Exploring the repeat protein universe through computational protein design TJ Brunette, F Parmeggiani, PS Huang, G Bhabha, DC Ekiert, ... Nature 528 (7583), 580-584, 2015 | 221 | 2015 |
Synthesis of D‐ and L‐Phenylalanine Derivatives by Phenylalanine Ammonia Lyases: A Multienzymatic Cascade Process F Parmeggiani, SL Lovelock, NJ Weise, ST Ahmed, NJ Turner Angewandte Chemie 127 (15), 4691-4694, 2015 | 119 | 2015 |
Synthetic and therapeutic applications of ammonia-lyases and aminomutases F Parmeggiani, NJ Weise, ST Ahmed, NJ Turner Chemical reviews 118 (1), 73-118, 2018 | 111 | 2018 |
Thermodynamic benchmark study using Biacore technology I Navratilova, GA Papalia, RL Rich, D Bedinger, S Brophy, B Condon, ... Analytical Biochemistry 364 (1), 67-77, 2007 | 108 | 2007 |
Computational design of self-assembling cyclic protein homo-oligomers JA Fallas, G Ueda, W Sheffler, V Nguyen, DE McNamara, B Sankaran, ... Nature chemistry 9 (4), 353-360, 2017 | 105 | 2017 |
Biosynthesis and Characterization of Copper Nanoparticles Using Shewanella oneidensis: Application for Click Chemistry RL Kimber, EA Lewis, F Parmeggiani, K Smith, H Bagshaw, T Starborg, ... Small 14 (10), 1703145, 2018 | 102 | 2018 |
Biotechnological Development of a Practical Synthesis of Ethyl (S)-2-Ethoxy-3-(p-methoxyphenyl)propanoate (EEHP): Over 100-Fold Productivity Increase from … M Bechtold, E Brenna, C Femmer, FG Gatti, S Panke, F Parmeggiani, ... Organic Process Research & Development 16 (2), 269-276, 2012 | 78 | 2012 |
Enoate Reductase-Mediated Preparation of Methyl (S)-2-Bromobutanoate, a Useful Key Intermediate for the Synthesis of Chiral Active Pharmaceutical Ingredients E Brenna, FG Gatti, A Manfredi, D Monti, F Parmeggiani Organic Process Research & Development 16 (2), 262-268, 2012 | 71 | 2012 |
The bacterial ammonia lyase EncP: a tunable biocatalyst for the synthesis of unnatural amino acids NJ Weise, F Parmeggiani, ST Ahmed, NJ Turner Journal of the American Chemical Society 137 (40), 12977-12983, 2015 | 66 | 2015 |
Biocatalytic transamination with near-stoichiometric inexpensive amine donors mediated by bifunctional mono-and di-amine transaminases JL Galman, I Slabu, NJ Weise, C Iglesias, F Parmeggiani, RC Lloyd, ... Green Chemistry 19 (2), 361-366, 2017 | 64 | 2017 |
Cascade coupling of ene reductases with alcohol dehydrogenases: Enantioselective reduction of prochiral unsaturated aldehydes E Brenna, FG Gatti, D Monti, F Parmeggiani, A Sacchetti ChemCatChem 4 (5), 653-659, 2012 | 64 | 2012 |
Adenylation activity of carboxylic acid reductases enables the synthesis of amides AJL Wood, NJ Weise, JD Frampton, MS Dunstan, MA Hollas, ... Angewandte Chemie 129 (46), 14690-14693, 2017 | 60 | 2017 |
Chemoenzymatic Synthesis of Optically Pure l- and d-Biarylalanines through Biocatalytic Asymmetric Amination and Palladium-Catalyzed Arylation ST Ahmed, F Parmeggiani, NJ Weise, SL Flitsch, NJ Turner ACS Catalysis 5 (9), 5410-5413, 2015 | 60 | 2015 |
Real-time screening of biocatalysts in live bacterial colonies C Yan, F Parmeggiani, EA Jones, E Claude, SA Hussain, NJ Turner, ... Journal of the American Chemical Society 139 (4), 1408-1411, 2017 | 53 | 2017 |
Synthesis of robalzotan, ebalzotan, and rotigotine precursors via the stereoselective multienzymatic cascade reduction of α, β-unsaturated aldehydes E Brenna, FG Gatti, L Malpezzi, D Monti, F Parmeggiani, A Sacchetti The Journal of Organic Chemistry 78 (10), 4811-4822, 2013 | 48 | 2013 |
Opposite Enantioselectivity in the Bioreduction of (Z)‐β‐Aryl‐β‐cyanoacrylates Mediated by the Tryptophan 116 Mutants of Old Yellow Enzyme 1: Synthetic Approach to (R)‐and (S … E Brenna, M Crotti, FG Gatti, D Monti, F Parmeggiani, RW Powell III, ... Advanced Synthesis & Catalysis 357 (8), 1849-1860, 2015 | 46 | 2015 |
Single‐Biocatalyst Synthesis of Enantiopure d‐Arylalanines Exploiting an Engineered d‐Amino Acid Dehydrogenase F Parmeggiani, ST Ahmed, MP Thompson, NJ Weise, JL Galman, ... Advanced Synthesis & Catalysis 358 (20), 3298-3306, 2016 | 45 | 2016 |
Old Yellow Enzyme-mediated reduction of β-cyano-α, β-unsaturated esters for the synthesis of chiral building blocks: stereochemical analysis of the reaction E Brenna, FG Gatti, A Manfredi, D Monti, F Parmeggiani Catalysis Science & Technology 3 (4), 1136-1146, 2013 | 41 | 2013 |
Preparation and luminescence thermochromism of tetranuclear copper (I)–pyridine–iodide clusters F Parmeggiani, A Sacchetti Journal of Chemical Education 89 (7), 946-949, 2012 | 39 | 2012 |
Productivity enhancement of C= C bioreductions by coupling the in situ substrate feeding product removal technology with isolated enzymes. E Brenna, FG Gatti, D Monti, F Parmeggiani, A Sacchetti Chemical Communications (Cambridge, England) 48 (1), 79-81, 2011 | 38 | 2011 |