Author

S. Damerow

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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Microbiology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:drug response / drug discovery· 2 Organism:mouse· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1

Frequent Co-Authors

H. Guo· 2 shared M. A. J. Ferguson· 2 shared S. M. Beverley· 2 shared A. G. Coyne· 1 shared A. Mehlert· 1 shared C. Abell· 1 shared C. E. Barry· 1 shared C. Spry· 1 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersMicrobiology

H. Guo

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

An essential, kinetoplastid-specific GDP-Fuc: β-D-Gal α-1,2-fucosyltransferase is located in the mitochondrion of Trypanosoma brucei

G. Bandini, S. Damerow, M. L. Sempaio Güther, H. Guo, A. Mehlert, S. M. Beverley, M. A. J. Ferguson

This study identifies TbFUT1 as an essential mitochondrial fucosyltransferase in Trypanosoma brucei, critical for both bloodstream and procyclic forms and potentially therapeutically relevant across trypanosomatids.

bioRxiv · May 11, 2021Microbiology

A broadly active fucosyltransferase LmjFUT1 whose mitochondrial localization and catalytic activity is essential in the parasitic protozoan Leishmania

H. Guo, S. Damerow, L. Penha, S. Menzies, G. Polanco, H. Zegzouti, M. A. J. Ferguson, S. M. Beverley

This paper identifies FUT1 as an essential fucosyltransferase in Leishmania, localized to mitochondria, with enzymatic activity required for viability and mitochondrial function.

bioRxiv · May 10, 2021Microbiology

Inhibiting Mycobacterium tuberculosis CoaBC by targeting a new allosteric site.

V. Mendes, S. R. Green, J. C. Evans, J. Hess, M. Blaszczyk, C. Spry, O. Bryant, J. Cory-Wright, D. S.-H. Chan, P. H. M. Torres, Z. Wang, S. O'Neill, S. Damerow, J. Post, T. Bayliss, , T. L. Blundell

The paper identifies potent inhibitors of Mycobacterium tuberculosis CoaB by targeting a novel allosteric site, based on structural and biochemical analyses of CoaBC.

bioRxiv · Jan 15, 2020 · PreprintBiochemistry