Journal of Structural Biology. 169(3), 294-303 Structures of two elapid snake venom metalloproteases with distinct activities highlight the disulfide patterns in the D domain of ADAMalysin family proteins. |
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Molecular & Cellular Proteomics. 8(9), 2034-50 Complementary quantitative proteomics reveals that transcription factor AP-4 mediates E-box-dependent complex formation for transcriptional repression of HDM2. |
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Chemphyschem. 10, 549-558. Fluorescence Single-Molecule Study of Cobra Phospholipase A(2) Action on a Supported Gel-Phase Lipid Bilayer. |
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Biochemistry 46, 12111-12123 Role of Glycosphingolipid conformational change in membrane pore forming activity of Cobra cardiotoxin. |
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Biochemistry 46, 9941-9952 Structures of heparin-derived tetrasaccharide bound to cobra cardiotoxins: heparin binding at a single protein site with diverse side chain interactions. |
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J.Mol. Biol. 367, 456-472 PWWP module of human Hepatoma-derived growth factor forms a domain-swapped dimer with much higher affinity for heparin. |
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J. Biol. Chem. 281, 7937-7945. Non-cytotoxic cobra cardiotoxin A5 binds to integrin αv β3 and inhibits bone resorption: Identification of cardiotoxins as non-RGD integrin- binding proteins of the Ly-6 family |
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J. Biol. Chem. 281, 656-667 Glycosphingolipid-facilitated membrane insertion and internalization of cobra cardiotoxin: The sulfatide/ cardiotoxin complex structure in a membrane-like environment suggests a lipid-dependent cell-penetrating mechanism for membenae binding polypetides. |
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Toxicon 46, 430-40 Cobra cardiotoxin-induced cell death in fetal rat cardiomyocytes and cortical neurons: different pathway but similar cell surface target. |
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FEBS Lett. 579,3169-74. Amphiphilic beta-sheet cobra cardiotoxin targets mitochondria and disrupts its network. FEBS Lett. |
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Biochemistry 44, 7414-26 Structural difference between group I and group II cobra cardiotoxins: X-ray, NMR, and CD analysis of the effect of cis-proline conformation on three-fingered toxins. |
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Carbohydr. Res. 340, 355-372 Development of specific inhibitors for heparin-binding proteins based on the cobra cardiotoxin structure: an effective synthetic strategy for rationally modified heparin-like disaccharides and a trisaccharide. |
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J. Biol. Chem. 280, 9567-9577 Structural basis of citrate-dependent and heparan sulfate-mediated cell surface retention of cobra cardiotoxin A3. |
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J. Mol. Biol. 343, 1365-1377 Solution structure and heparin interaction of human hepatoma-derived growth factor. |
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Acta Crystallogr. D Biol. Crystallogr. 60, 1912-1915. Purification, crystallization and preliminary X-ray crystallographic analysis of a cysteine-rich secretory protein (CRISP) from Naja atra venom. |
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NMR of Glyco-Conjugates, edited by J.Jimenez-Barbero, et al, Wiley-VCH, Weinhem. NMR of carbohydrates: 1D homonuclear selective methods. |
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Proteins: Membrane Binding and Pore Formation, edited by G. Anderluh, et al, Landes Biosciences, Austin. Role of Heparan Sulfate and Glycosphingolipid in the Pore Formation of Basic polypeptides of Cobra Cardiotoxin. |