-
1
-
-
84860741240
-
Engineering the third wave of biocatalysis
-
Bornscheuer U.T., Huisman G.W., Kazlauskas R.J., Lutz S., Moore J.C., Robins K. Engineering the third wave of biocatalysis. Nature 2012, 485:185-194.
-
(2012)
Nature
, vol.485
, pp. 185-194
-
-
Bornscheuer, U.T.1
Huisman, G.W.2
Kazlauskas, R.J.3
Lutz, S.4
Moore, J.C.5
Robins, K.6
-
2
-
-
84921037626
-
Synthetic biology for the directed evolution of protein biocatalysts: navigating sequence space intelligently
-
Currin A., Swainston N., Day P.J., Kell D.B. Synthetic biology for the directed evolution of protein biocatalysts: navigating sequence space intelligently. Chem Soc Rev 2015, 44:1172-1239.
-
(2015)
Chem Soc Rev
, vol.44
, pp. 1172-1239
-
-
Currin, A.1
Swainston, N.2
Day, P.J.3
Kell, D.B.4
-
3
-
-
84908548338
-
Recent advances in biocatalyst discovery, development and applications
-
Yang G., Ding Y. Recent advances in biocatalyst discovery, development and applications. Bioorg Med Chem 2014, 22:5604-5612.
-
(2014)
Bioorg Med Chem
, vol.22
, pp. 5604-5612
-
-
Yang, G.1
Ding, Y.2
-
4
-
-
84878025107
-
Computational enzyme design
-
Kiss G., Çelebi-Ölçüm N., Moretti R., Baker D., Houk K. Computational enzyme design. Angew Chem 2013, 52:5700-5725.
-
(2013)
Angew Chem
, vol.52
, pp. 5700-5725
-
-
Kiss, G.1
Çelebi-Ölçüm, N.2
Moretti, R.3
Baker, D.4
Houk, K.5
-
5
-
-
84891421517
-
Computational tools for designing and engineering enzymes
-
Damborsky J., Brezovsky J. Computational tools for designing and engineering enzymes. Curr Opin Chem Biol 2014, 19:8-16.
-
(2014)
Curr Opin Chem Biol
, vol.19
, pp. 8-16
-
-
Damborsky, J.1
Brezovsky, J.2
-
6
-
-
84929497651
-
A promiscuous de novo retro-aldolase catalyzes asymmetric Michael additions via Schiff Base intermediates
-
Garrabou X., Beck T., Hilvert D. A promiscuous de novo retro-aldolase catalyzes asymmetric Michael additions via Schiff Base intermediates. Angew Chem Int Ed 2015, 54:5609-5612.
-
(2015)
Angew Chem Int Ed
, vol.54
, pp. 5609-5612
-
-
Garrabou, X.1
Beck, T.2
Hilvert, D.3
-
7
-
-
84940453195
-
Mechanistic analysis of an engineered enzyme that catalyzes the formose reaction
-
Poust S., Piety J., Bar-Even A., Louw C., Baker D., Keasling J.D., Siegel J.B. Mechanistic analysis of an engineered enzyme that catalyzes the formose reaction. ChemBioChem 2015, 16:1950-1954.
-
(2015)
ChemBioChem
, vol.16
, pp. 1950-1954
-
-
Poust, S.1
Piety, J.2
Bar-Even, A.3
Louw, C.4
Baker, D.5
Keasling, J.D.6
Siegel, J.B.7
-
8
-
-
84928310608
-
Molecular dynamics explorations of active site structure in designed and evolved enzymes
-
Osuna S., Jimenez-Oses G., Noey E.L., Houk K. Molecular dynamics explorations of active site structure in designed and evolved enzymes. Acc Chem Res 2015, 48:1080-1089.
-
(2015)
Acc Chem Res
, vol.48
, pp. 1080-1089
-
-
Osuna, S.1
Jimenez-Oses, G.2
Noey, E.L.3
Houk, K.4
-
9
-
-
84915803232
-
RApid Parallel Protein EvaluatoR (RAPPER), from gene to enzyme function in one day
-
Quertinmont L.T., Orru R., Lutz S. RApid Parallel Protein EvaluatoR (RAPPER), from gene to enzyme function in one day. Chem Commun 2015, 51:122-124.
-
(2015)
Chem Commun
, vol.51
, pp. 122-124
-
-
Quertinmont, L.T.1
Orru, R.2
Lutz, S.3
-
10
-
-
84955206087
-
High-throughput analysis and protein engineering using microcapillary arrays
-
Chen B., Lim S., Kannan A., Alford S.C., Sunden F., Herschlag D., Dimov I.K., Baer T.M., Cochran J.R. High-throughput analysis and protein engineering using microcapillary arrays. Nat Chem Biol 2016, 12:76-81.
-
(2016)
Nat Chem Biol
, vol.12
, pp. 76-81
-
-
Chen, B.1
Lim, S.2
Kannan, A.3
Alford, S.C.4
Sunden, F.5
Herschlag, D.6
Dimov, I.K.7
Baer, T.M.8
Cochran, J.R.9
-
11
-
-
84907246904
-
Reprogramming the specificity of sortase enzymes
-
Dorr B.M., Ham H.O., An C., Chaikof E.L., Liu D.R. Reprogramming the specificity of sortase enzymes. Proc Natl Acad Sci U S A 2015, 111:13343-13348.
-
(2015)
Proc Natl Acad Sci U S A
, vol.111
, pp. 13343-13348
-
-
Dorr, B.M.1
Ham, H.O.2
An, C.3
Chaikof, E.L.4
Liu, D.R.5
-
12
-
-
84908513108
-
Next generation sequencing technology: advances and applications
-
Buermans H.P.J., den Dunnen J.T. Next generation sequencing technology: advances and applications. Biochem Biophys Acta 2014, 1842:1932-1941.
-
(2014)
Biochem Biophys Acta
, vol.1842
, pp. 1932-1941
-
-
Buermans, H.P.J.1
den Dunnen, J.T.2
-
13
-
-
84906536651
-
A computational approach to enzyme design: predicting ω-aminotransferase catalytic activity using docking and MM-GBSA scoring
-
Sirin S., Kumar R., Martinez C., Karmilowicz M., Ghosh P., Abramov Y., Martin V., Sherman W. A computational approach to enzyme design: predicting ω-aminotransferase catalytic activity using docking and MM-GBSA scoring. J Chem Inform Model 2014, 54:2334-2346.
-
(2014)
J Chem Inform Model
, vol.54
, pp. 2334-2346
-
-
Sirin, S.1
Kumar, R.2
Martinez, C.3
Karmilowicz, M.4
Ghosh, P.5
Abramov, Y.6
Martin, V.7
Sherman, W.8
-
14
-
-
84872552315
-
Navigating the protein fitness landscape with Gaussian processes
-
Romero P.A., Krause A., Arnold F.H. Navigating the protein fitness landscape with Gaussian processes. Proc Natl Acad Sci U S A 2013, 110:E193-E201.
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. E193-E201
-
-
Romero, P.A.1
Krause, A.2
Arnold, F.H.3
-
16
-
-
84876710917
-
On the development of new biocatalytic processes for practical pharmaceutical synthesis
-
Huisman G.W., Collier S.J. On the development of new biocatalytic processes for practical pharmaceutical synthesis. Curr Opin Chem Biol 2013, 17:284-292.
-
(2013)
Curr Opin Chem Biol
, vol.17
, pp. 284-292
-
-
Huisman, G.W.1
Collier, S.J.2
-
17
-
-
77949894197
-
Practical chiral alcohol manufacture using ketoreductases
-
Huisman G.W., Liang J., Krebber A. Practical chiral alcohol manufacture using ketoreductases. Curr Opin Chem Biol 2010, 14:122-129.
-
(2010)
Curr Opin Chem Biol
, vol.14
, pp. 122-129
-
-
Huisman, G.W.1
Liang, J.2
Krebber, A.3
-
18
-
-
77149176912
-
Highly enantioselective reduction of a small heterocyclic ketone: biocatalytic reduction of tetrahydrothiophene-3-one to the corresponding (R)-alcohol
-
Liang J., Mundorff E., Voladri R., Jenne S., Gilson L., Conway A., Krebber A., Wong J., Huisman G., Truesdell S., et al. Highly enantioselective reduction of a small heterocyclic ketone: biocatalytic reduction of tetrahydrothiophene-3-one to the corresponding (R)-alcohol. Organ Process Res Dev 2009, 14:188-192.
-
(2009)
Organ Process Res Dev
, vol.14
, pp. 188-192
-
-
Liang, J.1
Mundorff, E.2
Voladri, R.3
Jenne, S.4
Gilson, L.5
Conway, A.6
Krebber, A.7
Wong, J.8
Huisman, G.9
Truesdell, S.10
-
19
-
-
84903205486
-
Development of a practical, biocatalytic reduction for the manufacture of (S)-licarbazepine using an evolved ketoreductase
-
Modukuru N.K., Sukumaran J., Collier S.J., Chan A.S., Gohel A., Huisman G.W., Keledjian R., Narayanaswamy K., Novick S.J., Palanivel S. Development of a practical, biocatalytic reduction for the manufacture of (S)-licarbazepine using an evolved ketoreductase. Organ Process Res Dev 2014, 18:810-815.
-
(2014)
Organ Process Res Dev
, vol.18
, pp. 810-815
-
-
Modukuru, N.K.1
Sukumaran, J.2
Collier, S.J.3
Chan, A.S.4
Gohel, A.5
Huisman, G.W.6
Keledjian, R.7
Narayanaswamy, K.8
Novick, S.J.9
Palanivel, S.10
-
20
-
-
77149160599
-
Development of a biocatalytic process as an alternative to the (α)-DIP-Cl-mediated asymmetric reduction of a key intermediate of montelukast
-
Liang J., Lalonde J., Borup B., Mitchell V., Mundorff E., Trinh N., Kochrekar D., Nair Cherat R., Pai G.G. Development of a biocatalytic process as an alternative to the (α)-DIP-Cl-mediated asymmetric reduction of a key intermediate of montelukast. Organ Process Res Dev 2009, 14:193-198.
-
(2009)
Organ Process Res Dev
, vol.14
, pp. 193-198
-
-
Liang, J.1
Lalonde, J.2
Borup, B.3
Mitchell, V.4
Mundorff, E.5
Trinh, N.6
Kochrekar, D.7
Nair Cherat, R.8
Pai, G.G.9
-
21
-
-
84952705870
-
Origins of stereoselectivity in evolved ketoreductases
-
Noey E.L., Tibrewal N., Jimenez-Oses G., Osuna S., Park J., Bond C.M., Cascio D., Liang J., Zhang X., Huisman G.W., et al. Origins of stereoselectivity in evolved ketoreductases. Proc Natl Acad Sci U S A 2015, 112:E7065-E7072.
-
(2015)
Proc Natl Acad Sci U S A
, vol.112
, pp. E7065-E7072
-
-
Noey, E.L.1
Tibrewal, N.2
Jimenez-Oses, G.3
Osuna, S.4
Park, J.5
Bond, C.M.6
Cascio, D.7
Liang, J.8
Zhang, X.9
Huisman, G.W.10
-
22
-
-
84960090140
-
Catalytic asymmetric reduction of difficult-to-reduce ketones: triple code saturation mutagenesis of an alcohol dehydrogenase
-
Sun Z., Lonsdale R., Ilie A., Li G., Zhou J., Reetz M.T. Catalytic asymmetric reduction of difficult-to-reduce ketones: triple code saturation mutagenesis of an alcohol dehydrogenase. ACS Catal 2016.
-
(2016)
ACS Catal
-
-
Sun, Z.1
Lonsdale, R.2
Ilie, A.3
Li, G.4
Zhou, J.5
Reetz, M.T.6
-
24
-
-
77149171446
-
Efficient production of enantiomerically pure chiral amines at concentrations of 50 g/L using transaminases
-
Truppo M.D., Rozzell J.D., Turner N.J. Efficient production of enantiomerically pure chiral amines at concentrations of 50 g/L using transaminases. Organ Process Res Dev 2010, 14:234-237.
-
(2010)
Organ Process Res Dev
, vol.14
, pp. 234-237
-
-
Truppo, M.D.1
Rozzell, J.D.2
Turner, N.J.3
-
25
-
-
77954797329
-
Biocatalytic asymmetric synthesis of chiral amines from ketones applied to sitagliptin manufacture
-
Savile C., Janey J., Mundorff E., Moore J., Tam S., Jarvis W., Colbeck J., Krebber A., Fleitz F., Brands J., et al. Biocatalytic asymmetric synthesis of chiral amines from ketones applied to sitagliptin manufacture. Science 2010, 329:305-309.
-
(2010)
Science
, vol.329
, pp. 305-309
-
-
Savile, C.1
Janey, J.2
Mundorff, E.3
Moore, J.4
Tam, S.5
Jarvis, W.6
Colbeck, J.7
Krebber, A.8
Fleitz, F.9
Brands, J.10
-
26
-
-
84971307144
-
-
US 8,932,838
-
Cabirol FL, Gohel A, Oh SH, Smith DJ, Wong B, Lalonde JJ: Biocatalysts and methods for the synthesis of (S)-3-(1-aminoethyl)-phenol. US 8,932,838 2015.
-
(2015)
Biocatalysts and methods for the synthesis of (S)-3-(1-aminoethyl)-phenol
-
-
Cabirol, F.L.1
Gohel, A.2
Oh, S.H.3
Smith, D.J.4
Wong, B.5
Lalonde, J.J.6
-
27
-
-
84900859109
-
A highly efficient asymmetric synthesis of vernakalant
-
Limanto J., Ashley E.R., Yin J., Beutner G.L., Grau B.T., Kassim A.M., Kim M.M., Klapars A., Liu Z., Strotman H.R., et al. A highly efficient asymmetric synthesis of vernakalant. Org Lett 2014, 16:2716-2719.
-
(2014)
Org Lett
, vol.16
, pp. 2716-2719
-
-
Limanto, J.1
Ashley, E.R.2
Yin, J.3
Beutner, G.L.4
Grau, B.T.5
Kassim, A.M.6
Kim, M.M.7
Klapars, A.8
Liu, Z.9
Strotman, H.R.10
-
28
-
-
84971356601
-
Process for preparing aminocyclohexyl ether compounds
-
US 20150259284 A1
-
Limanto J, Beutner GL, Yin J, Klapars A, Ashley ER, Strotman HR, Truppo MD, Chung CK, Hughes G, Liu Z: Process for preparing aminocyclohexyl ether compounds. US 20150259284 A1 2015.
-
(2015)
-
-
Limanto, J.1
Beutner, G.L.2
Yin, J.3
Klapars, A.4
Ashley, E.R.5
Strotman, H.R.6
Truppo, M.D.7
Chung, C.K.8
Hughes, G.9
Liu, Z.10
-
29
-
-
84893855937
-
Development of a concise, asymmetric synthesis of a smoothened receptor (SMO) inhibitor: enzymatic transamination of a 4-piperidinone with dynamic kinetic resolution
-
Peng Z., Wong J.W., Hansen E.C., Puchlopek-Dermenci A.L., Clarke H.J. Development of a concise, asymmetric synthesis of a smoothened receptor (SMO) inhibitor: enzymatic transamination of a 4-piperidinone with dynamic kinetic resolution. Org Lett 2014, 16:860-863.
-
(2014)
Org Lett
, vol.16
, pp. 860-863
-
-
Peng, Z.1
Wong, J.W.2
Hansen, E.C.3
Puchlopek-Dermenci, A.L.4
Clarke, H.J.5
-
30
-
-
84908628081
-
A novel chimeric amine dehydrogenase shows altered substrate specificity compared to its parent enzymes
-
Bommarius B.R., Schurmann M., Bommarius A.S. A novel chimeric amine dehydrogenase shows altered substrate specificity compared to its parent enzymes. Chem Commun 2014, 50:14953-14955.
-
(2014)
Chem Commun
, vol.50
, pp. 14953-14955
-
-
Bommarius, B.R.1
Schurmann, M.2
Bommarius, A.S.3
-
31
-
-
0032731656
-
Biocatalysis for industrial production of fine chemicals
-
Schulze B., Wubbolts M.G. Biocatalysis for industrial production of fine chemicals. Curr Opin Biotechnol 1999, 10:609-615.
-
(1999)
Curr Opin Biotechnol
, vol.10
, pp. 609-615
-
-
Schulze, B.1
Wubbolts, M.G.2
-
32
-
-
84879209057
-
The evolution of an amine dehydrogenase biocatalyst for the asymmetric production of chiral amines
-
Abrahamson M.J., Wong J.W., Bommarius A.S. The evolution of an amine dehydrogenase biocatalyst for the asymmetric production of chiral amines. Adv Synth Catal 2013, 355.
-
(2013)
Adv Synth Catal
, pp. 355
-
-
Abrahamson, M.J.1
Wong, J.W.2
Bommarius, A.S.3
-
33
-
-
84865841265
-
Redox self-sufficient biocatalyst network for the amination of primary alcohols
-
Sattler J.H., Fuchs M., Tauber K., Mutti F.G., Faber K., Pfeffer J., Haas T., Kroutil W. Redox self-sufficient biocatalyst network for the amination of primary alcohols. Angew Chem Int Ed 2012, 51:9156-9159.
-
(2012)
Angew Chem Int Ed
, vol.51
, pp. 9156-9159
-
-
Sattler, J.H.1
Fuchs, M.2
Tauber, K.3
Mutti, F.G.4
Faber, K.5
Pfeffer, J.6
Haas, T.7
Kroutil, W.8
-
34
-
-
84943353055
-
Amination of functionalized aliphatic primary alcohols by a biocatalytic oxidation-transamination cascade
-
Pickl M., Fuchs M., Glueck S.M., Faber K. Amination of functionalized aliphatic primary alcohols by a biocatalytic oxidation-transamination cascade. ChemCatChem 2015, 7:3121-3124.
-
(2015)
ChemCatChem
, vol.7
, pp. 3121-3124
-
-
Pickl, M.1
Fuchs, M.2
Glueck, S.M.3
Faber, K.4
-
35
-
-
84942357824
-
Conversion of alcohols to enantiopure amines through dual-enzyme hydrogen-borrowing cascades
-
Mutti F.G., Knaus T., Scrutton N.S., Breuer M., Turner N.J. Conversion of alcohols to enantiopure amines through dual-enzyme hydrogen-borrowing cascades. Science 2015, 349:1525-1529.
-
(2015)
Science
, vol.349
, pp. 1525-1529
-
-
Mutti, F.G.1
Knaus, T.2
Scrutton, N.S.3
Breuer, M.4
Turner, N.J.5
-
36
-
-
84954505910
-
Asymmetric amination of secondary alcohols by using a redox-neutral two-enzyme cascade
-
Chen F.-F., Liu Y.-Y., Zheng G.-W., Xu J.-H. Asymmetric amination of secondary alcohols by using a redox-neutral two-enzyme cascade. ChemCatChem 2016, 7:3838-3841.
-
(2016)
ChemCatChem
, vol.7
, pp. 3838-3841
-
-
Chen, F.-F.1
Liu, Y.-Y.2
Zheng, G.-W.3
Xu, J.-H.4
-
37
-
-
84894450875
-
A regio and stereoselective omega-transaminase/monoamine oxidase cascade for the synthesis of chiral 2, 5 disubstituted pyrrolidines
-
O'Reilly E., Iglesias C., Ghislieri D., Hopwood J., Galman J.L., Lloyd R.C., Turner N.J. A regio and stereoselective omega-transaminase/monoamine oxidase cascade for the synthesis of chiral 2, 5 disubstituted pyrrolidines. Angew Chem Int Ed 2014, 53:2447-2450.
-
(2014)
Angew Chem Int Ed
, vol.53
, pp. 2447-2450
-
-
O'Reilly, E.1
Iglesias, C.2
Ghislieri, D.3
Hopwood, J.4
Galman, J.L.5
Lloyd, R.C.6
Turner, N.J.7
-
38
-
-
84971255758
-
InspIRED by nature: NADPH-dependent imine reductases (IREDs) as catalysts for the preparation of chiral amines
-
Grogan G., Turner N.J. InspIRED by nature: NADPH-dependent imine reductases (IREDs) as catalysts for the preparation of chiral amines. Chem: Eur J 2015.
-
(2015)
Chem: Eur J
-
-
Grogan, G.1
Turner, N.J.2
-
39
-
-
0024720392
-
A new NAD+-dependent opine dehydrogenase from Arthrobacter sp. strain 1C
-
Asano Y., Yamaguchi K., Kondo K. A new NAD+-dependent opine dehydrogenase from Arthrobacter sp. strain 1C. J Bacteriol 1989, 171:4466-4471.
-
(1989)
J Bacteriol
, vol.171
, pp. 4466-4471
-
-
Asano, Y.1
Yamaguchi, K.2
Kondo, K.3
-
40
-
-
84905574413
-
Direct reductive amination of ketones: structure and activity of S-selective imine reductases from Streptomyces
-
Huber T., Schneider L., Praeg A., Gerhardt S., Einsle O., Mueller M. Direct reductive amination of ketones: structure and activity of S-selective imine reductases from Streptomyces. ChemCatChem 2014, 6:2248-2252.
-
(2014)
ChemCatChem
, vol.6
, pp. 2248-2252
-
-
Huber, T.1
Schneider, L.2
Praeg, A.3
Gerhardt, S.4
Einsle, O.5
Mueller, M.6
-
41
-
-
84944149519
-
Imine reductase-catalyzed intermolecular reductive amination of aldehydes and ketones
-
Scheller P.N., Lenz M., Hammer S.C., Hauer B., Nestl B.M. Imine reductase-catalyzed intermolecular reductive amination of aldehydes and ketones. ChemCatChem 2015, 7:3239-3242.
-
(2015)
ChemCatChem
, vol.7
, pp. 3239-3242
-
-
Scheller, P.N.1
Lenz, M.2
Hammer, S.C.3
Hauer, B.4
Nestl, B.M.5
-
42
-
-
84971261333
-
Engineered imine reductases and methods for the reductive animation of ketone and amine compounds
-
US 20130302859 A1
-
Haibin C, Collier SJ, Nazor J, Sukumaran J, Smith D, Moore JC, Hughes G, Janey J, Huisman G, Novick S: Engineered imine reductases and methods for the reductive animation of ketone and amine compounds. US 20130302859 A1 2013.
-
(2013)
-
-
Haibin, C.1
Collier, S.J.2
Nazor, J.3
Sukumaran, J.4
Smith, D.5
Moore, J.C.6
Hughes, G.7
Janey, J.8
Huisman, G.9
Novick, S.10
-
43
-
-
84971321223
-
Engineered imine reductases and methods for the reductive amination of ketone and amine compounds
-
WO 2015073555 A1
-
Agard NJ, Alvizo O, Mayo MA, Minor SN, Riggins JN, Moore JC: Engineered imine reductases and methods for the reductive amination of ketone and amine compounds. WO 2015073555 A1 2015.
-
(2015)
-
-
Agard, N.J.1
Alvizo, O.2
Mayo, M.A.3
Minor, S.N.4
Riggins, J.N.5
Moore, J.C.6
-
44
-
-
71149114259
-
Directed evolution and structural characterization of a simvastatin synthase
-
Gao X., Xie X., Pashkov I., Sawaya M.R., Laidman J., Zhang W., Cacho R., Yeates T.O., Tang Y. Directed evolution and structural characterization of a simvastatin synthase. Chem Biol 2009, 16:1064-1074.
-
(2009)
Chem Biol
, vol.16
, pp. 1064-1074
-
-
Gao, X.1
Xie, X.2
Pashkov, I.3
Sawaya, M.R.4
Laidman, J.5
Zhang, W.6
Cacho, R.7
Yeates, T.O.8
Tang, Y.9
-
46
-
-
84903494800
-
Variant LovD polypeptides and their uses
-
US 8383382 B2
-
Gilson L, Collier SJ, Sukumaran J, Yeo WL, Alvizo O, Teo EL, Wilson RJ, Junye X: Variant LovD polypeptides and their uses. US 8383382 B2 2014.
-
(2014)
-
-
Gilson, L.1
Collier, S.J.2
Sukumaran, J.3
Yeo, W.L.4
Alvizo, O.5
Teo, E.L.6
Wilson, R.J.7
Junye, X.8
-
47
-
-
84901195603
-
The role of distant mutations and allosteric regulation on LovD active site dynamics
-
Jimenez-Oses G., Osuna S., Gao X., Sawaya M.R., Gilson L., Collier S.J., Huisman G.W., Yeates T.O., Tang Y., Houk K. The role of distant mutations and allosteric regulation on LovD active site dynamics. Nat Chem Biol 2014, 10:431-436.
-
(2014)
Nat Chem Biol
, vol.10
, pp. 431-436
-
-
Jimenez-Oses, G.1
Osuna, S.2
Gao, X.3
Sawaya, M.R.4
Gilson, L.5
Collier, S.J.6
Huisman, G.W.7
Yeates, T.O.8
Tang, Y.9
Houk, K.10
-
48
-
-
10044248344
-
Catalytic promiscuity in biocatalysis: using old enzymes to form new bonds and follow new pathways
-
Bornscheuer U.T., Kazlauskas R.J. Catalytic promiscuity in biocatalysis: using old enzymes to form new bonds and follow new pathways. Angew Chem Int Ed 2004, 43:6032-6040.
-
(2004)
Angew Chem Int Ed
, vol.43
, pp. 6032-6040
-
-
Bornscheuer, U.T.1
Kazlauskas, R.J.2
-
49
-
-
84959155451
-
Evolving new protein-protein interaction specificity through promiscuous intermediates
-
Aakre C., Herrou J., Phung T., Perchuk B., Crosson S., Laub M. Evolving new protein-protein interaction specificity through promiscuous intermediates. Cell 2015, 163:594-606.
-
(2015)
Cell
, vol.163
, pp. 594-606
-
-
Aakre, C.1
Herrou, J.2
Phung, T.3
Perchuk, B.4
Crosson, S.5
Laub, M.6
-
50
-
-
84947447600
-
Chemomimetic biocatalysis: exploiting the synthetic potential of cofactor-dependent enzymes to create new catalysts
-
Prier C.K., Arnold F.H. Chemomimetic biocatalysis: exploiting the synthetic potential of cofactor-dependent enzymes to create new catalysts. J Am Chem Soc 2015, 137:13992-14006.
-
(2015)
J Am Chem Soc
, vol.137
, pp. 13992-14006
-
-
Prier, C.K.1
Arnold, F.H.2
-
51
-
-
84896520980
-
Expanding P450 catalytic reaction space through evolution and engineering
-
McIntosh J.A., Farwell C.C., Arnold F.H. Expanding P450 catalytic reaction space through evolution and engineering. Curr Opin Chem Biol 2014, 19:126-134.
-
(2014)
Curr Opin Chem Biol
, vol.19
, pp. 126-134
-
-
McIntosh, J.A.1
Farwell, C.C.2
Arnold, F.H.3
-
52
-
-
84949190783
-
The nature of chemical innovation: new enzymes by evolution
-
Arnold F.H. The nature of chemical innovation: new enzymes by evolution. Q Rev Biophys 2015, 48:404-410.
-
(2015)
Q Rev Biophys
, vol.48
, pp. 404-410
-
-
Arnold, F.H.1
-
53
-
-
84872495336
-
Olefin cyclopropanation via carbene transfer catalyzed by engineered cytochrome P450 enzymes
-
Coelho P.S., Brustad E.M., Kannan A., Arnold F.H. Olefin cyclopropanation via carbene transfer catalyzed by engineered cytochrome P450 enzymes. Science 2013, 339:307-310.
-
(2013)
Science
, vol.339
, pp. 307-310
-
-
Coelho, P.S.1
Brustad, E.M.2
Kannan, A.3
Arnold, F.H.4
-
54
-
-
84903155038
-
Enantioselective intramolecular CH amination catalyzed by engineered cytochrome P450 enzymes in vitro and in vivo
-
McIntosh J.A., Coelho P.S., Farwell C.C., Wang Z.J., Lewis J.C., Brown T.R., Arnold F.H. Enantioselective intramolecular CH amination catalyzed by engineered cytochrome P450 enzymes in vitro and in vivo. Angew Chem 2013, 125:9479-9482.
-
(2013)
Angew Chem
, vol.125
, pp. 9479-9482
-
-
McIntosh, J.A.1
Coelho, P.S.2
Farwell, C.C.3
Wang, Z.J.4
Lewis, J.C.5
Brown, T.R.6
Arnold, F.H.7
-
55
-
-
84947430009
-
Enantioselective enzyme-catalyzed aziridination enabled by active-site evolution of a cytochrome P450
-
Farwell C.C., Zhang R.K., McIntosh J.A., Hyster T.K., Arnold F.H. Enantioselective enzyme-catalyzed aziridination enabled by active-site evolution of a cytochrome P450. ACS Central Sci 2015, 1:89-93.
-
(2015)
ACS Central Sci
, vol.1
, pp. 89-93
-
-
Farwell, C.C.1
Zhang, R.K.2
McIntosh, J.A.3
Hyster, T.K.4
Arnold, F.H.5
-
56
-
-
84903168457
-
Improved cyclopropanation activity of histidine-ligated cytochrome P450 enables the enantioselective formal synthesis of levomilnacipran
-
Wang Z.J., Renata H., Peck N.E., Farwell C.C., Coelho P.S., Arnold F.H. Improved cyclopropanation activity of histidine-ligated cytochrome P450 enables the enantioselective formal synthesis of levomilnacipran. Angew Chem Int Ed 2014, 53:6810-6813.
-
(2014)
Angew Chem Int Ed
, vol.53
, pp. 6810-6813
-
-
Wang, Z.J.1
Renata, H.2
Peck, N.E.3
Farwell, C.C.4
Coelho, P.S.5
Arnold, F.H.6
-
57
-
-
84937889484
-
Engineering a dirhodium artificial metalloenzyme for selective olefin cyclopropanation
-
Srivastava P., Yang H., Ellis-Guardiola K., Lewis J.C. Engineering a dirhodium artificial metalloenzyme for selective olefin cyclopropanation. Nat Commun 2015, 6.
-
(2015)
Nat Commun
, vol.6
-
-
Srivastava, P.1
Yang, H.2
Ellis-Guardiola, K.3
Lewis, J.C.4
-
58
-
-
84961382184
-
Expanding the enzyme universe: accessing non-natural reactions by mechanism-guided directed evolution
-
Renata H., Wang Z.J., Arnold F.H. Expanding the enzyme universe: accessing non-natural reactions by mechanism-guided directed evolution. Angew Chem Int Ed 2015, 54:3351-3367.
-
(2015)
Angew Chem Int Ed
, vol.54
, pp. 3351-3367
-
-
Renata, H.1
Wang, Z.J.2
Arnold, F.H.3
-
59
-
-
21444454396
-
Synthetic biology offers alternative pathways to natural products
-
Herrera S. Synthetic biology offers alternative pathways to natural products. Nat Biotechnol 2005, 23:270-271.
-
(2005)
Nat Biotechnol
, vol.23
, pp. 270-271
-
-
Herrera, S.1
-
60
-
-
84922067763
-
A microbial biomanufacturing platform for natural and semisynthetic opioids
-
Thodey K., Galanie S., Smolke C.D. A microbial biomanufacturing platform for natural and semisynthetic opioids. Nat Chem Biol 2014, 10:837-844.
-
(2014)
Nat Chem Biol
, vol.10
, pp. 837-844
-
-
Thodey, K.1
Galanie, S.2
Smolke, C.D.3
|