Author

M. J. Roth

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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Biophysics· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Assay:protein structure· 2 Approach:statistical model· 2 Research Focus:chromatin & epigenetic regulation· 1 Approach:deep learning· 1 Approach:experimental assay· 1 Research Focus:host-pathogen & immune response· 1 Organism:mouse· 1 Research Focus:protein structure prediction· 1

Frequent Co-Authors

G. T. Montelione· 2 shared G. V. T. Swapna· 2 shared J. Hao· 2 shared A. Mondal· 1 shared A. Perez· 1 shared B. Jacobs· 1 shared G. Chalmers· 1 shared G. Liu· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersBiophysics

G. T. Montelione

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2 papers

Recent·Most cited

Structure determination of protein-peptide complexes from NMR chemical shift data using MELD.

A. Mondal, G. V. T. Swapna, J. Hao, L. Ma, M. J. Roth, G. T. Montelione, A. Perez

The paper develops a hybrid MELD-NMR approach to determine structures of flexible protein-polypeptide complexes using only NMR chemical shift data, achieving accurate results for ET domain-BET protein interactions.

bioRxiv · Dec 31, 2021 · PreprintBiophysics

A common binding motif in the ET domain of BRD3 forms polymorphic structural interfaces with host and viral proteins

S. Aiyer, G. V. T. Swapna, G. Liu, L.-C. Ma, J. Hao, G. Chalmers, B. Jacobs, G. T. Montelione, M. J. Roth

This paper investigates the structural interactions of the BRD3 ET domain with host and viral proteins, revealing polymorphic structural interfaces and conformational plasticity.

bioRxiv · Sep 21, 2020Microbiology