-
1
-
-
0029916122
-
A human peptidyl-prolyl isomerase essential for regulation of mitosis
-
Lu KP, Hanes SD, Hunter T, (1996) A human peptidyl-prolyl isomerase essential for regulation of mitosis. Nature 380: 544-547.
-
(1996)
Nature
, vol.380
, pp. 544-547
-
-
Lu, K.P.1
Hanes, S.D.2
Hunter, T.3
-
2
-
-
33847656165
-
Substrate recognition reduces side-chain flexibility for conserved hydrophobic residues in human Pin1
-
Namanja AT, Peng T, Zintsmaster JS, Elson AC, Shakour MG, et al. (2007) Substrate recognition reduces side-chain flexibility for conserved hydrophobic residues in human Pin1. Structure 15: 313-327.
-
(2007)
Structure
, vol.15
, pp. 313-327
-
-
Namanja, A.T.1
Peng, T.2
Zintsmaster, J.S.3
Elson, A.C.4
Shakour, M.G.5
-
3
-
-
0031438929
-
Sequence-specific and phosphorylation-dependent proline isomerization: a potential mitotic regulatory mechanism
-
Yaffe MB, Schutkowski M, Shen M, Zhou XZ, Stukenberg PT, et al. (1997) Sequence-specific and phosphorylation-dependent proline isomerization: a potential mitotic regulatory mechanism. Science 278: 1957-1960.
-
(1997)
Science
, vol.278
, pp. 1957-1960
-
-
Yaffe, M.B.1
Schutkowski, M.2
Shen, M.3
Zhou, X.Z.4
Stukenberg, P.T.5
-
4
-
-
0027135981
-
Role of the cyclosporin-A-cyclophilin complex, FK506-FK506-binding protein complex and calcineurin in the inhibition of T-cell signal transduction
-
Etzkorn FA, Stolz LA, Chang ZY, Walsh CT, (1993) Role of the cyclosporin-A-cyclophilin complex, FK506-FK506-binding protein complex and calcineurin in the inhibition of T-cell signal transduction. Curr Opin Struct Biol 3: 929-933.
-
(1993)
Curr Opin Struct Biol
, vol.3
, pp. 929-933
-
-
Etzkorn, F.A.1
Stolz, L.A.2
Chang, Z.Y.3
Walsh, C.T.4
-
5
-
-
34548660854
-
Prolyl cis-trans isomerization as a molecular timer
-
Lu KP, Finn G, Lee TH, Nicholson LK, (2007) Prolyl cis-trans isomerization as a molecular timer. Nat Chem Biol 3: 619-629.
-
(2007)
Nat Chem Biol
, vol.3
, pp. 619-629
-
-
Lu, K.P.1
Finn, G.2
Lee, T.H.3
Nicholson, L.K.4
-
6
-
-
0037351048
-
Prolyl isomerase Pin1: a catalyst for oncogenesis and a potential therapeutic target in cancer
-
Ryo A, Liou YC, Lu KP, Wulf G, (2003) Prolyl isomerase Pin1: a catalyst for oncogenesis and a potential therapeutic target in cancer. J Cell Sci 116: 773-783.
-
(2003)
J Cell Sci
, vol.116
, pp. 773-783
-
-
Ryo, A.1
Liou, Y.C.2
Lu, K.P.3
Wulf, G.4
-
7
-
-
72449205615
-
Pin1 as an anticancer drug target
-
Xu GG, Etzkorn FA, (2009) Pin1 as an anticancer drug target. Drug News Perspect 22: 399-407.
-
(2009)
Drug News Perspect
, vol.22
, pp. 399-407
-
-
Xu, G.G.1
Etzkorn, F.A.2
-
8
-
-
34247490735
-
PIN1, the cell cycle and cancer
-
Yeh ES, Means AR, (2007) PIN1, the cell cycle and cancer. Nat Rev Cancer 7: 381-388.
-
(2007)
Nat Rev Cancer
, vol.7
, pp. 381-388
-
-
Yeh, E.S.1
Means, A.R.2
-
9
-
-
0036786838
-
Substrate-based design of reversible Pin1 inhibitors
-
Zhang Y, Fussel S, Reimer U, Schutkowski M, Fischer G, (2002) Substrate-based design of reversible Pin1 inhibitors. Biochemistry 41: 11868-11877.
-
(2002)
Biochemistry
, vol.41
, pp. 11868-11877
-
-
Zhang, Y.1
Fussel, S.2
Reimer, U.3
Schutkowski, M.4
Fischer, G.5
-
10
-
-
9644302270
-
Conformationally locked isostere of phosphoSer-cis-Pro inhibits Pin1 23-fold better than phosphoSer-trans-Pro isostere
-
Wang XJ, Xu B, Mullins AB, Neiler FK, Etzkorn FA, (2004) Conformationally locked isostere of phosphoSer-cis-Pro inhibits Pin1 23-fold better than phosphoSer-trans-Pro isostere. J Am Chem Soc 126: 15533-15542.
-
(2004)
J Am Chem Soc
, vol.126
, pp. 15533-15542
-
-
Wang, X.J.1
Xu, B.2
Mullins, A.B.3
Neiler, F.K.4
Etzkorn, F.A.5
-
11
-
-
33751234234
-
Aryl indanyl ketones: efficient inhibitors of the human peptidyl prolyl cis/trans isomerase Pin1
-
Daum S, Erdmann F, Fischer G, Feaux de Lacroix B, Hessamian-Alinejad A, et al. (2006) Aryl indanyl ketones: efficient inhibitors of the human peptidyl prolyl cis/trans isomerase Pin1. Angew Chem Int Ed Engl 45: 7454-7458.
-
(2006)
Angew Chem Int Ed Engl
, vol.45
, pp. 7454-7458
-
-
Daum, S.1
Erdmann, F.2
Fischer, G.3
Feaux de Lacroix, B.4
Hessamian-Alinejad, A.5
-
12
-
-
33645680245
-
Nanomolar inhibitors of the peptidyl prolyl cis/trans isomerase Pin1 from combinatorial peptide libraries
-
Wildemann D, Erdmann F, Alvarez BH, Stoller G, Zhou XZ, et al. (2006) Nanomolar inhibitors of the peptidyl prolyl cis/trans isomerase Pin1 from combinatorial peptide libraries. J Med Chem 49: 2147-2150.
-
(2006)
J Med Chem
, vol.49
, pp. 2147-2150
-
-
Wildemann, D.1
Erdmann, F.2
Alvarez, B.H.3
Stoller, G.4
Zhou, X.Z.5
-
13
-
-
35648979497
-
A phosphorylated prodrug for the inhibition of Pin1
-
Zhao S, Etzkorn FA, (2007) A phosphorylated prodrug for the inhibition of Pin1. Bioorg Med Chem Lett 17: 6615-6618.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 6615-6618
-
-
Zhao, S.1
Etzkorn, F.A.2
-
14
-
-
76849108650
-
Convergent synthesis of alpha-ketoamide inhibitors of Pin1
-
Xu GG, Etzkorn FA, (2010) Convergent synthesis of alpha-ketoamide inhibitors of Pin1. Org Lett 12: 696-699.
-
(2010)
Org Lett
, vol.12
, pp. 696-699
-
-
Xu, G.G.1
Etzkorn, F.A.2
-
15
-
-
0032574832
-
Selective inactivation of parvulin-like peptidyl-prolyl cis/trans isomerases by juglone
-
Hennig L, Christner C, Kipping M, Schelbert B, Rucknagel KP, et al. (1998) Selective inactivation of parvulin-like peptidyl-prolyl cis/trans isomerases by juglone. Biochemistry 37: 5953-5960.
-
(1998)
Biochemistry
, vol.37
, pp. 5953-5960
-
-
Hennig, L.1
Christner, C.2
Kipping, M.3
Schelbert, B.4
Rucknagel, K.P.5
-
16
-
-
0037256548
-
Pin1 and Par14 peptidyl prolyl isomerase inhibitors block cell proliferation
-
Uchida T, Takamiya M, Takahashi M, Miyashita H, Ikeda H, et al. (2003) Pin1 and Par14 peptidyl prolyl isomerase inhibitors block cell proliferation. Chem Biol 10: 15-24.
-
(2003)
Chem Biol
, vol.10
, pp. 15-24
-
-
Uchida, T.1
Takamiya, M.2
Takahashi, M.3
Miyashita, H.4
Ikeda, H.5
-
17
-
-
0025004246
-
Confirmation of the secondary deuterium isotope effect for the peptidyl prolyl cis-trans isomerase activity of cyclophilin by a competitive, double-label technique
-
Harrison RK, Caldwell CG, Rosegay A, Melillo D, Stein RL, (1990) Confirmation of the secondary deuterium isotope effect for the peptidyl prolyl cis-trans isomerase activity of cyclophilin by a competitive, double-label technique. J Am Chem Soc 112: 7063-7064.
-
(1990)
J Am Chem Soc
, vol.112
, pp. 7063-7064
-
-
Harrison, R.K.1
Caldwell, C.G.2
Rosegay, A.3
Melillo, D.4
Stein, R.L.5
-
18
-
-
0025005004
-
Mechanistic Studies of Peptidyl Prolyl Cis-Trans Isomerase: Evidence for Catalysis by Distortion
-
Harrison RK, Stein RL, (1990) Mechanistic Studies of Peptidyl Prolyl Cis-Trans Isomerase: Evidence for Catalysis by Distortion. Biochemistry 29: 1684-1689.
-
(1990)
Biochemistry
, vol.29
, pp. 1684-1689
-
-
Harrison, R.K.1
Stein, R.L.2
-
19
-
-
0025302066
-
Inhibition of FKBP Rotamase Activity by Immunosuppressant FK506: Twisted Amide Surrogate
-
Rosen MK, Standaert RF, Galat A, Nakatsuka M, Schreiber SL, (1990) Inhibition of FKBP Rotamase Activity by Immunosuppressant FK506: Twisted Amide Surrogate. Science 248: 863-866.
-
(1990)
Science
, vol.248
, pp. 863-866
-
-
Rosen, M.K.1
Standaert, R.F.2
Galat, A.3
Nakatsuka, M.4
Schreiber, S.L.5
-
20
-
-
0026649497
-
PPIase catalysis by human FK506-binding protein proceeds through a conformational twist mechanism
-
Park ST, Aldape RA, Futer O, DeCenzo MT, Livingston DJ, (1992) PPIase catalysis by human FK506-binding protein proceeds through a conformational twist mechanism. J Biol Chem 267: 3316-3324.
-
(1992)
J Biol Chem
, vol.267
, pp. 3316-3324
-
-
Park, S.T.1
Aldape, R.A.2
Futer, O.3
DeCenzo, M.T.4
Livingston, D.J.5
-
21
-
-
0027071803
-
Active site mutants of human cyclophilin A separate peptidyl-prolyl isomerase activity from cyclosporin A binding and calcineurin inhibition
-
Zydowsky LD, Etzkorn FA, Chang HY, Ferguson SB, Stolz LA, et al. (1992) Active site mutants of human cyclophilin A separate peptidyl-prolyl isomerase activity from cyclosporin A binding and calcineurin inhibition. Protein Sci 1: 1092-1099.
-
(1992)
Protein Sci
, vol.1
, pp. 1092-1099
-
-
Zydowsky, L.D.1
Etzkorn, F.A.2
Chang, H.Y.3
Ferguson, S.B.4
Stolz, L.A.5
-
22
-
-
0027742843
-
A Mechanism for Rotamase Catalysis by the FK506 Binding Protein (FKBP)
-
Fischer S, Michnick S, Karplus M, (1993) A Mechanism for Rotamase Catalysis by the FK506 Binding Protein (FKBP). Biochemistry 32: 13830-13837.
-
(1993)
Biochemistry
, vol.32
, pp. 13830-13837
-
-
Fischer, S.1
Michnick, S.2
Karplus, M.3
-
24
-
-
0037178118
-
The mechanism of cis-trans isomerization of prolyl peptides by cyclophilin
-
Hur S, Bruice TC, (2002) The mechanism of cis-trans isomerization of prolyl peptides by cyclophilin. J Am Chem Soc 124: 7303-7313.
-
(2002)
J Am Chem Soc
, vol.124
, pp. 7303-7313
-
-
Hur, S.1
Bruice, T.C.2
-
25
-
-
33745800493
-
Theoretical and experimental investigation of the energetics of cis-trans proline isomerization in peptide models
-
Schroeder OE, Carper E, Wind JJ, Poutsma JL, Etzkorn FA, et al. (2006) Theoretical and experimental investigation of the energetics of cis-trans proline isomerization in peptide models. J Phys Chem A 110: 6522-6530.
-
(2006)
J Phys Chem A
, vol.110
, pp. 6522-6530
-
-
Schroeder, O.E.1
Carper, E.2
Wind, J.J.3
Poutsma, J.L.4
Etzkorn, F.A.5
-
26
-
-
0008233581
-
Structural and functional analysis of the mitotic rotamase Pin1 suggests substrate recognition is phosphorylation dependent
-
Ranganathan R, Lu KP, Hunter T, Noel JP, (1997) Structural and functional analysis of the mitotic rotamase Pin1 suggests substrate recognition is phosphorylation dependent. Cell 89: 875-886.
-
(1997)
Cell
, vol.89
, pp. 875-886
-
-
Ranganathan, R.1
Lu, K.P.2
Hunter, T.3
Noel, J.P.4
-
27
-
-
80155166010
-
A Reduced-Amide Inhibitor of Pin1 Binds in a Conformation Resembling a Twisted-Amide Transition State
-
Xu GG, Zhang Y, Mercedes-Camacho AY, Etzkorn FA, (2011) A Reduced-Amide Inhibitor of Pin1 Binds in a Conformation Resembling a Twisted-Amide Transition State. Biochemistry 50: 9545-9550.
-
(2011)
Biochemistry
, vol.50
, pp. 9545-9550
-
-
Xu, G.G.1
Zhang, Y.2
Mercedes-Camacho, A.Y.3
Etzkorn, F.A.4
-
28
-
-
9844229891
-
Synthesis and biological activity of a series of potent fluoromethyl ketone inhibitors of recombinant human calpain I
-
Chatterjee S, Ator MA, Bozyczko-Coyne D, Josef K, Wells G, et al. (1997) Synthesis and biological activity of a series of potent fluoromethyl ketone inhibitors of recombinant human calpain I. J Med Chem 40: 3820-3828.
-
(1997)
J Med Chem
, vol.40
, pp. 3820-3828
-
-
Chatterjee, S.1
Ator, M.A.2
Bozyczko-Coyne, D.3
Josef, K.4
Wells, G.5
-
29
-
-
0034732951
-
Inactivation of cysteine proteases by (acyloxy)methyl ketones using S′-P′ interactions
-
Dai Y, Hedstrom L, Abeles RH, (2000) Inactivation of cysteine proteases by (acyloxy)methyl ketones using S′-P′ interactions. Biochemistry 39: 6498-6502.
-
(2000)
Biochemistry
, vol.39
, pp. 6498-6502
-
-
Dai, Y.1
Hedstrom, L.2
Abeles, R.H.3
-
30
-
-
0034618705
-
Difluoro ketone peptidomimetics suggest a large S1 pocket for Alzheimer's gamma-secretase: implications for inhibitor design
-
Moore CL, Leatherwood DD, Diehl TS, Selkoe DJ, Wolfe MS, (2000) Difluoro ketone peptidomimetics suggest a large S1 pocket for Alzheimer's gamma-secretase: implications for inhibitor design. J Med Chem 43: 3434-3442.
-
(2000)
J Med Chem
, vol.43
, pp. 3434-3442
-
-
Moore, C.L.1
Leatherwood, D.D.2
Diehl, T.S.3
Selkoe, D.J.4
Wolfe, M.S.5
-
31
-
-
0033551099
-
Peptidomimetic probes and molecular modeling suggest that Alzheimer's gamma-secretase is an intramembrane-cleaving aspartyl protease
-
Wolfe MS, Xia W, Moore CL, Leatherwood DD, Ostaszewski B, et al. (1999) Peptidomimetic probes and molecular modeling suggest that Alzheimer's gamma-secretase is an intramembrane-cleaving aspartyl protease. Biochemistry 38: 4720-4727.
-
(1999)
Biochemistry
, vol.38
, pp. 4720-4727
-
-
Wolfe, M.S.1
Xia, W.2
Moore, C.L.3
Leatherwood, D.D.4
Ostaszewski, B.5
-
32
-
-
34347384233
-
Structural basis for high-affinity peptide inhibition of human Pin1
-
Zhang Y, Daum S, Wildemann D, Zhou XZ, Verdecia MA, et al. (2007) Structural basis for high-affinity peptide inhibition of human Pin1. ACS Chem Biol 2: 320-328.
-
(2007)
ACS Chem Biol
, vol.2
, pp. 320-328
-
-
Zhang, Y.1
Daum, S.2
Wildemann, D.3
Zhou, X.Z.4
Verdecia, M.A.5
-
33
-
-
84865249209
-
Structural and kinetic analysis of prolyl-isomerization/phosphorylation cross-talk in the CTD code
-
Zhang M, Wang XJ, Chen X, Bowman ME, Luo Y, et al. (2012) Structural and kinetic analysis of prolyl-isomerization/phosphorylation cross-talk in the CTD code. ACS Chem Biol doi: 10.1021/cb3000887.
-
(2012)
ACS Chem Biol
-
-
Zhang, M.1
Wang, X.J.2
Chen, X.3
Bowman, M.E.4
Luo, Y.5
-
34
-
-
0344951058
-
Serine-cis-proline and serine-trans-proline isosteres: stereoselective synthesis of (Z)- and (E)-alkene mimics by Still-Wittig and Ireland-Claisen rearrangements
-
Wang XJ, Hart SA, Xu B, Mason MD, Goodell JR, et al. (2003) Serine-cis-proline and serine-trans-proline isosteres: stereoselective synthesis of (Z)- and (E)-alkene mimics by Still-Wittig and Ireland-Claisen rearrangements. J Org Chem 68: 2343-2349.
-
(2003)
J Org Chem
, vol.68
, pp. 2343-2349
-
-
Wang, X.J.1
Hart, S.A.2
Xu, B.3
Mason, M.D.4
Goodell, J.R.5
-
35
-
-
85027851932
-
Preparation and reactions of 2-tert-butyl-1,1,3,3-tetramethylguanidine: 2,2,6-trimethylcyclohexen-1-yl iodide
-
Barton DHR, Chen M, Jaszberenyi JC, Taylor DK, (1997) Preparation and reactions of 2-tert-butyl-1,1,3,3-tetramethylguanidine: 2,2,6-trimethylcyclohexen-1-yl iodide. Org Synth 74: 101-107.
-
(1997)
Org Synth
, vol.74
, pp. 101-107
-
-
Barton, D.H.R.1
Chen, M.2
Jaszberenyi, J.C.3
Taylor, D.K.4
-
36
-
-
33646426403
-
Enantioselective butenolide preparation for straightforward asymmetric syntheses of gamma -lactones - paraconic acids, avenaciolide, and hydroxylated eleutherol
-
Braukmueller S, Brueckner R, (2006) Enantioselective butenolide preparation for straightforward asymmetric syntheses of gamma-lactones- paraconic acids, avenaciolide, and hydroxylated eleutherol. Eur J Org Chem pp. 2110-2118.
-
(2006)
Eur J Org Chem
, pp. 2110-2118
-
-
Braukmueller, S.1
Brueckner, R.2
-
37
-
-
0024544606
-
Studies of Stemona alkaloids. Total synthesis of (+)-croomine
-
Williams DR, Brown DL, Benbow JW, (1989) Studies of Stemona alkaloids. Total synthesis of (+)-croomine. J Am Chem Soc 111: 1923-1925.
-
(1989)
J Am Chem Soc
, vol.111
, pp. 1923-1925
-
-
Williams, D.R.1
Brown, D.L.2
Benbow, J.W.3
-
38
-
-
13244267171
-
Regioselective debenzylation of C-glycosyl compounds by boron trichloride
-
Xie J, Menand M, Valery J-M, (2005) Regioselective debenzylation of C-glycosyl compounds by boron trichloride. Carbohydr Res 340: 481-487.
-
(2005)
Carbohydr Res
, vol.340
, pp. 481-487
-
-
Xie, J.1
Menand, M.2
Valery, J.-M.3
-
39
-
-
0024564139
-
Synthesis of a substrate of protein kinase C and its corresponding phosphopeptide
-
de Bont HB, Liskamp RM, O'Brian CA, Erkelens C, Veeneman GH, et al. (1989) Synthesis of a substrate of protein kinase C and its corresponding phosphopeptide. Int J Pept Protein Res 33: 115-123.
-
(1989)
Int J Pept Protein Res
, vol.33
, pp. 115-123
-
-
de Bont, H.B.1
Liskamp, R.M.2
O'Brian, C.A.3
Erkelens, C.4
Veeneman, G.H.5
-
40
-
-
84866527326
-
-
CrysAlis v1.171, Wroclaw, Poland: Oxford Diffraction
-
CrysAlis v1.171 (2004). Wroclaw, Poland: Oxford Diffraction.
-
(2004)
-
-
-
41
-
-
37549039510
-
A short history of SHELX
-
Sheldrick GM, (2008) A short history of SHELX. Acta Cryst A64: 112-122.
-
(2008)
Acta Cryst
, vol.A64
, pp. 112-122
-
-
Sheldrick, G.M.1
-
42
-
-
84866527589
-
-
1699 South Hanley Rd., St. Louis, MO, 63144USA: Tripos International
-
(2008) SYBYL. 1699 South Hanley Rd., St. Louis, MO, 63144USA: Tripos International.
-
(2008)
SYBYL
-
-
-
43
-
-
79952177721
-
-
Wallingford CT: Gaussian, Inc
-
Frisch MJ, Trucks GW, Schlegel HB, Scuseria GE, Robb MA, et al. (2009) Gaussian. Wallingford CT: Gaussian, Inc.
-
(2009)
Gaussian
-
-
Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
-
44
-
-
49749094973
-
-
San Carlos, CAUSA: DeLano Scientific LLC
-
DeLano WL (2006) MacPyMol. San Carlos, CAUSA: DeLano Scientific LLC.
-
(2006)
MacPyMol
-
-
DeLano, W.L.1
|