Author

A. B. D. Barshap

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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Organism:E. coli· 2 Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:gene regulatory network inference· 1 Approach:genetic perturbation / CRISPR· 1 Organism:human· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

H. Peled-Zehavi· 2 shared N. Fluman· 2 shared A. Bsoul· 1 shared I. A. Kalinin· 1 shared M. Chai-Danino· 1 shared M. Plohn· 1 shared N. Ravensary· 1 shared R. Nevo· 1 shared

Activity by Year

2023-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersBiochemistry

H. Peled-Zehavi

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2 papers

Recent·Most cited

Membrane-embedded polar residues target membrane proteins for degradation by the quality control protease FtsH

M. Chai-Danino, N. Ravensary, T. Onyshchuk, M. Plohn, A. B. D. Barshap, A. Bsoul, H. Peled-Zehavi, N. Fluman

The paper identifies how lipid-facing polar residues direct membrane proteins to FtsH-mediated degradation in E. coli, revealing a mechanism for recognizing misfolded proteins.

bioRxiv · Dec 12, 2023Biochemistry

Membrane protein sequence features direct post-translational insertion

I. A. Kalinin, H. Peled-Zehavi, A. B. D. Barshap, S. A. Tamari, Y. Weiss, R. Nevo, N. Fluman

The paper shows that C-terminal tails of membrane proteins influence post-translational insertion of transmembrane helices, with sequence changes causing functional defects and disease.

bioRxiv · Dec 12, 2023Biochemistry