-
1
-
-
0035282334
-
Mammalian MAP kinase signaling cascades
-
Chang, L. and Karin, M. (2001) Mammalian MAP kinase signaling cascades. Nature 410, 37-40
-
(2001)
Nature
, vol.410
, pp. 37-40
-
-
Chang, L.1
Karin, M.2
-
2
-
-
0026799441
-
Affinity-purified c-Jun amino-terminal protein kinase requires serine/ threonine phosphorylation for activity
-
Adler, V., Polotskaya, A., Wagner, F. and Kraft, A. S. (1992) Affinity-purified c-Jun amino-terminal protein kinase requires serine/ threonine phosphorylation for activity. J. Biol. Chem. 267, 17001-17005
-
(1992)
J. Biol. Chem
, vol.267
, pp. 17001-17005
-
-
Adler, V.1
Polotskaya, A.2
Wagner, F.3
Kraft, A.S.4
-
3
-
-
0026004501
-
Phosphorylation of c-Jun mediated by MAP kinases
-
Pulverer, B. J., Kyriakis, J. M., Avruch, J., Nikolakaki, E. and Woodgett, J. R. (1991) Phosphorylation of c-Jun mediated by MAP kinases. Nature 353, 670-674
-
(1991)
Nature
, vol.353
, pp. 670-674
-
-
Pulverer, B.J.1
Kyriakis, J.M.2
Avruch, J.3
Nikolakaki, E.4
Woodgett, J.R.5
-
4
-
-
1542269020
-
Targeting the JNK MAPK cascade for inhibition: Basic science and therapeutic potential
-
Bogoyevitch, M. A., Boehm, I., Oakley, A., Ketterman, A. J. and Barr, R. K. (2004) Targeting the JNK MAPK cascade for inhibition: basic science and therapeutic potential. Biochim. Biophys. Acta 1697, 89-101
-
(2004)
Biochim. Biophys. Acta
, vol.1697
, pp. 89-101
-
-
Bogoyevitch, M.A.1
Boehm, I.2
Oakley, A.3
Ketterman, A.J.4
Barr, R.K.5
-
5
-
-
0033231020
-
From receptors to stress-activated MAP kinases
-
Ichijo, H. (1999) From receptors to stress-activated MAP kinases. Oncogene 18, 6087-6093
-
(1999)
Oncogene
, vol.18
, pp. 6087-6093
-
-
Ichijo, H.1
-
6
-
-
0034644522
-
Signal transduction by the JNK group of MAP kinases
-
Davis, R. J. (2000) Signal transduction by the JNK group of MAP kinases. Cell 103, 239-252
-
(2000)
Cell
, vol.103
, pp. 239-252
-
-
Davis, R.J.1
-
7
-
-
21344474327
-
From JNK to pay dirt: Jun kinases, their biochemistry, physiology and clinical importance
-
Karin, M. and Gallagher, E. (2005) From JNK to pay dirt: Jun kinases, their biochemistry, physiology and clinical importance. IUBMB Life 57, 283-295
-
(2005)
IUBMB Life
, vol.57
, pp. 283-295
-
-
Karin, M.1
Gallagher, E.2
-
8
-
-
33746101818
-
Functional in vivo interactions between JNK1 and JNK2 isoforms in obesity and insulin resistance
-
Tuncman, G., Hirosumi, J., Solinas, G., Chang, L., Karin, M. and Hotamisligil, G. S. (2006) Functional in vivo interactions between JNK1 and JNK2 isoforms in obesity and insulin resistance. Proc. Natl. Acad. Sci. U.S.A. 103, 10741-10746
-
(2006)
Proc. Natl. Acad. Sci. U.S.A
, vol.103
, pp. 10741-10746
-
-
Tuncman, G.1
Hirosumi, J.2
Solinas, G.3
Chang, L.4
Karin, M.5
Hotamisligil, G.S.6
-
9
-
-
0038004740
-
Targeting JNK for therapeutic benefit: From Junk to gold?
-
Manning, A. M. and Davis, R. J. (2003) Targeting JNK for therapeutic benefit: from Junk to gold? Nat. Rev. Drug Discov. 2, 554-565
-
(2003)
Nat. Rev. Drug Discov
, vol.2
, pp. 554-565
-
-
Manning, A.M.1
Davis, R.J.2
-
10
-
-
0041302157
-
JNK: A new therapeutic target for diabetes. Curr. Opin. Pharmacol
-
Bennett, B. L., Satoh, Y. and Lewis, A. J. (2003) JNK: a new therapeutic target for diabetes. Curr. Opin. Pharmacol. 3, 420-425
-
(2003)
, vol.3
, pp. 420-425
-
-
Bennett, B.L.1
Satoh, Y.2
Lewis, A.J.3
-
11
-
-
0037153158
-
A central role for JNK in obesity and insulin resistance
-
Hirosumi, J., Tuncman, G., Chang, L., Gorgun, C. Z., Uysal, K. T., Maeda, K., Karin, M. and Hotamisligil, G. S. (2002) A central role for JNK in obesity and insulin resistance. Nature 420, 333-336
-
(2002)
Nature
, vol.420
, pp. 333-336
-
-
Hirosumi, J.1
Tuncman, G.2
Chang, L.3
Gorgun, C.Z.4
Uysal, K.T.5
Maeda, K.6
Karin, M.7
Hotamisligil, G.S.8
-
12
-
-
0030826412
-
A cytoplasmic inhibitor of the JNK signal transduction pathway
-
Dickens, M., Rogers, J. S., Cavanagh, J., Raitano, A., Xia, Z., Halpern, J. R., Greenberg, M. E., Sawyers, C. L. and Davis, R. J. (1997) A cytoplasmic inhibitor of the JNK signal transduction pathway. Science 277, 693-696
-
(1997)
Science
, vol.277
, pp. 693-696
-
-
Dickens, M.1
Rogers, J.S.2
Cavanagh, J.3
Raitano, A.4
Xia, Z.5
Halpern, J.R.6
Greenberg, M.E.7
Sawyers, C.L.8
Davis, R.J.9
-
13
-
-
33751274234
-
The JIP family of MAPK scaffold proteins
-
Whitmarsh, A. J. (2006) The JIP family of MAPK scaffold proteins. Biochem. Soc. Trans. 34, 828-832
-
(2006)
Biochem. Soc. Trans
, vol.34
, pp. 828-832
-
-
Whitmarsh, A.J.1
-
14
-
-
0032508714
-
A mammalian scaffold complex that selectively mediates MAP kinase activation
-
Whitmarsh, A. J., Cavanagh, J., Tournier, C., Yasuda, J. and Davis, R. J. (1998) A mammalian scaffold complex that selectively mediates MAP kinase activation. Science 281, 1671-1674
-
(1998)
Science
, vol.281
, pp. 1671-1674
-
-
Whitmarsh, A.J.1
Cavanagh, J.2
Tournier, C.3
Yasuda, J.4
Davis, R.J.5
-
15
-
-
0035883958
-
Requirement of the JIP1 scaffold protein for stress-induced JNK activation
-
Whitmarsh, A. J., Kuan, C. Y., Kennedy, N. J., Kelkar, N., Haydar, T. F., Mordes, J. P., Appel, M., Rossini, A. A., Jones, S. N., Flavell, R. A. et al. (2001) Requirement of the JIP1 scaffold protein for stress-induced JNK activation. Genes Dev. 15, 2421-2432
-
(2001)
Genes Dev
, vol.15
, pp. 2421-2432
-
-
Whitmarsh, A.J.1
Kuan, C.Y.2
Kennedy, N.J.3
Kelkar, N.4
Haydar, T.F.5
Mordes, J.P.6
Appel, M.7
Rossini, A.A.8
Jones, S.N.9
Flavell, R.A.10
-
16
-
-
0037192843
-
Identification of the critical features of a small peptide inhibitor of JNK activity
-
Barr, R. K., Kendrick, T. S. and Bogoyevitch, M. A. (2002) Identification of the critical features of a small peptide inhibitor of JNK activity. J. Biol. Chem. 277, 10987-10997
-
(2002)
J. Biol. Chem
, vol.277
, pp. 10987-10997
-
-
Barr, R.K.1
Kendrick, T.S.2
Bogoyevitch, M.A.3
-
17
-
-
3042689209
-
Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125
-
Heo, Y. S., Kim, S. K., Seo, C. I., Kim, Y. K., Sung, B. J., Lee, H. S., Lee, J. I., Park, S. Y., Kim, J. H., Hwang, K. Y. et al. (2004) Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125. EMBO J. 23, 2185-2195
-
(2004)
EMBO J
, vol.23
, pp. 2185-2195
-
-
Heo, Y.S.1
Kim, S.K.2
Seo, C.I.3
Kim, Y.K.4
Sung, B.J.5
Lee, H.S.6
Lee, J.I.7
Park, S.Y.8
Kim, J.H.9
Hwang, K.Y.10
-
18
-
-
7044230885
-
Possible novel therapy for diabetes with cell-permeable JNK-inhibitory peptide
-
Kaneto, H., Nakatani, Y., Miyatsuka, T., Kawamori, D., Matsuoka, T., Matsuhisa, M., Kajimoto, Y., Ichijo, H., Yamasaki, Y. and Hori, M. (2004) Possible novel therapy for diabetes with cell-permeable JNK-inhibitory peptide. Nat. Med. 10, 1128-1132
-
(2004)
Nat. Med
, vol.10
, pp. 1128-1132
-
-
Kaneto, H.1
Nakatani, Y.2
Miyatsuka, T.3
Kawamori, D.4
Matsuoka, T.5
Matsuhisa, M.6
Kajimoto, Y.7
Ichijo, H.8
Yamasaki, Y.9
Hori, M.10
-
19
-
-
3142781225
-
Small-molecule inhibitors of protein-protein interactions: Progressing towards the dream
-
Arkin, M. R. and Wells, J. A. (2004) Small-molecule inhibitors of protein-protein interactions: progressing towards the dream. Nat. Rev. Drug Discov. 3, 301-317
-
(2004)
Nat. Rev. Drug Discov
, vol.3
, pp. 301-317
-
-
Arkin, M.R.1
Wells, J.A.2
-
20
-
-
33846155913
-
Structure-based maximal affinity model predicts small-molecule druggability
-
Cheng, A. C., Coleman, R. G., Smyth, K. T., Cao, Q., Soulard, P., Caffrey, D. R., Salzberg, A. C. and Huang, E. S. (2007) Structure-based maximal affinity model predicts small-molecule druggability. Nat. Biotechnol. 25, 71-75
-
(2007)
Nat. Biotechnol
, vol.25
, pp. 71-75
-
-
Cheng, A.C.1
Coleman, R.G.2
Smyth, K.T.3
Cao, Q.4
Soulard, P.5
Caffrey, D.R.6
Salzberg, A.C.7
Huang, E.S.8
-
21
-
-
4344576752
-
The critical features and the mechanism of inhibition of a kinase interaction motif-based peptide inhibitor of JNK
-
Barr, R. K., Boehm, I., Attwood, P. V., Watt, P. M. and Bogoyevitch, M. A. (2004) The critical features and the mechanism of inhibition of a kinase interaction motif-based peptide inhibitor of JNK. J. Biol. Chem. 279, 36327-36338
-
(2004)
J. Biol. Chem
, vol.279
, pp. 36327-36338
-
-
Barr, R.K.1
Boehm, I.2
Attwood, P.V.3
Watt, P.M.4
Bogoyevitch, M.A.5
-
22
-
-
55949100580
-
Identification of a new JNK inhibitor targeting the JNK-JIP interaction site
-
Stebbins, J. L., De, S. K., Machleidt, T., Becattini, B., Vazquez, J., Kuntzen, C., Chen, L., Cellitti, J. F., Riel-Mehan, M., Emdadi, A. et al. (2008) Identification of a new JNK inhibitor targeting the JNK-JIP interaction site. Proc. Natl. Acad. Sci. U.S.A. 105, 16809-16813
-
(2008)
Proc. Natl. Acad. Sci. U.S.A
, vol.105
, pp. 16809-16813
-
-
Stebbins, J.L.1
De, S.K.2
Machleidt, T.3
Becattini, B.4
Vazquez, J.5
Kuntzen, C.6
Chen, L.7
Cellitti, J.F.8
Riel-Mehan, M.9
Emdadi, A.10
-
23
-
-
0001930769
-
A spectrophotometric assay for biotin-binding sites of immobilized avidin
-
Janolino, V. G., Fontecha, J. and Swaisgood, H. E. (1996) A spectrophotometric assay for biotin-binding sites of immobilized avidin. Appl. Biochem. Biotechnol. 56, 1-7
-
(1996)
Appl. Biochem. Biotechnol
, vol.56
, pp. 1-7
-
-
Janolino, V.G.1
Fontecha, J.2
Swaisgood, H.E.3
-
24
-
-
0034668860
-
Synergistic activation of stress-activated protein kinase 1/c-Jun N-terminal kinase (SAPK1/JNK) isoforms by mitogen-activated protein kinase kinase 4 (MKK4) and MKK7
-
Fleming, Y., Armstrong, C. G., Morrice, N., Paterson, A., Goedert, M. and Cohen, P. (2000) Synergistic activation of stress-activated protein kinase 1/c-Jun N-terminal kinase (SAPK1/JNK) isoforms by mitogen-activated protein kinase kinase 4 (MKK4) and MKK7. Biochem. J. 352, 145-154
-
(2000)
Biochem. J
, vol.352
, pp. 145-154
-
-
Fleming, Y.1
Armstrong, C.G.2
Morrice, N.3
Paterson, A.4
Goedert, M.5
Cohen, P.6
-
25
-
-
66949114096
-
-
Wasilko, D. J. and Lee, S. E. (2006) TIPS: titerless infected-cells preservation and scale-up. BioProcess. J. 5, 29-32
-
Wasilko, D. J. and Lee, S. E. (2006) TIPS: titerless infected-cells preservation and scale-up. BioProcess. J. 5, 29-32
-
-
-
-
26
-
-
33751558665
-
Homogeneous and nonradioactive high-throughput screening platform for the characterization of kinase inhibitors in cell lysates
-
Guenat, S., Rouleau, N., Bielmann, C., Bedard, J., Maurer, F., Allaman-Pillet, N., Nicod, P., Bielefeld-Sevigny, M., Beckmann, J. S., Bonny, C. et al. (2006) Homogeneous and nonradioactive high-throughput screening platform for the characterization of kinase inhibitors in cell lysates. J. Biomol. Screening 11, 1015-1026
-
(2006)
J. Biomol. Screening
, vol.11
, pp. 1015-1026
-
-
Guenat, S.1
Rouleau, N.2
Bielmann, C.3
Bedard, J.4
Maurer, F.5
Allaman-Pillet, N.6
Nicod, P.7
Bielefeld-Sevigny, M.8
Beckmann, J.S.9
Bonny, C.10
-
27
-
-
0034306450
-
Specificity and mechanism of action of some commonly used protein kinase inhibitors
-
Davies, S. P., Reddy, H., Caivano, M. and Cohen, P. (2000) Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem. J. 351, 95-105
-
(2000)
Biochem. J
, vol.351
, pp. 95-105
-
-
Davies, S.P.1
Reddy, H.2
Caivano, M.3
Cohen, P.4
-
28
-
-
50349089225
-
Mechanistic characterization for c-Jun-N-terminal kinase 1α1
-
Ember, B. and LoGrasso, P. (2008) Mechanistic characterization for c-Jun-N-terminal kinase 1α1. Arch. Biochem. Biophys. 477, 324-329
-
(2008)
Arch. Biochem. Biophys
, vol.477
, pp. 324-329
-
-
Ember, B.1
LoGrasso, P.2
-
29
-
-
0018735516
-
Statistical analysis of enzyme kinetic data
-
Cleland, W. W. (1979) Statistical analysis of enzyme kinetic data. Methods Enzymol. 63, 103-138
-
(1979)
Methods Enzymol
, vol.63
, pp. 103-138
-
-
Cleland, W.W.1
-
30
-
-
0016700753
-
Tight-binding inhibitors - I. Kinetic behavior
-
Cha, S. (1975) Tight-binding inhibitors - I. Kinetic behavior. Biochem. Pharmacol. 24, 2177-2185
-
(1975)
Biochem. Pharmacol
, vol.24
, pp. 2177-2185
-
-
Cha, S.1
-
31
-
-
0033003760
-
A simple statistical parameter for use in evaluation and validation of high throughput screening assays
-
Zhang, J. H., Chung, T. D. and Oldenburg, K. R. (1999) A simple statistical parameter for use in evaluation and validation of high throughput screening assays. J. Biomol. Screening 4, 67-73
-
(1999)
J. Biomol. Screening
, vol.4
, pp. 67-73
-
-
Zhang, J.H.1
Chung, T.D.2
Oldenburg, K.R.3
-
32
-
-
33746614110
-
Discovery of novel isothiazole inhibitors of the TrkA kinase: Structure-activity relationship, computer modeling, optimization, and identification of highly potent antagonists
-
Lippa, B., Morris, J., Corbett, M., Kwan, T. A., Noe, M. C., Snow, S. L., Gant, T. G., Mangiaracina, M., Coffey, H. A. and Foster, B. (2006) Discovery of novel isothiazole inhibitors of the TrkA kinase: structure-activity relationship, computer modeling, optimization, and identification of highly potent antagonists. Bioorg. Med. Chem. Lett. 16, 3444-3448
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 3444-3448
-
-
Lippa, B.1
Morris, J.2
Corbett, M.3
Kwan, T.A.4
Noe, M.C.5
Snow, S.L.6
Gant, T.G.7
Mangiaracina, M.8
Coffey, H.A.9
Foster, B.10
-
33
-
-
34247517344
-
-
Niu, L., Chang, K. C., Wilson, S., Tran, P., Zuo, F. and and Swinney, D. C. (2007) Kinetic characterization of human JNK2α2 reaction mechanism using substrate competitive inhibitors. Biochemistry 46, 4775-4784
-
Niu, L., Chang, K. C., Wilson, S., Tran, P., Zuo, F. and and Swinney, D. C. (2007) Kinetic characterization of human JNK2α2 reaction mechanism using substrate competitive inhibitors. Biochemistry 46, 4775-4784
-
-
-
-
34
-
-
66949128039
-
-
kinase inhibitors, Int. Pat. WO/2000/031063
-
G. D. Searle & Co. (2000) Substituted pyrazoles as p38 kinase inhibitors, Int. Pat. WO/2000/031063
-
(2000)
Substituted pyrazoles as
, pp. 38
-
-
Searle, G.D.1
Co2
-
35
-
-
0029885419
-
Selective interaction of JNK protein kinase isoforms with transcription factors
-
Gupta, S., Barrett, T., Whitmarsh, A. J., Cavanagh, J., Sluss, H. K., Derijard, B. and Davis, R. J. (1996) Selective interaction of JNK protein kinase isoforms with transcription factors. EMBO J. 15, 2760-2770
-
(1996)
EMBO J
, vol.15
, pp. 2760-2770
-
-
Gupta, S.1
Barrett, T.2
Whitmarsh, A.J.3
Cavanagh, J.4
Sluss, H.K.5
Derijard, B.6
Davis, R.J.7
-
36
-
-
0035923665
-
SP600125, an anthrapyrazolone inhibitor of Jun N-terminal kinase
-
Bennett, B. L., Sasaki, D. T., Murray, B. W., O'Leary, E. C., Sakata, S. T., Xu, W., Leisten, J. C., Motiwala, A., Pierce, S., Satoh, Y. et al. (2001) SP600125, an anthrapyrazolone inhibitor of Jun N-terminal kinase. Proc. Natl. Acad. Sci. U.S.A. 98, 13681-13686
-
(2001)
Proc. Natl. Acad. Sci. U.S.A
, vol.98
, pp. 13681-13686
-
-
Bennett, B.L.1
Sasaki, D.T.2
Murray, B.W.3
O'Leary, E.C.4
Sakata, S.T.5
Xu, W.6
Leisten, J.C.7
Motiwala, A.8
Pierce, S.9
Satoh, Y.10
-
37
-
-
33744798469
-
Docking interactions induce exposure of activation loop in the MAP kinase ERK2
-
Zhou, T., Sun, L., Humphrey, J. and Goldsmith, E. J. (2006) Docking interactions induce exposure of activation loop in the MAP kinase ERK2. Structure 14, 1011-1019
-
(2006)
Structure
, vol.14
, pp. 1011-1019
-
-
Zhou, T.1
Sun, L.2
Humphrey, J.3
Goldsmith, E.J.4
-
38
-
-
34447295963
-
Molecular basis of MAPK-activated protein kinase 2: P38 assembly
-
White, A., Pargellis, C. A., Studts, J. M., Werneburg, B. G. and Farmer, II, B. T. (2007) Molecular basis of MAPK-activated protein kinase 2: p38 assembly. Proc. Natl. Acad. Sci. U.S.A. 104, 6353-6358
-
(2007)
Proc. Natl. Acad. Sci. U.S.A
, vol.104
, pp. 6353-6358
-
-
White, A.1
Pargellis, C.A.2
Studts, J.M.3
Werneburg, B.G.4
Farmer II, B.T.5
-
39
-
-
40549109546
-
Kinetic mechanism and inhibitor characterization for c-Jun-N-terminal kinase 3α1
-
Ember, B., Kamenecka, T. and LoGrasso, P. (2008) Kinetic mechanism and inhibitor characterization for c-Jun-N-terminal kinase 3α1. Biochemistry 47, 3076-3084
-
(2008)
Biochemistry
, vol.47
, pp. 3076-3084
-
-
Ember, B.1
Kamenecka, T.2
LoGrasso, P.3
|