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Computational study of non-catalytic T-loop pocket on CDK proteins for drug development 被引量:1

Computational study of non-catalytic T-loop pocket on CDK proteins for drug development
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摘要 Cyclin-dependent kinases (CDKs) are critical to the cell cycle and many other biological processes, and as such, are considered as one of the promising targets for therapy against cancer and other diseases. Most pan-CDK inhibitors bind to the highly conserved catalytic ATP-binding pocket and therefore lack the specificity to prevent side effects. It is desirable to develop drugs targeting non-catalytic pockets for specificity towards individual CDKs. Here we performed a systematic analysis of non-catalytic pockets on CDKs and identified a region underneath the T-loop, which we term TL pocket, for potential inhibitor development. Specifically, we compared the TL pockets of human CDK2 and CDK7-homolog Pfmrk of Plasmodium falciparum, a malaria-causing parasite. Molecular dynamics simulations of several short peptides revealed that this less conserved TL pocket could be used to design potentially specific inhibitors against malaria disease. Cyclin-dependent kinases (CDKs) are critical to the cell cycle and many other biological processes, and as such, are considered as one of the promising targets for therapy against cancer and other diseases. Most pan-CDK inhibitors bind to the highly conserved catalytic ATP-binding pocket and therefore lack the specificity to prevent side effects. It is desirable to develop drugs targeting non-catalytic pockets for specificity towards individual CDKs. Here we performed a systematic analysis of non-catalytic pockets on CDKs and identified a region underneath the T-loop, which we term TL pocket, for potential inhibitor development. Specifically, we compared the TL pockets of human CDK2 and CDK7-homolog Pfmrk of Plasmodium falciparum, a malaria-causing parasite. Molecular dynamics simulations of several short peptides revealed that this less conserved TL pocket could be used to design potentially specific inhibitors against malaria disease.
出处 《Chinese Physics B》 SCIE EI CAS CSCD 2017年第12期32-40,共9页 中国物理B(英文版)
基金 Project supported by the National Natural Science Foundation of China(Grant No.11704140) the Natural Science Foundation of Hubei Province,China(Grant No.2017CFB116) the Thousand Talents Plan(Grant No.31103201603) the Self-determined Research Funds of CCNU from the Colleges’Basic Research and Operation of MOE 20205170045 to YZ
关键词 cyclin-dependent kinases NON-CATALYTIC TL pocket inhibitor design cyclin-dependent kinases non-catalytic TL pocket inhibitor design
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