Author

K. P. 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

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Biochemistry· 1 Biophysics· 1 Pharmacology & Toxicology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 3 Organism:human· 3 Approach:experimental assay· 2 Assay:proteomics· 2 Approach:statistical model· 2 Research Focus:cancer & tumor microenvironment· 1 Approach:deep learning· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

B. Han· 1 shared C. M. Khoo· 1 shared C. Seok· 1 shared D. Han· 1 shared D. Ryu· 1 shared E. Chan· 1 shared E. S. Tai· 1 shared G. X. Li· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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1 shared paperPhysiology

B. Han

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

PhysiologybioRxivPreprintJun 30, 2023

Unbiased phosphoproteomics analysis unveils modulation of insulin signaling by extramitotic CDK1 kinase activity in human myotubes

B. Han, G. X. Li, W. L. Liew…·E. S. Tai

The paper uses phosphoproteomics to show that CDK1 activity modulates insulin signaling and glucose uptake in human myotubes, with group-specific phosphorylation changes observed.

DOI 10.1101/2023.06.30.547176

humanproteomics

𝕏 PostBluesky

BiochemistrybioRxivJun 6, 2022

ECPAS/Ecm29-Mediated 26S Proteasome Disassembly Is an Adaptive Response to Glucose Starvation

W. H. Choi, Y. Yun, I. Byun…·M. J. Lee

This study shows that ECPAS-mediated 26S proteasome disassembly into 20S and 19S subcomplexes occurs during glucose starvation, enhancing proteolysis and cell survival.

DOI 10.1016/j.celrep.2023.112701

humanproteomics

𝕏 PostBluesky

BiophysicsbioRxivPreprintMay 31, 2022

P176S polymorphism in Maspin rewires electrostatic interaction that alters Maspin functionality

M. A. Anwar, M. Haseeb, S. Choi, K. P. Kim

This study shows that the P176S polymorphism in Maspin alters electrostatic interactions, affecting its function and binding properties in cancer.

DOI 10.1101/2022.05.31.494110

humanprotein structure

𝕏 PostBluesky

Pharmacology & ToxicologybioRxivPreprintOct 1, 2021

Synthetic glabridin derivatives mitigate steatohepatitis in a diet-induced biopsy-confirmed non-alcoholic steatosis hepatitis mouse model through paraoxonase-2

G.-C. Shin, H. M. Lee, N. Y. Kim…·K.-H. Kim

This study shows synthetic glabridin derivatives reduce NASH symptoms in mice by activating autophagy and antioxidant defenses through targeting paraoxonase-2.

DOI 10.1101/2021.10.01.462722

mouseexperimental assay

𝕏 PostBluesky