1bx6
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(New page: 200px<br /><applet load="1bx6" size="450" color="white" frame="true" align="right" spinBox="true" caption="1bx6, resolution 2.1Å" /> '''CRYSTAL STRUCTURE OF ...)
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Revision as of 09:52, 20 November 2007
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CRYSTAL STRUCTURE OF THE POTENT NATURAL PRODUCT INHIBITOR BALANOL IN COMPLEX WITH THE CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE
Overview
Endogenous protein kinase inhibitors are essential for a wide range of, physiological functions. These endogenous inhibitors may mimic peptide, substrates as in the case of the heat-stable protein kinase inhibitor, (PKI), or they may mimic nucleotide triphosphates. Natural product, inhibitors, endogenous to the unique organisms producing them, can be, potent exogenous inhibitors against foreign protein kinases. Balanol is a, natural product inhibitor exhibiting low nanomolar Ki values against, serine and threonine specific kinases, while being ineffective against, protein tyrosine kinases. To elucidate balanol's specific inhibitory, effects and provide a basis for understanding inhibition-regulated, biological processes, a 2.1 A resolution crystal structure of balanol in, complex with cAMP-dependent protein kinase (cAPK) was determined. The, structure reveals conserved binding regions and displays extensive, complementary interactions between balanol and conserved cAPK residues., This report describes the structure of a protein kinase crystallized with, a natural ATP mimetic in the absence of metal ions and peptide inhibitor.
About this Structure
1BX6 is a Single protein structure of sequence from Mus musculus with BA1 as ligand. Active as Non-specific serine/threonine protein kinase, with EC number 2.7.11.1 Full crystallographic information is available from OCA.
Reference
Crystal structure of the potent natural product inhibitor balanol in complex with the catalytic subunit of cAMP-dependent protein kinase., Narayana N, Diller TC, Koide K, Bunnage ME, Nicolaou KC, Brunton LL, Xuong NH, Ten Eyck LF, Taylor SS, Biochemistry. 1999 Feb 23;38(8):2367-76. PMID:10029530
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