Author

R. W. Reed

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 Research Focus:drug response / drug discovery· 1 Research Focus:protein structure prediction· 1 Assay:structural biology· 1

Frequent Co-Authors

C. T. Chaton· 2 shared K. V. Korotkov· 2 shared A. H. A. Parret· 1 shared A. T. Tuukkanen· 1 shared C. W. Kenner· 1 shared D. Eisenberg· 1 shared D. Freire· 1 shared E. S. Rodriguez· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersBiochemistry

C. T. Chaton

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2 papers

Recent·Most cited

Structural analysis of mycobacterial homoserine transacetylases central to methionine biosynthesis reveals druggable active site

C. T. Chaton, E. S. Rodriguez, R. W. Reed, J. Li, C. W. Kenner, K. V. Korotkov

The paper determines the crystal structures of three homoserine transacetylases and identifies MtMetX as highly druggable.

bioRxiv · Dec 10, 2019Biochemistry

Structural variability of EspG chaperones from mycobacterial ESX-1, ESX-3 and ESX-5 type VII secretion systems

A. T. Tuukkanen, D. Freire, S. Chan, M. A. Arbing, R. W. Reed, T. J. Evans, G. Zenkeviciute, J. Kim, S. Kahng, M. R. Sawaya, C. T. Chaton, M. Wilmanns, D. Eisenberg, A. H. A. Parret, K. V. Korotkov

The paper reports crystal and SAXS structures of EspG chaperones from mycobacterial ESX systems, revealing structural variability and potential substrate binding modes.

bioRxiv · Oct 13, 2018Biochemistry