| Year |
Citation |
Score |
| 2023 |
Deletti G, Green SD, Weber C, Patterson KN, Joshi SS, Khopade TM, Coban M, Veek-Wilson J, Caulfield TR, Viswanathan R, Lane AL. Unveiling an indole alkaloid diketopiperazine biosynthetic pathway that features a unique stereoisomerase and multifunctional methyltransferase. Nature Communications. 14: 2558. PMID 37137876 DOI: 10.1038/s41467-023-38168-3 |
0.583 |
|
| 2019 |
Carey J, Nguyen T, Korchak J, Beecher C, de Jong F, Lane AL. An Isotopic Ratio Outlier Analysis Approach for Global Metabolomics of Biosynthetically Talented Actinomycetes. Metabolites. 9. PMID 31510039 DOI: 10.3390/Metabo9090181 |
0.392 |
|
| 2019 |
Borgman P, Lopez RD, Lane AL. The expanding spectrum of diketopiperazine natural product biosynthetic pathways containing cyclodipeptide synthases. Organic & Biomolecular Chemistry. PMID 30688950 DOI: 10.1039/C8Ob03063D |
0.457 |
|
| 2015 |
James ED, Knuckley B, Alqahtani N, Porwal S, Ban J, Karty JA, Viswanathan R, Lane AL. Two distinct cyclodipeptide synthases from a marine actinomycete catalyze biosynthesis of the same diketopiperazine natural product. Acs Synthetic Biology. PMID 26641496 DOI: 10.1021/Acssynbio.5B00120 |
0.424 |
|
| 2015 |
Alqahtani N, Porwal SK, James ED, Bis DM, Karty JA, Lane AL, Viswanathan R. Synergism between genome sequencing, tandem mass spectrometry and bio-inspired synthesis reveals insights into nocardioazine B biogenesis. Organic & Biomolecular Chemistry. 13: 7177-92. PMID 26022437 DOI: 10.1039/C5Ob00537J |
0.514 |
|
| 2015 |
Bis DM, Ban YH, James ED, Alqahtani N, Viswanathan R, Lane AL. Characterization of the nocardiopsin biosynthetic gene cluster reveals similarities to and differences from the rapamycin and FK-506 pathways. Chembiochem : a European Journal of Chemical Biology. 16: 990-7. PMID 25755076 DOI: 10.1002/Cbic.201500007 |
0.43 |
|
| 2015 |
Trevathan-Tackett SM, Lane AL, Bishop N, Ross C. Metabolites derived from the tropical seagrass Thalassia testudinum are bioactive against pathogenic Labyrinthula sp Aquatic Botany. 122: 1-8. DOI: 10.1016/J.Aquabot.2014.12.005 |
0.361 |
|
| 2014 |
Xu M, Hillwig ML, Lane AL, Tiernan MS, Moore BS, Peters RJ. Characterization of an orphan diterpenoid biosynthetic operon from Salinispora arenicola. Journal of Natural Products. 77: 2144-7. PMID 25203741 DOI: 10.1021/Np500422D |
0.568 |
|
| 2013 |
Kersten RD, Lane AL, Nett M, Richter TK, Duggan BM, Dorrestein PC, Moore BS. Bioactivity-guided genome mining reveals the lomaiviticin biosynthetic gene cluster in Salinispora tropica. Chembiochem : a European Journal of Chemical Biology. 14: 955-62. PMID 23649992 DOI: 10.1002/Cbic.201300147 |
0.673 |
|
| 2013 |
Lane AL, Nam SJ, Fukuda T, Yamanaka K, Kauffman CA, Jensen PR, Fenical W, Moore BS. Structures and comparative characterization of biosynthetic gene clusters for cyanosporasides, enediyne-derived natural products from marine actinomycetes. Journal of the American Chemical Society. 135: 4171-4. PMID 23458364 DOI: 10.1021/Ja311065V |
0.593 |
|
| 2011 |
Lane AL, Moore BS. A sea of biosynthesis: marine natural products meet the molecular age. Natural Product Reports. 28: 411-28. PMID 21170424 DOI: 10.1039/C0Np90032J |
0.587 |
|
| 2010 |
Lane AL, Mular L, Drenkard EJ, Shearer TL, Engel S, Fredericq S, Fairchild CR, Prudhomme J, Le Roch K, Hay ME, Aalbersberg W, Kubanek J. Ecological leads for natural product discovery: Novel sesquiterpene hydroquinones from the red macroalga Peyssonnelia sp. Tetrahedron. 66: 455-461. PMID 20661312 DOI: 10.1016/J.Tet.2009.11.042 |
0.652 |
|
| 2010 |
Whalen KE, Lane AL, Kubanek J, Hahn ME. Biochemical warfare on the reef: the role of glutathione transferases in consumer tolerance of dietary prostaglandins. Plos One. 5: e8537. PMID 20052279 DOI: 10.1371/Journal.Pone.0008537 |
0.553 |
|
| 2009 |
Lane AL, Nyadong L, Galhena AS, Shearer TL, Stout EP, Parry RM, Kwasnik M, Wang MD, Hay ME, Fernandez FM, Kubanek J. Desorption electrospray ionization mass spectrometry reveals surface-mediated antifungal chemical defense of a tropical seaweed. Proceedings of the National Academy of Sciences of the United States of America. 106: 7314-9. PMID 19366672 DOI: 10.1073/Pnas.0812020106 |
0.726 |
|
| 2009 |
Nyadong L, Hohenstein EG, Galhena A, Lane AL, Kubanek J, Sherrill CD, Fernández FM. Reactive desorption electrospray ionization mass spectrometry (DESI-MS) of natural products of a marine alga. Analytical and Bioanalytical Chemistry. 394: 245-54. PMID 19277616 DOI: 10.1007/S00216-009-2674-3 |
0.589 |
|
| 2009 |
Lane AL, Stout EP, Lin AS, Prudhomme J, Le Roch K, Fairchild CR, Franzblau SG, Hay ME, Aalbersberg W, Kubanek J. Antimalarial bromophycolides J-Q from the Fijian red alga Callophycus serratus. The Journal of Organic Chemistry. 74: 2736-42. PMID 19271727 DOI: 10.1021/Jo900008W |
0.724 |
|
| 2009 |
Stout EP, Hasemeyer AP, Lane AL, Davenport TM, Engel S, Hay ME, Fairchild CR, Prudhomme J, Le Roch K, Aalbersberg W, Kubanek J. Antibacterial neurymenolides from the Fijian red alga Neurymenia fraxinifolia. Organic Letters. 11: 225-8. PMID 19053716 DOI: 10.1021/Ol8024814 |
0.707 |
|
| 2008 |
Jiang RW, Lane AL, Mylacraine L, Hardcastle KI, Fairchild CR, Aalbersberg W, Hay ME, Kubanek J. Structures and absolute configurations of sulfate-conjugated triterpenoids including an antifungal chemical defense of the green macroalga Tydemania expeditionis. Journal of Natural Products. 71: 1616-9. PMID 18763828 DOI: 10.1021/Np800307H |
0.644 |
|
| 2008 |
Lane AL, Kubanek J. Secondary metabolite defenses against pathogens and biofoulers Algal Chemical Ecology. 229-243. DOI: 10.1007/978-3-540-74181-7_11 |
0.525 |
|
| 2007 |
Lane AL, Stout EP, Hay ME, Prusak AC, Hardcastle K, Fairchild CR, Franzblau SG, Le Roch K, Prudhomme J, Aalbersberg W, Kubanek J. Callophycoic acids and callophycols from the Fijian red alga Callophycus serratus. The Journal of Organic Chemistry. 72: 7343-51. PMID 17715978 DOI: 10.1021/Jo071210Y |
0.737 |
|
| 2006 |
Lane AL, Kubanek J. Structure-activity relationship of chemical defenses from the freshwater plant Micranthemum umbrosum. Phytochemistry. 67: 1224-31. PMID 16793072 DOI: 10.1016/J.Phytochem.2006.05.007 |
0.604 |
|
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