Author

J. M. Kim

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Biochemistry· 1 Biophysics· 1 Microbiology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 3 Research Focus:cell signaling & trafficking· 2 Research Focus:chromatin & epigenetic regulation· 1 Assay:DNA methylation· 1 Organism:E. coli· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Approach:microscopy & imaging analysis· 1

Frequent Co-Authors

C. C. Carcamo· 1 shared C. Wu· 1 shared D. K. Sasmal· 1 shared E. Balleza· 1 shared E. Hui· 1 shared H. A. Wallweber· 1 shared I. Mellman· 1 shared J. B. Grimm· 1 shared

Activity by Year

2016-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperBiophysics

C. C. Carcamo

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Dynamic 1D Search and Processive Nucleosome Translocations by RSC and ISW2 Chromatin Remodelers

J. M. Kim, C. C. Carcamo, S. Jazani, Z. Xie, X. A. Feng, M. Yamadi, M. F. Poyton, K. L. Holland, J. B. Grimm, L. D. Lavis, T. Ha, C. Wu

This study investigates the dynamic search and processive nucleosome translocation mechanisms of RSC and ISW2 chromatin remodelers using optical tweezers and single-particle imaging.

bioRxiv · Jun 13, 2023Biophysics

Stochastic transcriptional pulses orchestrate flagellum biosynthesis in E. coli

J. M. Kim, M. Alcala-Garcia, E. Balleza, P. Cluzel

The paper shows that flagellum biosynthesis in E. coli is driven by stochastic transcriptional pulses rather than a deterministic program, revealing a post-translational regulatory mechanism.

bioRxiv · Jan 29, 2019 · PreprintMicrobiology

T cell co-stimulatory receptor CD28 is a primary target for PD-1-mediated inhibition

E. Hui, J. Cheung, J. Zhu, X. Su, M. J. Taylor, H. A. Wallweber, D. K. Sasmal, J. Huang, J. M. Kim, I. Mellman, R. D. Vale

This study shows PD-1 inhibits T cell activation by preferentially dephosphorylating CD28 over TCR, revealing CD28 as a primary target for PD-1-mediated suppression.

bioRxiv · Nov 9, 2016Biochemistry