2gni: Difference between revisions

New page: left|200px<br /><applet load="2gni" size="450" color="white" frame="true" align="right" spinBox="true" caption="2gni, resolution 2.27Å" /> '''PKA fivefold mutant ...
 
No edit summary
Line 1: Line 1:
[[Image:2gni.gif|left|200px]]<br /><applet load="2gni" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2gni.gif|left|200px]]<br /><applet load="2gni" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2gni, resolution 2.27&Aring;" />
caption="2gni, resolution 2.27&Aring;" />
'''PKA fivefold mutant model of Rho-kinase with inhibitor Fasudil (HA1077)'''<br />
'''PKA fivefold mutant model of Rho-kinase with inhibitor Fasudil (HA1077)'''<br />


==Overview==
==Overview==
Controlling aberrant kinase-mediated cellular signaling is a major, strategy in cancer therapy; successful protein kinase inhibitors such as, Tarceva and Gleevec verify this approach. Specificity of inhibitors for, the targeted kinase(s), however, is a crucial factor for therapeutic, success. Based on homology modeling, we previously identified four amino, acids in the active site of Rho-kinase that likely determine inhibitor, specificities observed for Rho-kinase relative to protein kinase A (PKA), (in PKA numbering: T183A, L49I, V123M, and E127D), and a fifth (Q181K), that played a surprising role in PKA-PKB hybrid proteins. We have, systematically mutated these residues in PKA to their counterparts in, Rho-kinase, individually and in combination. Using four, Rho-kinase-specific, one PKA-specific, and one pan-kinase-specific, inhibitor, we measured the inhibitor-binding properties of the mutated, proteins and identify the roles of individual residues as specificity, determinants. Two combined mutant proteins, containing the combination of, mutations T183A and L49I, closely mimic Rho-kinase. Kinetic results, corroborate the hypothesis that side-chain identities form the major, determinants of selectivity. An unexpected result of the analysis is the, consistent contribution of the individual mutations by simple factors., Crystal structures of the surrogate kinase inhibitor complexes provide a, detailed basis for an understanding of these selectivity determinant, residues. The ability to obtain kinetic and structural data from these PKA, mutants, combined with their Rho-kinase-like selectivity profiles, make, them valuable for use as surrogate kinases for structure-based inhibitor, design.
Controlling aberrant kinase-mediated cellular signaling is a major strategy in cancer therapy; successful protein kinase inhibitors such as Tarceva and Gleevec verify this approach. Specificity of inhibitors for the targeted kinase(s), however, is a crucial factor for therapeutic success. Based on homology modeling, we previously identified four amino acids in the active site of Rho-kinase that likely determine inhibitor specificities observed for Rho-kinase relative to protein kinase A (PKA) (in PKA numbering: T183A, L49I, V123M, and E127D), and a fifth (Q181K) that played a surprising role in PKA-PKB hybrid proteins. We have systematically mutated these residues in PKA to their counterparts in Rho-kinase, individually and in combination. Using four Rho-kinase-specific, one PKA-specific, and one pan-kinase-specific inhibitor, we measured the inhibitor-binding properties of the mutated proteins and identify the roles of individual residues as specificity determinants. Two combined mutant proteins, containing the combination of mutations T183A and L49I, closely mimic Rho-kinase. Kinetic results corroborate the hypothesis that side-chain identities form the major determinants of selectivity. An unexpected result of the analysis is the consistent contribution of the individual mutations by simple factors. Crystal structures of the surrogate kinase inhibitor complexes provide a detailed basis for an understanding of these selectivity determinant residues. The ability to obtain kinetic and structural data from these PKA mutants, combined with their Rho-kinase-like selectivity profiles, make them valuable for use as surrogate kinases for structure-based inhibitor design.


==About this Structure==
==About this Structure==
2GNI is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with M77 as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/cAMP-dependent_protein_kinase cAMP-dependent protein kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.11.11 2.7.11.11] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2GNI OCA].  
2GNI is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with <scene name='pdbligand=M77:'>M77</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/cAMP-dependent_protein_kinase cAMP-dependent protein kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.11.11 2.7.11.11] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2GNI OCA].  


==Reference==
==Reference==
Line 16: Line 16:
[[Category: Bonn, S.]]
[[Category: Bonn, S.]]
[[Category: Bossemeyer, D.]]
[[Category: Bossemeyer, D.]]
[[Category: Breitenlechner, C.B.]]
[[Category: Breitenlechner, C B.]]
[[Category: Engh, R.A.]]
[[Category: Engh, R A.]]
[[Category: Gassel, M.]]
[[Category: Gassel, M.]]
[[Category: Herrero, S.]]
[[Category: Herrero, S.]]
Line 29: Line 29:
[[Category: surrogate]]
[[Category: surrogate]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 11:17:42 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:33:28 2008''

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA