-kinase interaction map for clinical kinase inhibitors
-
Fabian MA, Biggs WH 3rd, Treiber DK, Atteridge CE, Azimioara MD, Benedetti MG, et al.: A small molecule-kinase interaction map for clinical kinase inhibitors. Nat Biotechnol 2005;23:329-336.
-
(2005)
Nat Biotechnol
, vol.23
, pp. 329-336
-
-
Fabian, M.A.1
Biggs III, W.H.2
Treiber, D.K.3
Atteridge, C.E.4
Azimioara, M.D.5
Benedetti, M.G.6
-
34
-
-
0033003760
-
A simple statistical parameter for use in evaluation and validation of high-throughput screening assays
-
Zhang JH, Chung TDY, Oldenburg KR: A simple statistical parameter for use in evaluation and validation of high-throughput screening assays. J Biomol Screen 1999; 4:67-73.
-
(1999)
J Biomol Screen
, vol.4
, pp. 67-73
-
-
Zhang, J.H.1
Chung, T.D.Y.2
Oldenburg, K.R.3
-
35
-
-
4644223114
-
Discovery and characterization of a substrate selective p38α inhibitor
-
Davidson W, Frego L, Peet GW, Kroe RR, Labadia ME, Lukas SM, et al.: Discovery and characterization of a substrate selective p38α inhibitor. Biochemistry 2004; 43:11658-11671.
-
(2004)
Biochemistry
, vol.43
, pp. 11658-11671
-
-
Davidson, W.1
Frego, L.2
Peet, G.W.3
Kroe, R.R.4
Labadia, M.E.5
Lukas, S.M.6
-
36
-
-
18844370417
-
G protein-coupled receptor assays: To measure affinity or efficacy that is the question
-
William C, Sewing A: G protein-coupled receptor assays: to measure affinity or efficacy that is the question. Comb Chem HTS 2005;8:285-292.
-
(2005)
Comb Chem HTS
, vol.8
, pp. 285-292
-
-
William, C.1
Sewing, A.2
-
37
-
-
20544445672
-
High-throughput screening using β-lactamase reporter-gene technology for identification of low-molecular-weight antagonists of the human gonadotropin releasing hormone receptor
-
Oosterom, J, van Doornmalen EJP, Lobregt S, Blomenröhr M, Zaman GJR: High-throughput screening using β-lactamase reporter-gene technology for identification of low-molecular-weight antagonists of the human gonadotropin releasing hormone receptor. Assay Drug Dev Technol 2005;3:143-154.
-
(2005)
Assay Drug Dev Technol
, vol.3
, pp. 143-154
-
-
Oosterom, J.1
van Doornmalen, E.J.P.2
Lobregt, S.3
Blomenröhr, M.4
Zaman, G.J.R.5
-
38
-
-
0035991330
-
Comparison of assay technologies for a tyrosine kinase assay generates different results in high throughput screening
-
Sills MA, Weiss D, Pham Q, Schweitzer R, Wu X, Wu JJ: Comparison of assay technologies for a tyrosine kinase assay generates different results in high throughput screening. J Biomol Screen 2002;7:191-199.
-
(2002)
J Biomol Screen
, vol.7
, pp. 191-199
-
-
Sills, M.A.1
Weiss, D.2
Pham, Q.3
Schweitzer, R.4
Wu, X.5
Wu, J.J.6
|