|

|
| 
|
Sanguk Kim, Ph.D.
|
|
Associate Professor Department of Life Science Division
of Molecular and Life Sciences Bioinformatics
|
|

|
|
E-mail sukim@postech.ac.kr Phone +82-54-279-2348(office)
+82-54-279-8171(lab.) Laboratory
Structural Bioinformatics Laboratory
|
|

|
|
Profile
| Research Interests
| Selected Publications
|
|

|
|
Profile
|
2002 2002-2005
|
Ph.D., Molecular
Biophysics, Florida
State University Post-doc, Univ.
of California, Los Angeles
|
|
|
TOP
|
|
|
Research Interests
Computational structural biology and bioinformatics - Structural and functional characterization of membrane proteins - Development of prediction methods for protein structure and protein-protein interaction Structural Bioinformatics of Membrane Proteins Membrane proteins serve many important cellular functions including cell-cell communications, signal transductions, and ion/nutrient transportations. Defects in membrane proteins are related to the diseases in cancer, heart diseases, immunological and neurological disorders. Thus, improving our understanding of membrane protein structure and function should have a significant impact on medicine. In spite of their importance, our understanding of membrane protein is limited due to the difficulties in current methods of structural biology. Thus, effective structure prediction methods combined with designed biophysical and biochemical experiments should have an enormous impact on our understanding of membrane protein structure and function. Keywords from research publications Channel architecture, open-close & ion transport mechanism, functional & structural motif, drug binding, cell surface receptor, transmembrane cell signaling, GPCR, receptor tyrosine kinase, integrin, cell adhesion molecules, Alzheimer amyloid pore, glycine zipper, mechanosensitive channel, and tight junction protein
|
|
Selected Publications
- Lee, D.W. Kim, J.K. Lee, S. Choi, S. Kim,
S.* Hwang, I.* (2008). “Nuclear-encoded plastid
transit peptides contain multiple sequence subgroups
with distinctive chloroplast-targeting sequence
motifs.” Plant Cell In press. *Corresponding
authors
- Kim, Y.Y. Kim, D.Y. Shim, D. Song, W.Y.
Lee, J. Schroeder, J.I. Kim, S. Moran, N. Lee,
Y. (2008). “Expression of the novel wheat gene
TM20 confers enhanced cadmium tolerance to baker’s
yeast.” J. Biol. Chem. 283(23):15893-15902.
- Kim, H.R. Lee, G.H. Ha, K.C. Ahn, T. Lee,
B.J. Choo, S.G. Kim, S. Seo, Y.R. Shin, Y.J.
Chae, S.W. Reed, J.C. Chae, H.J. (2008). “Bax
inhibitor-1 (BI-1) is a pH-dependent regulator
of Ca2+ channel activity in the endoplasmic
reticulum.” J. Biol. Chem. 283(23):15946-15955.
- Page, R.C. Kim, S. Cross, T.A. (2008). “Transmembrane
helix uniformity examined by spectral mapping
of torsion angles.” Structure 16: 787-797.
- Gorman, P.M. Kim, S. Guo, M. Melnyk, R.
McLaurin, J. Fraser, P.E. Bowie, J. Chakrabartty,
A. (2008). “Dimerization of the transmembrane
domain of amyloid precursor proteins and familial
Alzheimer’s disease mutants.” BMC Neuroscience
9, 1-11.
- Choi, S. Jeon, J. Yang, J.S. Kim, S. (2008).
“Common occurrence of internal repeat symmetry
in membrane proteins.” Proteins 71, 68-80.
- Plotkowski, M.L. Kim, S. Phillips, M.L.
Partridge, A.W. Deber, C.M. Bowie, J.U. (2007).
“The transmembrane domain of Myelin Protein
Zero can form dimers: Possible implications
for Myelin construction.” Biochemistry 46,
12164-12173.
- Kim, Y.K. Park, H.W. Yang, J.S. Oh, S.Y.
Chang Y.S, Shin, E.S. Lee, J.E. Kim, S.* Gho
Y.S. Cho, S.H. Min, K.U. Kim, Y.Y. (2007). “Association
and functional relevance of E237G, a polymorphism
of the high-affinity IgE-receptor beta chain
gene, to airway hyperresponsiveness.” Clin
Exp Allergy 37, 592-598.
- Barwe, S.P.* Kim, S.* Rajasekaran, S.A.
Bowie, J.U. Rajasekaran, A.K. (2007). “Janus
model of the Na,K-ATPase β-subunit transmembrane
domain: Distinct faces mediate α/β assembly
and β-β homo-oligomerization.” J. Mol. Biol.
365, 706-714.
- Jeong, M.Y.* Kim, S.* Yun, C.W. Choi, Y.J.
Cho, S.G. (2007). “Engineering a de novo internal
disulfide disulfide bridge to improve the thermal
stability of xylanase from Bacillus stearothermophilus
No. 236.” J. Biotechnol.127, 300-309.
|
|
|
|

|
|
Division
of Molecular & Life Sciences| POSTECH |
|