Cyclin-dependent kinase

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Cyclin-dependent kinase
EC no.
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MetaCycmetabolic pathway
PDB structuresRCSB PDB PDBe PDBsum
Tertiary structure of human Cdk2, determined by X-ray crystallography. Like other protein kinases, Cdk2 is composed of two lobes: a smaller amino-terminal lobe (top) that is composed primarily of beta sheet and the PSTAIRE helix, and a large carboxy-terminal lobe (bottom) that is primarily made up of alpha helices. The ATP substrate is shown as a ball-and-stick model, located deep within the active-site cleft between the two lobes. The phosphates are oriented outward, toward the mouth of the cleft, which is blocked in this structure by the T-loop (highlighted in green). (PDB 1hck)
Schematic of the cell cycle. outer ring: I = Interphase, M = Mitosis; inner ring: M = Mitosis; G1 = Gap phase 1; S = Synthesis; G2 = Gap phase 2.

Cyclin-dependent kinases (CDKs) are the families of protein kinases first discovered for their role in regulating the cell cycle. They are also involved in regulating transcription, mRNA processing, and the differentiation of nerve cells.[1] They are present in all known eukaryotes, and their regulatory function in the cell cycle has been evolutionarily conserved. In fact, yeast cells can proliferate normally when their CDK gene has been replaced with the homologous human gene.[1][2] CDKs are relatively small proteins, with molecular weights ranging from 34 to 40 kDa, and contain little more than the kinase domain.[1] By definition, a CDK binds a regulatory protein called a cyclin. Without cyclin, CDK has little kinase activity; only the cyclin-CDK complex is an active kinase but its activity can be typically further modulated by phosphorylation and other binding proteins, like p27. CDKs phosphorylate their substrates on serines and threonines, so they are serine-threonine kinases.[1] The consensus sequence for the phosphorylation site in the amino acid sequence of a CDK substrate is [S/T*]PX[K/R], where S/T* is the phosphorylated serine or threonine, P is proline, X is any amino acid, K is lysine, and R is arginine.[1]


Table 1: Known CDKs, their cyclin partners, and their functions in the human[3] and consequences of deletion in mice[4]
CDK Cyclin partner Function Deletion Phenotype in Mice
Cdk1 Cyclin B M phase None
Cdk2 Cyclin E G1/S transition Reduced size, imparted neural progenitor cell proliferation. Viable, but both males & females sterile.
Cdk2 Cyclin A S phase, G2 phase
Cdk3 Cyclin C G1 phase No defects. Viable, fertile.
Cdk4 Cyclin D G1 phase Reduced size, insulin deficient diabetes. Viable, but both male & female infertile.

CDKs and cyclins in the cell cycle[edit]

Most of the known cyclin-CDK complexes regulate the progression through the cell cycle. Animal cells contain at least nine CDKs, four of which, CDK1, 2, 3, and 4, are directly involved in cell cycle regulation.[1] In mammalian cells, CDK1, with its partners cyclin A2 and B1, alone can drive the cell cycle.[4] Another one, CDK7, is involved indirectly as the CDK-activating kinase.[1] Cyclin-CDK complexes phosphorylate substrates appropriate for the particular cell cycle phase.[3] Cyclin-CDK complexes of earlier cell-cycle phase help activate cyclin-CDK complexes in later phase.[1]

Table 2: Cyclins and CDKs by Cell-Cycle Phase
Phase Cyclin CDK
G0 C Cdk3
G1 D, E Cdk4, Cdk2, Cdk6
S A, E Cdk2
G2 A Cdk2, Cdk1
M B Cdk1
Table 3: Cyclin-dependent kinases that control the cell cycle in model organisms[1]
Species Name Original name Size (amino acids) Function
Saccharomyces cerevisiae Cdk1 Cdc28 298 All cell-cycle stages
Schizosaccharomyces pombe Cdk1 Cdc2 297 All cell-cycle stages
Drosophila melanogaster Cdk1 Cdc2 297 M
Cdk2 Cdc2c 314 G1/S, S, possibly M
Cdk4 Cdk4/6 317 G1, promotes growth
Xenopus laevis Cdk1 Cdc2 301 M
Cdk2 297 S, possibly M
Homo sapiens Cdk1 Cdc2 297 M
Cdk2 298 G1, S, possibly M
Cdk4 301 G1
Cdk6 326 G1

A list of CDKs with their regulator protein, cyclin or other:

Regulation of activity[edit]

CDK levels remain relatively constant throughout the cell cycle and most regulation is post-translational. Most knowledge of CDK structure and function is based on CDKs of S. pombe (Cdc2), S. cerevisiae (CDC28), and vertebrates (CDC2 and CDK2). The four major mechanisms of CDK regulation are cyclin binding, CAK phosphorylation, regulatory inhibitory phosphorylation, and binding of CDK inhibitory subunits (CKIs).[5]

Cyclin binding[edit]

The active site, or ATP-binding site, of all kinases is a cleft between a small amino-terminal lobe and a larger carboxy-terminal lobe.[1] The structure of human Cdk2 revealed that CDKs have a modified ATP-binding site that can be regulated by cyclin binding.[1] Phosphorylation by CDK-activating kinase (CAK) at Thr 161 on the T-loop increases the complex activity. Without cyclin, a flexible loop called the activation loop or T-loop blocks the cleft, and the position of several key amino acid residues is not optimal for ATP-binding.[1] With cyclin, two alpha helices change position to permit ATP binding. One of them, the L12 helix that comes just before the T-loop in the primary sequence, becomes a beta strand and helps rearrange the T-loop, so it no longer blocks the active site.[1] The other alpha helix called the PSTAIRE helix rearranges and helps change the position of the key amino acid residues in the active site.[1]

There is considerable specificity in which cyclin binds with CDK.[3] Furthermore, cyclin binding determines the specificity of the cyclin-CDK complex for particular substrates.[3] Cyclins can directly bind the substrate or localize the CDK to a subcellular area where the substrate is found. Substrate specificity of S cyclins is imparted by the hydrophobic batch (centered on the MRAIL sequence), which has affinity for substrate proteins that contain a hydrophobic RXL (or Cy) motif. Cyclin B1 and B2 can localize Cdk1 to the nucleus and the Golgi, respectively, through a localization sequence outside the CDK-binding region.[1]


Cyclin binding alone causes partial activation of Cdks, but complete activation also requires activating phosphorylation by a CAK. In animal cells, CAK phosphorylates the Cdk subunit only after cyclin binding, as shown here. Budding yeast contains a different version of CAK that can phosphorylate the Cdk even in the absence of cyclin, and so the two activation steps can occur in either order.

Full kinase activity requires an activating phosphorylation on a threonine adjacent to the CDK's active site.[1] The identity of the CDK-activating kinase (CAK) that performs this phosphorylation varies across the model organisms.[1] The timing of this phosphorylation varies as well. In mammalian cells, the activating phosphorylation occurs after cyclin binding.[1] In yeast cells, it occurs before cyclin binding.[1] CAK activity is not regulated by known cell-cycle pathways and cyclin binding is the limiting step for CDK activation.[1]

Unlike activating phosphorylation, CDK inhibitory phosphorylation is vital for regulation of the cell cycle. Various kinases and phosphatases regulate their phosphorylation state. One of the kinases that place the tyrosine phosphate is Wee1, a kinase conserved in all eukaryotes.[1] Fission yeast also contains a second kinase Mik1 that can phosphorylate the tyrosine.[1] Vertebrates contain a different second kinase called Myt1 that is related to Wee1 but can phosphorylate both the threonine and the tyrosine.[1] Phosphatases from the Cdc25 family dephosphorylate both the threonine and the tyrosine.[1]

CDK inhibitors[edit]

A cyclin-dependent kinase inhibitor (CKI) is a protein that interacts with a cyclin-CDK complex to block kinase activity, usually during G1 or in response to signals from the environment or from damaged DNA.[1] In animal cells, there are two major CKI families: the INK4 family and the CIP/KIP family.[1] The INK4 family proteins are strictly inhibitory and bind CDK monomers. Crystal structures of CDK6-INK4 complexes show that INK4 binding twists the CDK to distort cyclin binding and kinase activity. The CIP/KIP family proteins bind both the cyclin and the CDK of a complex and can be inhibitory or activating. CIP/KIP family proteins activate cyclin D and CDK4 or CDK6 complexes by enhancing complex formation.[1]

In yeast and Drosophila, CKIs are strong inhibitors of S- and M-CDK, but do not inhibit G1/S-CDKs. During G1, high levels of CKIs prevent cell cycle events from occurring out of order, but do not prevent transition through the Start checkpoint, which is initiated through G1/S-CDKs. Once the cell cycle is initiated, phosphorylation by early G1/S-CDKs leads to destruction of CKIs, relieving inhibition on later cell cycle transitions. In mammalian cells, the CKI regulation works differently. Mammalian protein p27 (Dacapo in Drosophila) inhibits G1/S- and S-CDKs, but does not inhibit S- and M-CDKs.[1]

Based on molecular docking results, Ligands-3, 5, 14, and 16 were screened among 17 different Pyrrolone-fused benzosuberene compounds as potent and specific inhibitors without any cross-reactivity against different CDK isoforms. Analysis of MD simulations and MM-PBSA studies, revealed the binding energy profiles of all the selected complexes. Selected ligands performed better than the experimental drug candidate (Roscovitine). Ligands-3 and 14 show specificity for CDK7 and Ligands-5 and 16 were specific against CDK9. These ligands are expected to possess lower risk of side effects due to their natural origin. [6]

Interpretation of dynamic simulations and binding free energy studies unveiled that Ligand2 (Out of 17 in-house synthesized pyrrolone-fused benzosuberene (PBS) compounds) has a stable and equivalent free energy to Flavopiridol, SU9516, and CVT-313 inhibitors. Ligand2 scrutinized as a selective inhibitor of CDK2 without off-target binding (CDK1 and CDK9) based on ligand efficiency and binding affinity. [7]

Graphical abstract of CDK2 [7]

Suk1 or Cks[edit]

The CDKs directly involved in the regulation of the cell cycle associate with small, 9- to 13-kiloDalton proteins called Suk1 or Cks.[3] These proteins are required for CDK function, but their precise role is unknown.[3] Cks1 binds the carboxy lobe of the CDK, and recognizes phosphorylated residues. It may help the cyclin-CDK complex with substrates that have multiple phosphorylation sites by increasing affinity for the substrate.[3]

Non-cyclin activators[edit]

Viral cyclins[edit]

Viruses can encode proteins with sequence homology to cyclins. One much-studied example is K-cyclin (or v-cyclin) from Kaposi sarcoma herpes virus (see Kaposi’s sarcoma), which activates CDK6. Viral cyclin-CDK complexes have different substrate specificities and regulation sensitivities.[8]

CDK5 activators[edit]

The proteins p35 and p39 activate CDK5. Although they lack cyclin sequence homology, crystal structures show that p35 folds in a similar way as the cyclins. However, activation of CDK5 does not require activation loop phosphorylation.[8]


Proteins with no homology to the cyclin family can be direct activators of CDKs.[9] One family of such activators is the RINGO/Speedy family,[9] which was originally discovered in Xenopus. All five members discovered so far directly activate Cdk1 and Cdk2, but the RINGO/Speedy-CDK2 complex recognizes different substrates than cyclin A-CDK2 complex.[8]


Leland H. Hartwell, R. Timothy Hunt, and Paul M. Nurse received the 2001 Nobel Prize in Physiology or Medicine for their complete description of cyclin and cyclin-dependent kinase mechanisms, which are central to the regulation of the cell cycle.

Medical significance[edit]

Diseases of CDK[edit]

As drug targets[edit]

CDKs are considered a potential target for anti-cancer medication. If it is possible to selectively interrupt the cell cycle regulation in cancer cells by interfering with CDK action, the cell will die. At present, some CDK inhibitors such as seliciclib are undergoing clinical trials. Although it was originally developed as a potential anti-cancer drug, seliciclib has also proven to induce apoptosis in neutrophil granulocytes, which mediate inflammation.[10] This means that novel drugs for treatment of chronic inflammation diseases such as arthritis and cystic fibrosis could be developed.

Flavopiridol (alvocidib) is the first CDK inhibitor to be tested in clinical trials after being identified in an anti-cancer agent screen in 1992. It competes for the ATP site of the CDKs.[11] Palbociclib and abemaciclib have been approved for the management of hormone receptor (estrogen receptor/progestogen receptor) expressing metastatic breast cancer in combination with endocrine therapy.[12][13]

More research is required, however, because disruption of the CDK-mediated pathway has potentially serious consequences; while CDK inhibitors seem promising, it has to be determined how side-effects can be limited so that only target cells are affected. As such diseases are currently treated with glucocorticoids, which have often serious side-effects, even a minor success would be an improvement.[12]

Complications of developing a CDK drug include the fact that many CDKs are not involved in the cell cycle, but other processes such as transcription, neural physiology, and glucose homeostasis.[14]

Cyclin-dependent kinase inhibitor drugs[14]: Table 4 
Drug CDKs Inhibited
Flavopiridol (alvocidib) 1, 2, 4, 6, 7, 9
Olomoucine 1, 2, 5
Roscovitine (Seliciclib) 1, 2, 5, 7, 9[15][16][6]
Purvalanol 1, 2, 5
Paullones 1, 2, 5
Butryolactone 1, 2, 5
Palbociclib 4, 6
Thio/oxoflavopiridols 1
Oxindoles 2
Fadraciclib 2, 9[17]
Aminothiazoles 4
Benzocarbazoles 4
Pyrimidines 4


  1. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab Morgan DO (2007). The Cell Cycle: Principles of Control (1st ed.). London: New Science Press. ISBN 978-0-87893-508-6.
  2. ^ Lee MG, Nurse P (1987). "Complementation used to clone a human homologue of the fission yeast cell cycle control gene cdc2". Nature. 327 (6117): 31–5. Bibcode:1987Natur.327...31L. doi:10.1038/327031a0. PMID 3553962. S2CID 4300190.
  3. ^ a b c d e f g Morgan DO (1997). "Cyclin-dependent kinases: engines, clocks, and microprocessors". Annual Review of Cell and Developmental Biology. 13: 261–91. doi:10.1146/annurev.cellbio.13.1.261. PMID 9442875.
  4. ^ a b Satyanarayana A, Kaldis P (August 2009). "Mammalian cell-cycle regulation: several Cdks, numerous cyclins and diverse compensatory mechanisms". Oncogene. 28 (33): 2925–39. doi:10.1038/onc.2009.170. PMID 19561645.
  5. ^ Morgan DO (March 1995). "Principles of CDK regulation". Nature. 374 (6518): 131–4. Bibcode:1995Natur.374..131M. doi:10.1038/374131a0. PMID 7877684. S2CID 4323623.
  6. ^ a b Singh R, Bhardwaj VK, Das P, Purohit R (November 2019). "Natural analogues inhibiting selective cyclin-dependent kinase protein isoforms: a computational perspective". Journal of Biomolecular Structure and Dynamics. 38 (17): 5126–5135. doi:10.1080/07391102.2019.1696709. PMID 3176087. S2CID 208276454.
  7. ^ a b Singh R, Bhardwaj VK, Sharma J, Das P, Purohit R (March 2021). "Identification of selective cyclin-dependent kinase 2 inhibitor from the library of pyrrolone-fused benzosuberene compounds: an in silico exploration". Journal of Biomolecular Structure and Dynamics. 40 (17): 7693–7701. doi:10.1080/07391102.2021.1900918. PMID 33749525. S2CID 232309609.
  8. ^ a b c Nebreda AR (April 2006). "CDK activation by non-cyclin proteins". Current Opinion in Cell Biology. 18 (2): 192–8. doi:10.1016/ PMID 16488127.
  9. ^ a b Mourón S, de Cárcer G, Seco E, Fernández-Miranda G, Malumbres M, Nebreda AR (August 2010). "RINGO C is required to sustain the spindle-assembly checkpoint". Journal of Cell Science. 123 (Pt 15): 2586–95. doi:10.1242/jcs.059964. PMID 20605920.
  10. ^ Rossi AG, Sawatzky DA, Walker A, Ward C, Sheldrake TA, Riley NA, et al. (September 2006). "Cyclin-dependent kinase inhibitors enhance the resolution of inflammation by promoting inflammatory cell apoptosis". Nature Medicine. 12 (9): 1056–64. doi:10.1038/nm1468. PMID 16951685. S2CID 5875865.
  11. ^ Senderowicz AM (1999). "Flavopiridol: the first cyclin-dependent kinase inhibitor in human clinical trials". Investigational New Drugs. 17 (3): 313–20. doi:10.1023/a:1006353008903. PMID 10665481. S2CID 23551260.
  12. ^ a b "FDA Grants Palbociclib Accelerated Approval for Advanced Breast Cancer". National Cancer Institute. 11 February 2015. Retrieved 2017-11-30.
  13. ^ "Approved Drugs - FDA approves abemaciclib for HR-positive, HER2-negative breast cancer". Center for Drug Evaluation and Research. U.S Food and Drug Administration. Retrieved 2017-11-30.
  14. ^ a b Sausville EA (2002). "Complexities in the development of cyclin-dependent kinase inhibitor drugs". Trends in Molecular Medicine. 8 (4 Suppl): S32-7. doi:10.1016/s1471-4914(02)02308-0. PMID 11927285.
  15. ^ Kolodziej M, Goetz C, Di Fazio P, Montalbano R, Ocker M, Strik H, Quint K. Roscovitine has anti-proliferative and pro-apoptotic effects on glioblastoma cell lines: A pilot study. Oncology reports. 2015 Sep 1;34(3):1549-56.
  16. ^ Otyepka M, Bártová I, Kříž Z, Koča J. Different mechanisms of CDK5 and CDK2 activation as revealed by CDK5/p25 and CDK2/cyclin A dynamics. Journal of Biological Chemistry. 2006 Mar 17;281(11):7271-81.
  17. ^ Oral fadraciclib starts clinical trials. Sep 2021

Further reading[edit]

  • Loyer P, Trembley JH, Katona R, Kidd VJ, Lahti JM (September 2005). "Role of CDK/cyclin complexes in transcription and RNA splicing". Cellular Signalling. 17 (9): 1033–51. doi:10.1016/j.cellsig.2005.02.005. PMID 15935619.

External links[edit]