Please use this identifier to cite or link to this item:
https://doi.org/10.1007/s00894-006-0127-x
DC Field | Value | |
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dc.title | Study of the inhibition of cyclin-dependent kinases with roscovitine and indirubin-3′-oxime from molecular dynamics simulations | |
dc.contributor.author | Zhang, B. | |
dc.contributor.author | Tan, V.B.C. | |
dc.contributor.author | Lim, K.M. | |
dc.contributor.author | Tay, T.E. | |
dc.contributor.author | Zhuang, S. | |
dc.date.accessioned | 2014-06-17T06:34:41Z | |
dc.date.available | 2014-06-17T06:34:41Z | |
dc.date.issued | 2007-01 | |
dc.identifier.citation | Zhang, B., Tan, V.B.C., Lim, K.M., Tay, T.E., Zhuang, S. (2007-01). Study of the inhibition of cyclin-dependent kinases with roscovitine and indirubin-3′-oxime from molecular dynamics simulations. Journal of Molecular Modeling 13 (1) : 79-89. ScholarBank@NUS Repository. https://doi.org/10.1007/s00894-006-0127-x | |
dc.identifier.issn | 16102940 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/61403 | |
dc.description.abstract | Molecular dynamics simulations were performed to elucidate the interactions of CDK2 and CDK5 complexes with three inhibitors: R-roscovitine, S-roscovitine, and indirubin-3′-oxime. The preference of the two complexes for R-roscovitine over the S enantiomer, as reported by the experiment, was also found by the simulations. More importantly, the simulations showed that the cause of the stronger affinity for the R enantiomer is the presence of an important hydrogen bond between R-roscovitine and the kinases not found with S-roscovitine. The simulations also showed two amino acid mutations in the active site of CDK5/R-roscovitine that favor binding-enhanced electrostatic contributions, making the inhibitor more effective for CDK5 than for CDK2. This suggests that the effectiveness of roscovitine-like inhibitors can be improved by enhancing their electrostatic interaction with the kinases. Finally, molecular mechanics-Possion-Boltzmann/surface area calculations of the CDK5/indirubin-3′-oxime system in both water-excluded and water-included environments gave significantly different electrostatic contributions to the binding. The simulations detected the displacement of a water molecule in the active site of the water-included CDK/indirubin-3′-oxime system. This resulted in a more conserved binding pattern than the water-excluded structure. Hence, in the design of new indirubin-like inhibitors, it is important to include the water molecule in the analysis. © Springer-Verlag 2006. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1007/s00894-006-0127-x | |
dc.source | Scopus | |
dc.subject | Binding energy | |
dc.subject | Binding pattern | |
dc.subject | Cycline-dependent kinase | |
dc.subject | Hydrogen bond | |
dc.subject | Molecular dynamics simulation | |
dc.type | Article | |
dc.contributor.department | MECHANICAL ENGINEERING | |
dc.description.doi | 10.1007/s00894-006-0127-x | |
dc.description.sourcetitle | Journal of Molecular Modeling | |
dc.description.volume | 13 | |
dc.description.issue | 1 | |
dc.description.page | 79-89 | |
dc.description.coden | JMMOF | |
dc.identifier.isiut | 000242326700009 | |
Appears in Collections: | Staff Publications |
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