TY - JOUR
T1 - Substrate specificity of protein kinases and computational prediction of substrates
AU - Kobe, B
AU - Kampmann, T.
AU - Forwood, Jade
AU - Listwan, P.
AU - Brinkworth, R.I.
N1 - Imported on 12 Apr 2017 - DigiTool details were: Journal title (773t) = Biochimica et Biophysica Acta: international journal of biochemistry and biophysics. ISSNs: 0006-3002;
PY - 2005
Y1 - 2005
N2 - To ensure signalling fidelity, kinases must act only on a defined subset of cellular targets. Appreciating the basis for this substrate specificity is essential for understanding the role of an individual protein kinase in a particular cellular process. The specificity in the cell is determined by a combination of "peptide specificity" of the kinase (the molecular recognition of the sequence surrounding the phosphorylation site), substrate recruitment and phosphatase activity. Peptide specificity plays a crucial role and depends on the complementarity between the kinase and the substrate and therefore on their three-dimensional structures. Methods for experimental identification of kinase substrates and characterization of specificity are expensive and laborious, therefore, computational approaches are being developed to reduce the amount of experimental work required in substrate identification. We discuss the structural basis of substrate specificity of protein kinases and review the experimental and computational methods used to obtain specificity information.
AB - To ensure signalling fidelity, kinases must act only on a defined subset of cellular targets. Appreciating the basis for this substrate specificity is essential for understanding the role of an individual protein kinase in a particular cellular process. The specificity in the cell is determined by a combination of "peptide specificity" of the kinase (the molecular recognition of the sequence surrounding the phosphorylation site), substrate recruitment and phosphatase activity. Peptide specificity plays a crucial role and depends on the complementarity between the kinase and the substrate and therefore on their three-dimensional structures. Methods for experimental identification of kinase substrates and characterization of specificity are expensive and laborious, therefore, computational approaches are being developed to reduce the amount of experimental work required in substrate identification. We discuss the structural basis of substrate specificity of protein kinases and review the experimental and computational methods used to obtain specificity information.
U2 - 10.1016/j.bbapap.2005.07.036
DO - 10.1016/j.bbapap.2005.07.036
M3 - Article
C2 - 16172032
SN - 0006-3002
VL - 1754
SP - 200
EP - 209
JO - Biochimica et Biophysica Acta: international journal of biochemistry and biophysics
JF - Biochimica et Biophysica Acta: international journal of biochemistry and biophysics
IS - 1-2
ER -