-
1
-
-
14244272868
-
PHENIX: Building new software for automated crystallographic structure determination
-
P.D. Adams, R.W. Grosse-Kunstleve, L.W. Hung, T.R. Ioerger, A.J. McCoy, N.W. Moriarty, R.J. Read, J.C. Sacchettini, N.K. Sauter, and T.C. Terwilliger PHENIX: building new software for automated crystallographic structure determination Acta Crystallogr. D Biol. Crystallogr. 58 2002 1948 1954
-
(2002)
Acta Crystallogr. D Biol. Crystallogr.
, vol.58
, pp. 1948-1954
-
-
Adams, P.D.1
Grosse-Kunstleve, R.W.2
Hung, L.W.3
Ioerger, T.R.4
McCoy, A.J.5
Moriarty, N.W.6
Read, R.J.7
Sacchettini, J.C.8
Sauter, N.K.9
Terwilliger, T.C.10
-
2
-
-
0036753953
-
Structure of a Sir2 enzyme bound to an acetylated p53 peptide
-
J.L. Avalos, I. Celic, S. Muhammad, M.S. Cosgrove, J.D. Boeke, and C. Wolberger Structure of a Sir2 enzyme bound to an acetylated p53 peptide Mol. Cell 10 2002 523 535
-
(2002)
Mol. Cell
, vol.10
, pp. 523-535
-
-
Avalos, J.L.1
Celic, I.2
Muhammad, S.3
Cosgrove, M.S.4
Boeke, J.D.5
Wolberger, C.6
-
3
-
-
84861852370
-
Are sirtuins viable targets for improving healthspan and lifespan?
-
J.A. Baur, Z. Ungvari, R.K. Minor, D.G. Le Couteur, and R. de Cabo Are sirtuins viable targets for improving healthspan and lifespan? Nat. Rev. Drug Discov. 11 2012 443 461
-
(2012)
Nat. Rev. Drug Discov.
, vol.11
, pp. 443-461
-
-
Baur, J.A.1
Ungvari, Z.2
Minor, R.K.3
Le Couteur, D.G.4
De Cabo, R.5
-
4
-
-
79957968813
-
Medicinal chemistry of sirtuin inhibitors
-
L. Chen Medicinal chemistry of sirtuin inhibitors Curr. Med. Chem. 18 2011 1936 1946
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 1936-1946
-
-
Chen, L.1
-
5
-
-
84871706585
-
The sirtuin 2 inhibitor AK-7 is neuroprotective in Huntington's disease mouse models
-
V. Chopra, L. Quinti, J. Kim, L. Vollor, K.L. Narayanan, C. Edgerly, P.M. Cipicchio, M.A. Lauver, S.H. Choi, and R.B. Silverman et al. The sirtuin 2 inhibitor AK-7 is neuroprotective in Huntington's disease mouse models Cell Rep. 2 2012 1492 1497
-
(2012)
Cell Rep.
, vol.2
, pp. 1492-1497
-
-
Chopra, V.1
Quinti, L.2
Kim, J.3
Vollor, L.4
Narayanan, K.L.5
Edgerly, C.6
Cipicchio, P.M.7
Lauver, M.A.8
Choi, S.H.9
Silverman, R.B.10
-
6
-
-
33745119442
-
The structural basis of sirtuin substrate affinity
-
M.S. Cosgrove, K. Bever, J.L. Avalos, S. Muhammad, X. Zhang, and C. Wolberger The structural basis of sirtuin substrate affinity Biochemistry 45 2006 7511 7521
-
(2006)
Biochemistry
, vol.45
, pp. 7511-7521
-
-
Cosgrove, M.S.1
Bever, K.2
Avalos, J.L.3
Muhammad, S.4
Zhang, X.5
Wolberger, C.6
-
7
-
-
84877714749
-
Discovery of thieno[3,2-d]pyrimidine-6-carboxamides as potent inhibitors of SIRT1, SIRT2, and SIRT3
-
J.S. Disch, G. Evindar, C.H. Chiu, C.A. Blum, H. Dai, L. Jin, E. Schuman, K.E. Lind, S.L. Belyanskaya, and J. Deng et al. Discovery of thieno[3,2-d]pyrimidine-6-carboxamides as potent inhibitors of SIRT1, SIRT2, and SIRT3 J. Med. Chem. 56 2013 3666 3679
-
(2013)
J. Med. Chem.
, vol.56
, pp. 3666-3679
-
-
Disch, J.S.1
Evindar, G.2
Chiu, C.H.3
Blum, C.A.4
Dai, H.5
Jin, L.6
Schuman, E.7
Lind, K.E.8
Belyanskaya, S.L.9
Deng, J.10
-
8
-
-
81055122671
-
Sirt5 is a NAD-dependent protein lysine demalonylase and desuccinylase
-
J. Du, Y. Zhou, X. Su, J.J. Yu, S. Khan, H. Jiang, J. Kim, J. Woo, J.H. Kim, and B.H. Choi et al. Sirt5 is a NAD-dependent protein lysine demalonylase and desuccinylase Science 334 2011 806 809
-
(2011)
Science
, vol.334
, pp. 806-809
-
-
Du, J.1
Zhou, Y.2
Su, X.3
Yu, J.J.4
Khan, S.5
Jiang, H.6
Kim, J.7
Woo, J.8
Kim, J.H.9
Choi, B.H.10
-
12
-
-
84858657128
-
In vitro selection of anti-Akt2 thioether-macrocyclic peptides leading to isoform-selective inhibitors
-
Y. Hayashi, J. Morimoto, and H. Suga In vitro selection of anti-Akt2 thioether-macrocyclic peptides leading to isoform-selective inhibitors ACS Chem. Biol. 7 2012 607 613
-
(2012)
ACS Chem. Biol.
, vol.7
, pp. 607-613
-
-
Hayashi, Y.1
Morimoto, J.2
Suga, H.3
-
13
-
-
84859627442
-
Ribosomal production and in vitro selection of natural product-like peptidomimetics: The FIT and RaPID systems
-
C.J. Hipolito, and H. Suga Ribosomal production and in vitro selection of natural product-like peptidomimetics: the FIT and RaPID systems Curr. Opin. Chem. Biol. 16 2012 196 203
-
(2012)
Curr. Opin. Chem. Biol.
, vol.16
, pp. 196-203
-
-
Hipolito, C.J.1
Suga, H.2
-
15
-
-
0037126026
-
Crystal structure of calcineurin-cyclophilin-cyclosporin shows common but distinct recognition of immunophilin-drug complexes
-
Q. Huai, H.Y. Kim, Y. Liu, Y. Zhao, A. Mondragon, J.O. Liu, and H. Ke Crystal structure of calcineurin-cyclophilin-cyclosporin shows common but distinct recognition of immunophilin-drug complexes Proc. Natl. Acad. Sci. USA 99 2002 12037 12042
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 12037-12042
-
-
Huai, Q.1
Kim, H.Y.2
Liu, Y.3
Zhao, Y.4
Mondragon, A.5
Liu, J.O.6
Ke, H.7
-
16
-
-
34248151365
-
The molecular biology of mammalian SIRT proteins: SIRT2 in cell cycle regulation
-
T. Inoue, M. Hiratsuka, M. Osaki, and M. Oshimura The molecular biology of mammalian SIRT proteins: SIRT2 in cell cycle regulation Cell Cycle 6 2007 1011 1018
-
(2007)
Cell Cycle
, vol.6
, pp. 1011-1018
-
-
Inoue, T.1
Hiratsuka, M.2
Osaki, M.3
Oshimura, M.4
-
17
-
-
69949151709
-
Crystal structures of human SIRT3 displaying substrate-induced conformational changes
-
L. Jin, W. Wei, Y. Jiang, H. Peng, J. Cai, C. Mao, H. Dai, W. Choy, J.E. Bemis, and M.R. Jirousek et al. Crystal structures of human SIRT3 displaying substrate-induced conformational changes J. Biol. Chem. 284 2009 24394 24405
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 24394-24405
-
-
Jin, L.1
Wei, W.2
Jiang, Y.3
Peng, H.4
Cai, J.5
Mao, C.6
Dai, H.7
Choy, W.8
Bemis, J.E.9
Jirousek, M.R.10
-
18
-
-
78650638268
-
SIRT2 down-regulation in HeLa can induce p53 accumulation via p38 MAPK activation-dependent p300 decrease, eventually leading to apoptosis
-
Y. Li, H. Matsumori, Y. Nakayama, M. Osaki, H. Kojima, A. Kurimasa, H. Ito, S. Mori, M. Katoh, M. Oshimura, and T. Inoue SIRT2 down-regulation in HeLa can induce p53 accumulation via p38 MAPK activation-dependent p300 decrease, eventually leading to apoptosis Genes Cells 16 2011 34 45
-
(2011)
Genes Cells
, vol.16
, pp. 34-45
-
-
Li, Y.1
Matsumori, H.2
Nakayama, Y.3
Osaki, M.4
Kojima, H.5
Kurimasa, A.6
Ito, H.7
Mori, S.8
Katoh, M.9
Oshimura, M.10
Inoue, T.11
-
19
-
-
84876715762
-
Crystal structure analysis of human Sirt2 and its ADP-ribose complex
-
S. Moniot, M. Schutkowski, and C. Steegborn Crystal structure analysis of human Sirt2 and its ADP-ribose complex J. Struct. Biol. 182 2013 136 143
-
(2013)
J. Struct. Biol.
, vol.182
, pp. 136-143
-
-
Moniot, S.1
Schutkowski, M.2
Steegborn, C.3
-
20
-
-
84859239807
-
Discovery of macrocyclic peptides armed with a mechanism-based warhead: Isoform-selective inhibition of human deacetylase SIRT2
-
J. Morimoto, Y. Hayashi, and H. Suga Discovery of macrocyclic peptides armed with a mechanism-based warhead: isoform-selective inhibition of human deacetylase SIRT2 Angew. Chem. Int. Ed. Engl. 51 2012 3423 3427
-
(2012)
Angew. Chem. Int. Ed. Engl.
, vol.51
, pp. 3423-3427
-
-
Morimoto, J.1
Hayashi, Y.2
Suga, H.3
-
21
-
-
29144501185
-
Discovery of indoles as potent and selective inhibitors of the deacetylase SIRT1
-
A.D. Napper, J. Hixon, T. McDonagh, K. Keavey, J.F. Pons, J. Barker, W.T. Yau, P. Amouzegh, A. Flegg, and E. Hamelin et al. Discovery of indoles as potent and selective inhibitors of the deacetylase SIRT1 J. Med. Chem. 48 2005 8045 8054
-
(2005)
J. Med. Chem.
, vol.48
, pp. 8045-8054
-
-
Napper, A.D.1
Hixon, J.2
McDonagh, T.3
Keavey, K.4
Pons, J.F.5
Barker, J.6
Yau, W.T.7
Amouzegh, P.8
Flegg, A.9
Hamelin, E.10
-
22
-
-
84870999850
-
The NAD-dependent deacetylase SIRT2 is required for programmed necrosis
-
N. Narayan, I.H. Lee, R. Borenstein, J. Sun, R. Wong, G. Tong, M.M. Fergusson, J. Liu, I.I. Rovira, and H.L. Cheng et al. The NAD-dependent deacetylase SIRT2 is required for programmed necrosis Nature 492 2012 199 204
-
(2012)
Nature
, vol.492
, pp. 199-204
-
-
Narayan, N.1
Lee, I.H.2
Borenstein, R.3
Sun, J.4
Wong, R.5
Tong, G.6
Fergusson, M.M.7
Liu, J.8
Rovira, I.I.9
Cheng, H.L.10
-
25
-
-
34547599329
-
Sirtuin 2 inhibitors rescue alpha-synuclein-mediated toxicity in models of Parkinson's disease
-
T.F. Outeiro, E. Kontopoulos, S.M. Altmann, I. Kufareva, K.E. Strathearn, A.M. Amore, C.B. Volk, M.M. Maxwell, J.C. Rochet, and P.J. McLean et al. Sirtuin 2 inhibitors rescue alpha-synuclein-mediated toxicity in models of Parkinson's disease Science 317 2007 516 519
-
(2007)
Science
, vol.317
, pp. 516-519
-
-
Outeiro, T.F.1
Kontopoulos, E.2
Altmann, S.M.3
Kufareva, I.4
Strathearn, K.E.5
Amore, A.M.6
Volk, C.B.7
Maxwell, M.M.8
Rochet, J.C.9
McLean, P.J.10
-
27
-
-
33847635635
-
+-dependent deacetylase SIRT5 by suramin
-
+-dependent deacetylase SIRT5 by suramin Structure 15 2007 377 389
-
(2007)
Structure
, vol.15
, pp. 377-389
-
-
Schuetz, A.1
Min, J.2
Antoshenko, T.3
Wang, C.L.4
Allali-Hassani, A.5
Dong, A.6
Loppnau, P.7
Vedadi, M.8
Bochkarev, A.9
Sternglanz, R.10
Plotnikov, A.N.11
-
28
-
-
37549067781
-
Acetyl-lysine analog peptides as mechanistic probes of protein deacetylases
-
B.C. Smith, and J.M. Denu Acetyl-lysine analog peptides as mechanistic probes of protein deacetylases J. Biol. Chem. 282 2007 37256 37265
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 37256-37265
-
-
Smith, B.C.1
Denu, J.M.2
-
29
-
-
84876297961
-
Structural basis for the drug extrusion mechanism by a MATE multidrug transporter
-
Y. Tanaka, C.J. Hipolito, A.D. Maturana, K. Ito, T. Kuroda, T. Higuchi, K. Takayuki, H.E. Kato, M. Hattori, and K. Kumazaki et al. Structural basis for the drug extrusion mechanism by a MATE multidrug transporter Nature 496 2013 247 251
-
(2013)
Nature
, vol.496
, pp. 247-251
-
-
Tanaka, Y.1
Hipolito, C.J.2
Maturana, A.D.3
Ito, K.4
Kuroda, T.5
Higuchi, T.6
Takayuki, K.7
Kato, H.E.8
Hattori, M.9
Kumazaki, K.10
-
31
-
-
33646550204
-
SirT2 is a histone deacetylase with preference for histone H4 Lys 16 during mitosis
-
A. Vaquero, M.B. Scher, D.H. Lee, A. Sutton, H.L. Cheng, F.W. Alt, L. Serrano, R. Sternglanz, and D. Reinberg SirT2 is a histone deacetylase with preference for histone H4 Lys 16 during mitosis Genes Dev. 20 2006 1256 1261
-
(2006)
Genes Dev.
, vol.20
, pp. 1256-1261
-
-
Vaquero, A.1
Scher, M.B.2
Lee, D.H.3
Sutton, A.4
Cheng, H.L.5
Alt, F.W.6
Serrano, L.7
Sternglanz, R.8
Reinberg, D.9
-
32
-
-
84555190565
-
Natural product-like macrocyclic N-methyl-peptide inhibitors against a ubiquitin ligase uncovered from a ribosome-expressed de novo library
-
Y. Yamagishi, I. Shoji, S. Miyagawa, T. Kawakami, T. Katoh, Y. Goto, and H. Suga Natural product-like macrocyclic N-methyl-peptide inhibitors against a ubiquitin ligase uncovered from a ribosome-expressed de novo library Chem. Biol. 18 2011 1562 1570
-
(2011)
Chem. Biol.
, vol.18
, pp. 1562-1570
-
-
Yamagishi, Y.1
Shoji, I.2
Miyagawa, S.3
Kawakami, T.4
Katoh, T.5
Goto, Y.6
Suga, H.7
-
33
-
-
84875033669
-
Mechanism-based modulator discovery for sirtuin-catalyzed deacetylation reaction
-
W. Zheng Mechanism-based modulator discovery for sirtuin-catalyzed deacetylation reaction Mini Rev. Med. Chem. 13 2013 132 154
-
(2013)
Mini Rev. Med. Chem.
, vol.13
, pp. 132-154
-
-
Zheng, W.1
-
34
-
-
84865225339
-
The bicyclic intermediate structure provides insights into the desuccinylation mechanism of human sirtuin 5 (SIRT5)
-
Y. Zhou, H. Zhang, B. He, J. Du, H. Lin, R.A. Cerione, and Q. Hao The bicyclic intermediate structure provides insights into the desuccinylation mechanism of human sirtuin 5 (SIRT5) J. Biol. Chem. 287 2012 28307 28314
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 28307-28314
-
-
Zhou, Y.1
Zhang, H.2
He, B.3
Du, J.4
Lin, H.5
Cerione, R.A.6
Hao, Q.7
|