Author

I. A. Gak

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· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Assay:proteomics· 2 Organism:human· 1 Research Focus:protein folding & dynamics· 1 Organism:yeast· 1

Frequent Co-Authors

G. Bakos· 2 shared J. Mansfeld· 2 shared J. S. Choudhary· 2 shared L. Yu· 2 shared T. I. Roumeliotis· 2 shared A. Herrmann· 1 shared C. Horenburg· 1 shared D. Liakopoulos· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersCell Biology

G. Bakos

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2 papers

Recent·Most cited

UFMylation regulates translational homeostasis and cell cycle progression

I. A. Gak, D. Vasiljevic, T. Zerjatke, L. Yu, M. Brosch, T. I. Roumeliotis, C. Horenburg, N. Klemm, G. Bakos, A. Herrmann, J. Hampe, I. Glauche, J. S. Choudhary, J. Mansfeld

This study shows UFMylation regulates translation and cell cycle progression by controlling eIF4F complex assembly and ribosome recruitment, independent of stress response pathways.

bioRxiv · Feb 3, 2020 · PreprintCell Biology

An E2-ubiquitin thioester-driven approach to identify substrates modified with ubiquitin and ubiquitin-like molecules

G. Bakos, L. Yu, I. A. Gak, T. I. Roumeliotis, D. Liakopoulos, J. S. Choudhary, J. Mansfeld

This paper introduces E2~dID, a method to identify substrates modified by ubiquitin and ubiquitin-like molecules using E2-thioester conjugates, validated in human and yeast systems.

bioRxiv · Oct 10, 2018Biochemistry