-
1
-
-
0033570996
-
Cloning and molecular characterization of a soluble epoxide hydrolase from Aspergillus niger that is related to mammalian microsomal epoxide hydrolase
-
Arand M., Hemmer H., Dürk H., Baratti J., Archelas A., Furstoss R., Oesch F. Cloning and molecular characterization of a soluble epoxide hydrolase from Aspergillus niger that is related to mammalian microsomal epoxide hydrolase. Biochem. J. 1999, 344:273-280.
-
(1999)
Biochem. J.
, vol.344
, pp. 273-280
-
-
Arand, M.1
Hemmer, H.2
Dürk, H.3
Baratti, J.4
Archelas, A.5
Furstoss, R.6
Oesch, F.7
-
2
-
-
0030798603
-
Synthesis of enantiopure epoxides through biocatalytic approaches
-
Archelas A., Furstoss R. Synthesis of enantiopure epoxides through biocatalytic approaches. Annu. Rev. Microbiol. 1997, 51:491-525.
-
(1997)
Annu. Rev. Microbiol.
, vol.51
, pp. 491-525
-
-
Archelas, A.1
Furstoss, R.2
-
3
-
-
0032031614
-
Epoxide hydrolases: new tools for the synthesis of fine organic chemicals
-
Archelas A., Furstoss R. Epoxide hydrolases: new tools for the synthesis of fine organic chemicals. Trends Biotechnol. 1998, 16:108-116.
-
(1998)
Trends Biotechnol.
, vol.16
, pp. 108-116
-
-
Archelas, A.1
Furstoss, R.2
-
4
-
-
32144432437
-
The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling
-
Arnold K., Bordoli L., Kopp J., Schwede T. The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling. Bioinformatics 2006, 22:195-201.
-
(2006)
Bioinformatics
, vol.22
, pp. 195-201
-
-
Arnold, K.1
Bordoli, L.2
Kopp, J.3
Schwede, T.4
-
5
-
-
33646865510
-
Enantioselective catalysis and analysis on a chip
-
Belder D., Ludwig M., Wang L.-W., Reetz M.T. Enantioselective catalysis and analysis on a chip. Angew. Chem. Int. Ed. 2006, 45:2463-2466.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 2463-2466
-
-
Belder, D.1
Ludwig, M.2
Wang, L.-W.3
Reetz, M.T.4
-
6
-
-
43049123356
-
Advances in laboratory evolution of enzymes
-
Bershtein S., Tawfik D.S. Advances in laboratory evolution of enzymes. Curr. Opin. Chem. Biol. 2008, 12:151-158.
-
(2008)
Curr. Opin. Chem. Biol.
, vol.12
, pp. 151-158
-
-
Bershtein, S.1
Tawfik, D.S.2
-
7
-
-
33745211891
-
Enantioconvergent production of (R)-1-phenyl-1,2-ethanediol from styrene oxide by combining the Solanum tuberosum and an evolved Agrobacterium radiobacter AD1 epoxide hydrolases
-
Cao L., Lee J., Chen W., Wood T.K. Enantioconvergent production of (R)-1-phenyl-1,2-ethanediol from styrene oxide by combining the Solanum tuberosum and an evolved Agrobacterium radiobacter AD1 epoxide hydrolases. Biotechnol. Bioeng. 2006, 124:522-529.
-
(2006)
Biotechnol. Bioeng.
, vol.124
, pp. 522-529
-
-
Cao, L.1
Lee, J.2
Chen, W.3
Wood, T.K.4
-
8
-
-
0346101759
-
Modification of activity and specificity of haloalkane dehalogenase from Sphingomonas paucimobilis UT26 by engineering of its entrance tunnel
-
Chaloupková R., Sýkorová J., Prokop Z., Jesenská A., Monincová M., Pavlová M., Tsuda M., Nagata Y., Damborský J. Modification of activity and specificity of haloalkane dehalogenase from Sphingomonas paucimobilis UT26 by engineering of its entrance tunnel. J. Biol. Chem. 2003, 278:52622-52628.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 52622-52628
-
-
Chaloupková, R.1
Sýkorová, J.2
Prokop, Z.3
Jesenská, A.4
Monincová, M.5
Pavlová, M.6
Tsuda, M.7
Nagata, Y.8
Damborský, J.9
-
9
-
-
23444450226
-
Semi-rational approaches to engineering enzyme activity: combining the benefits of directed evolution and rational design
-
Chica R.A., Doucet N., Pelletier J.N. Semi-rational approaches to engineering enzyme activity: combining the benefits of directed evolution and rational design. Curr. Opin. Biotechnol. 2005, 16:378-384.
-
(2005)
Curr. Opin. Biotechnol.
, vol.16
, pp. 378-384
-
-
Chica, R.A.1
Doucet, N.2
Pelletier, J.N.3
-
10
-
-
0032054698
-
Enantioselective epoxide hydrolysis: catalysis involving microbes, mammals and metals
-
Finney N.S. Enantioselective epoxide hydrolysis: catalysis involving microbes, mammals and metals. Chem. Biol. 1998, 5:R73-R79.
-
(1998)
Chem. Biol.
, vol.5
-
-
Finney, N.S.1
-
11
-
-
43949114931
-
Directed evolution library creation
-
Humana Press, Totowa
-
Georgescu R., Bandara G., Sun L. Directed evolution library creation. Methods in Molecular Biology 2003, vol. 231:75-83. Humana Press, Totowa.
-
(2003)
Methods in Molecular Biology
, vol.231
, pp. 75-83
-
-
Georgescu, R.1
Bandara, G.2
Sun, L.3
-
12
-
-
0018697931
-
Activation of vinyl chloride to covalently bound metabolites: roles of 2-chloroethylene oxide and 2-chloroacetaldehyde
-
Guengerich F.P., Crawford W.M., Watanabe P.G. Activation of vinyl chloride to covalently bound metabolites: roles of 2-chloroethylene oxide and 2-chloroacetaldehyde. Biochemistry 1979, 18:5178-5182.
-
(1979)
Biochemistry
, vol.18
, pp. 5178-5182
-
-
Guengerich, F.P.1
Crawford, W.M.2
Watanabe, P.G.3
-
13
-
-
77954358041
-
Modification of substrate specificity resulting in an epoxide hydrolase with shifted enantiopreference for (2,3-epoxypropyl)benzene
-
Gurell A., Widersten M. Modification of substrate specificity resulting in an epoxide hydrolase with shifted enantiopreference for (2,3-epoxypropyl)benzene. ChemBioChem 2010, 11:1422-1429.
-
(2010)
ChemBioChem
, vol.11
, pp. 1422-1429
-
-
Gurell, A.1
Widersten, M.2
-
14
-
-
0002051540
-
BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT
-
Hall T.A. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucl. Acids Symp. Ser. 1999, 41:95-98.
-
(1999)
Nucl. Acids Symp. Ser.
, vol.41
, pp. 95-98
-
-
Hall, T.A.1
-
15
-
-
0028843882
-
Asymmetric synthesis of FR165914: a novel β3-adrenergic agonist with a benzocycloheptene structure
-
Hattori K., Nagano M., Kato T., Nakanishi I., Imai K., Kinoshita T., Sakane K. Asymmetric synthesis of FR165914: a novel β3-adrenergic agonist with a benzocycloheptene structure. Bioorg. Med. Chem. Lett. 1995, 5:2821-2824.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 2821-2824
-
-
Hattori, K.1
Nagano, M.2
Kato, T.3
Nakanishi, I.4
Imai, K.5
Kinoshita, T.6
Sakane, K.7
-
16
-
-
44949203597
-
Enantioconvergent bioconversion of p-chlorostyrene oxide to (R)-p-chlorophenyl-1,2-ethandiol by the bacterial epoxide hydrolase of Caulobacter crescentus
-
Hwang S., Choi C.H., Lee E.Y. Enantioconvergent bioconversion of p-chlorostyrene oxide to (R)-p-chlorophenyl-1,2-ethandiol by the bacterial epoxide hydrolase of Caulobacter crescentus. Biotechnol. Lett. 2008, 30:1219-1225.
-
(2008)
Biotechnol. Lett.
, vol.30
, pp. 1219-1225
-
-
Hwang, S.1
Choi, C.H.2
Lee, E.Y.3
-
17
-
-
52749090358
-
One-pot biotransformation of racemic styrene oxide into (R)-1,2-phenylethanediol by two recombinant microbial epoxide hydrolases
-
Hwang S., Choi C.Y., Lee E.Y. One-pot biotransformation of racemic styrene oxide into (R)-1,2-phenylethanediol by two recombinant microbial epoxide hydrolases. Biotechnol. Bioprocess Eng. 2008, 13:453-457.
-
(2008)
Biotechnol. Bioprocess Eng.
, vol.13
, pp. 453-457
-
-
Hwang, S.1
Choi, C.Y.2
Lee, E.Y.3
-
18
-
-
30844440518
-
Immobilization of the Solanum tuberosum epoxide hydrolase and its application in an enantioconvergent process
-
Karboune S., Archelas A., Furstoss R., Baratti J.C. Immobilization of the Solanum tuberosum epoxide hydrolase and its application in an enantioconvergent process. Biocatal. Biotransform. 2005, 23:397-405.
-
(2005)
Biocatal. Biotransform.
, vol.23
, pp. 397-405
-
-
Karboune, S.1
Archelas, A.2
Furstoss, R.3
Baratti, J.C.4
-
19
-
-
0032479816
-
Chiral C3 epoxides and halohydrins: their preparation and synthetic application
-
Kasai N., Suzuki T., Furukawa Y. Chiral C3 epoxides and halohydrins: their preparation and synthetic application. J. Mol. Catal. B: Enzym. 1998, 4:237-252.
-
(1998)
J. Mol. Catal. B: Enzym.
, vol.4
, pp. 237-252
-
-
Kasai, N.1
Suzuki, T.2
Furukawa, Y.3
-
20
-
-
36649004271
-
Biosynthesis of (R)-phenyl-1,2-ethanediol from racemic styrene oxide by using bacterial and marine fish epoxide hydrolases
-
Kim H.S., Lee O.K., Hwang S., Kim B.J., Lee E.Y. Biosynthesis of (R)-phenyl-1,2-ethanediol from racemic styrene oxide by using bacterial and marine fish epoxide hydrolases. Biotechnol. Lett. 2008, 30:127-133.
-
(2008)
Biotechnol. Lett.
, vol.30
, pp. 127-133
-
-
Kim, H.S.1
Lee, O.K.2
Hwang, S.3
Kim, B.J.4
Lee, E.Y.5
-
21
-
-
0026495369
-
A simplified procedure for the stereospecific transformation of 1,2-diols into epoxides
-
Kolb H.C., Sharpless K.B. A simplified procedure for the stereospecific transformation of 1,2-diols into epoxides. Tetrahedron 1992, 48:10515-10530.
-
(1992)
Tetrahedron
, vol.48
, pp. 10515-10530
-
-
Kolb, H.C.1
Sharpless, K.B.2
-
23
-
-
33644618258
-
Purification and characterisation of a novel enantioselective epoxide hydrolase from Aspergillus niger M200
-
Kotik M., Kyslík P. Purification and characterisation of a novel enantioselective epoxide hydrolase from Aspergillus niger M200. Biochim. Biophys. Acta: Gen. Subj. 2006, 1760:245-252.
-
(2006)
Biochim. Biophys. Acta: Gen. Subj.
, vol.1760
, pp. 245-252
-
-
Kotik, M.1
Kyslík, P.2
-
24
-
-
27744517396
-
Novel microbial epoxide hydrolases for biohydrolysis of glycidyl derivatives
-
Kotik M., Brichac J., Kyslík P. Novel microbial epoxide hydrolases for biohydrolysis of glycidyl derivatives. J. Biotechnol. 2005, 120:364-375.
-
(2005)
J. Biotechnol.
, vol.120
, pp. 364-375
-
-
Kotik, M.1
Brichac, J.2
Kyslík, P.3
-
25
-
-
34848893919
-
Cloning of an epoxide hydrolase-encoding gene from Aspergillus niger M200, overexpression in E. coli, and modification of activity and enantioselectivity of the enzyme by protein engineering
-
Kotik M., Štěpánek V., Kyslík P., Marešová H. Cloning of an epoxide hydrolase-encoding gene from Aspergillus niger M200, overexpression in E. coli, and modification of activity and enantioselectivity of the enzyme by protein engineering. J. Biotechnol. 2007, 132:8-15.
-
(2007)
J. Biotechnol.
, vol.132
, pp. 8-15
-
-
Kotik, M.1
Štěpánek, V.2
Kyslík, P.3
Marešová, H.4
-
26
-
-
58249089337
-
Environmental DNA as a source of a novel epoxide hydrolase reacting with aliphatic terminal epoxides
-
Kotik M., Štěpánek V., Marešová H., Kyslík P., Archelas A. Environmental DNA as a source of a novel epoxide hydrolase reacting with aliphatic terminal epoxides. J. Mol. Catal. B: Enzym. 2009, 56:288-293.
-
(2009)
J. Mol. Catal. B: Enzym.
, vol.56
, pp. 288-293
-
-
Kotik, M.1
Štěpánek, V.2
Marešová, H.3
Kyslík, P.4
Archelas, A.5
-
27
-
-
77952583553
-
Access to enantiopure aromatic epoxides and diols using epoxide hydrolases derived from total biofilter DNA
-
Kotik M., Štěpánek V., Grulich M., Kyslík P., Archelas A. Access to enantiopure aromatic epoxides and diols using epoxide hydrolases derived from total biofilter DNA. J. Mol. Catal. B: Enzym. 2010, 65:41-48.
-
(2010)
J. Mol. Catal. B: Enzym.
, vol.65
, pp. 41-48
-
-
Kotik, M.1
Štěpánek, V.2
Grulich, M.3
Kyslík, P.4
Archelas, A.5
-
28
-
-
34948826046
-
Molecular engineering of epoxide hydrolase and its application to asymmetric and enantioconvergent hydrolysis
-
Lee E.Y., Shuler M.L. Molecular engineering of epoxide hydrolase and its application to asymmetric and enantioconvergent hydrolysis. Biotechnol. Bioeng. 2007, 98:318-327.
-
(2007)
Biotechnol. Bioeng.
, vol.98
, pp. 318-327
-
-
Lee, E.Y.1
Shuler, M.L.2
-
29
-
-
0035924935
-
Microbiological transformations. Part 45. A green chemistry preparative scale synthesis of enantiopure building blocks of Eliprodil: elaboration of a high substrate concentration epoxide hydrolase-catalyzed hydrolytic kinetic resolution process
-
Manoj K.M., Archelas A., Baratti J., Furstoss R. Microbiological transformations. Part 45. A green chemistry preparative scale synthesis of enantiopure building blocks of Eliprodil: elaboration of a high substrate concentration epoxide hydrolase-catalyzed hydrolytic kinetic resolution process. Tetrahedron 2001, 57:695-701.
-
(2001)
Tetrahedron
, vol.57
, pp. 695-701
-
-
Manoj, K.M.1
Archelas, A.2
Baratti, J.3
Furstoss, R.4
-
30
-
-
8744220371
-
Inverse thinking about double mutants of enzymes
-
Mildvan A.S. Inverse thinking about double mutants of enzymes. Biochemistry 2004, 43:14517-14520.
-
(2004)
Biochemistry
, vol.43
, pp. 14517-14520
-
-
Mildvan, A.S.1
-
31
-
-
4644259619
-
Enzymatic transformations. Part 58. Enantioconvergent biohydrolysis of styrene oxide derivatives catalysed by the Solanum tuberosum epoxide hydrolase
-
Monterde M.I., Lombard M., Archelas A., Cronin A., Arand M., Furstoss R. Enzymatic transformations. Part 58. Enantioconvergent biohydrolysis of styrene oxide derivatives catalysed by the Solanum tuberosum epoxide hydrolase. Tetrahedron: Asymmetr. 2004, 15:2801-2805.
-
(2004)
Tetrahedron: Asymmetr.
, vol.15
, pp. 2801-2805
-
-
Monterde, M.I.1
Lombard, M.2
Archelas, A.3
Cronin, A.4
Arand, M.5
Furstoss, R.6
-
32
-
-
11644261806
-
Automated docking using a Lamarckian genetic algorithm and empirical binding free energy function
-
Morris G.M., Goodsell D.S., Halliday R.S., Huey R., Hart W.E., Belew R.K., Olson A.J. Automated docking using a Lamarckian genetic algorithm and empirical binding free energy function. J. Comput. Chem. 1998, 19:1639-1662.
-
(1998)
J. Comput. Chem.
, vol.19
, pp. 1639-1662
-
-
Morris, G.M.1
Goodsell, D.S.2
Halliday, R.S.3
Huey, R.4
Hart, W.E.5
Belew, R.K.6
Olson, A.J.7
-
33
-
-
0032496192
-
Microbial transformations. Part 39. Determination of the regioselectivity occurring during oxirane ring opening by epoxide hydrolases: a theoretical analysis and a new method for its determination
-
Moussou P., Archelas A., Baratti J., Furstoss R. Microbial transformations. Part 39. Determination of the regioselectivity occurring during oxirane ring opening by epoxide hydrolases: a theoretical analysis and a new method for its determination. Tetrahedron: Asymmetr. 1998, 9:1539-1547.
-
(1998)
Tetrahedron: Asymmetr.
, vol.9
, pp. 1539-1547
-
-
Moussou, P.1
Archelas, A.2
Baratti, J.3
Furstoss, R.4
-
34
-
-
0033994961
-
Clues for the existence of two different epoxide hydrolase activities in the fungus Beauveria bassiana
-
Moussou P., Archelas A., Furstoss R., Baratti J.C. Clues for the existence of two different epoxide hydrolase activities in the fungus Beauveria bassiana. Enzyme Microb. Technol. 2000, 26:414-420.
-
(2000)
Enzyme Microb. Technol.
, vol.26
, pp. 414-420
-
-
Moussou, P.1
Archelas, A.2
Furstoss, R.3
Baratti, J.C.4
-
35
-
-
0041765676
-
User-friendly algorithms for estimating completeness and diversity in randomized protein-encoding libraries
-
Patrick W.M., Firth A.E., Blackburn J.M. User-friendly algorithms for estimating completeness and diversity in randomized protein-encoding libraries. Protein Eng. Des. Sel. 2003, 16:451-457.
-
(2003)
Protein Eng. Des. Sel.
, vol.16
, pp. 451-457
-
-
Patrick, W.M.1
Firth, A.E.2
Blackburn, J.M.3
-
36
-
-
70349330482
-
Redesigning dehalogenase access tunnels as a strategy for degrading an anthropogenic substrate
-
Pavlova M., Klvana M., Prokop Z., Chaloupkova R., Banas P., Otyepka M., Wade R.C., Tsuda M., Nagata Y., Damborsky J. Redesigning dehalogenase access tunnels as a strategy for degrading an anthropogenic substrate. Nat. Chem. Biol. 2009, 5:727-733.
-
(2009)
Nat. Chem. Biol.
, vol.5
, pp. 727-733
-
-
Pavlova, M.1
Klvana, M.2
Prokop, Z.3
Chaloupkova, R.4
Banas, P.5
Otyepka, M.6
Wade, R.C.7
Tsuda, M.8
Nagata, Y.9
Damborsky, J.10
-
37
-
-
0029881420
-
Microbial transformations 32: use of epoxide hydrolase mediated biohydrolysis as a way to enantiopure epoxides and vicinal diols: application to substituted styrene oxide derivatives
-
Pedragosa-Moreau S., Archelas A., Furstoss R. Microbial transformations 32: use of epoxide hydrolase mediated biohydrolysis as a way to enantiopure epoxides and vicinal diols: application to substituted styrene oxide derivatives. Tetrahedron 1996, 52:4593-4606.
-
(1996)
Tetrahedron
, vol.52
, pp. 4593-4606
-
-
Pedragosa-Moreau, S.1
Archelas, A.2
Furstoss, R.3
-
38
-
-
1942503297
-
Controlling the enantioselectivity of enzymes by directed evolution: practical and theoretical ramifications
-
Reetz M.T. Controlling the enantioselectivity of enzymes by directed evolution: practical and theoretical ramifications. Proc. Natl. Acad. Sci. U.S.A. 2004, 101:5716-5722.
-
(2004)
Proc. Natl. Acad. Sci. U.S.A.
, vol.101
, pp. 5716-5722
-
-
Reetz, M.T.1
-
39
-
-
54349117265
-
Constructing and analyzing the fitness landscape of an experimental evolutionary process
-
Reetz M.T., Sanchis J. Constructing and analyzing the fitness landscape of an experimental evolutionary process. ChemBioChem 2008, 9:2260-2267.
-
(2008)
ChemBioChem
, vol.9
, pp. 2260-2267
-
-
Reetz, M.T.1
Sanchis, J.2
-
40
-
-
0035477024
-
Directed evolution of an enantioselective enzyme through combinatorial multiple-cassette mutagenesis
-
Reetz M.T., Wilensek S., Zha D., Jaeger K.-E. Directed evolution of an enantioselective enzyme through combinatorial multiple-cassette mutagenesis. Angew. Chem. Int. Ed. 2001, 40:3589-3591.
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 3589-3591
-
-
Reetz, M.T.1
Wilensek, S.2
Zha, D.3
Jaeger, K.-E.4
-
41
-
-
0842325300
-
Enhancing the enantioselectivity of an epoxide hydrolase by directed evolution
-
Reetz M.T., Torre C., Eipper A., Lohmer R., Hermes M., Brunner B., Maichele A., Bocola M., Arand M., Cronin A., Genzel Y., Archelas A., Furstoss R. Enhancing the enantioselectivity of an epoxide hydrolase by directed evolution. Org. Lett. 2004, 6:177-180.
-
(2004)
Org. Lett.
, vol.6
, pp. 177-180
-
-
Reetz, M.T.1
Torre, C.2
Eipper, A.3
Lohmer, R.4
Hermes, M.5
Brunner, B.6
Maichele, A.7
Bocola, M.8
Arand, M.9
Cronin, A.10
Genzel, Y.11
Archelas, A.12
Furstoss, R.13
-
42
-
-
33744475011
-
Directed evolution of enantioselective enzymes: iterative cycles of CASTing for probing protein-sequence space
-
Reetz M.T., Wang L.-W., Bocola M. Directed evolution of enantioselective enzymes: iterative cycles of CASTing for probing protein-sequence space. Angew. Chem. Int. Ed. 2006, 45:1236-1241.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 1236-1241
-
-
Reetz, M.T.1
Wang, L.-W.2
Bocola, M.3
-
43
-
-
54349090614
-
Addressing the numbers problem in directed evolution
-
Reetz M.T., Kahakeaw D., Lohmer D. Addressing the numbers problem in directed evolution. ChemBioChem 2008, 9:1797-1804.
-
(2008)
ChemBioChem
, vol.9
, pp. 1797-1804
-
-
Reetz, M.T.1
Kahakeaw, D.2
Lohmer, D.3
-
44
-
-
67650547522
-
Directed evolution of an enantioselective epoxide hydrolase: uncovering the source of enantioselectivity at each evolutionary stage
-
Reetz M.T., Bocola M., Wang L.-W., Sanchis J., Cronin A., Arand M., Zou J., Archelas A., Bottalla A.-L., Naworyta A., Mowbray S.L. Directed evolution of an enantioselective epoxide hydrolase: uncovering the source of enantioselectivity at each evolutionary stage. J. Am. Chem. Soc. 2009, 131:7334-7343.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 7334-7343
-
-
Reetz, M.T.1
Bocola, M.2
Wang, L.-W.3
Sanchis, J.4
Cronin, A.5
Arand, M.6
Zou, J.7
Archelas, A.8
Bottalla, A.-L.9
Naworyta, A.10
Mowbray, S.L.11
-
45
-
-
78149432825
-
Laboratory evolution of stereoselective enzymes: a prolific source of catalysts for asymmetric reactions
-
Reetz M.T. Laboratory evolution of stereoselective enzymes: a prolific source of catalysts for asymmetric reactions. Angew. Chem. Int. Ed. 2011, 50:138-174.
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 138-174
-
-
Reetz, M.T.1
-
46
-
-
0030969017
-
Primary structure and catalytic mechanism of the epoxide hydrolase from Agrobacterium radiobacter AD1
-
Rink R., Fennema M., Smids M., Dehmel U., Janssen D.B. Primary structure and catalytic mechanism of the epoxide hydrolase from Agrobacterium radiobacter AD1. J. Biol. Chem. 1997, 272:14650-14657.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 14650-14657
-
-
Rink, R.1
Fennema, M.2
Smids, M.3
Dehmel, U.4
Janssen, D.B.5
-
47
-
-
22144457118
-
Protein engineering of epoxide hydrolase from Agrobacterium radiobacter AD1 for enhanced activity and enantioselective production of (R)-1-phenylethane-1,2-diol
-
Rui L., Cao L., Chen W., Reardon K.F., Wood T.K. Protein engineering of epoxide hydrolase from Agrobacterium radiobacter AD1 for enhanced activity and enantioselective production of (R)-1-phenylethane-1,2-diol. Appl. Environ. Microbiol. 2005, 71:3995-4003.
-
(2005)
Appl. Environ. Microbiol.
, vol.71
, pp. 3995-4003
-
-
Rui, L.1
Cao, L.2
Chen, W.3
Reardon, K.F.4
Wood, T.K.5
-
48
-
-
0033397980
-
Python: a programming language for software integration and development
-
Sanner M.F. Python: a programming language for software integration and development. J. Mol. Graph. 1999, 17:57-61.
-
(1999)
J. Mol. Graph.
, vol.17
, pp. 57-61
-
-
Sanner, M.F.1
-
49
-
-
1942517067
-
Reaction mechanism of soluble epoxide hydrolase: insights from molecular dynamics simulations
-
Schiøtt B., Bruice T.C. Reaction mechanism of soluble epoxide hydrolase: insights from molecular dynamics simulations. J. Am. Chem. Soc. 2002, 124:14558-14570.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 14558-14570
-
-
Schiøtt, B.1
Bruice, T.C.2
-
50
-
-
0042622380
-
SWISS-MODEL: an automated protein homology-modeling server
-
Schwede T., Kopp J., Guex N., Peitsch M.C. SWISS-MODEL: an automated protein homology-modeling server. Nucleic Acids Res. 2003, 31:3381-3385.
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 3381-3385
-
-
Schwede, T.1
Kopp, J.2
Guex, N.3
Peitsch, M.C.4
-
51
-
-
0033556602
-
Biocatalytic transformation of racemates into chiral building blocks in 100% chemical yield and 100% enantiomeric excess
-
Strauss U.T., Felfer U., Faber K. Biocatalytic transformation of racemates into chiral building blocks in 100% chemical yield and 100% enantiomeric excess. Tetrahedron: Asymmetr. 1999, 10:107-117.
-
(1999)
Tetrahedron: Asymmetr.
, vol.10
, pp. 107-117
-
-
Strauss, U.T.1
Felfer, U.2
Faber, K.3
-
52
-
-
3342911436
-
Directed evolution of epoxide hydrolase from A. radiobacter toward higher enantioselectivity by error-prone PCR and DNA shuffling
-
van Loo B., Lutje Spelberg J.H., Kingma J., Sonke T., Wubbolts M.G., Janssen D.B. Directed evolution of epoxide hydrolase from A. radiobacter toward higher enantioselectivity by error-prone PCR and DNA shuffling. Chem. Biol. 2004, 11:981-990.
-
(2004)
Chem. Biol.
, vol.11
, pp. 981-990
-
-
van Loo, B.1
Lutje Spelberg, J.H.2
Kingma, J.3
Sonke, T.4
Wubbolts, M.G.5
Janssen, D.B.6
-
53
-
-
0035711459
-
High-throughput screening for biocatalysis
-
Wahler D., Raymond J.-L. High-throughput screening for biocatalysis. Curr. Opin. Biotechnol. 2001, 12:535-544.
-
(2001)
Curr. Opin. Biotechnol.
, vol.12
, pp. 535-544
-
-
Wahler, D.1
Raymond, J.-L.2
-
54
-
-
33646443800
-
Enantioconvergent hydrolysis of styrene epoxides by newly discovered epoxide hydrolases in mung bean
-
Xu W., Xu J.-H., Pan J., Gu Q., Wu X.-Y. Enantioconvergent hydrolysis of styrene epoxides by newly discovered epoxide hydrolases in mung bean. Org. Lett. 2006, 8:1737-1740.
-
(2006)
Org. Lett.
, vol.8
, pp. 1737-1740
-
-
Xu, W.1
Xu, J.-H.2
Pan, J.3
Gu, Q.4
Wu, X.-Y.5
-
56
-
-
78149259021
-
Manipulating the stereoselectivity of limonene epoxide hydrolase by directed evolution based on iterative saturation mutagenesis
-
Zheng H., Reetz M.T. Manipulating the stereoselectivity of limonene epoxide hydrolase by directed evolution based on iterative saturation mutagenesis. J. Am. Chem. Soc. 2010, 132:15744-15751.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 15744-15751
-
-
Zheng, H.1
Reetz, M.T.2
-
57
-
-
78149264575
-
Directed evolution of enantioconvergency: the case of an epoxide hydrolase-catalyzed reaction of a racemic epoxide
-
Zheng H., Kahakeaw D., Acevedo J.P., Reetz M.T. Directed evolution of enantioconvergency: the case of an epoxide hydrolase-catalyzed reaction of a racemic epoxide. ChemCatChem 2010, 2:958-961.
-
(2010)
ChemCatChem
, vol.2
, pp. 958-961
-
-
Zheng, H.1
Kahakeaw, D.2
Acevedo, J.P.3
Reetz, M.T.4
-
58
-
-
0034651639
-
Structure of Aspergillus niger epoxide hydrolase at 1.8Å resolution: implications for the structure and function of the mammalian microsomal class of epoxide hydrolases
-
Zou J.Y., Hallberg B.M., Bergfors T., Oesch F., Arand M., Mowbray S.L., Jones T.A. Structure of Aspergillus niger epoxide hydrolase at 1.8Å resolution: implications for the structure and function of the mammalian microsomal class of epoxide hydrolases. Structure 2000, 8:111-122.
-
(2000)
Structure
, vol.8
, pp. 111-122
-
-
Zou, J.Y.1
Hallberg, B.M.2
Bergfors, T.3
Oesch, F.4
Arand, M.5
Mowbray, S.L.6
Jones, T.A.7
|