Please use this identifier to cite or link to this item:
|Title:||Influences of phosphorylation on Thr14/Tyr15 in CDK5 in the presence of roscovitine/ATP and HHASPRK|
|Citation:||Jin, H.-X., Zhang, B., Jun, Y.-X., Xu, J.-L., Tan, V.B.C. (2012-03-01). Influences of phosphorylation on Thr14/Tyr15 in CDK5 in the presence of roscovitine/ATP and HHASPRK. Molecular Simulation 38 (3) : 248-257. ScholarBank@NUS Repository. https://doi.org/10.1080/08927022.2011.616503|
|Abstract:||Binding details of roscovitine, ATP and HHASPRK peptide in complex with both unphosphorylated and phosphorylated cyclin-dependent kinase 5 (CDK5) from molecular dynamics simulations using a crystal structure of CDK2/cyclinA/ATP/ HHASPRK and three CDK5/p25/roscovitine systems as references are presented. The influence of phosphorylation on well-conserved amino acids (Thr14 and Tyr15) on the conformation of the inhibition loop (G-loop) is investigated. The simulations suggest that the long ATP phosphate group affects the conformation of the loop differently in different complexes. Binding patterns of ATP in CDK5 are then studied and compared with those in CDK2. The residues on the G-loop affect the conformation of the ATP phosphate group and thus influence the hydrogen bonding network around the ligand. In addition, bindings of the peptide in CDK5 are investigated and compared with that in the crystal structure. Also, the possible conformation of the terminal lysine side chain of the peptide is analysed and suggested. © 2012 Copyright Taylor and Francis Group, LLC.|
|Source Title:||Molecular Simulation|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Aug 3, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.