Max J. Cryle

Affiliations: 
Monash University (Australia) 
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"Max Cryle"
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Padva L, Gullick J, Coe L, et al. (2024) The biarylitides: understanding the structure and biosynthesis of a fascinating class of Cytochrome P450 modified RiPP natural products. Chembiochem : a European Journal of Chemical Biology. e202400916
Zhao Y, Gullick J, Hansen MH, et al. (2024) Loss of fluorine during crosslinking by the biarylitide P450 proceeds due to restricted peptide orientation. Chemical Communications (Cambridge, England). 60: 13951-13954
Voitsekhovskaia I, Ho YTC, Klatt C, et al. (2024) Altering glycopeptide antibiotic biosynthesis through mutasynthesis allows incorporation of fluorinated phenylglycine residues. Rsc Chemical Biology
Ratnayake M, Ho YTC, Jian X, et al. (2024) An in vitro assay to explore condensation domain specificity from non-ribosomal peptide synthesis. Methods in Enzymology. 702: 89-119
Coe LJ, Zhao Y, Padva L, et al. (2024) REASSIGNMENT OF THE STRUCTURE OF A TRYPTOPHAN-CONTAINING CYCLIC TRIPEPTIDE PRODUCED BY THE BIARYLITIDE CROSSLINKING CYTOCHROME P450BLT. Chemistry (Weinheim An Der Bergstrasse, Germany). e202400988
Ratnayake MS, Hansen MH, Cryle MJ. (2024) Enzyme engineering lets us play with new building blocks in non-ribosomal peptide synthesis. Structure (London, England : 1993). 32: 520-522
Treisman M, Coe L, Zhao Y, et al. (2024) An Engineered Biarylitide Cross-Linking P450 from RiPP Biosynthesis Generates Alternative Cyclic Peptides. Organic Letters
Marschall E, Cass RW, Prasad KM, et al. (2023) Synthetic ramoplanin analogues are accessible by effective incorporation of arylglycines in solid-phase peptide synthesis. Chemical Science. 15: 195-203
Zhang S, Zhang L, Greule A, et al. (2023) P450-mediated dehydrotyrosine formation during WS9326 biosynthesis proceeds dehydrogenation of a specific acylated dipeptide substrate. Acta Pharmaceutica Sinica. B. 13: 3561-3574
Ho YTC, Kaczmarski JA, Tailhades J, et al. (2023) Not always an innocent bystander: the impact of stabilised phosphopantetheine moieties when studying nonribosomal peptide biosynthesis. Chemical Communications (Cambridge, England)
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