-
1
-
-
33947226782
-
Structural and functional diversity of the microbial kinome
-
Kannan, N., and Taylor., S. S., Zhai, Y., Venter, J. C. and Manning, G. (2007) Structural and functional diversity of the microbial kinome. PLoS Biol. 5, e17
-
(2007)
PLoS Biol.
, vol.5
, pp. e17
-
-
Kannan, N.1
Taylor, S.S.2
Zhai, Y.3
Venter, J.C.4
Manning, G.5
-
2
-
-
0037032835
-
The protein kinase complement of the human genome
-
Manning, G., and Whyte., D. B., Martinez, R., Hunter, T. and Sudarsanam, S. (2002) The protein kinase complement of the human genome. Science 298, 1912-1934
-
(2002)
Science
, vol.298
, pp. 1912-1934
-
-
Manning, G.1
Whyte, D.B.2
Martinez, R.3
Hunter, T.4
Sudarsanam, S.5
-
3
-
-
4143139896
-
The mouse kinome: Discovery and comparative genomics of all mouse protein kinases
-
Caenepeel, S., Charydczak, G., Sudarsanam, S., Hunter, T. and Manning, G. (2004) The mouse kinome: discovery and comparative genomics of all mouse protein kinases. Proc. Natl. Acad. Sci. U.S.A. 101, 11707-11712
-
(2004)
Proc. Natl. Acad. Sci. U.S.A.
, vol.101
, pp. 11707-11712
-
-
Caenepeel, S.1
Charydczak, G.2
Sudarsanam, S.3
Hunter, T.4
Manning, G.5
-
4
-
-
79960603102
-
The minimal kinome of giardia lambliailluminates early kinase evolution and unique parasite biology
-
Manning, G., and Reiner., D. S., Lauwaet, T., Dacre, M., Smith, A., Zhai, Y., Svard, S. and Gillin, F. D. (2011) The minimal kinome of Giardia lambliailluminates early kinase evolution and unique parasite biology. Genome Biol. 12, R66
-
(2011)
Genome Biol.
, vol.12
, pp. R66
-
-
Manning, G.1
Reiner, D.S.2
Lauwaet, T.3
Dacre, M.4
Smith, A.5
Zhai, Y.6
Svard, S.7
Gillin, F.D.8
-
5
-
-
84878518682
-
Structural and evolutionary adaptation of rhoptry kinases and pseudokinases, a family of coccidian virulence factors
-
Talevich, E. and Kannan, N. (2013) Structural and evolutionary adaptation of rhoptry kinases and pseudokinases, a family of coccidian virulence factors. BMC Evol. Biol. 13, 117
-
(2013)
BMC Evol. Biol.
, vol.13
, pp. 117
-
-
Talevich, E.1
Kannan, N.2
-
6
-
-
84880534837
-
Dawn of the dead: Protein pseudokinases signal new adventures in cell biology
-
Eyers, P. A. and Murphy, J. M. (2013) Dawn of the dead: protein pseudokinases signal new adventures in cell biology. Biochem. Soc. Trans. 41, 969-974
-
(2013)
Biochem. Soc. Trans.
, vol.41
, pp. 969-974
-
-
Eyers, P.A.1
Murphy, J.M.2
-
7
-
-
58149204174
-
Structure of the pseudokinase VRK3 reveals a degraded catalytic site, a highly conserved kinase fold, and a putative regulatory binding site
-
Scheeff, E. D., Eswaran, J., Bunkoczi, G., Knapp, S. and Manning, G. (2009) Structure of the pseudokinase VRK3 reveals a degraded catalytic site, a highly conserved kinase fold, and a putative regulatory binding site. Structure 17, 128-138
-
(2009)
Structure
, vol.17
, pp. 128-138
-
-
Scheeff, E.D.1
Eswaran, J.2
Bunkoczi, G.3
Knapp, S.4
Manning, G.5
-
8
-
-
33747886526
-
Emerging roles of pseudokinases
-
Boudeau, J., Miranda-Saavedra, D., Barton, G. J. and Alessi, D. R. (2006) Emerging roles of pseudokinases. Trends Cell Biol. 16, 443-452
-
(2006)
Trends Cell Biol.
, vol.16
, pp. 443-452
-
-
Boudeau, J.1
Miranda-Saavedra, D.2
Barton, G.J.3
Alessi, D.R.4
-
9
-
-
84890921845
-
A robust methodology to subclassify pseudokinases based on their nucleotide-binding properties
-
Murphy, J. M., Zhang, Q., Young, S. N., Reese, M. L., Bailey, F. P., Eyers, P. A., Ungureanu, D., Hammaren, H., Silvennoinen, O., Varghese, L. N. et al. (2014) A robust methodology to subclassify pseudokinases based on their nucleotide-binding properties. Biochem. J. 457, 323-334
-
(2014)
Biochem. J.
, vol.457
, pp. 323-334
-
-
Murphy, J.M.1
Zhang, Q.2
Young, S.N.3
Reese, M.L.4
Bailey, F.P.5
Eyers, P.A.6
Ungureanu, D.7
Hammaren, H.8
Silvennoinen, O.9
Varghese, L.N.10
-
10
-
-
79955044151
-
Mutation that blocks ATP binding creates a pseudokinase stabilizing the scaffolding function of kinase suppressor of ras, CRAF and BRAF
-
Hu, J., Yu, H., Kornev, A. P., Zhao, J., Filbert, E. L., Taylor, S. S. and Shaw, A. S. (2011) Mutation that blocks ATP binding creates a pseudokinase stabilizing the scaffolding function of kinase suppressor of Ras, CRAF and BRAF. Proc. Natl. Acad. Sci. U.S.A. 108, 6067-6072
-
(2011)
Proc. Natl. Acad. Sci. U.S.A.
, vol.108
, pp. 6067-6072
-
-
Hu, J.1
Yu, H.2
Kornev, A.P.3
Zhao, J.4
Filbert, E.L.5
Taylor, S.S.6
Shaw, A.S.7
-
11
-
-
84880530413
-
New insights into the structure and function of the pseudokinase domain in JAK2
-
Silvennoinen, O., Ungureanu, D., Niranjan, Y., Hammaren, H., Bandaranayake, R. and Hubbard, S. R. (2013) New insights into the structure and function of the pseudokinase domain in JAK2. Biochem. Soc. Trans. 41, 1002-1007
-
(2013)
Biochem. Soc. Trans.
, vol.41
, pp. 1002-1007
-
-
Silvennoinen, O.1
Ungureanu, D.2
Niranjan, Y.3
Hammaren, H.4
Bandaranayake, R.5
Hubbard, S.R.6
-
12
-
-
67649950358
-
ATP and MO25alpha regulate the conformational state of the STRADalpha pseudokinase and activation of the LKB1 tumour suppressor
-
Zeqiraj, E., and Filippi., B. M., Goldie, S., Navratilova, I., Boudeau, J., Deak, M., Alessi, D. R. and van Aalten, D. M. (2009) ATP and MO25alpha regulate the conformational state of the STRADalpha pseudokinase and activation of the LKB1 tumour suppressor. PLoS Biol. 7, e1000126
-
(2009)
PLoS Biol.
, vol.7
-
-
Zeqiraj, E.1
Filippi, B.M.2
Goldie, S.3
Navratilova, I.4
Boudeau, J.5
Deak, M.6
Alessi, D.R.7
Van Aalten, D.M.8
-
13
-
-
84884308522
-
The pseudokinase MLKL mediates necroptosis via a molecular switch mechanism
-
Murphy, J. M., and Czabotar., P. E., Hildebrand, J. M., Lucet, I. S., Zhang, J. G., Alvarez-Diaz, S., Lewis, R., Lalaoui, N., Metcalf, D., Webb, A. I. et al. (2013) The pseudokinase MLKL mediates necroptosis via a molecular switch mechanism. Immunity 39, 443-453
-
(2013)
Immunity
, vol.39
, pp. 443-453
-
-
Murphy, J.M.1
Czabotar, P.E.2
Hildebrand, J.M.3
Lucet, I.S.4
Zhang, J.G.5
Alvarez-Diaz, S.6
Lewis, R.7
Lalaoui, N.8
Metcalf, D.9
Webb, A.I.10
-
14
-
-
84906938626
-
Day of the dead: Pseudokinases and pseudophosphatases in physiology and disease
-
Reiterer, V., Eyers, P. A. and Farhan, H. (2014) Day of the dead: pseudokinases and pseudophosphatases in physiology and disease. Trends Cell Biol. 24, 489-505
-
(2014)
Trends Cell Biol.
, vol.24
, pp. 489-505
-
-
Reiterer, V.1
Eyers, P.A.2
Farhan, H.3
-
15
-
-
58149287842
-
A conserved salt bridge in the G loop of multiple protein kinases is important for catalysis and for in vivo lyn function
-
Barouch-Bentov, R., Che, J., and Lee., C. C., Yang, Y., Herman, A., Jia, Y., Velentza, A., Watson, J., Sternberg, L., Kim, S. et al. (2009) A conserved salt bridge in the G loop of multiple protein kinases is important for catalysis and for in vivo Lyn function. Mol. Cell 33, 43-52
-
(2009)
Mol. Cell
, vol.33
, pp. 43-52
-
-
Barouch-Bentov, R.1
Che, J.2
Lee, C.C.3
Yang, Y.4
Herman, A.5
Jia, Y.6
Velentza, A.7
Watson, J.8
Sternberg, L.9
Kim, S.10
-
16
-
-
79551594605
-
Protein kinases: Evolution of dynamic regulatory proteins
-
Taylor, S. S. and Kornev, A. P. (2011) Protein kinases: evolution of dynamic regulatory proteins. Trends Biochem Sci. 36, 65-77
-
(2011)
Trends Biochem Sci.
, vol.36
, pp. 65-77
-
-
Taylor, S.S.1
Kornev, A.P.2
-
17
-
-
84862131533
-
The vertebrate mitotic checkpoint protein BUBR1 is an unusual pseudokinase
-
Suijkerbuijk, S. J., van Dam, T. J., Karagoz, G. E., von Castelmur, E., Hubner, N. C., Duarte, A. M., Vleugel, M., Perrakis, A., Rudiger, S. G., Snel, B. et al. (2012) The vertebrate mitotic checkpoint protein BUBR1 is an unusual pseudokinase. Dev. Cell 22, 1321-1329
-
(2012)
Dev. Cell
, vol.22
, pp. 1321-1329
-
-
Suijkerbuijk, S.J.1
Van Dam, T.J.2
Karagoz, G.E.3
Von Castelmur, E.4
Hubner, N.C.5
Duarte, A.M.6
Vleugel, M.7
Perrakis, A.8
Rudiger, S.G.9
Snel, B.10
-
18
-
-
0034924175
-
Haspin-like proteins: A new family of evolutionarily conserved putative eukaryotic protein kinases
-
Higgins, J. M. (2001) Haspin-like proteins: a new family of evolutionarily conserved putative eukaryotic protein kinases. Protein Sci. 10, 1677-1684
-
(2001)
Protein Sci.
, vol.10
, pp. 1677-1684
-
-
Higgins, J.M.1
-
19
-
-
0037013143
-
The conformational plasticity of protein kinases
-
Huse, M. and Kuriyan, J. (2002) The conformational plasticity of protein kinases. Cell 109, 275-282
-
(2002)
Cell
, vol.109
, pp. 275-282
-
-
Huse, M.1
Kuriyan, J.2
-
20
-
-
77952338791
-
ErbB3/HER3 intracellular domain is competent to bind ATP and catalyze autophosphorylation
-
Shi, F. M., and Telesco., S. E., Liu, Y. T., Radhakrishnan, R. and Lemmon, M. A. (2010) ErbB3/HER3 intracellular domain is competent to bind ATP and catalyze autophosphorylation. Proc. Natl. Acad. Sci. U.S.A. 107, 7692-7697
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 7692-7697
-
-
Shi, F.M.1
Telesco, S.E.2
Liu, Y.T.3
Radhakrishnan, R.4
Lemmon, M.A.5
-
21
-
-
80052492285
-
The pseudokinase domain of JAK2 is a dual-specificity protein kinase that negatively regulates cytokine signaling
-
Ungureanu, D., Wu, J., Pekkala, T., Niranjan, Y., Young, C., Jensen, O. N., Xu, C.-F., Neubert, T. A., Skoda, R. C., Hubbard, S. R. et al. (2011) The pseudokinase domain of JAK2 is a dual-specificity protein kinase that negatively regulates cytokine signaling. Nat. Struct. Mol. Biol. 18, 971-U921
-
(2011)
Nat. Struct. Mol. Biol.
, vol.18
, pp. 971-U921
-
-
Ungureanu, D.1
Wu, J.2
Pekkala, T.3
Niranjan, Y.4
Young, C.5
Jensen, O.N.6
Xu, C.-F.7
Neubert, T.A.8
Skoda, R.C.9
Hubbard, S.R.10
-
22
-
-
41949128173
-
2+ -independent neurexin kinase
-
2+ -independent neurexin kinase. Cell 133, 328-339
-
(2008)
Cell
, vol.133
, pp. 328-339
-
-
Mukherjee, K.1
Sharma, M.2
Urlaub, H.3
Bourenkov, G.P.4
Jahn, R.5
Sudhof, T.C.6
Wahl, M.C.7
-
23
-
-
84882923644
-
SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function
-
Yoshida-Moriguchi, T., Willer, T., and Anderson., M. E., Venzke, D., Whyte, T., Muntoni, F., Lee, H., Nelson, S. F., Yu, L. and Campbell, K. P. (2013) SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function. Science 341, 896-899
-
(2013)
Science
, vol.341
, pp. 896-899
-
-
Yoshida-Moriguchi, T.1
Willer, T.2
Anderson, M.E.3
Venzke, D.4
Whyte, T.5
Muntoni, F.6
Lee, H.7
Nelson, S.F.8
Yu, L.9
Campbell, K.P.10
-
24
-
-
84875194085
-
Affinity profiling of the cellular kinome for the nucleotide cofactors ATP, ADP, and GTP
-
Becher, I., and Savitski., M. M., Savitski, M. F., Hopf, C., Bantscheff, M. and Drewes, G. (2013) Affinity profiling of the cellular kinome for the nucleotide cofactors ATP, ADP, and GTP. ACS Chem. Biol. 8, 599-607
-
(2013)
ACS Chem. Biol.
, vol.8
, pp. 599-607
-
-
Becher, I.1
Savitski, M.M.2
Savitski, M.F.3
Hopf, C.4
Bantscheff, M.5
Drewes, G.6
-
25
-
-
77249164281
-
The (un)targeted cancer kinome
-
Fedorov, O., Muller, S. and Knapp, S. (2010) The (un)targeted cancer kinome. Nat. Chem. Biol. 6, 166-169
-
(2010)
Nat. Chem. Biol.
, vol.6
, pp. 166-169
-
-
Fedorov, O.1
Muller, S.2
Knapp, S.3
-
26
-
-
84871312669
-
A public-private partnership to unlock the untargeted kinome
-
Knapp, S., Arruda, P., Blagg, J., Burley, S., and Drewry., D. H., Edwards, A., Fabbro, D., Gillespie, P., and Gray., N. S., Kuster, B. et al. (2013) A public-private partnership to unlock the untargeted kinome. Nat. Chem. Biol. 9, 3-6
-
(2013)
Nat. Chem. Biol.
, vol.9
, pp. 3-6
-
-
Knapp, S.1
Arruda, P.2
Blagg, J.3
Burley, S.4
Drewry, D.H.5
Edwards, A.6
Fabbro, D.7
Gillespie, P.8
Gray, N.S.9
Kuster, B.10
-
27
-
-
84880549135
-
Receptor tyrosine kinases with intracellular pseudokinase domains
-
Mendrola, J. M., Shi, F., Park, J. H. and Lemmon, M. A. (2013) Receptor tyrosine kinases with intracellular pseudokinase domains. Biochem. Soc. Trans. 41, 1029-1036
-
(2013)
Biochem. Soc. Trans.
, vol.41
, pp. 1029-1036
-
-
Mendrola, J.M.1
Shi, F.2
Park, J.H.3
Lemmon, M.A.4
-
28
-
-
78649642175
-
Pseudokinases-remnants of evolution or key allosteric regulators?
-
Zeqiraj, E. and van Aalten, D. M. (2010) Pseudokinases-remnants of evolution or key allosteric regulators? Curr. Opin. Struct. Biol. 20, 772-781
-
(2010)
Curr. Opin. Struct. Biol.
, vol.20
, pp. 772-781
-
-
Zeqiraj, E.1
Van Aalten, D.M.2
-
29
-
-
76049128717
-
Structural analysis of the catalytically inactive kinase domain of the human EGF receptor 3
-
Jura, N., Shan, Y., Cao, X., Shaw, D. E. and Kuriyan, J. (2009) Structural analysis of the catalytically inactive kinase domain of the human EGF receptor 3. Proc. Natl. Acad. Sci. U.S.A. 106, 21608-21613
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 21608-21613
-
-
Jura, N.1
Shan, Y.2
Cao, X.3
Shaw, D.E.4
Kuriyan, J.5
-
30
-
-
48649092620
-
A central role for HER3 in HER2-amplified breast cancer: Implications for targeted therapy
-
Lee-Hoeflich, S. T., Crocker, L., Yao, E., Pham, T., Munroe, X., Hoeflich, K. P., Sliwkowski, M. X. and Stern, H. M. (2008) A central role for HER3 in HER2-amplified breast cancer: implications for targeted therapy. Cancer Res. 68, 5878-5887
-
(2008)
Cancer Res.
, vol.68
, pp. 5878-5887
-
-
Lee-Hoeflich, S.T.1
Crocker, L.2
Yao, E.3
Pham, T.4
Munroe, X.5
Hoeflich, K.P.6
Sliwkowski, M.X.7
Stern, H.M.8
-
31
-
-
0042307325
-
The ErbB2/ErbB3 heterodimer functions as an oncogenic unit: ErbB2 requires ErbB3 to drive breast tumor cell proliferation
-
Holbro, T., and Beerli., R. R., Maurer, F., Koziczak, M., Barbas, 3rd, C. F. and Hynes, N. E. (2003) The ErbB2/ErbB3 heterodimer functions as an oncogenic unit: ErbB2 requires ErbB3 to drive breast tumor cell proliferation. Proc. Natl. Acad. Sci. U.S.A. 100, 8933-8938
-
(2003)
Proc. Natl. Acad. Sci. U.S.A.
, vol.100
, pp. 8933-8938
-
-
Holbro, T.1
Beerli, R.R.2
Maurer, F.3
Koziczak, M.4
Barbas, C.F.5
Hynes, N.E.6
-
32
-
-
77649314140
-
An activated ErbB3/NRG1 autocrine loop supports in vivo proliferation in ovarian cancer cells
-
Sheng, Q., Liu, X., Fleming, E., Yuan, K., Piao, H., Chen, J., Moustafa, Z., and Thomas., R. K., Greulich, H., Schinzel, A. et al. (2010) An activated ErbB3/NRG1 autocrine loop supports in vivo proliferation in ovarian cancer cells. Cancer Cell 17, 298-310
-
(2010)
Cancer Cell
, vol.17
, pp. 298-310
-
-
Sheng, Q.1
Liu, X.2
Fleming, E.3
Yuan, K.4
Piao, H.5
Chen, J.6
Moustafa, Z.7
Thomas, R.K.8
Greulich, H.9
Schinzel, A.10
-
33
-
-
77649285474
-
The rebirth of a phoenix: Ovarian cancers are addicted to ErbB-3
-
Mills, G. B. and Yarden, Y. (2010) The rebirth of a phoenix: ovarian cancers are addicted to ErbB-3. Cancer Cell 17, 217-218
-
(2010)
Cancer Cell
, vol.17
, pp. 217-218
-
-
Mills, G.B.1
Yarden, Y.2
-
34
-
-
34249075147
-
MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling
-
Engelman, J. A., Zejnullahu, K., Mitsudomi, T., Song, Y., Hyland, C., Park, J. O., Lindeman, N., Gale, C. M., Zhao, X., Christensen, J. et al. (2007) MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling. Science 316, 1039-1043
-
(2007)
Science
, vol.316
, pp. 1039-1043
-
-
Engelman, J.A.1
Zejnullahu, K.2
Mitsudomi, T.3
Song, Y.4
Hyland, C.5
Park, J.O.6
Lindeman, N.7
Gale, C.M.8
Zhao, X.9
Christensen, J.10
-
35
-
-
84872525097
-
Dual targeting of EGFR and HER3 with MEHD7945A overcomes acquired resistance to EGFR inhibitors and radiation
-
Huang, S., Li, C., Armstrong, E. A., Peet, C. R., Saker, J., Amler, L. C., Sliwkowski, M. X. and Harari, P. M. (2013) Dual targeting of EGFR and HER3 with MEHD7945A overcomes acquired resistance to EGFR inhibitors and radiation. Cancer Res. 73, 824-833
-
(2013)
Cancer Res.
, vol.73
, pp. 824-833
-
-
Huang, S.1
Li, C.2
Armstrong, E.A.3
Peet, C.R.4
Saker, J.5
Amler, L.C.6
Sliwkowski, M.X.7
Harari, P.M.8
-
36
-
-
80755125575
-
Comprehensive analysis of kinase inhibitor selectivity
-
Davis, M. I., and Hunt., J. P., Herrgard, S., Ciceri, P., Wodicka, L. M., Pallares, G., Hocker, M., Treiber, D. K. and Zarrinkar, P. P. (2011) Comprehensive analysis of kinase inhibitor selectivity. Nat. Biotechnol. 29, 1046-51
-
(2011)
Nat. Biotechnol
, vol.29
, pp. 1046-1051
-
-
Davis, M.I.1
Hunt, J.P.2
Herrgard, S.3
Ciceri, P.4
Wodicka, L.M.5
Pallares, G.6
Hocker, M.7
Treiber, D.K.8
Zarrinkar, P.P.9
-
37
-
-
84920594371
-
Bosutinib: A novel src/abl kinase inhibitor for chronic myelogenous leukemia
-
Steinbach, A., Clark, S. M. and Clemmons, A. B. (2013) Bosutinib: a novel src/abl kinase inhibitor for chronic myelogenous leukemia. J. Adv. Pract. Oncol. 4, 451-455
-
(2013)
J. Adv. Pract. Oncol.
, vol.4
, pp. 451-455
-
-
Steinbach, A.1
Clark, S.M.2
Clemmons, A.B.3
-
38
-
-
84866175467
-
Bosutinib versus imatinib in newly diagnosed chronic-phase chronic myeloid leukemia: Results from the BELA trial
-
Cortes, J. E., and Kim., D. W., Kantarjian, H. M., Brummendorf, T. H., Dyagil, I., Griskevicius, L., Malhotra, H., Powell, C., Gogat, K., Countouriotis, A. M. et al. (2012) Bosutinib versus imatinib in newly diagnosed chronic-phase chronic myeloid leukemia: results from the BELA trial. J. Clin. Oncol. 30, 3486-3492
-
(2012)
J. Clin. Oncol.
, vol.30
, pp. 3486-3492
-
-
Cortes, J.E.1
Kim, D.W.2
Kantarjian, H.M.3
Brummendorf, T.H.4
Dyagil, I.5
Griskevicius, L.6
Malhotra, H.7
Powell, C.8
Gogat, K.9
Countouriotis, A.M.10
-
39
-
-
84899638504
-
An ATP-competitive inhibitor modulates the allosteric function of the HER3 pseudokinase
-
Littlefield, P., Moasser, Mark, M. and Jura, N. (2014) An ATP-competitive inhibitor modulates the allosteric function of the HER3 pseudokinase. Chem. Biol. 21, 453-458
-
(2014)
Chem. Biol.
, vol.21
, pp. 453-458
-
-
Littlefield, P.1
Moasser, M.M.2
Jura, N.3
-
40
-
-
84880529916
-
Pseudokinase drug intervention: A potentially poisoned chalice
-
Claus, J., Cameron, A. J. and Parker, P. J. (2013) Pseudokinase drug intervention: a potentially poisoned chalice. Biochem. Soc. Transact. 41, 1083-1088
-
(2013)
Biochem. Soc. Transact.
, vol.41
, pp. 1083-1088
-
-
Claus, J.1
Cameron, A.J.2
Parker, P.J.3
-
41
-
-
84863922124
-
Comprehensive molecular characterization of human colon and rectal cancer
-
The Cancer Genome Atlas Network (2012) Comprehensive molecular characterization of human colon and rectal cancer. Nature 487, 330-337
-
(2012)
Nature
, vol.487
, pp. 330-337
-
-
The Cancer Genome Atlas Network1
-
42
-
-
20244369569
-
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
-
Levine, R. L., Wadleigh, M., Cools, J., Ebert, B. L., Wernig, G., Huntly, B. J., Boggon, T. J., Wlodarska, I., Clark, J. J., Moore, S. et al. (2005) Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell 7, 387-397
-
(2005)
Cancer Cell
, vol.7
, pp. 387-397
-
-
Levine, R.L.1
Wadleigh, M.2
Cools, J.3
Ebert, B.L.4
Wernig, G.5
Huntly, B.J.6
Boggon, T.J.7
Wlodarska, I.8
Clark, J.J.9
Moore, S.10
-
43
-
-
17844383458
-
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
-
James, C., Ugo, V., Le Couedic, J. P., Staerk, J., Delhommeau, F., Lacout, C., Garcon, L., Raslova, H., Berger, R., Bennaceur-Griscelli, A. et al. (2005) A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature 434, 1144-1148
-
(2005)
Nature
, vol.434
, pp. 1144-1148
-
-
James, C.1
Ugo, V.2
Le Couedic, J.P.3
Staerk, J.4
Delhommeau, F.5
Lacout, C.6
Garcon, L.7
Raslova, H.8
Berger, R.9
Bennaceur-Griscelli, A.10
-
44
-
-
17644424955
-
A gain-of-function mutation of JAK2 in myeloproliferative disorders
-
Kralovics, R., Passamonti, F., Buser, A. S., Teo, S. S., Tiedt, R., Passweg, J. R., Tichelli, A., Cazzola, M. and Skoda, R. C. (2005) A gain-of-function mutation of JAK2 in myeloproliferative disorders. N. Engl. J. Med. 352, 1779-1790
-
(2005)
N. Engl. J. Med.
, vol.352
, pp. 1779-1790
-
-
Kralovics, R.1
Passamonti, F.2
Buser, A.S.3
Teo, S.S.4
Tiedt, R.5
Passweg, J.R.6
Tichelli, A.7
Cazzola, M.8
Skoda, R.C.9
-
45
-
-
20144363192
-
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
-
Baxter, E. J., and Scott., L. M., Campbell, P. J., East, C., Fourouclas, N., Swanton, S., Vassiliou, G. S., Bench, A. J., Boyd, E. M., Curtin, N. et al. (2005) Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet 365, 1054-1061
-
(2005)
Lancet
, vol.365
, pp. 1054-1061
-
-
Baxter, E.J.1
Scott, L.M.2
Campbell, P.J.3
East, C.4
Fourouclas, N.5
Swanton, S.6
Vassiliou, G.S.7
Bench, A.J.8
Boyd, E.M.9
Curtin, N.10
-
46
-
-
84904638434
-
The molecular regulation of janus kinase (JAK) activation
-
Babon, J. J., and Lucet., I. S., Murphy, J. M., Nicola, N. A. and Varghese, L. N. (2014) The molecular regulation of Janus kinase (JAK) activation. Biochem. J. 462, 1-13
-
(2014)
Biochem. J.
, vol.462
, pp. 1-13
-
-
Babon, J.J.1
Lucet, I.S.2
Murphy, J.M.3
Nicola, N.A.4
Varghese, L.N.5
-
47
-
-
0034012330
-
Regulation of the jak2 tyrosine kinase by its pseudokinase domain
-
Saharinen, P., Takaluoma, K. and Silvennoinen, O. (2000) Regulation of the Jak2 tyrosine kinase by its pseudokinase domain. Mol. Cell. Biol. 20, 3387-3395
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 3387-3395
-
-
Saharinen, P.1
Takaluoma, K.2
Silvennoinen, O.3
-
48
-
-
33846660947
-
JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis
-
Scott, L. M., Tong, W., Levine, R. L., Scott, M. A., Beer, P. A., Stratton, M. R., Futreal, P. A., Erber, W. N., McMullin, M. F., Harrison, C. N. et al. (2007) JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis. N. Engl. J. Med. 356, 459-468
-
(2007)
N. Engl. J. Med.
, vol.356
, pp. 459-468
-
-
Scott, L.M.1
Tong, W.2
Levine, R.L.3
Scott, M.A.4
Beer, P.A.5
Stratton, M.R.6
Futreal, P.A.7
Erber, W.N.8
Mcmullin, M.F.9
Harrison, C.N.10
-
49
-
-
84865735256
-
Heterodimeric JAK-STAT activation as a mechanism of persistence to JAK2 inhibitor therapy
-
Koppikar, P., Bhagwat, N., Kilpivaara, O., Manshouri, T., Adli, M., Hricik, T., Liu, F., and Saunders., L. M., Mullally, A., Abdel-Wahab, O. et al. (2012) Heterodimeric JAK-STAT activation as a mechanism of persistence to JAK2 inhibitor therapy. Nature 489, 155-159
-
(2012)
Nature
, vol.489
, pp. 155-159
-
-
Koppikar, P.1
Bhagwat, N.2
Kilpivaara, O.3
Manshouri, T.4
Adli, M.5
Hricik, T.6
Liu, F.7
Saunders, L.M.8
Mullally, A.9
Abdel-Wahab, O.10
-
50
-
-
84900432315
-
Mechanism of activation of protein kinase JAK2 by the growth hormone receptor
-
Brooks, A. J., Dai, W., O'Mara, M. L., Abankwa, D., Chhabra, Y., Pelekanos, R. A., Gardon, O., Tunny, K. A., Blucher, K. M., Morton, C. J. et al. (2014) Mechanism of activation of protein kinase JAK2 by the growth hormone receptor. Science 344, 1249783
-
(2014)
Science
, vol.344
-
-
Brooks, A.J.1
Dai, W.2
O'Mara, M.L.3
Abankwa, D.4
Chhabra, Y.5
Pelekanos, R.A.6
Gardon, O.7
Tunny, K.A.8
Blucher, K.M.9
Morton, C.J.10
-
51
-
-
84903899364
-
Molecular basis for pseudokinase-dependent autoinhibition of JAK2 tyrosine kinase
-
Shan, Y., Gnanasambandan, K., Ungureanu, D., Kim, E. T., Hammaren, H., Yamashita, K., Silvennoinen, O., Shaw, D. E. and Hubbard, S. R. (2014) Molecular basis for pseudokinase-dependent autoinhibition of JAK2 tyrosine kinase. Nat. Struct. Mol. Biol. 21, 579-584
-
(2014)
Nat. Struct. Mol. Biol.
, vol.21
, pp. 579-584
-
-
Shan, Y.1
Gnanasambandan, K.2
Ungureanu, D.3
Kim, E.T.4
Hammaren, H.5
Yamashita, K.6
Silvennoinen, O.7
Shaw, D.E.8
Hubbard, S.R.9
-
52
-
-
80755140046
-
SB1518, a novel macrocyclic pyrimidine-based JAK2 inhibitor for the treatment of myeloid and lymphoid Malignancies
-
Hart, S., and Goh., K. C., Novotny-Diermayr, V., Hu, C. Y., Hentze, H., and Tan., Y. C., Madan, B., Amalini, C., Loh, Y. K., Ong, L. C. et al. (2011) SB1518, a novel macrocyclic pyrimidine-based JAK2 inhibitor for the treatment of myeloid and lymphoid malignancies. Leukemia 25, 1751-1759
-
(2011)
Leukemia
, vol.25
, pp. 1751-1759
-
-
Hart, S.1
Goh, K.C.2
Novotny-Diermayr, V.3
Hu, C.Y.4
Hentze, H.5
Tan, Y.C.6
Madan, B.7
Amalini, C.8
Loh, Y.K.9
Ong, L.C.10
-
53
-
-
84887870449
-
Ruxolitinib for myelofibrosis-an update of its clinical effects
-
Kantarjian, H. M., and Silver., R. T., Komrokji, R. S., Mesa, R. A., Tacke, R. and Harrison, C. N. (2013) Ruxolitinib for myelofibrosis-an update of its clinical effects. Clin. Lymphoma Myeloma Leuk. 13, 638-645
-
(2013)
Clin. Lymphoma Myeloma Leuk.
, vol.13
, pp. 638-645
-
-
Kantarjian, H.M.1
Silver, R.T.2
Komrokji, R.S.3
Mesa, R.A.4
Tacke, R.5
Harrison, C.N.6
-
54
-
-
84878284776
-
Discovery and characterization of LY2784544, a small-molecule tyrosine kinase inhibitor of JAK2V617F
-
Ma, L., and Clayton., J. R., Walgren, R. A., Zhao, B., Evans, R. J., Smith, M. C., Heinz-Taheny, K. M., Kreklau, E. L., Bloem, L., Pitou, C. et al. (2013) Discovery and characterization of LY2784544, a small-molecule tyrosine kinase inhibitor of JAK2V617F. Blood Cancer J. 3, e109
-
(2013)
Blood Cancer J.
, vol.3
, pp. e109
-
-
Ma, L.1
Clayton, J.R.2
Walgren, R.A.3
Zhao, B.4
Evans, R.J.5
Smith, M.C.6
Heinz-Taheny, K.M.7
Kreklau, E.L.8
Bloem, L.9
Pitou, C.10
-
55
-
-
84867851649
-
JAK2 the future: Therapeutic strategies for JAK-dependent Malignancies
-
LaFave, L. M. and Levine, R. L. (2012) JAK2 the future: therapeutic strategies for JAK-dependent malignancies. Trends Pharmacol. Sci. 33, 574-582
-
(2012)
Trends Pharmacol. Sci.
, vol.33
, pp. 574-582
-
-
Lafave, L.M.1
Levine, R.L.2
-
56
-
-
2242435334
-
Regulation of WNK1 by an autoinhibitory domain and autophosphorylation
-
Xu, B. E., Min, X., Stippec, S., Lee, B. H., Goldsmith, E. J. and Cobb, M. H. (2002) Regulation of WNK1 by an autoinhibitory domain and autophosphorylation. J. Biol. Chem. 277, 48456-48462
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 48456-48462
-
-
Xu, B.E.1
Min, X.2
Stippec, S.3
Lee, B.H.4
Goldsmith, E.J.5
Cobb, M.H.6
-
57
-
-
3142600709
-
Crystal structure of the kinase domain of WNK1, a kinase that causes a hereditary form of hypertension
-
Min, X., and Lee., B. H., Cobb, M. H. and Goldsmith, E. J. (2004) Crystal structure of the kinase domain of WNK1, a kinase that causes a hereditary form of hypertension. Structure 12, 1303-1311
-
(2004)
Structure
, vol.12
, pp. 1303-1311
-
-
Min, X.1
Lee, B.H.2
Cobb, M.H.3
Goldsmith, E.J.4
-
58
-
-
0034595634
-
WNK1, a novel Mammalian serine/threonine protein kinase lacking the catalytic lysine in subdomain II
-
Xu, B., and English., J. M., Wilsbacher, J. L., Stippec, S., Goldsmith, E. J. and Cobb, M. H. (2000) WNK1, a novel mammalian serine/threonine protein kinase lacking the catalytic lysine in subdomain II. J. Biol. Chem. 275, 16795-16801
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 16795-16801
-
-
Xu, B.1
English, J.M.2
Wilsbacher, J.L.3
Stippec, S.4
Goldsmith, E.J.5
Cobb, M.H.6
-
59
-
-
22844441657
-
Properties of WNK1 and implications for other family members
-
Lenertz, L. Y., and Lee., B. H., Min, X. S., Xu, B. E., Wedin, K., Earnest, S., Goldsmith, E. J. and Cobb, M. H. (2005) Properties of WNK1 and implications for other family members. J. Biol. Chem. 280, 26653-26658
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 26653-26658
-
-
Lenertz, L.Y.1
Lee, B.H.2
Min, X.S.3
Xu, B.E.4
Wedin, K.5
Earnest, S.6
Goldsmith, E.J.7
Cobb, M.H.8
-
60
-
-
84900543727
-
Chloride sensing by WNK1 involves inhibition of autophosphorylation
-
Piala, A. T., and Moon., T. M., Akella, R., He, H., Cobb, M. H. and Goldsmith, E. J. (2014) Chloride sensing by WNK1 involves inhibition of autophosphorylation. Sci. Signal. 7, ra41
-
(2014)
Sci. Signal.
, vol.7
, pp. ra41
-
-
Piala, A.T.1
Moon, T.M.2
Akella, R.3
He, H.4
Cobb, M.H.5
Goldsmith, E.J.6
-
61
-
-
0034595634
-
WNK1, a novel Mammalian serine/threonine protein kinase lacking the catalytic lysine in subdomain II
-
Xu, B. E., and English., J. M., Wilsbacher, J. L., Stippec, S., Goldsmith, E. J. and Cobb, M. H. (2000) WNK1, a novel mammalian serine/threonine protein kinase lacking the catalytic lysine in subdomain II. J. Biol. Chem. 275, 16795-16801
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 16795-16801
-
-
Xu, B.E.1
English, J.M.2
Wilsbacher, J.L.3
Stippec, S.4
Goldsmith, E.J.5
Cobb, M.H.6
-
62
-
-
0035817725
-
WNK kinases, a novel protein kinase subfamily in multi-cellular organisms
-
Verissimo, F. and Jordan, P. (2001) WNK kinases, a novel protein kinase subfamily in multi-cellular organisms. Oncogene 20, 5562-5569
-
(2001)
Oncogene
, vol.20
, pp. 5562-5569
-
-
Verissimo, F.1
Jordan, P.2
-
63
-
-
33746644724
-
- cotransporter in HeLa cells
-
- cotransporter in HeLa cells. Proc. Natl. Acad. Sci. U.S.A. 103, 10883-10888
-
(2006)
Proc. Natl. Acad. Sci. U.S.A.
, vol.103
, pp. 10883-10888
-
-
Anselmo, A.N.1
Earnest, S.2
Chen, W.3
Juang, Y.C.4
Kim, S.C.5
Zhao, Y.6
Cobb, M.H.7
-
64
-
-
84904397693
-
The WNK-SPAK/OSR1 pathway: Master regulator of cation-chloride cotransporters
-
Alessi, D. R., Zhang, J., Khanna, A., Hochdorfer, T., Shang, Y. and Kahle, K. T. (2014) The WNK-SPAK/OSR1 pathway: master regulator of cation-chloride cotransporters. Sci. Signal. 7, re3
-
(2014)
Sci. Signal.
, vol.7
, pp. re3
-
-
Alessi, D.R.1
Zhang, J.2
Khanna, A.3
Hochdorfer, T.4
Shang, Y.5
Kahle, K.T.6
-
65
-
-
84896718225
-
- cotransporter facilitates glioma migration
-
- cotransporter facilitates glioma migration. Mol. Cancer 13, 31
-
(2014)
Mol. Cancer
, vol.13
, pp. 31
-
-
Zhu, W.1
Begum, G.2
Pointer, K.3
Clark, P.A.4
Yang, S.S.5
Lin, S.H.6
Kahle, K.T.7
Kuo, J.S.8
Sun, D.9
-
66
-
-
12144287284
-
LKB1 is a master kinase that activates 13 kinases of the AMPK subfamily, including MARK/PAR-1
-
Lizcano, J. M., Goransson, O., Toth, R., Deak, M., and Morrice., N. A., Boudeau, J., Hawley, S. A., Udd, L., Makela, T. P., Hardie, D. G. et al. (2004) LKB1 is a master kinase that activates 13 kinases of the AMPK subfamily, including MARK/PAR-1. EMBO J. 23, 833-843
-
(2004)
EMBO J.
, vol.23
, pp. 833-843
-
-
Lizcano, J.M.1
Goransson, O.2
Toth, R.3
Deak, M.4
Morrice, N.A.5
Boudeau, J.6
Hawley, S.A.7
Udd, L.8
Makela, T.P.9
Hardie, D.G.10
-
67
-
-
72949115493
-
Structure of the LKB1-STRAD-MO25 complex reveals an allosteric mechanism of kinase activation
-
Zeqiraj, E., and Filippi., B. M., Deak, M., Alessi, D. R. and van Aalten, D. M. F. (2009) Structure of the LKB1-STRAD-MO25 complex reveals an allosteric mechanism of kinase activation. Science 326, 1707-1711
-
(2009)
Science
, vol.326
, pp. 1707-1711
-
-
Zeqiraj, E.1
Filippi, B.M.2
Deak, M.3
Alessi, D.R.4
Van Aalten, D.M.F.5
-
68
-
-
0037173013
-
Role of lkb1, the causative gene of peutz-jeghers syndrome, in embryogenesis and polyposis
-
Jishage, K., Nezu, J., Kawase, Y., Iwata, T., Watanabe, M., Miyoshi, A., Ose, A., Habu, K., Kake, T., Kamada, N. et al. (2002) Role of Lkb1, the causative gene of Peutz-Jeghers syndrome, in embryogenesis and polyposis. Proc. Natl. Acad. Sci. U.S.A. 99, 8903-8908
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 8903-8908
-
-
Jishage, K.1
Nezu, J.2
Kawase, Y.3
Iwata, T.4
Watanabe, M.5
Miyoshi, A.6
Ose, A.7
Habu, K.8
Kake, T.9
Kamada, N.10
-
69
-
-
84892185626
-
Insights into the evolution of divergent nucleotide-binding mechanisms among pseudokinases revealed by crystal structures of human and mouse MLKL
-
Murphy, J. M., and Lucet., I. S., Hildebrand, J. M., Tanzer, M. C., Young, S. N., Sharma, P., Lessene, G., Alexander, W. S., Babon, J. J., Silke, J. et al. (2014) Insights into the evolution of divergent nucleotide-binding mechanisms among pseudokinases revealed by crystal structures of human and mouse MLKL. Biochem. J. 457, 369-377
-
(2014)
Biochem. J.
, vol.457
, pp. 369-377
-
-
Murphy, J.M.1
Lucet, I.S.2
Hildebrand, J.M.3
Tanzer, M.C.4
Young, S.N.5
Sharma, P.6
Lessene, G.7
Alexander, W.S.8
Babon, J.J.9
Silke, J.10
-
70
-
-
84908072785
-
Activation of the pseudokinase MLKL unleashes the four-helix bundle domain to induce membrane localization and necroptotic cell death
-
Hildebrand, J. M., and Tanzer., M. C., Lucet, I. S., Young, S. N., Spall, S. K., Sharma, P., Pierotti, C., Garnier, J. M., Dobson, R. C., Webb, A. I. et al. (2014) Activation of the pseudokinase MLKL unleashes the four-helix bundle domain to induce membrane localization and necroptotic cell death. Proc. Natl. Acad. Sci. U.S.A. 111, 15072-15077
-
(2014)
Proc. Natl. Acad. Sci. U.S.A.
, vol.111
, pp. 15072-15077
-
-
Hildebrand, J.M.1
Tanzer, M.C.2
Lucet, I.S.3
Young, S.N.4
Spall, S.K.5
Sharma, P.6
Pierotti, C.7
Garnier, J.M.8
Dobson, R.C.9
Webb, A.I.10
-
71
-
-
84862907788
-
Mixed lineage kinase domain-like protein mediates necrosis signaling downstream of RIP3 kinase
-
Sun, L. M., and Wang., H. Y., Wang, Z. G., He, S. D., Chen, S., Liao, D. H., Wang, L., Yan, J. C., Liu, W. L., Lei, X. G. et al. (2012) Mixed lineage kinase domain-like protein mediates necrosis signaling downstream of RIP3 kinase. Cell 148, 213-227
-
(2012)
Cell
, vol.148
, pp. 213-227
-
-
Sun, L.M.1
Wang, H.Y.2
Wang, Z.G.3
He, S.D.4
Chen, S.5
Liao, D.H.6
Wang, L.7
Yan, J.C.8
Liu, W.L.9
Lei, X.G.10
-
72
-
-
57549098807
-
The catalogue of somatic mutations in cancer (COSMIC)
-
Chapter 10, Unit 10.11
-
Forbes, S. A., Bhamra, G., Bamford, S., Dawson, E., Kok, C., Clements, J., Menzies, A., and Teague., J. W., Futreal, P. A. and Stratton, M. R. (2008) The catalogue of somatic mutations in cancer (COSMIC). Curr. Protoc. Hum. Genet., Chapter 10, Unit 10.11
-
(2008)
Curr. Protoc. Hum. Genet.
-
-
Forbes, S.A.1
Bhamra, G.2
Bamford, S.3
Dawson, E.4
Kok, C.5
Clements, J.6
Menzies, A.7
Teague, J.W.8
Futreal, P.A.9
Stratton, M.R.10
-
73
-
-
84897540766
-
Kinases and pseudokinases: Lessons from RAF
-
Shaw, A. S., and Kornev., A. P., Hu, J., Ahuja, L. G. and Taylor, S. S. (2014) Kinases and pseudokinases: lessons from RAF. Mol. Cell. Biol. 34, 1538-1546
-
(2014)
Mol. Cell. Biol.
, vol.34
, pp. 1538-1546
-
-
Shaw, A.S.1
Kornev, A.P.2
Hu, J.3
Ahuja, L.G.4
Taylor, S.S.5
-
74
-
-
84880522418
-
The dual function of KSR1: A pseudokinase and beyond
-
Zhang, H., and Koo., C. Y., Stebbing, J. and Giamas, G. (2013) The dual function of KSR1: a pseudokinase and beyond. Biochem. Soc. Trans. 41, 1078-1082
-
(2013)
Biochem. Soc. Trans.
, vol.41
, pp. 1078-1082
-
-
Zhang, H.1
Koo, C.Y.2
Stebbing, J.3
Giamas, G.4
-
75
-
-
0035930343
-
C-TAK1 regulates ras signaling by phosphorylating the MAPK scaffold, KSR1
-
Muller, J., Ory, S., Copeland, T., Piwnica-Worms, H. and Morrison, D. K. (2001) C-TAK1 regulates Ras signaling by phosphorylating the MAPK scaffold, KSR1. Mol. Cell 8, 983-993
-
(2001)
Mol. Cell
, vol.8
, pp. 983-993
-
-
Muller, J.1
Ory, S.2
Copeland, T.3
Piwnica-Worms, H.4
Morrison, D.K.5
-
76
-
-
0037083988
-
KSR is a scaffold required for activation of the ERK/MAPK module
-
Roy, F., Laberge, G., Douziech, M., Ferland-McCollough, D. and Therrien, M. (2002) KSR is a scaffold required for activation of the ERK/MAPK module. Genes Dev. 16, 427-438
-
(2002)
Genes Dev.
, vol.16
, pp. 427-438
-
-
Roy, F.1
Laberge, G.2
Douziech, M.3
Ferland-Mccollough, D.4
Therrien, M.5
-
77
-
-
0031149850
-
The protein kinase KSR interacts with 14-3-3 protein and raf
-
Xing, H., Kornfeld, K. and Muslin, A. J. (1997) The protein kinase KSR interacts with 14-3-3 protein and Raf. Curr. Biol. 7, 294-300
-
(1997)
Curr. Biol.
, vol.7
, pp. 294-300
-
-
Xing, H.1
Kornfeld, K.2
Muslin, A.J.3
-
78
-
-
79955472800
-
A raf-induced allosteric transition of KSR stimulates phosphorylation of MEK
-
Brennan, D. F., and Dar., A. C., Hertz, N. T., Chao, W. C., Burlingame, A. L., Shokat, K. M. and Barford, D. (2011) A Raf-induced allosteric transition of KSR stimulates phosphorylation of MEK. Nature 472, 366-369
-
(2011)
Nature
, vol.472
, pp. 366-369
-
-
Brennan, D.F.1
Dar, A.C.2
Hertz, N.T.3
Chao, W.C.4
Burlingame, A.L.5
Shokat, K.M.6
Barford, D.7
-
79
-
-
77949685981
-
RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth
-
Hatzivassiliou, G., Song, K., Yen, I., Brandhuber, B. J., Anderson, D. J., Alvarado, R., Ludlam, M. J. C., Stokoe, D., Gloor, S. L., Vigers, G. et al. (2010) RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth. Nature 464, 431-435
-
(2010)
Nature
, vol.464
, pp. 431-435
-
-
Hatzivassiliou, G.1
Song, K.2
Yen, I.3
Brandhuber, B.J.4
Anderson, D.J.5
Alvarado, R.6
Ludlam, M.J.C.7
Stokoe, D.8
Gloor, S.L.9
Vigers, G.10
-
80
-
-
0035971073
-
Kinase suppressor of ras signals through thr269 of c-raf-1
-
Xing, H. R. and Kolesnick, R. (2001) Kinase suppressor of Ras signals through Thr269 of c-Raf-1. J. Biol. Chem. 276, 9733-9741
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 9733-9741
-
-
Xing, H.R.1
Kolesnick, R.2
-
81
-
-
70449720533
-
Kinase suppressor of ras transphosphorylates c-raf-1
-
Zafrullah, M., Yin, X., Haimovitz-Friedman, A., Fuks, Z. and Kolesnick, R. (2009) Kinase suppressor of Ras transphosphorylates c-Raf-1. Biochem. Biophys. Res. Commun. 390, 434-440
-
(2009)
Biochem. Biophys. Res. Commun.
, vol.390
, pp. 434-440
-
-
Zafrullah, M.1
Yin, X.2
Haimovitz-Friedman, A.3
Fuks, Z.4
Kolesnick, R.5
-
82
-
-
15244361961
-
Kinase suppressor of ras-1 protects intestinal epithelium from cytokine-mediated apoptosis during inflammation
-
Yan, F., and John., S. K., Wilson, G., Jones, D. S., Washington, M. K. and Polk, D. B. (2004) Kinase suppressor of Ras-1 protects intestinal epithelium from cytokine-mediated apoptosis during inflammation. J. Clin. Invest. 114, 1272-1280
-
(2004)
J. Clin. Invest.
, vol.114
, pp. 1272-1280
-
-
Yan, F.1
John, S.K.2
Wilson, G.3
Jones, D.S.4
Washington, M.K.5
Polk, D.B.6
-
83
-
-
0035116903
-
Kinase suppressor of ras is necessary for tumor necrosis factor alpha activation of extracellular signal-regulated kinase/mitogen-activated protein kinase in intestinal epithelial cells
-
Yan, F. and Polk, D. B. (2001) Kinase suppressor of ras is necessary for tumor necrosis factor alpha activation of extracellular signal-regulated kinase/mitogen-activated protein kinase in intestinal epithelial cells. Cancer Res. 61, 963-969
-
(2001)
Cancer Res.
, vol.61
, pp. 963-969
-
-
Yan, F.1
Polk, D.B.2
-
84
-
-
0142137239
-
Pharmacologic inactivation of kinase suppressor of ras-1 abrogates ras-mediated pancreatic cancer
-
Xing, H. R., Cordon-Cardo, C., Deng, X., Tong, W., Campodonico, L., Fuks, Z. and Kolesnick, R. (2003) Pharmacologic inactivation of kinase suppressor of ras-1 abrogates Ras-mediated pancreatic cancer. Nat. Med. 9, 1266-1268
-
(2003)
Nat. Med.
, vol.9
, pp. 1266-1268
-
-
Xing, H.R.1
Cordon-Cardo, C.2
Deng, X.3
Tong, W.4
Campodonico, L.5
Fuks, Z.6
Kolesnick, R.7
-
85
-
-
2942531229
-
The molecular scaffold KSR1 regulates the proliferative and oncogenic potential of cells
-
Kortum, R. L. and Lewis, R. E. (2004) The molecular scaffold KSR1 regulates the proliferative and oncogenic potential of cells. Mol. Cell. Biol. 24, 4407-4416
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 4407-4416
-
-
Kortum, R.L.1
Lewis, R.E.2
-
86
-
-
79958035502
-
Kinase suppressor of ras 1 (KSR1) regulates PGC1alpha and estrogen-related receptor alpha to promote oncogenic ras-dependent anchorage-independent growth
-
Fisher, K. W., Das, B., Kortum, R. L., Chaika, O. V. and Lewis, R. E. (2011) Kinase suppressor of ras 1 (KSR1) regulates PGC1alpha and estrogen-related receptor alpha to promote oncogenic Ras-dependent anchorage-independent growth. Mol. Cell. Biol. 31, 2453-2461
-
(2011)
Mol. Cell. Biol.
, vol.31
, pp. 2453-2461
-
-
Fisher, K.W.1
Das, B.2
Kortum, R.L.3
Chaika, O.V.4
Lewis, R.E.5
-
87
-
-
84866385871
-
Kinase suppressor of ras 2 (KSR2) regulates tumor cell transformation via AMPK
-
Fernandez, M. R., Henry, M. D. and Lewis, R. E. (2012) Kinase suppressor of Ras 2 (KSR2) regulates tumor cell transformation via AMPK. Mol. Cell. Biol. 32, 3718-3731
-
(2012)
Mol. Cell. Biol.
, vol.32
, pp. 3718-3731
-
-
Fernandez, M.R.1
Henry, M.D.2
Lewis, R.E.3
-
88
-
-
84873523703
-
The kinase domain of drosophila tribbles is required for turnover of fly C/EBP during cell migration
-
Masoner, V., Das, R., Pence, L., Anand, G., LaFerriere, H., Zars, T., Bouyain, S. and Dobens, L. L. (2013) The kinase domain of Drosophila Tribbles is required for turnover of fly C/EBP during cell migration. Dev. Biol. 375, 33-44
-
(2013)
Dev. Biol.
, vol.375
, pp. 33-44
-
-
Masoner, V.1
Das, R.2
Pence, L.3
Anand, G.4
Laferriere, H.5
Zars, T.6
Bouyain, S.7
Dobens, L.L.8
-
89
-
-
0033637113
-
The level of C/EBP protein is critical for cell migration during drosophila oogenesis and is tightly controlled by regulated degradation
-
Rorth, P., Szabo, K. and Texido, G. (2000) The level of C/EBP protein is critical for cell migration during Drosophila oogenesis and is tightly controlled by regulated degradation. Mol. Cell 6, 23-30
-
(2000)
Mol. Cell
, vol.6
, pp. 23-30
-
-
Rorth, P.1
Szabo, K.2
Texido, G.3
-
90
-
-
78649732085
-
Transformation by tribbles homolog 2 (Trib2) requires both the trib2 kinase domain and COP1 binding
-
Keeshan, K., Bailis, W., Dedhia, P. H., Vega, M. E., Shestova, O., Xu, L., Toscano, K., Uljon, S. N., Blacklow, S. C. and Pear, W. S. (2010) Transformation by Tribbles homolog 2 (Trib2) requires both the Trib2 kinase domain and COP1 binding. Blood 116, 4948-4957
-
(2010)
Blood
, vol.116
, pp. 4948-4957
-
-
Keeshan, K.1
Bailis, W.2
Dedhia, P.H.3
Vega, M.E.4
Shestova, O.5
Xu, L.6
Toscano, K.7
Uljon, S.N.8
Blacklow, S.C.9
Pear, W.S.10
-
91
-
-
84920596326
-
Tribbles homolog 2 (Trib2) inactivates C/EBPalpha and causes acute myelogenous leukemia
-
Keeshan, K., and He., Y. P., Wouters, B. J., Shestova, O., Xu, L. W., Sai, H., Rodriguez, C. G., Maillard, I., Valk, P., Carroll, M. et al. (2006) Tribbles homolog 2 (Trib2) inactivates C/EBPalpha and causes acute myelogenous leukemia. Blood 108, 233a
-
(2006)
Blood
, vol.108
, pp. 233a
-
-
Keeshan, K.1
He, Y.P.2
Wouters, B.J.3
Shestova, O.4
Xu, L.W.5
Sai, H.6
Rodriguez, C.G.7
Maillard, I.8
Valk, P.9
Carroll, M.10
-
92
-
-
79960847407
-
Overexpression of TRIB2 in human lung cancers contributes to tumorigenesis through downregulation of C/EBP alpha
-
Grandinetti, K. B., and Stevens., T. A., Ha, S., Salamone, R. J., Walker, J. R., Zhang, J., Agarwalla, S., Tenen, D. G., Peters, E. C. and Reddy, V. A. (2011) Overexpression of TRIB2 in human lung cancers contributes to tumorigenesis through downregulation of C/EBP alpha. Oncogene 30, 3328-3335
-
(2011)
Oncogene
, vol.30
, pp. 3328-3335
-
-
Grandinetti, K.B.1
Stevens, T.A.2
Ha, S.3
Salamone, R.J.4
Walker, J.R.5
Zhang, J.6
Agarwalla, S.7
Tenen, D.G.8
Peters, E.C.9
Reddy, V.A.10
-
93
-
-
77952672913
-
Human TRIB2 is a repressor of FOXO that contributes to the Malignant phenotype of melanoma cells
-
Zanella, F., Renner, O., Garcia, B., Callejas, S., Dopazo, A., Peregrina, S., Carnero, A. and Link, W. (2010) Human TRIB2 is a repressor of FOXO that contributes to the malignant phenotype of melanoma cells. Oncogene 29, 2973-2982
-
(2010)
Oncogene
, vol.29
, pp. 2973-2982
-
-
Zanella, F.1
Renner, O.2
Garcia, B.3
Callejas, S.4
Dopazo, A.5
Peregrina, S.6
Carnero, A.7
Link, W.8
-
94
-
-
84880515015
-
TRIB2 acts downstream of wnt/TCF in liver cancer cells to regulate YAP and C/EBP alpha function
-
Wang, J., Park, J.-S., Wei, Y., Rajurkar, M., Cotton, J. L., Fan, Q., Lewis, B. C., Ji, H. and Mao, J. (2013) TRIB2 acts downstream of Wnt/TCF in liver cancer cells to regulate YAP and C/EBP alpha function. Mol. Cell 51, 211-225
-
(2013)
Mol. Cell
, vol.51
, pp. 211-225
-
-
Wang, J.1
Park, J.-S.2
Wei, Y.3
Rajurkar, M.4
Cotton, J.L.5
Fan, Q.6
Lewis, B.C.7
Ji, H.8
Mao, J.9
-
95
-
-
34247391073
-
Trib1 and evi1 cooperate with hoxa and meis1 in myeloid leukemogenesis
-
Jin, G., Yamazaki, Y., Takuwa, M., Takahara, T., Kaneko, K., Kuwata, T., Miyata, S. and Nakamura, T. (2007) Trib1 and Evi1 cooperate with Hoxa and Meis1 in myeloid leukemogenesis. Blood 109, 3998-4005
-
(2007)
Blood
, vol.109
, pp. 3998-4005
-
-
Jin, G.1
Yamazaki, Y.2
Takuwa, M.3
Takahara, T.4
Kaneko, K.5
Kuwata, T.6
Miyata, S.7
Nakamura, T.8
-
96
-
-
77957963658
-
Trib1 links the MEK1/ERK pathway in myeloid leukemogenesis
-
Yokoyama, T., Kanno, Y., Yamazaki, Y., Takahara, T., Miyata, S. and Nakamura, T. (2010) Trib1 links the MEK1/ERK pathway in myeloid leukemogenesis. Blood 116, 2768-2775
-
(2010)
Blood
, vol.116
, pp. 2768-2775
-
-
Yokoyama, T.1
Kanno, Y.2
Yamazaki, Y.3
Takahara, T.4
Miyata, S.5
Nakamura, T.6
-
97
-
-
84863391280
-
Identification of TRIB1 R107L gain-of-function mutation in human acute megakaryocytic leukemia
-
Yokoyama, T., Toki, T., Aoki, Y., Kanezaki, R., and Park., M. J., Kanno, Y., Takahara, T., Yamazaki, Y., Ito, E., Hayashi, Y. et al. (2012) Identification of TRIB1 R107L gain-of-function mutation in human acute megakaryocytic leukemia. Blood 119, 2608-2611
-
(2012)
Blood
, vol.119
, pp. 2608-2611
-
-
Yokoyama, T.1
Toki, T.2
Aoki, Y.3
Kanezaki, R.4
Park, M.J.5
Kanno, Y.6
Takahara, T.7
Yamazaki, Y.8
Ito, E.9
Hayashi, Y.10
-
98
-
-
84905187459
-
Association of polymorphisms in GCKR and TRIB1 with nonalcoholic fatty liver disease and metabolic syndrome traits
-
Kitamoto, A., Kitamoto, T., Nakamura, T., Ogawa, Y., Yoneda, M., Hyogo, H., Ochi, H., Mizusawa, S., Ueno, T., Nakao, K. et al. (2014) Association of polymorphisms in GCKR and TRIB1 with nonalcoholic fatty liver disease and metabolic syndrome traits. Endocr. J. 61, 683-689
-
(2014)
Endocr. J.
, vol.61
, pp. 683-689
-
-
Kitamoto, A.1
Kitamoto, T.2
Nakamura, T.3
Ogawa, Y.4
Yoneda, M.5
Hyogo, H.6
Ochi, H.7
Mizusawa, S.8
Ueno, T.9
Nakao, K.10
-
99
-
-
77956495743
-
Differential ability of tribbles family members to promote degradation of C/EBP alpha and induce acute myelogenous leukemia
-
Dedhia, P. H., Keeshan, K., Uljon, S., Xu, L. W., Vega, M. E., Shestova, O., Zaks-Zilberman, M., Romany, C., Blacklow, S. C. and Pear, W. S. (2010) Differential ability of Tribbles family members to promote degradation of C/EBP alpha and induce acute myelogenous leukemia. Blood 116, 1321-1328
-
(2010)
Blood
, vol.116
, pp. 1321-1328
-
-
Dedhia, P.H.1
Keeshan, K.2
Uljon, S.3
Xu, L.W.4
Vega, M.E.5
Shestova, O.6
Zaks-Zilberman, M.7
Romany, C.8
Blacklow, S.C.9
Pear, W.S.10
-
100
-
-
70449346285
-
Abnormal expression of TRIB3 in colorectal cancer: A novel marker for prognosis
-
Miyoshi, N., Ishii, H., Mimori, K., Takatsuno, Y., Kim, H., Hirose, H., Sekimoto, M., Doki, Y. and Mori, M. (2009) Abnormal expression of TRIB3 in colorectal cancer: a novel marker for prognosis. Br. J. Cancer 101, 1664-1670
-
(2009)
Br. J. Cancer
, vol.101
, pp. 1664-1670
-
-
Miyoshi, N.1
Ishii, H.2
Mimori, K.3
Takatsuno, Y.4
Kim, H.5
Hirose, H.6
Sekimoto, M.7
Doki, Y.8
Mori, M.9
-
101
-
-
84873161936
-
High throughput kinase inhibitor screens reveal TRB3 and MAPK-ERK/TGFbeta pathways as fundamental notch regulators in breast cancer
-
Izrailit, J., and Berman., H. K., Datti, A., Wrana, J. L. and Reedijk, M. (2013) High throughput kinase inhibitor screens reveal TRB3 and MAPK-ERK/TGFbeta pathways as fundamental Notch regulators in breast cancer. Proc. Natl. Acad. Sci. U.S.A. 110, 1714-1719
-
(2013)
Proc. Natl. Acad. Sci. U.S.A.
, vol.110
, pp. 1714-1719
-
-
Izrailit, J.1
Berman, H.K.2
Datti, A.3
Wrana, J.L.4
Reedijk, M.5
-
102
-
-
80052025916
-
Tribbles homolog 3 denotes a poor prognosis in breast cancer and is involved in hypoxia response
-
Wennemers, M., Bussink, J., Scheijen, B., Nagtegaal, I. D., van Laarhoven, H. W., Raleigh, J. A., Varia, M. A., Heuvel, J. J., Rouschop, K. M., Sweep, F. C. et al. (2011) Tribbles homolog 3 denotes a poor prognosis in breast cancer and is involved in hypoxia response. Breast Cancer Res. 13, R82
-
(2011)
Breast Cancer Res.
, vol.13
, pp. R82
-
-
Wennemers, M.1
Bussink, J.2
Scheijen, B.3
Nagtegaal, I.D.4
Van Laarhoven, H.W.5
Raleigh, J.A.6
Varia, M.A.7
Heuvel, J.J.8
Rouschop, K.M.9
Sweep, F.C.10
-
103
-
-
84891793531
-
TRIB3 mediates glucose-induced insulin resistance via a mechanism that requires the hexosamine biosynthetic pathway
-
Zhang, W., Liu, J., Tian, L., Liu, Q., Fu, Y. and Garvey, W. T. (2013) TRIB3 mediates glucose-induced insulin resistance via a mechanism that requires the hexosamine biosynthetic pathway. Diabetes 62, 4192-4200
-
(2013)
Diabetes
, vol.62
, pp. 4192-4200
-
-
Zhang, W.1
Liu, J.2
Tian, L.3
Liu, Q.4
Fu, Y.5
Garvey, W.T.6
-
104
-
-
84874302744
-
Deletion of STK40 protein in mice causes respiratory failure and death at birth
-
Yu, H., He, K., Li, L., Sun, L., Tang, F., Li, R., Ning, W. and Jin, Y. (2013) Deletion of STK40 protein in mice causes respiratory failure and death at birth. J. Biol. Chem. 288, 5342-5352
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 5342-5352
-
-
Yu, H.1
He, K.2
Li, L.3
Sun, L.4
Tang, F.5
Li, R.6
Ning, W.7
Jin, Y.8
-
105
-
-
2442690630
-
A novel protein tyrosine kinase NOK that shares homology with platelet-derived growth factor/fibroblast growth factor receptors induces tumorigenesis and metastasis in nude mice
-
Liu, L., and Yu., X. Z., Li, T. S., Song, L. X., Chen, P. L., Suo, T. L., Li, Y. H., Wang, S. D., Chen, Y., Ren, Y. M. et al. (2004) A novel protein tyrosine kinase NOK that shares homology with platelet-derived growth factor/fibroblast growth factor receptors induces tumorigenesis and metastasis in nude mice. Cancer Res. 64, 3491-3499
-
(2004)
Cancer Res.
, vol.64
, pp. 3491-3499
-
-
Liu, L.1
Yu, X.Z.2
Li, T.S.3
Song, L.X.4
Chen, P.L.5
Suo, T.L.6
Li, Y.H.7
Wang, S.D.8
Chen, Y.9
Ren, Y.M.10
-
106
-
-
28244476479
-
Point mutation at single tyrosine residue of novel oncogene NOK abrogates tumorigenesis in nude mice
-
Chen, Y., and Li., Y. H., Chen, X. P., Gong, L. N., Zhang, S. P., Chang, Z. J., Zhang, X. F., Fu, X. Y. and Liu, L. (2005) Point mutation at single tyrosine residue of novel oncogene NOK abrogates tumorigenesis in nude mice. Cancer Res. 65, 10838-10846
-
(2005)
Cancer Res.
, vol.65
, pp. 10838-10846
-
-
Chen, Y.1
Li, Y.H.2
Chen, X.P.3
Gong, L.N.4
Zhang, S.P.5
Chang, Z.J.6
Zhang, X.F.7
Fu, X.Y.8
Liu, L.9
-
107
-
-
67049173046
-
Overexpression of serine threonine tyrosine kinase 1/novel oncogene with kinase domain mRNA in patients with acute leukemia
-
Kondoh, T., Kobayashi, D., Tsuji, N., Kuribayashi, K. and Watanabe, N. (2009) Overexpression of serine threonine tyrosine kinase 1/novel oncogene with kinase domain mRNA in patients with acute leukemia. Exp. Hematol. 37, 824-830
-
(2009)
Exp. Hematol.
, vol.37
, pp. 824-830
-
-
Kondoh, T.1
Kobayashi, D.2
Tsuji, N.3
Kuribayashi, K.4
Watanabe, N.5
-
108
-
-
34247583954
-
Diagnostic relevance of overexpressed mRNA of novel oncogene with kinase-domain (NOK) in lung cancers
-
Amachika, T., Kobayashi, D., Moriai, R., Tsuji, N. and Watanabe, N. (2007) Diagnostic relevance of overexpressed mRNA of novel oncogene with kinase-domain (NOK) in lung cancers. Lung Cancer 56, 337-340
-
(2007)
Lung Cancer
, vol.56
, pp. 337-340
-
-
Amachika, T.1
Kobayashi, D.2
Moriai, R.3
Tsuji, N.4
Watanabe, N.5
-
109
-
-
77953419895
-
Aberrant STYK1 expression in ovarian cancer tissues and cell lines
-
Jackson, K. A., Oprea, G., Handy, J. and Kimbro, K. S. (2009) Aberrant STYK1 expression in ovarian cancer tissues and cell lines. J. Ovarian Res. 2, 15
-
(2009)
J. Ovarian Res.
, vol.2
, pp. 15
-
-
Jackson, K.A.1
Oprea, G.2
Handy, J.3
Kimbro, K.S.4
-
110
-
-
71049181019
-
Overexpression of the potential kinase serine/threonine/tyrosine kinase 1 (STYK 1) in castration-resistant prostate cancer
-
Chung, S. Y., Tamura, K., Furihata, M., Uemura, M., Daigo, Y., Nasu, Y., Miki, T., Shuin, T., Fujioka, T., Nakamura, Y. et al. (2009) Overexpression of the potential kinase serine/threonine/tyrosine kinase 1 (STYK 1) in castration-resistant prostate cancer. Cancer Sci. 100, 2109-2114
-
(2009)
Cancer Sci.
, vol.100
, pp. 2109-2114
-
-
Chung, S.Y.1
Tamura, K.2
Furihata, M.3
Uemura, M.4
Daigo, Y.5
Nasu, Y.6
Miki, T.7
Shuin, T.8
Fujioka, T.9
Nakamura, Y.10
-
111
-
-
38349141902
-
A novel gene STYK1/NOK is upregulated in estrogen receptor-alpha negative estrogen receptor-beta positive breast cancer cells following estrogen treatment
-
Kimbro, K. S., Duschene, K., Willard, M., Moore, J.-A. and Freeman, S. (2008) A novel gene STYK1/NOK is upregulated in estrogen receptor-alpha negative estrogen receptor-beta positive breast cancer cells following estrogen treatment. Mol. Biol. Rep. 35, 23-27
-
(2008)
Mol. Biol. Rep.
, vol.35
, pp. 23-27
-
-
Kimbro, K.S.1
Duschene, K.2
Willard, M.3
Moore, J.-A.4
Freeman, S.5
-
112
-
-
84907189436
-
Significance of serine threonine tyrosine kinase 1 as a drug resistance factor and therapeutic predictor in acute leukemia
-
Nirasawa, S., Kobayashi, D., Kondoh, T., Kuribayashi, K., Tanaka, M., Yanagihara, N. and Watanabe, N. (2014) Significance of serine threonine tyrosine kinase 1 as a drug resistance factor and therapeutic predictor in acute leukemia. Int. J. Oncol. 45, 1867-1874
-
(2014)
Int. J. Oncol.
, vol.45
, pp. 1867-1874
-
-
Nirasawa, S.1
Kobayashi, D.2
Kondoh, T.3
Kuribayashi, K.4
Tanaka, M.5
Yanagihara, N.6
Watanabe, N.7
-
113
-
-
84872515516
-
Kinase drug discovery - What's next in the field?
-
Cohen, P. and Alessi, D. R. (2013) Kinase drug discovery - what's next in the field? ACS Chem. Biol. 8, 96-104
-
(2013)
ACS Chem. Biol.
, vol.8
, pp. 96-104
-
-
Cohen, P.1
Alessi, D.R.2
-
114
-
-
77955299093
-
JAK2 V617F constitutive activation requires JH2 residue F595: A pseudokinase domain target for specific inhibitors
-
Dusa, A., Mouton, C., Pecquet, C., Herman, M. and Constantinescu, S. N. (2010) JAK2 V617F constitutive activation requires JH2 residue F595: a pseudokinase domain target for specific inhibitors. PLoS ONE 5, e11157
-
(2010)
PLoS ONE
, vol.5
-
-
Dusa, A.1
Mouton, C.2
Pecquet, C.3
Herman, M.4
Constantinescu, S.N.5
-
115
-
-
84877839648
-
Oncogenic ERBB3 mutations in human cancers
-
Jaiswal, B. S., and Kljavin., N. M., Stawiski, E. W., Chan, E., Parikh, C., Durinck, S., Chaudhuri, S., Pujara, K., Guillory, J., Edgar, K. A. et al. (2013) Oncogenic ERBB3 mutations in human cancers. Cancer Cell 23, 603-617
-
(2013)
Cancer Cell
, vol.23
, pp. 603-617
-
-
Jaiswal, B.S.1
Kljavin, N.M.2
Stawiski, E.W.3
Chan, E.4
Parikh, C.5
Durinck, S.6
Chaudhuri, S.7
Pujara, K.8
Guillory, J.9
Edgar, K.A.10
-
116
-
-
0033179479
-
Paradoxical activation of raf by a novel raf inhibitor
-
Hall-Jackson, C. A., Eyers, P. A., Cohen, P., Goedert, M., and Boyle., F. T., Hewitt, N., Plant, H. and Hedge, P. (1999) Paradoxical activation of Raf by a novel Raf inhibitor. Chem. Biol. 6, 559-568
-
(1999)
Chem. Biol.
, vol.6
, pp. 559-568
-
-
Hall-Jackson, C.A.1
Eyers, P.A.2
Cohen, P.3
Goedert, M.4
Boyle, F.T.5
Hewitt, N.6
Plant, H.7
Hedge, P.8
-
117
-
-
84862273387
-
Identification of a novel family of BRAF(V600E) inhibitors
-
Qin, J., Xie, P., Ventocilla, C., Zhou, G., Vultur, A., Chen, Q., Liu, Q., Herlyn, M., Winkler, J. and Marmorstein, R. (2012) Identification of a novel family of BRAF(V600E) inhibitors. J. Med. Chem. 55, 5220-5230
-
(2012)
J. Med. Chem.
, vol.55
, pp. 5220-5230
-
-
Qin, J.1
Xie, P.2
Ventocilla, C.3
Zhou, G.4
Vultur, A.5
Chen, Q.6
Liu, Q.7
Herlyn, M.8
Winkler, J.9
Marmorstein, R.10
-
118
-
-
79955751512
-
BRAF(V600E): Implications for carcinogenesis and molecular therapy
-
Cantwell-Dorris, E. R., O'Leary, J. J. and Sheils, O. M. (2011) BRAF(V600E): implications for carcinogenesis and molecular therapy. Mol. Cancer Therap. 10, 385-394
-
(2011)
Mol. Cancer Therap.
, vol.10
, pp. 385-394
-
-
Cantwell-Dorris, E.R.1
O'Leary, J.J.2
Sheils, O.M.3
-
119
-
-
25144502820
-
Higher-order substrate recognition of eIF2alpha by the RNA-dependent protein kinase PKR
-
Dar, A. C., Dever, T. E. and Sicheri, F. (2005) Higher-order substrate recognition of eIF2alpha by the RNA-dependent protein kinase PKR. Cell 122, 887-900
-
(2005)
Cell
, vol.122
, pp. 887-900
-
-
Dar, A.C.1
Dever, T.E.2
Sicheri, F.3
-
120
-
-
33751539464
-
Protein-protein interactions in the allosteric regulation of protein kinases
-
Pellicena, P. and Kuriyan, J. (2006) Protein-protein interactions in the allosteric regulation of protein kinases. Curr. Opin. Struct. Biol. 16, 702-709
-
(2006)
Curr. Opin. Struct. Biol.
, vol.16
, pp. 702-709
-
-
Pellicena, P.1
Kuriyan, J.2
-
121
-
-
80051931772
-
New mutations and pathogenesis of myeloproliferative neoplasms
-
Vainchenker, W., Delhommeau, F., Constantinescu, S. N. and Bernard, O. A. (2011) New mutations and pathogenesis of myeloproliferative neoplasms. Blood 118, 1723-1735
-
(2011)
Blood
, vol.118
, pp. 1723-1735
-
-
Vainchenker, W.1
Delhommeau, F.2
Constantinescu, S.N.3
Bernard, O.A.4
-
122
-
-
84864668290
-
Crystal structures of the JAK2 pseudokinase domain and the pathogenic mutant V617F
-
Bandaranayake, R. M., Ungureanu, D., Shan, Y., Shaw, D. E., Silvennoinen, O. and Hubbard, S. R. (2012) Crystal structures of the JAK2 pseudokinase domain and the pathogenic mutant V617F. Nat. Struct. Mol. Biol. 19, 754-759
-
(2012)
Nat. Struct. Mol. Biol.
, vol.19
, pp. 754-759
-
-
Bandaranayake, R.M.1
Ungureanu, D.2
Shan, Y.3
Shaw, D.E.4
Silvennoinen, O.5
Hubbard, S.R.6
-
123
-
-
84901840527
-
Structure of the pseudokinase-kinase domains from protein kinase TYK2 reveals a mechanism for janus kinase (JAK) autoinhibition
-
Lupardus, P. J., Ultsch, M., Wallweber, H., Bir Kohli, P., Johnson, A. R. and Eigenbrot, C. (2014) Structure of the pseudokinase-kinase domains from protein kinase TYK2 reveals a mechanism for Janus kinase (JAK) autoinhibition. Proc. Natl. Acad. Sci. U.S.A. 111, 8025-8030
-
(2014)
Proc. Natl. Acad. Sci. U.S.A.
, vol.111
, pp. 8025-8030
-
-
Lupardus, P.J.1
Ultsch, M.2
Wallweber, H.3
Bir Kohli, P.4
Johnson, A.R.5
Eigenbrot, C.6
-
124
-
-
84880531829
-
Pseudokinases from a structural perspective
-
Taylor, S. S., Shaw, A., Hu, J., Meharena, H. S. and Kornev, A. (2013) Pseudokinases from a structural perspective. Biochem. Soc. Trans. 41, 981-986
-
(2013)
Biochem. Soc. Trans.
, vol.41
, pp. 981-986
-
-
Taylor, S.S.1
Shaw, A.2
Hu, J.3
Meharena, H.S.4
Kornev, A.5
-
125
-
-
58149189627
-
ROP2 from toxoplasma gondii: A virulence factor with a protein-kinase fold and no enzymatic activity
-
Labesse, G., Gelin, M., Bessin, Y., Lebrun, M., Papoin, J., Cerdan, R., Arold, S. T. and Dubremetz, J. F. (2009) ROP2 from Toxoplasma gondii: a virulence factor with a protein-kinase fold and no enzymatic activity. Structure 17, 139-146
-
(2009)
Structure
, vol.17
, pp. 139-146
-
-
Labesse, G.1
Gelin, M.2
Bessin, Y.3
Lebrun, M.4
Papoin, J.5
Cerdan, R.6
Arold, S.T.7
Dubremetz, J.F.8
-
126
-
-
71149097258
-
The pseudoactive site of ILK is essential for its binding to alpha-parvin and localization to focal adhesions
-
Fukuda, K., Gupta, S., Chen, K., Wu, C. and Qin, J. (2009) The pseudoactive site of ILK is essential for its binding to alpha-Parvin and localization to focal adhesions. Mol. Cell 36, 819-830
-
(2009)
Mol. Cell
, vol.36
, pp. 819-830
-
-
Fukuda, K.1
Gupta, S.2
Chen, K.3
Wu, C.4
Qin, J.5
-
127
-
-
38049155899
-
A systematic interaction map of validated kinase inhibitors with ser/Thr kinases
-
Fedorov, O., Marsden, B., Pogacic, V., Rellos, P., Muller, S., Bullock, A. N., Schwaller, J., Sundstrom, M. and Knapp, S. (2007) A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases. Proc. Natl. Acad. Sci. U.S.A. 104, 20523-20528
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 20523-20528
-
-
Fedorov, O.1
Marsden, B.2
Pogacic, V.3
Rellos, P.4
Muller, S.5
Bullock, A.N.6
Schwaller, J.7
Sundstrom, M.8
Knapp, S.9
-
128
-
-
77749304756
-
Biophysical and X-ray crystallographic analysis of mps1 kinase inhibitor complexes
-
Chu, M. L., Lang, Z., Chavas, L. M., Neres, J., Fedorova, O. S., Tabernero, L., Cherry, M., and Williams., D. H., Douglas, K. T. and Eyers, P. A. (2010) Biophysical and X-ray crystallographic analysis of Mps1 kinase inhibitor complexes. Biochemistry 49, 1689-1701
-
(2010)
Biochemistry
, vol.49
, pp. 1689-1701
-
-
Chu, M.L.1
Lang, Z.2
Chavas, L.M.3
Neres, J.4
Fedorova, O.S.5
Tabernero, L.6
Cherry, M.7
Williams, D.H.8
Douglas, K.T.9
Eyers, P.A.10
-
129
-
-
80555156183
-
Targeting cancer with small-molecular-weight kinase inhibitors
-
Fabbro, D., Cowan-Jacob, S. W., Mobitz, H. and Martiny-Baron, G. (2012) Targeting cancer with small-molecular-weight kinase inhibitors. Methods: Mol. Biol. 795, 1-34
-
(2012)
Methods: Mol. Biol.
, vol.795
, pp. 1-34
-
-
Fabbro, D.1
Cowan-Jacob, S.W.2
Mobitz, H.3
Martiny-Baron, G.4
-
130
-
-
58149102648
-
Type-II kinase inhibitor docking, screening, and profiling using modified structures of active kinase states
-
Kufareva, I. and Abagyan, R. (2008) Type-II kinase inhibitor docking, screening, and profiling using modified structures of active kinase states. J. Med. Chem. 51, 7921-7932
-
(2008)
J. Med. Chem.
, vol.51
, pp. 7921-7932
-
-
Kufareva, I.1
Abagyan, R.2
-
132
-
-
75749146563
-
Targeting bcr-abl by combining allosteric with ATP-binding-site inhibitors
-
Zhang, J., and Adrian., F. J., Jahnke, W., Cowan-Jacob, S. W., Li, A. G., Iacob, R. E., Sim, T., Powers, J., Dierks, C., Sun, F. et al. (2010) Targeting Bcr-Abl by combining allosteric with ATP-binding-site inhibitors. Nature 463, 501-506
-
(2010)
Nature
, vol.463
, pp. 501-506
-
-
Zhang, J.1
Adrian, F.J.2
Jahnke, W.3
Cowan-Jacob, S.W.4
Li, A.G.5
Iacob, R.E.6
Sim, T.7
Powers, J.8
Dierks, C.9
Sun, F.10
-
133
-
-
84904898065
-
AZD9291, an irreversible EGFR TKI, overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer
-
Cross, D. A., and Ashton., S. E., Ghiorghiu, S., Eberlein, C., Nebhan, C. A., Spitzler, P. J., Orme, J. P., Finlay, M. R., and Ward., R. A., Mellor, M. J. et al. (2014) AZD9291, an irreversible EGFR TKI, overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer. Cancer Discov. 4, 1046-1061
-
(2014)
Cancer Discov.
, vol.4
, pp. 1046-1061
-
-
Cross, D.A.1
Ashton, S.E.2
Ghiorghiu, S.3
Eberlein, C.4
Nebhan, C.A.5
Spitzler, P.J.6
Orme, J.P.7
Finlay, M.R.8
Ward, R.A.9
Mellor, M.J.10
-
134
-
-
33645233076
-
Targeted covalent inactivation of protein kinases by resorcylic acid lactone polyketides
-
Schirmer, A., Kennedy, J., Murli, S., Reid, R. and Santi, D. V. (2006) Targeted covalent inactivation of protein kinases by resorcylic acid lactone polyketides. Proc. Natl. Acad. Sci. U.S.A. 103, 4234-4239
-
(2006)
Proc. Natl. Acad. Sci. U.S.A.
, vol.103
, pp. 4234-4239
-
-
Schirmer, A.1
Kennedy, J.2
Murli, S.3
Reid, R.4
Santi, D.V.5
-
135
-
-
77955625479
-
The bruton tyrosine kinase inhibitor PCI-32765 blocks B-cell activation and is efficacious in models of autoimmune disease and B-cell Malignancy
-
Honigberg, L. A., and Smith., A. M., Sirisawad, M., Verner, E., Loury, D., Chang, B., Li, S., Pan, Z., and Thamm., D. H., Miller, R. A. et al. (2010) The Bruton tyrosine kinase inhibitor PCI-32765 blocks B-cell activation and is efficacious in models of autoimmune disease and B-cell malignancy. Proc. Natl. Acad. Sci. U.S.A. 107, 13075-13080
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 13075-13080
-
-
Honigberg, L.A.1
Smith, A.M.2
Sirisawad, M.3
Verner, E.4
Loury, D.5
Chang, B.6
Li, S.7
Pan, Z.8
Thamm, D.H.9
Miller, R.A.10
-
136
-
-
84887977876
-
Discovery of a mutant-selective covalent inhibitor of EGFR that overcomes T790M-mediated resistance in NSCLC
-
Walter, A. O., and Sjin., R. T., Haringsma, H. J., Ohashi, K., Sun, J., Lee, K., Dubrovskiy, A., Labenski, M., Zhu, Z., Wang, Z. et al. (2013) Discovery of a mutant-selective covalent inhibitor of EGFR that overcomes T790M-mediated resistance in NSCLC. Cancer Discov. 3, 1404-1415
-
(2013)
Cancer Discov.
, vol.3
, pp. 1404-1415
-
-
Walter, A.O.1
Sjin, R.T.2
Haringsma, H.J.3
Ohashi, K.4
Sun, J.5
Lee, K.6
Dubrovskiy, A.7
Labenski, M.8
Zhu, Z.9
Wang, Z.10
-
137
-
-
84874301754
-
Developing irreversible inhibitors of the protein kinase cysteinome
-
Liu, Q., Sabnis, Y., Zhao, Z., Zhang, T., and Buhrlage., S. J., Jones, L. H. and Gray, N. S. (2013) Developing irreversible inhibitors of the protein kinase cysteinome. Chem. Biol. 20, 146-159
-
(2013)
Chem. Biol.
, vol.20
, pp. 146-159
-
-
Liu, Q.1
Sabnis, Y.2
Zhao, Z.3
Zhang, T.4
Buhrlage, S.J.5
Jones, L.H.6
Gray, N.S.7
-
138
-
-
40049099220
-
The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP
-
Yun, C. H., and Mengwasser., K. E., Toms, A. V., Woo, M. S., Greulich, H., Wong, K. K., Meyerson, M. and Eck, M. J. (2008) The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP. Proc. Natl. Acad. Sci. U.S.A. 105, 2070-2075
-
(2008)
Proc. Natl. Acad. Sci. U.S.A.
, vol.105
, pp. 2070-2075
-
-
Yun, C.H.1
Mengwasser, K.E.2
Toms, A.V.3
Woo, M.S.4
Greulich, H.5
Wong, K.K.6
Meyerson, M.7
Eck, M.J.8
-
139
-
-
84893578349
-
Ponatinib in philadelphia chromosome-positive leukemias
-
Cortes, J. E., Talpaz, M. and Kantarjian, H. (2014) Ponatinib in Philadelphia chromosome-positive leukemias. N. Engl. J. Med. 370, 577
-
(2014)
N. Engl. J. Med.
, vol.370
, pp. 577
-
-
Cortes, J.E.1
Talpaz, M.2
Kantarjian, H.3
-
140
-
-
84920590896
-
Pharmacological targeting of the pseudokinase her3
-
Xie, T., and Lim., S. M., Westover, K. D., Dodge, M. E., Ercan, D., Ficarro, S. B., Udayakumar, D., Gurbani, D., and Tae., H. S., Riddle, S. M. et al. (2014) Pharmacological targeting of the pseudokinase Her3. Nat. Chem. Biol. 10, 1006-1012
-
(2014)
Nat. Chem. Biol.
, vol.10
, pp. 1006-1012
-
-
Xie, T.1
Lim, S.M.2
Westover, K.D.3
Dodge, M.E.4
Ercan, D.5
Ficarro, S.B.6
Udayakumar, D.7
Gurbani, D.8
Tae, H.S.9
Riddle, S.M.10
-
141
-
-
21744446065
-
Discovery of a novel and potent series of dianilinopyrimidineurea and urea isostere inhibitors of VEGFR2 tyrosine kinase
-
Sammond, D. M., and Nailor., K. E., Veal, J. M., Nolte, R. T., Wang, L., Knick, V. B., Rudolph, S. K., Truesdale, A. T., and Nartey., E. N., Stafford, J. A. et al. (2005) Discovery of a novel and potent series of dianilinopyrimidineurea and urea isostere inhibitors of VEGFR2 tyrosine kinase. Bioorg. Med. Chem. Lett. 15, 3519-3523
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 3519-3523
-
-
Sammond, D.M.1
Nailor, K.E.2
Veal, J.M.3
Nolte, R.T.4
Wang, L.5
Knick, V.B.6
Rudolph, S.K.7
Truesdale, A.T.8
Nartey, E.N.9
Stafford, J.A.10
-
142
-
-
83355168628
-
Pro kin O: An ontology for integrative analysis of protein kinases in cancer
-
Gosal, G., Kochut, K. J. and Kannan, N. (2011) Pro Kin O: an ontology for integrative analysis of protein kinases in cancer. PLoS ONE 6, e28782
-
(2011)
PLoS ONE
, vol.6
-
-
Gosal, G.1
Kochut, K.J.2
Kannan, N.3
-
143
-
-
84874306548
-
On the molecular mechanisms of mitotic kinase activation
-
Bayliss, R., Fry, A., Haq, T. and Yeoh, S. (2012) On the molecular mechanisms of mitotic kinase activation. Open Biol. 2, 120136
-
(2012)
Open Biol.
, vol.2
-
-
Bayliss, R.1
Fry, A.2
Haq, T.3
Yeoh, S.4
-
144
-
-
84887001050
-
A three-stage biophysical screening cascade for fragment-based drug discovery
-
Mashalidis, E. H., Sledz, P., Lang, S. and Abell, C. (2013) A three-stage biophysical screening cascade for fragment-based drug discovery. Nat. Protoc. 8, 2309-2324
-
(2013)
Nat. Protoc.
, vol.8
, pp. 2309-2324
-
-
Mashalidis, E.H.1
Sledz, P.2
Lang, S.3
Abell, C.4
-
145
-
-
84861542870
-
Use of differential scanning fluorimetry as a high-throughput assay to identify nuclear receptor ligands
-
DeSantis, K., Reed, A., Rahhal, R. and Reinking, J. (2012) Use of differential scanning fluorimetry as a high-throughput assay to identify nuclear receptor ligands. Nucl. Recept. Signal. 10, e002
-
(2012)
Nucl. Recept. Signal.
, vol.10
, pp. e002
-
-
Desantis, K.1
Reed, A.2
Rahhal, R.3
Reinking, J.4
-
146
-
-
84880536536
-
Techniques to examine nucleotide binding by pseudokinases
-
Lucet, I. S., Babon, J. J. and Murphy, J. M. (2013) Techniques to examine nucleotide binding by pseudokinases. Biochem. Soc. Trans. 41, 975-980
-
(2013)
Biochem. Soc. Trans.
, vol.41
, pp. 975-980
-
-
Lucet, I.S.1
Babon, J.J.2
Murphy, J.M.3
-
147
-
-
37249005205
-
The use of differential scanning fluorimetry to detect ligand interactions that promote protein stability
-
Niesen, F. H., Berglund, H. and Vedadi, M. (2007) The use of differential scanning fluorimetry to detect ligand interactions that promote protein stability. Nat. Protoc. 2, 2212-2221
-
(2007)
Nat. Protoc.
, vol.2
, pp. 2212-2221
-
-
Niesen, F.H.1
Berglund, H.2
Vedadi, M.3
-
148
-
-
84891938336
-
A fluorescence-based thermal shift assay identifies inhibitors of mitogen activated protein kinase kinase 4
-
Krishna, S. N., and Luan., C. H., Mishra, R. K., Xu, L., Scheidt, K. A., Anderson, W. F. and Bergan, R. C. (2013) A fluorescence-based thermal shift assay identifies inhibitors of mitogen activated protein kinase kinase 4. PLoS ONE 8, e81504
-
(2013)
PLoS ONE
, vol.8
-
-
Krishna, S.N.1
Luan, C.H.2
Mishra, R.K.3
Xu, L.4
Scheidt, K.A.5
Anderson, W.F.6
Bergan, R.C.7
-
149
-
-
78650847770
-
Selective inhibition of BET bromodomains
-
Filippakopoulos, P., Qi, J., Picaud, S., Shen, Y., and Smith., W. B., Fedorov, O., Morse, E. M., Keates, T., Hickman, T. T., Felletar, I. et al. (2010) Selective inhibition of BET bromodomains. Nature 468, 1067-1073
-
(2010)
Nature
, vol.468
, pp. 1067-1073
-
-
Filippakopoulos, P.1
Qi, J.2
Picaud, S.3
Shen, Y.4
Smith, W.B.5
Fedorov, O.6
Morse, E.M.7
Keates, T.8
Hickman, T.T.9
Felletar, I.10
-
150
-
-
84896611007
-
Dual kinase-bromodomain inhibitors for rationally designed polypharmacology
-
Ciceri, P., Muller, S., O'Mahony, A., Fedorov, O., Filippakopoulos, P., Hunt, J. P., Lasater, E. A., Pallares, G., Picaud, S., Wells, C. et al. (2014) Dual kinase-bromodomain inhibitors for rationally designed polypharmacology. Nat. Chem. Biol. 10, 305-312
-
(2014)
Nat. Chem. Biol.
, vol.10
, pp. 305-312
-
-
Ciceri, P.1
Muller, S.2
O'Mahony, A.3
Fedorov, O.4
Filippakopoulos, P.5
Hunt, J.P.6
Lasater, E.A.7
Pallares, G.8
Picaud, S.9
Wells, C.10
-
151
-
-
84894039568
-
Seeding collaborations to advance kinase science with the GSK published kinase inhibitor set (PKIS)
-
Drewry, D. H., Willson, T. M. and Zuercher, W. J. (2014) Seeding collaborations to advance kinase science with the GSK Published Kinase Inhibitor Set (PKIS). Curr. Top. Med. Chem. 14, 340-342
-
(2014)
Curr. Top. Med. Chem.
, vol.14
, pp. 340-342
-
-
Drewry, D.H.1
Willson, T.M.2
Zuercher, W.J.3
|