Ph.D. Program in Structural and
Computational Biology and
Molecular Biophysics

Choel Kim

Choel Kim

Baylor College of Medicine

Department: Pharmacology
Address: Building: BCM-Alkek Graduate School
Room: BCMN-520.07
Phone: 713-798-8411
Fax: 713-798-3415
Email: ckim@bcm.edu
Web: www.bcm.edu/pharmacology/?pmid=9685

Education

1995, Biology, University of California, San Diego
1996, Biology, University of California, San Diego
2002, Chemistry, Unviersity of California, San Diego
2002-2008, Howard Hughes Medical Institute at Susan Taylor Laboratory, University of California, San Diego

Honors

Research Topic

Pharmacology

Research Description

Signal transduction

Protein-Protein Recognition

Assembly of Higher Order Signal Transduction Complexes

Localized Cyclic Nucleotide Signaling

To survive, a cell must be able to sense its ever-changing environment and adapt with an appropriate response or a set of responses. In particular, cellular events that require rapid and amplified responses, such as neurotransmitter release, hormone secretion and muscle contraction, need highly organized and dynamic sets of proteins with coordinated interactions. While we are accumulating biochemical and structural information on individual signaling components, understanding these molecules in the context of larger signaling assembly remains an important challenge that has yet to be realized.



Cyclic nucleotide (cAMP and cGMP) dependent protein kinases are broad-specificity kinases that can phosphorylate a large range of substrates and require mechanisms to achieve their specificity. In this theme, we have come to appreciate that these proteins and their substrates are not randomly scattered throughout the cell. Instead they are localized and exist as part of larger signaling complexes that are assembled near the sites of phosphorylation such as ion channels and co-transporters or near organelles such as the mitochondria and golgi. Often this targeting is mediated by a family of scaffolding proteins, called Kinase Anchoring Proteins, which can bind not only kinases, but other signaling components such as phosphatases, phospodiesterases and other proteins.

Using cyclic nucleotide (cAMP and cGMP) dependent protein kinases as model systems, I am interested in understanding these signaling proteins not only as single proteins, but also as integral components of larger signaling assemblies. My lab will pursue the answers to the following questions:

What are the molecular determinants for binding cyclic nucleotides that lead to activation?
What are the anchoring proteins specific for NO/cGMP signaling pathway?
How do different anchoring proteins differentiate pathway-specific kinases?
How are different signaling components functionally organized and linked to other pathways?
We will answer these questions using interdisciplinary techniques such Biophysical and biochemical methods, Molecular biology, X-ray crystallography and NMR, Single molecule cryoEM and Small angle x-ray scattering.

Selected Publications

Lab Members

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Last edited on: September 21, 2009