Author

S. E. Strassler

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:bacteria (other)· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:protein folding & dynamics· 1 Assay:structural biology· 1 Organism:yeast· 1

Frequent Co-Authors

G. L. Conn· 2 shared A. Krishnamohan· 1 shared A. Mehrani· 1 shared C. B. Edgington· 1 shared C. J. Hancock· 1 shared C. M. Dunham· 1 shared D. Dey· 1 shared E. D. Hoffer· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersBiochemistry

G. L. Conn

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Author profile →

2 papers

Recent·Most cited

tRNA m1G9 modification depends on substrate-specific RNA conformational changes induced by the methyltransferase Trm10

S. E. Strassler, I. E. Bowles, A. Krishnamohan, H. Kim, C. B. Edgington, E. G. Kuiper, C. J. Hancock, L. Comstock, J. E. Jackman, G. L. Conn

This study identifies that Trm10 substrate recognition depends on tRNA conformational changes induced by the enzyme, revealing a novel mechanism for tRNA modification.

bioRxiv · Feb 1, 2023Biochemistry

Functionally critical residues in the aminoglycoside resistance-associated methyltransferase RmtC play distinct roles in 30S substrate recognition

M. Nosrati, D. Dey, A. Mehrani, S. E. Strassler, N. Zelinskaya, E. D. Hoffer, S. M. Stagg, C. M. Dunham, G. L. Conn

This study identifies functionally critical residues in RmtC that distinguish between 30S-binding affinity and 16S rRNA modification through structural and biochemical analysis.

bioRxiv · Oct 3, 2019Biochemistry