| Year |
Citation |
Score |
| 2023 |
Nett RS, Dho Y, Tsai C, Passow D, Martinez Grundman J, Low YY, Sattely ES. Plant carbonic anhydrase-like enzymes in neuroactive alkaloid biosynthesis. Nature. 624: 182-191. PMID 37938780 DOI: 10.1038/s41586-023-06716-y |
0.341 |
|
| 2023 |
Nagashima K, Zhao A, Atabakhsh K, Bae M, Blum JE, Weakley A, Jain S, Meng X, Cheng AG, Wang M, Higginbottom S, Dimas A, Murugkar P, Sattely ES, Moon JJ, et al. Mapping the T cell repertoire to a complex gut bacterial community. Nature. PMID 37587342 DOI: 10.1038/s41586-023-06431-8 |
0.631 |
|
| 2023 |
Carlson ED, Rajniak J, Sattely ES. Multiplicity of the Infection of for Transient DNA Delivery. Acs Synthetic Biology. 12: 2329-2338. PMID 37558215 DOI: 10.1021/acssynbio.3c00148 |
0.777 |
|
| 2023 |
Mehta N, Meng Y, Zare R, Kamenetsky-Goldstein R, Sattely E. A developmental gradient reveals biosynthetic pathways to eukaryotic toxins in monocot geophytes. Biorxiv : the Preprint Server For Biology. PMID 37214939 DOI: 10.1101/2023.05.12.540595 |
0.348 |
|
| 2023 |
De La Peña R, Hodgson H, Liu JC, Stephenson MJ, Martin AC, Owen C, Harkess A, Leebens-Mack J, Jimenez LE, Osbourn A, Sattely ES. Complex scaffold remodeling in plant triterpene biosynthesis. Science (New York, N.Y.). 379: 361-368. PMID 36701471 DOI: 10.1126/science.adf1017 |
0.348 |
|
| 2022 |
Kim SS, Wengier DL, Ragland CJ, Sattely ES. Transcriptional Reactivation of Lignin Biosynthesis for the Heterologous Production of Etoposide Aglycone in . Acs Synthetic Biology. PMID 36122905 DOI: 10.1021/acssynbio.2c00289 |
0.427 |
|
| 2021 |
Nett RS, Sattely ES. Total Biosynthesis of the Tubulin-Binding Alkaloid Colchicine. Journal of the American Chemical Society. 143: 19454-19465. PMID 34780686 DOI: 10.1021/jacs.1c08659 |
0.388 |
|
| 2021 |
Nett RS, Dho Y, Low YY, Sattely ES. A metabolic regulon reveals early and late acting enzymes in neuroactive Lycopodium alkaloid biosynthesis. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34112718 DOI: 10.1073/pnas.2102949118 |
0.418 |
|
| 2021 |
Schnabel T, Sattely E. Engineering Posttranslational Regulation of Glutamine Synthetase for Controllable Ammonia Production in the Plant Symbiont Azospirillum brasilense. Applied and Environmental Microbiology. 87: e0058221. PMID 33962983 DOI: 10.1128/AEM.00582-21 |
0.341 |
|
| 2021 |
Holmes EC, Chen YC, Mudgett MB, Sattely ES. Arabidopsis UGT76B1 glycosylates N-hydroxy-pipecolic acid and inactivates systemic acquired resistance in tomato. The Plant Cell. 33: 750-765. PMID 33955491 DOI: 10.1093/plcell/koaa052 |
0.347 |
|
| 2021 |
Holmes EC, Chen YC, Mudgett MB, Sattely ES. Arabidopsis UGT76B1 glycosylates N-hydroxy-pipecolic acid and inactivates systemic acquired resistance in tomato. The Plant Cell. PMID 33624103 DOI: 10.1093/plcell/koaa052 |
0.347 |
|
| 2020 |
De La Peña R, Sattely ES. Rerouting plant terpene biosynthesis enables momilactone pathway elucidation. Nature Chemical Biology. PMID 33106662 DOI: 10.1038/s41589-020-00669-3 |
0.388 |
|
| 2020 |
Calgaro-Kozina A, Vuu KM, Keasling JD, Loqué D, Sattely ES, Shih PM. Engineering Plant Synthetic Pathways for the Biosynthesis of Novel Antifungals. Acs Central Science. 6: 1394-1400. PMID 32875080 DOI: 10.1021/Acscentsci.0C00241 |
0.771 |
|
| 2020 |
Nett RS, Lau W, Sattely ES. Publisher Correction: Discovery and engineering of colchicine alkaloid biosynthesis. Nature. PMID 32728219 DOI: 10.1038/S41586-020-2606-0 |
0.751 |
|
| 2020 |
Nett RS, Lau W, Sattely ES. Discovery and engineering of colchicine alkaloid biosynthesis. Nature. PMID 32699417 DOI: 10.1038/S41586-020-2546-8 |
0.82 |
|
| 2020 |
Liou CS, Sirk SJ, Diaz CAC, Klein AP, Fischer CR, Higginbottom SK, Erez A, Donia MS, Sonnenburg JL, Sattely ES. A Metabolic Pathway for Activation of Dietary Glucosinolates by a Human Gut Symbiont. Cell. 180: 717-728.e19. PMID 32084341 DOI: 10.1016/J.Cell.2020.01.023 |
0.78 |
|
| 2020 |
Jeon JE, Kim JG, Fischer CR, Mehta N, Dufour-Schroif C, Wemmer K, Mudgett MB, Sattely E. A Pathogen-Responsive Gene Cluster for Highly Modified Fatty Acids in Tomato. Cell. 180: 176-187.e19. PMID 31923394 DOI: 10.1016/J.Cell.2019.11.037 |
0.422 |
|
| 2019 |
Schultz B, Kim SY, Lau W, Sattely ES. Total Biosynthesis for Milligram-Scale Production of Etoposide Inter-mediates in a Plant Chassis. Journal of the American Chemical Society. PMID 31755709 DOI: 10.1021/Jacs.9B10717 |
0.762 |
|
| 2019 |
Holmes EC, Chen YC, Sattely ES, Mudgett MB. An engineered pathway for -hydroxy-pipecolic acid synthesis enhances systemic acquired resistance in tomato. Science Signaling. 12. PMID 31641079 DOI: 10.1126/Scisignal.Aay3066 |
0.491 |
|
| 2019 |
Hodgson H, De La Peña R, Stephenson MJ, Thimmappa R, Vincent JL, Sattely ES, Osbourn A. Identification of key enzymes responsible for protolimonoid biosynthesis in plants: Opening the door to azadirachtin production. Proceedings of the National Academy of Sciences of the United States of America. PMID 31371503 DOI: 10.1073/Pnas.1906083116 |
0.473 |
|
| 2019 |
Voges MJEEE, Bai Y, Schulze-Lefert P, Sattely ES. Plant-derived coumarins shape the composition of an synthetic root microbiome. Proceedings of the National Academy of Sciences of the United States of America. PMID 31152139 DOI: 10.1073/Pnas.1820691116 |
0.407 |
|
| 2018 |
Nett RS, Guan X, Smith K, Faust AM, Sattely ES, Fischer CR. DO Labeling to Measure Active Biosynthesis of Natural Products in Medicinal Plants. Aiche Journal. American Institute of Chemical Engineers. 64: 4319-4330. PMID 31235979 DOI: 10.1002/Aic.16413 |
0.497 |
|
| 2018 |
Chen YC, Holmes EC, Rajniak J, Kim JG, Tang S, Fischer CR, Mudgett MB, Sattely ES. -hydroxy-pipecolic acid is a mobile metabolite that induces systemic disease resistance in . Proceedings of the National Academy of Sciences of the United States of America. PMID 29735713 DOI: 10.1073/Pnas.1805291115 |
0.753 |
|
| 2018 |
Harvey CJB, Tang M, Schlecht U, Horecka J, Fischer CR, Lin HC, Li J, Naughton B, Cherry J, Miranda M, Li YF, Chu AM, Hennessy JR, Vandova GA, Inglis D, ... ... Sattely E, et al. HEx: A heterologous expression platform for the discovery of fungal natural products. Science Advances. 4: eaar5459. PMID 29651464 DOI: 10.1126/Sciadv.Aar5459 |
0.37 |
|
| 2018 |
Rajniak J, Giehl RFH, Chang E, Murgia I, von Wirén N, Sattely ES. Biosynthesis of redox-active metabolites in response to iron deficiency in plants. Nature Chemical Biology. PMID 29581584 DOI: 10.1038/S41589-018-0019-2 |
0.763 |
|
| 2017 |
Klein AP, Sattely ES. Biosynthesis of cabbage phytoalexins from indole glucosinolate. Proceedings of the National Academy of Sciences of the United States of America. PMID 28154137 DOI: 10.1073/Pnas.1615625114 |
0.685 |
|
| 2015 |
LeFevre GH, Portmann AC, Müller CE, Sattely ES, Luthy RG. Plant Assimilation Kinetics and Metabolism of 2-Mercaptobenzothiazole Tire Rubber Vulcanizers by Arabidopsis. Environmental Science & Technology. PMID 26698834 DOI: 10.1021/Acs.Est.5B04716 |
0.453 |
|
| 2015 |
Klein AP, Sattely ES. Two cytochromes P450 catalyze S-heterocyclizations in cabbage phytoalexin biosynthesis. Nature Chemical Biology. 11: 837-9. PMID 26389737 DOI: 10.1038/Nchembio.1914 |
0.58 |
|
| 2015 |
Müller CE, LeFevre GH, Timofte AE, Hussain FA, Sattely ES, Luthy RG. Competing mechanisms for perfluoroalkyl-acid accumulation in plants revealed using an Arabidopsis model system. Environmental Toxicology and Chemistry / Setac. PMID 26383989 DOI: 10.1002/Etc.3251 |
0.374 |
|
| 2015 |
Lau W, Sattely ES. Six enzymes from mayapple that complete the biosynthetic pathway to the etoposide aglycone. Science (New York, N.Y.). 349: 1224-8. PMID 26359402 DOI: 10.1126/Science.Aac7202 |
0.785 |
|
| 2015 |
Rajniak J, Barco B, Clay NK, Sattely ES. A new cyanogenic metabolite in Arabidopsis required for inducible pathogen defence. Nature. 525: 376-9. PMID 26352477 DOI: 10.1038/Nature14907 |
0.818 |
|
| 2015 |
LeFevre GH, Müller CE, Li RJ, Luthy RG, Sattely ES. Rapid Phytotransformation of Benzotriazole Generates Synthetic Tryptophan and Auxin Analogs in Arabidopsis. Environmental Science & Technology. 49: 10959-68. PMID 26301449 DOI: 10.1021/Acs.Est.5B02749 |
0.804 |
|
| 2014 |
Lau W, Fischbach MA, Osbourn A, Sattely ES. Key applications of plant metabolic engineering. Plos Biology. 12: e1001879. PMID 24915445 DOI: 10.1371/Journal.Pbio.1001879 |
0.799 |
|
| 2014 |
Anarat-Cappillino G, Sattely ES. The chemical logic of plant natural product biosynthesis. Current Opinion in Plant Biology. 19: 51-8. PMID 24727074 DOI: 10.1016/J.Pbi.2014.03.007 |
0.819 |
|
| 2013 |
Klein AP, Anarat-Cappillino G, Sattely ES. Minimum set of cytochromes P450 for reconstituting the biosynthesis of camalexin, a major Arabidopsis antibiotic. Angewandte Chemie (International Ed. in English). 52: 13625-8. PMID 24151049 DOI: 10.1002/Anie.201307454 |
0.751 |
|
| 2009 |
Heemstra JR, Walsh CT, Sattely ES. Enzymatic tailoring of ornithine in the biosynthesis of the Rhizobium cyclic trihydroxamate siderophore vicibactin. Journal of the American Chemical Society. 131: 15317-29. PMID 19778043 DOI: 10.1021/Ja9056008 |
0.439 |
|
| 2009 |
Wuest WM, Sattely ES, Walsh CT. Three siderophores from one bacterial enzymatic assembly line. Journal of the American Chemical Society. 131: 5056-7. PMID 19320483 DOI: 10.1021/Ja900815W |
0.666 |
|
| 2009 |
Sattely ES, Meek SJ, Malcolmson SJ, Schrock RR, Hoveyda AH. Design and stereoselective preparation of a new class of chiral olefin metathesis catalysts and application to enantioselective synthesis of quebrachamine: catalyst development inspired by natural product synthesis. Journal of the American Chemical Society. 131: 943-53. PMID 19113867 DOI: 10.1021/Ja8084934 |
0.774 |
|
| 2009 |
Sattely ES, Meek SJ, Malcolmson SJ, Schrock RR, Hoveyda AH. Synthesis of (+)-Quebrachamine Synfacts. 2009: 817-817. DOI: 10.1055/S-0029-1217578 |
0.764 |
|
| 2009 |
Hoveyda A, Malcolmson S, Meek S, Sattely E, Schrock R. Molybdenum-Catalyzed Enantioselective Alkene Metathesis Synfacts. 2009: 0293-0293. DOI: 10.1055/S-0028-1087747 |
0.765 |
|
| 2008 |
Malcolmson SJ, Meek SJ, Sattely ES, Schrock RR, Hoveyda AH. Highly efficient molybdenum-based catalysts for enantioselective alkene metathesis. Nature. 456: 933-7. PMID 19011612 DOI: 10.1038/Nature07594 |
0.761 |
|
| 2008 |
Sattely ES, Walsh CT. A latent oxazoline electrophile for N-O-C bond formation in pseudomonine biosynthesis. Journal of the American Chemical Society. 130: 12282-4. PMID 18710233 DOI: 10.1021/Ja804499R |
0.441 |
|
| 2008 |
Sattely ES, Fischbach MA, Walsh CT. Total biosynthesis: in vitro reconstitution of polyketide and nonribosomal peptide pathways. Natural Product Reports. 25: 757-93. PMID 18663394 DOI: 10.1039/B801747F |
0.628 |
|
| 2005 |
Sattely ES, Cortez GA, Moebius DC, Schrock RR, Hoveyda AH. Enantioselective synthesis of cyclic amides and amines through mo-catalyzed asymmetric ring-closing metathesis. Journal of the American Chemical Society. 127: 8526-33. PMID 15941288 DOI: 10.1021/Ja051330S |
0.772 |
|
| 2002 |
Dolman SJ, Sattely ES, Hoveyda AH, Schrock RR. Efficient catalytic enantioselective synthesis of unsaturated amines: preparation of small- and medium-ring cyclic amines through mo-catalyzed asymmetric ring-closing metathesis in the absence of solvent. Journal of the American Chemical Society. 124: 6991-7. PMID 12059222 DOI: 10.1021/Ja012534L |
0.529 |
|
| 2001 |
La DS, Sattely ES, Ford JG, Schrock RR, Hoveyda AH. Catalytic asymmetric ring-opening metathesis/cross metathesis (AROM/CM) reactions. Mechanism and application to enantioselective synthesis of functionalized cyclopentanes. Journal of the American Chemical Society. 123: 7767-78. PMID 11493050 DOI: 10.1021/ja010684q |
0.73 |
|
| 1999 |
La DS, Gair Ford J, Sattely ES, Bonitatebus PJ, Schrock RR, Hoveyda AH. Tandem catalytic asymmetric ring-opening metathesis/cross metathesis [19] Journal of the American Chemical Society. 121: 11603-11604. DOI: 10.1021/Ja9931832 |
0.72 |
|
| Show low-probability matches. |