Try experiments. This perform was funded from the generous help of

From Cypher Gate Wiki
Jump to: navigation, search

This operate was funded with the generous guidance of a National PF-06821497 Technical Information Institutes of Overall health New Innovator Award one DP2 OD008696. Koryakina I, et al. (2013) Poly distinct trans-acyltransferase machinery exposed by way of engineered acyl-CoA synthetases. ACS Chem Biol eight(1):200?08. thirteen. Wu N, Tsuji SY, Cane DE, Khosla C (2001) Evaluating the harmony among proteinprotein interactions and enzyme-substrate interactions during the channeling of intermediates amongst polyketide synthase modules. J Am Chem Soc 123(27): 6465?474. 14. Chen AY, Schnarr NA, Kim PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/24107419 CY, Cane DE, Khosla C (2006) Extender device and acyl provider protein specificity PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/23721119 of ketosynthase domains in the 6-deoxyerythronolide B synthase. J Am Chem Soc 128(nine):3067?074. fifteen. Koryakina I, McArthur JB, Draelos MM, Williams GJ (2013) Promiscuity of the modular polyketide synthase toward purely natural and non-natural extender models. Org Biomol Chem eleven(27):4449?458. 16. Rocha DF, Wouters FC, Machado G, Marsaioli AJ (2013) First Kainic acid COA biosynthetic pathway of 1-hepten-3-one in Iporangaia pustulosa (Opiliones). Sci Rep three:3156. 17. Jenner M, et al. (2015) Acyl-chain elongation drives ketosynthase substrate selectivity in trans-acyltransferase polyketide synthases. Angew Chem Int Ed Engl 54(six): 1817?821. 18.Check out experiments. This get the job done was funded through the generous help of a Nationwide Institutes of Wellness New Innovator Award one DP2 OD008696. O.A. and B.W.T. also accept the support of a National Institutes of Well being Coaching Grant T32 GMO66698. The faculty of Chemistry NMR Grants within the University of California, Berkeley is supported partly by Countrywide Institutes of Health and fitness Grants 1S10RR023679-01 and S10 RR16634-01.1. Staunton J, Weissman KJ (2001) Polyketide biosynthesis: A millennium evaluation. Nat Prod Rep 18(4):380?sixteen. two. Khosla C, Tang Y, Chen AY, Schnarr NA, Cane DE (2007) Framework and mechanism of the 6-deoxyerythronolide B synthase. Annu Rev Biochem 76:195?21. three. Dunn BJ, Khosla C (2013) Engineering the acyltransferase substrate specificity of assembly line polyketide synthases. J R Soc Interface 10(85):20130297. 4. Ray L, Moore BS (2016) Latest advances within the biosynthesis of surprising polyketide synthase substrates. Nat Prod Rep 33(two):150?61. five. Hagmann WK (2008) The many roles for fluorine in medicinal chemistry. J Med Chem fifty one(15):4359?369. six. Keatinge-Clay AT (2012) The structures of variety I polyketide synthases. Nat Prod Rep 29(10):1050?073. 7. Bravo-Rodriguez K, et al. (2015) Substrate flexibility of the mutated acyltransferase domain and implications for polyketide biosynthesis. Chem Biol 22(eleven): 1425?430. 8. Sundermann U, et al. (2013) Enzyme-directed mutasynthesis: A blended experimental and theoretical method of substrate recognition of the polyketide synthase. ACS Chem Biol eight(2):443?50. nine. McDaniel R, et al. (1999) A number of genetic modifications with the erythromycin polyketide synthase to provide a library of novel "unnatural" natural merchandise. Dunn BJ, Watts KR, Robbins T, Cane DE, Khosla C (2014) Comparative PMA References evaluation in the substrate specificity of trans- versus cis-acyltransferases of assembly line polyketide synthases.