-
1
-
-
84878832998
-
OTU deubiquitinases reveal mechanisms of linkage specificity and enable ubiquitin chain restriction analysis
-
T. E. Mevissen, M. K. Hospenthal, P. P. Geurink, P. R. Elliott, M. Akutsu, N. Arnaudo, R. Ekkebus, Y. Kulathu, T. Wauer, F. El Oualid, S. M. V. Freund, H. Ovaa, D. Komander, OTU deubiquitinases reveal mechanisms of linkage specificity and enable ubiquitin chain restriction analysis. Cell 154, 169-184 (2013).
-
(2013)
Cell
, vol.154
, pp. 169-184
-
-
Mevissen, T.E.1
Hospenthal, M.K.2
Geurink, P.P.3
Elliott, P.R.4
Akutsu, M.5
Arnaudo, N.6
Ekkebus, R.7
Kulathu, Y.8
Wauer, T.9
El Oualid, F.10
Freund, S.M.V.11
Ovaa, H.12
Komander, D.13
-
2
-
-
68049084674
-
Breaking the chains: Structure and function of the deubiquitinases
-
D. Komander, M. J. Clague, S. Urbé, Breaking the chains: Structure and function of the deubiquitinases. Nat. Rev. Mol. Cell Biol. 10, 550-563 (2009).
-
(2009)
Nat. Rev. Mol. Cell Biol
, vol.10
, pp. 550-563
-
-
Komander, D.1
Clague, M.J.2
Urbé, S.3
-
3
-
-
0038449224
-
Otubains: A new family of cysteine proteases in the ubiquitin pathway
-
M. Y. Balakirev, S. O. Tcherniuk, M. Jaquinod, J. Chroboczek, Otubains: A new family of cysteine proteases in the ubiquitin pathway. EMBO Rep. 4, 517-522 (2003).
-
(2003)
EMBO Rep
, vol.4
, pp. 517-522
-
-
Balakirev, M.Y.1
Tcherniuk, S.O.2
Jaquinod, M.3
Chroboczek, J.4
-
4
-
-
61449120240
-
Structural basis and specificity of human otubain 1-mediated deubiquitination
-
M. J. Edelmann, A. Iphöfer, M. Akutsu, M. Altun, K. di Gleria, H. B. Kramer, E. Fiebiger, S. Dhe-Paganon, B. M. Kessler, Structural basis and specificity of human otubain 1-mediated deubiquitination. Biochem. J. 418, 379 (2009).
-
(2009)
Biochem. J
, vol.418
, pp. 379
-
-
Edelmann, M.J.1
Iphöfer, A.2
Akutsu, M.3
Altun, M.4
Di Gleria, K.5
Kramer, H.B.6
Fiebiger, E.7
Dhe-Paganon, S.8
Kessler, B.M.9
-
5
-
-
44849136272
-
Structural basis for ubiquitin recognition by the Otu1 ovarian tumor domain protein
-
T. E. Messick, N. S. Russell, A. J. Iwata, K. L. Sarachan, R. Shiekhattar, J. R. Shanks, F. E. Reyes-Turcu, K. D. Wilkinson, R. Marmorstein, Structural basis for ubiquitin recognition by the Otu1 ovarian tumor domain protein. J. Biol. Chem. 283, 11038-11049 (2008).
-
(2008)
J. Biol. Chem
, vol.283
, pp. 11038-11049
-
-
Messick, T.E.1
Russell, N.S.2
Iwata, A.J.3
Sarachan, K.L.4
Shiekhattar, R.5
Shanks, J.R.6
Reyes-Turcu, F.E.7
Wilkinson, K.D.8
Marmorstein, R.9
-
6
-
-
60149084572
-
Evidence for bidentate substrate binding as the basis for the K48 linkage specificity of otubain 1
-
T. Wang, L. Yin, E. M. Cooper, M. Y. Lai, S. Dickey, C. M. Pickart, D. Fushman, K. D. Wilkinson, R. E. Cohen, C. Wolberger, Evidence for bidentate substrate binding as the basis for the K48 linkage specificity of otubain 1. J. Mol. Biol. 386, 1011-1023 (2009).
-
(2009)
J. Mol. Biol
, vol.386
, pp. 1011-1023
-
-
Wang, T.1
Yin, L.2
Cooper, E.M.3
Lai, M.Y.4
Dickey, S.5
Pickart, C.M.6
Fushman, D.7
Wilkinson, K.D.8
Cohen, R.E.9
Wolberger, C.10
-
7
-
-
84883740585
-
E2 ubiquitin-conjugating enzymes regulate the deubiquitinating activity of OTUB1
-
R. Wiener,A. T.DiBello,P.M. Lombardi,C.M. Guzzo,X. Zhang, M. J. Matunis,C. Wolberger, E2 ubiquitin-conjugating enzymes regulate the deubiquitinating activity of OTUB1. Nat. Struct. Mol. Biol. 20, 1033-1039 (2013).
-
(2013)
Nat. Struct. Mol. Biol
, vol.20
, pp. 1033-1039
-
-
Wiener, R.1
DiBello, A.T.2
Lombardi, P.M.3
Guzzo, C.M.4
Zhang, X.5
Matunis, M.J.6
Wolberger, C.7
-
8
-
-
84862806447
-
The mechanism of OTUB1-mediated inhibition of ubiquitination
-
R. Wiener, X. Zhang, T. Wang, C. Wolberger, The mechanism of OTUB1-mediated inhibition of ubiquitination. Nature 483, 612-622 (2012).
-
(2012)
Nature
, vol.483
, pp. 612-622
-
-
Wiener, R.1
Zhang, X.2
Wang, T.3
Wolberger, C.4
-
9
-
-
84856801739
-
OTUB1 co-opts Lys48-linked ubiquitin recognition to suppress E2 enzyme function
-
Y. C. Juang, M.C. Landry, M. Sanches, V.Vittal, C.C. Leung, D. F. Ceccarelli, A. R. Mateo, J. N. Pruneda, D. Y. Mao, R. K. Szilard, S. Orlicky, M. Munro, P. S. Brzovic, R. E. Klevit, F. Sicheri, D. Durocher, OTUB1 co-opts Lys48-linked ubiquitin recognition to suppress E2 enzyme function. Mol. Cell 45, 384-397 (2012).
-
(2012)
Mol. Cell
, vol.45
, pp. 384-397
-
-
Juang, Y.C.1
Landry, M.C.2
Sanches, M.3
Vittal, V.4
Leung, C.C.5
Ceccarelli, D.F.6
Mateo, A.R.7
Pruneda, J.N.8
Mao, D.Y.9
Szilard, R.K.10
Orlicky, S.11
Munro, M.12
Brzovic, P.S.13
Klevit, R.E.14
Sicheri, F.15
Durocher, D.16
-
10
-
-
84864386119
-
Molecular basis of Lys-63-linked polyubiquitination inhibition by the interaction between human deubiquitinating enzyme OTUB1 and ubiquitin-conjugating enzyme UBC13
-
Y. Sato, A. Yamagata, S. Goto-Ito, K. Kubota, R. Miyamoto, S. Nakada, S. Fukai, Molecular basis of Lys-63-linked polyubiquitination inhibition by the interaction between human deubiquitinating enzyme OTUB1 and ubiquitin-conjugating enzyme UBC13. J. Biol. Chem. 287, 25860-25868 (2012).
-
(2012)
J. Biol. Chem
, vol.287
, pp. 25860-25868
-
-
Sato, Y.1
Yamagata, A.2
Goto-Ito, S.3
Kubota, K.4
Miyamoto, R.5
Nakada, S.6
Fukai, S.7
-
11
-
-
77951168849
-
Regulation of virus-triggered signaling by OTUB1-and OTUB2-mediated deubiquitination of TRAF3 and TRAF6
-
S. Li, H. Zheng, A. P. Mao, B. Zhong, Y. Li, Y. Liu, Y. Gao, Y. Ran, P. Tien, H. B. Shu, Regulation of virus-triggered signaling by OTUB1-and OTUB2-mediated deubiquitination of TRAF3 and TRAF6. J. Biol. Chem. 285, 4291-4297 (2010).
-
(2010)
J. Biol. Chem
, vol.285
, pp. 4291-4297
-
-
Li, S.1
Zheng, H.2
Mao, A.P.3
Zhong, B.4
Li, Y.5
Liu, Y.6
Gao, Y.7
Ran, Y.8
Tien, P.9
Shu, H.B.10
-
12
-
-
67650215581
-
OTU Domaincontaining ubiquitin aldehyde-binding protein 1 (OTUB1) deubiquitinates estrogen receptor (ER) a and affects ERa transcriptional activity
-
V. Stanisic, A. Malovannaya, J. Qin, D. M. Lonard, B. W. O'Malley, OTU Domaincontaining ubiquitin aldehyde-binding protein 1 (OTUB1) deubiquitinates estrogen receptor (ER) a and affects ERa transcriptional activity. J. Biol. Chem. 284, 16135-16145 (2009).
-
(2009)
J. Biol. Chem
, vol.284
, pp. 16135-16145
-
-
Stanisic, V.1
Malovannaya, A.2
Qin, J.3
Lonard, D.M.4
O'malley, B.W.5
-
13
-
-
84856415004
-
Positive regulation of p53 stability and activity by the deubiquitinating enzyme Otubain 1
-
X.-X. Sun, K. B. Challagundla, M.-S. Dai, Positive regulation of p53 stability and activity by the deubiquitinating enzyme Otubain 1. EMBO J. 31, 576-592 (2011).
-
(2011)
EMBO J
, vol.31
, pp. 576-592
-
-
Sun, X.-X.1
Challagundla, K.B.2
Dai, M.-S.3
-
14
-
-
84876412379
-
OTUB1 modulates c-IAP1 stability to regulate signalling pathways
-
T. Goncharov, K. Niessen, M. C. de Almagro, A. Izrael-Tomasevic, A. V. Fedorova, E. Varfolomeev, D. Arnott, K. Deshayes, D. S. Kirkpatrick, D. Vucic, OTUB1 modulates c-IAP1 stability to regulate signalling pathways. EMBO J. 32, 1103-1114 (2013).
-
(2013)
EMBO J
, vol.32
, pp. 1103-1114
-
-
Goncharov, T.1
Niessen, K.2
De Almagro, M.C.3
Izrael-Tomasevic, A.4
Fedorova, A.V.5
Varfolomeev, E.6
Arnott, D.7
Deshayes, K.8
Kirkpatrick, D.S.9
Vucic, D.10
-
15
-
-
77955867565
-
Non-canonical inhibition of DNA damage-dependent ubiquitination by OTUB1
-
S.Nakada, I.Tai,S.Panier, A. Al-Hakim,S.-. Iemura, Y.-C. Juang, L.O'Donnell,A.Kumakubo, M. Munro, F. Sicheri, A.-C. Gingras, T. Natsume, T. Suda, D. Durocher, Non-canonical inhibition of DNA damage-dependent ubiquitination by OTUB1. Nature 466, 941-946 (2010).
-
(2010)
Nature
, vol.466
, pp. 941-946
-
-
Nakada, S.1
Tai, I.2
Panier, S.3
Al-Hakim, A.4
Iemura, S.5
Juang, Y.-C.6
O'donnell, L.7
Kumakubo, A.8
Munro, M.9
Sicheri, F.10
Gingras, A.-C.11
Natsume, T.12
Suda, T.13
Durocher, D.14
-
16
-
-
84885106833
-
OTUB1 enhances TGFb signalling by inhibiting the ubiquitylation and degradation of active SMAD2/3
-
L. Herhaus, M. Al-Salihi, T. Macartney, S. Weidlich, G. P. Sapkota, OTUB1 enhances TGFb signalling by inhibiting the ubiquitylation and degradation of active SMAD2/3. Nat. Commun. 4, 2519 (2013).
-
(2013)
Nat. Commun
, vol.4
, pp. 2519
-
-
Herhaus, L.1
Al-Salihi, M.2
Macartney, T.3
Weidlich, S.4
Sapkota, G.P.5
-
17
-
-
84904489086
-
The emerging roles of deubiquitylating enzymes (DUBs) in the TGFb and BMP pathways
-
L. Herhaus, G. P. Sapkota, The emerging roles of deubiquitylating enzymes (DUBs) in the TGFb and BMP pathways. Cell. Signal. 26, 2186-2192 (2014).
-
(2014)
Cell. Signal
, vol.26
, pp. 2186-2192
-
-
Herhaus, L.1
Sapkota, G.P.2
-
18
-
-
77952715402
-
Post-translational modification of the deubiquitinating enzyme otubain 1 modulates active RhoA levels and susceptibility to Yersinia invasion
-
M. J. Edelmann, H. B. Kramer, M. Altun, B. M. Kessler, Post-translational modification of the deubiquitinating enzyme otubain 1 modulates active RhoA levels and susceptibility to Yersinia invasion. FEBS J. 277, 2515-2530 (2010).
-
(2010)
FEBS J
, vol.277
, pp. 2515-2530
-
-
Edelmann, M.J.1
Kramer, H.B.2
Altun, M.3
Kessler, B.M.4
-
19
-
-
80054033461
-
A proteome-wide, quantitative survey of in vivo ubiquitylation sites reveals widespread regulatory roles
-
S. A. Wagner, P. Beli, B. T. Weinert, M. L. Nielsen, J. Cox, M. Mann, C. Choudhary, A proteome-wide, quantitative survey of in vivo ubiquitylation sites reveals widespread regulatory roles. Mol. Cell. Proteomics 10, M111.013284 (2011).
-
(2011)
Mol. Cell. Proteomics
, vol.10
, pp. M111013284
-
-
Wagner, S.A.1
Beli, P.2
Weinert, B.T.3
Nielsen, M.L.4
Cox, J.5
Mann, M.6
Choudhary, C.7
-
20
-
-
82455179484
-
Systematic and quantitative assessment of the ubiquitin-modified proteome
-
W. Kim, E. J. Bennett, E. L. Huttlin, A. Guo, J. Li, A. Possemato, M. E. Sowa, R. Rad, J. Rush, M. J. Comb, J. W. Harper, S. P. Gygi, Systematic and quantitative assessment of the ubiquitin-modified proteome. Mol. Cell 44, 325-340 (2011).
-
(2011)
Mol. Cell
, vol.44
, pp. 325-340
-
-
Kim, W.1
Bennett, E.J.2
Huttlin, E.L.3
Guo, A.4
Li, J.5
Possemato, A.6
Sowa, M.E.7
Rad, R.8
Rush, J.9
Comb, M.J.10
Harper, J.W.11
Gygi, S.P.12
-
21
-
-
2342651419
-
14-3-3-affinity purification of over 200 human phosphoproteins reveals new links to regulation of cellular metabolism, proliferation and trafficking
-
M. PozueloRubio,K. M. Geraghty, B. H. C. Wong, N. T. Wood, D. G. Campbell, N. Morrice, C. Mackintosh, 14-3-3-affinity purification of over 200 human phosphoproteins reveals new links to regulation of cellular metabolism, proliferation and trafficking. Biochem. J. 379, 395-408 (2004).
-
(2004)
Biochem. J
, vol.379
, pp. 395-408
-
-
Pozuelo Rubio, M.1
Geraghty, K.M.2
Wong, B.H.C.3
Wood, N.T.4
Campbell, D.G.5
Morrice, N.6
Mackintosh, C.7
-
22
-
-
0037334895
-
One-thousand-and-one substrates of protein kinase CK2?
-
F. Meggio, L. A. Pinna, One-thousand-and-one substrates of protein kinase CK2? FASEB J. 17, 349-368 (2003).
-
(2003)
FASEB J
, vol.17
, pp. 349-368
-
-
Meggio, F.1
Pinna, L.A.2
-
23
-
-
84855219821
-
Structural and functional determinants of protein kinase CK2a: Facts and open questions
-
R. Battistutta, G. Lolli, Structural and functional determinants of protein kinase CK2a: Facts and open questions. Mol. Cell. Biochem. 356, 67-73 (2011).
-
(2011)
Mol. Cell. Biochem
, vol.356
, pp. 67-73
-
-
Battistutta, R.1
Lolli, G.2
-
24
-
-
78649335829
-
Cellular regulators of protein kinase CK2
-
M. Montenarh, Cellular regulators of protein kinase CK2. Cell Tissue Res. 342, 139-146 (2010).
-
(2010)
Cell Tissue Res
, vol.342
, pp. 139-146
-
-
Montenarh, M.1
-
25
-
-
0037107552
-
Protein kinase CK2: A challenge to canons
-
L. A. Pinna, Protein kinase CK2: A challenge to canons. J. Cell Sci. 115, 3873-3878 (2002).
-
(2002)
J. Cell Sci
, vol.115
, pp. 3873-3878
-
-
Pinna, L.A.1
-
26
-
-
0038340907
-
The raison d'être of constitutively active protein kinases: The lesson of CK2
-
L. A. Pinna, The raison d'être of constitutively active protein kinases: The lesson of CK2. Acc. Chem. Res. 36, 378-384 (2003).
-
(2003)
Acc. Chem. Res
, vol.36
, pp. 378-384
-
-
Pinna, L.A.1
-
27
-
-
0037269847
-
Protein kinase CK2: Structure, regulation and role in cellular decisions of life and death
-
D. W. Litchfield, Protein kinase CK2: Structure, regulation and role in cellular decisions of life and death. Biochem. J. 369, 1-15 (2003).
-
(2003)
Biochem. J
, vol.369
, pp. 1-15
-
-
Litchfield, D.W.1
-
28
-
-
75349084777
-
Addiction to protein kinase CK2: A common denominator of diverse cancer cells?
-
M. Ruzzene, L. A. Pinna, Addiction to protein kinase CK2: A common denominator of diverse cancer cells? Biochim. Biophys. Acta 1804, 499-504 (2010).
-
(2010)
Biochim. Biophys. Acta
, vol.1804
, pp. 499-504
-
-
Ruzzene, M.1
Pinna, L.A.2
-
29
-
-
68749103450
-
CK2-dependent phosphorylation determines cellular localization and stability of ataxin-3
-
T. Mueller, P. Breuer, I. Schmitt, J. Walter, B. O. Evert, U. Wüllner, CK2-dependent phosphorylation determines cellular localization and stability of ataxin-3. Hum. Mol. Genet. 18, 3334-3343 (2009).
-
(2009)
Hum. Mol. Genet
, vol.18
, pp. 3334-3343
-
-
Mueller, T.1
Breuer, P.2
Schmitt, I.3
Walter, J.4
Evert, B.O.5
Wüllner, U.6
-
30
-
-
84856708042
-
Phosphorylationdependent activity of the deubiquitinase DUBA
-
O. W. Huang, X. Ma, J. Yin, J. Flinders, T. Maurer, N. Kayagaki, Q. Phung, I. Bosanac, D. Arnott, V. M. Dixit, S. G. Hymowitz, M. A. Starovasnik, A. G. Cochran, Phosphorylationdependent activity of the deubiquitinase DUBA. Nat. Struct. Mol. Biol. 19, 171-175 (2012).
-
(2012)
Nat. Struct. Mol. Biol
, vol.19
, pp. 171-175
-
-
Huang, O.W.1
Ma, X.2
Yin, J.3
Flinders, J.4
Maurer, T.5
Kayagaki, N.6
Phung, Q.7
Bosanac, I.8
Arnott, D.9
Dixit, V.M.10
Hymowitz, S.G.11
Starovasnik, M.A.12
Cochran, A.G.13
-
31
-
-
80051471864
-
The specificities of small molecule inhibitors of the TGFb and BMP pathways
-
J. Vogt, R. Traynor, G. P. Sapkota, The specificities of small molecule inhibitors of the TGFb and BMP pathways. Cell. Signal. 23, 1831-1842 (2011).
-
(2011)
Cell. Signal
, vol.23
, pp. 1831-1842
-
-
Vogt, J.1
Traynor, R.2
Sapkota, G.P.3
-
32
-
-
84864188557
-
Regulation of the transforming growth factor b pathway by reversible ubiquitylation
-
M. A. Al-Salihi, L. Herhaus, G. P. Sapkota, Regulation of the transforming growth factor b pathway by reversible ubiquitylation. Open Biol. 2, 120082 (2012).
-
(2012)
Open Biol
, vol.2
, pp. 120082
-
-
Al-Salihi, M.A.1
Herhaus, L.2
Sapkota, G.P.3
-
33
-
-
17744397294
-
Abnormal angiogenesis but intact hematopoietic potential in TGF-b type i receptor-deficient mice
-
J. Larsson, M. J. Goumans, L. J. Sjostrand, M. A. van Rooijen, D. Ward, P. Leveen, X. Xu, P. ten Dijke, C. L. Mummery, S. Karlsson, Abnormal angiogenesis but intact hematopoietic potential in TGF-b type I receptor-deficient mice. EMBO J. 20, 1663-1673 (2001).
-
(2001)
EMBO J
, vol.20
, pp. 1663-1673
-
-
Larsson, J.1
Goumans, M.J.2
Sjostrand, L.J.3
Van Rooijen, M.A.4
Ward, D.5
Leveen, P.6
Xu, X.7
Ten Dijke, P.8
Mummery, C.L.9
Karlsson, S.10
-
34
-
-
84878887568
-
Exploiting the repertoire of CK2 inhibitors to target DYRK and PIM kinases
-
G. Cozza, S. Sarno, M. Ruzzene, C. Girardi, A. Orzeszko, Z. Kazimierczuk, G. Zagotto, E. Bonaiuto, M. L. Di Paolo, L. A. Pinna, Exploiting the repertoire of CK2 inhibitors to target DYRK and PIM kinases. Biochim. Biophys. Acta 1834, 1402-1409 (2013).
-
(2013)
Biochim. Biophys. Acta
, vol.1834
, pp. 1402-1409
-
-
Cozza, G.1
Sarno, S.2
Ruzzene, M.3
Girardi, C.4
Orzeszko, A.5
Kazimierczuk, Z.6
Zagotto, G.7
Bonaiuto, E.8
Di Paolo, M.L.9
Pinna, L.A.10
-
35
-
-
20044377997
-
Protein kinase CK2 phosphorylates and upregulates Akt//PKB
-
G. Di Maira, M. Salvi, G. Arrigoni,O.Marin,S.Sarno, F. Brustolon, L. A. Pinna, M.Ruzzene, Protein kinase CK2 phosphorylates and upregulates Akt//PKB. Cell Death Differ. 12, 668-677 (2005).
-
(2005)
Cell Death Differ
, vol.12
, pp. 668-677
-
-
Di Maira, G.1
Salvi, M.2
Arrigoni, G.3
Marin, O.4
Sarno, S.5
Brustolon, F.6
Pinna, L.A.7
Ruzzene, M.8
-
36
-
-
1942486312
-
CK2 controls multiple protein kinases by phosphorylating a kinase-targeting molecular chaperone
-
Y. Miyata, E. Nishida, CK2 controls multiple protein kinases by phosphorylating a kinase-targeting molecular chaperone, Cdc37. Mol. Cell. Biol. 24, 4065-4074 (2004).
-
(2004)
Cdc37. Mol. Cell. Biol
, vol.24
, pp. 4065-4074
-
-
Miyata, Y.1
Nishida, E.2
-
37
-
-
84905119768
-
Cell-permeable dual inhibitors of protein kinases CK2 and PIM-1: Structural features and pharmacological potential
-
G. Cozza, C. Girardi, A. Ranchio, G. Lolli, S. Sarno, A. Orzeszko, Z. Kazimierczuk, R. Battistutta, M. Ruzzene, L. Pinna, Cell-permeable dual inhibitors of protein kinases CK2 and PIM-1: Structural features and pharmacological potential. Cell. Mol. Life Sci. 3173-3185 (2014).
-
(2014)
Cell. Mol. Life Sci
, pp. 3173-3185
-
-
Cozza, G.1
Girardi, C.2
Ranchio, A.3
Lolli, G.4
Sarno, S.5
Orzeszko, A.6
Kazimierczuk, Z.7
Battistutta, R.8
Ruzzene, M.9
Pinna, L.10
-
38
-
-
68249130300
-
Quinalizarin as a potent, selective and cell-permeable inhibitor of protein kinase CK2
-
G. Cozza, M. Mazzorana, E. Papinutto, J. Bain, M. Elliott, G. di Maira, A. Gianoncelli, M. A. Pagano, S. Sarno, M. Ruzzene, R. Battistutta, F. Meggio, S. Moro, G. Zagotto, L. A. Pinna, Quinalizarin as a potent, selective and cell-permeable inhibitor of protein kinase CK2. Biochem. J. 421, 387-395 (2009).
-
(2009)
Biochem. J
, vol.421
, pp. 387-395
-
-
Cozza, G.1
Mazzorana, M.2
Papinutto, E.3
Bain, J.4
Elliott, M.5
Di Maira, G.6
Gianoncelli, A.7
Pagano, M.A.8
Sarno, S.9
Ruzzene, M.10
Battistutta, R.11
Meggio, F.12
Moro, S.13
Zagotto, G.14
Pinna, L.A.15
-
39
-
-
70349321218
-
Protein kinase CK2 in health and disease: Structural bases of protein kinase CK2 inhibition
-
R. Battistutta, Protein kinase CK2 in health and disease: Structural bases of protein kinase CK2 inhibition. Cell. Mol. Life Sci. 66, 1868-1889 (2009).
-
(2009)
Cell. Mol. Life Sci
, vol.66
, pp. 1868-1889
-
-
Battistutta, R.1
-
40
-
-
77951980137
-
How druggable is protein kinase CK2?
-
G. Cozza, A. Bortolato, S. Moro, How druggable is protein kinase CK2? Med. Res. Rev. 30, 419-462 (2010).
-
(2010)
Med. Res. Rev
, vol.30
, pp. 419-462
-
-
Cozza, G.1
Bortolato, A.2
Moro, S.3
-
41
-
-
63449124343
-
The selectivity of inhibitors of protein kinase CK2: An update
-
M. A. Pagano, J. Bain, Z. Kazimierczuk, S. Sarno, M. Ruzzene, G. Di Maira, M. Elliott, A. Orzeszko, G. Cozza, F. Meggio, L. A. Pinna, The selectivity of inhibitors of protein kinase CK2: An update. Biochem. J. 415, 353-365 (2008).
-
(2008)
Biochem. J
, vol.415
, pp. 353-365
-
-
Pagano, M.A.1
Bain, J.2
Kazimierczuk, Z.3
Sarno, S.4
Ruzzene, M.5
Di Maira, G.6
Elliott, M.7
Orzeszko, A.8
Cozza, G.9
Meggio, F.10
Pinna, L.A.11
-
42
-
-
53049109206
-
Conjugation of complex polyubiquitin chains to WRNIP1
-
R. A. Bish, O. I. Fregoso, A. Piccini, M. P. Myers, Conjugation of complex polyubiquitin chains to WRNIP1. J. Proteome Res. 7, 3481-3489 (2008).
-
(2008)
J. Proteome Res
, vol.7
, pp. 3481-3489
-
-
Bish, R.A.1
Fregoso, O.I.2
Piccini, A.3
Myers, M.P.4
-
43
-
-
0032146749
-
Leptomycin B inhibition of signal-mediated nuclear export by direct binding to CRM1
-
N. Kudo, B. Wolff, T. Sekimoto, E. P. Schreiner, Y. Yoneda, M. Yanagida, S. Horinouchi, M. Yoshida, Leptomycin B inhibition of signal-mediated nuclear export by direct binding to CRM1. Exp. Cell Res. 242, 540-547 (1998).
-
(1998)
Exp. Cell Res
, vol.242
, pp. 540-547
-
-
Kudo, N.1
Wolff, B.2
Sekimoto, T.3
Schreiner, E.P.4
Yoneda, Y.5
Yanagida, M.6
Horinouchi, S.7
Yoshida, M.8
-
44
-
-
79959692369
-
Importazole, a small molecule inhibitor of the transport receptor importin-b
-
J. F. Soderholm, S. L. Bird, P. Kalab, Y. Sampathkumar, K.Hasegawa, M. Uehara-Bingen, K. Weis, R. Heald, Importazole, a small molecule inhibitor of the transport receptor importin-b. ACS Chem. Biol. 6, 700-708 (2011).
-
(2011)
ACS Chem. Biol
, vol.6
, pp. 700-708
-
-
Soderholm, J.F.1
Bird, S.L.2
Kalab, P.3
Sampathkumar, Y.4
Hasegawa, K.5
Uehara-Bingen, M.6
Weis, K.7
Heald, R.8
-
45
-
-
84856776536
-
Plk1 and CK2 act in concert to regulate Rad51 during DNA double strand break repair
-
K. Yata, J. Lloyd, S. Maslen, J. Y. Bleuyard, M. Skehel, S. J. Smerdon, F. Esashi, Plk1 and CK2 act in concert to regulate Rad51 during DNA double strand break repair. Mol. Cell 45, 371-383 (2012).
-
(2012)
Mol. Cell
, vol.45
, pp. 371-383
-
-
Yata, K.1
Lloyd, J.2
Maslen, S.3
Bleuyard, J.Y.4
Skehel, M.5
Smerdon, S.J.6
Esashi, F.7
-
46
-
-
84893787930
-
Protein kinase CK2 is required for the recruitment of 53BP1 to sites of DNA double-strand break induced by radiomimetic drugs
-
B. Guerra, K. Iwabuchi, O. G. Issinger, Protein kinase CK2 is required for the recruitment of 53BP1 to sites of DNA double-strand break induced by radiomimetic drugs. Cancer Lett. 345, 115-123 (2014).
-
(2014)
Cancer Lett
, vol.345
, pp. 115-123
-
-
Guerra, B.1
Iwabuchi, K.2
Issinger, O.G.3
-
47
-
-
0037082158
-
High-level and high-throughput recombinant protein production by transient transfection of suspension-growing human 293-EBNA1 cells
-
Y. Durocher, S. Perret, A. Kamen, High-level and high-throughput recombinant protein production by transient transfection of suspension-growing human 293-EBNA1 cells. Nucleic Acids Res. 30, E9 (2002).
-
(2002)
Nucleic Acids Res
, vol.30
, pp. E9
-
-
Durocher, Y.1
Perret, S.2
Kamen, A.3
-
48
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
M. M. Bradford, A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248-254 (1976).
-
(1976)
Anal. Biochem
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
49
-
-
84864240454
-
USP11 augments TGFb signalling by deubiquitylating ALK5
-
M. A. Al-Salihi, L. Herhaus, T. Macartney, G. P. Sapkota, USP11 augments TGFb signalling by deubiquitylating ALK5. Open Biol. 2, 120063 (2012).
-
(2012)
Open Biol
, vol.2
, pp. 120063
-
-
Al-Salihi, M.A.1
Herhaus, L.2
Macartney, T.3
Sapkota, G.P.4
-
50
-
-
84937413187
-
Protein associated with SMAD1 (PAWS1/FAM83G) is a substrate for type i bone morphogenetic protein receptors and modulates bone morphogenetic protein signalling
-
J. Vogt, K. S. Dingwell, L. Herhaus, R. Gourlay, T. Macartney, D. Campbell, J. C. Smith, G. P. Sapkota, Protein associated with SMAD1 (PAWS1/FAM83G) is a substrate for type I bone morphogenetic protein receptors and modulates bone morphogenetic protein signalling. Open Biol. 4, 130210 (2014).
-
(2014)
Open Biol
, vol.4
, pp. 130210
-
-
Vogt, J.1
Dingwell, K.S.2
Herhaus, L.3
Gourlay, R.4
Macartney, T.5
Campbell, D.6
Smith, J.C.7
Sapkota, G.P.8
-
51
-
-
0012059894
-
Identification of protein phosphorylation sites by a combination of mass spectrometry and solid phase Edman sequencing
-
D. Campbell, N. Morrice, Identification of protein phosphorylation sites by a combination of mass spectrometry and solid phase Edman sequencing. J. Biomol. Tech. 13, 119-130 (2002).
-
(2002)
J. Biomol. Tech
, vol.13
, pp. 119-130
-
-
Campbell, D.1
Morrice, N.2
-
52
-
-
84902386193
-
USP15 targets ALK3/ BMPR1A for deubiquitylation to enhance bone morphogenetic protein signalling
-
L. Herhaus, M. Al-Salihi, K. S. Dingwell, T. D. Cummins, L. Wasmus, J. Vogt, R. Ewan, D. Bruce, T. Macartney, S. Weidlich, J. C. Smith, G. P. Sapkota, USP15 targets ALK3/ BMPR1A for deubiquitylation to enhance bone morphogenetic protein signalling. Open Biol. 4, 140065 (2014).
-
(2014)
Open Biol
, vol.4
, pp. 140065
-
-
Herhaus, L.1
Al-Salihi, M.2
Dingwell, K.S.3
Cummins, T.D.4
Wasmus, L.5
Vogt, J.6
Ewan, R.7
Bruce, D.8
Macartney, T.9
Weidlich, S.10
Smith, J.C.11
Sapkota, G.P.12
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