CDK2
Serine/threonine-protein kinase involved in the control of the cell cycle; essential for meiosis, but dispensable for mitosis. Phosphorylates CTNNB1, USP37, p53/TP53, NPM1, CDK7, RB1, BRCA2, MYC, NPAT, EZH2. Triggers duplication of centrosomes and DNA. Acts at the G1-S transition to promote the E2F ...
Serine/threonine-protein kinase involved in the control of the cell cycle; essential for meiosis, but dispensable for mitosis. Phosphorylates CTNNB1, USP37, p53/TP53, NPM1, CDK7, RB1, BRCA2, MYC, NPAT, EZH2. Triggers duplication of centrosomes and DNA. Acts at the G1-S transition to promote the E2F transcriptional program and the initiation of DNA synthesis, and modulates G2 progression; controls the timing of entry into mitosis/meiosis by controlling the subsequent activation of cyclin B/CDK1 by phosphorylation, and coordinates the activation of cyclin B/CDK1 at the centrosome and in the nucleus. Crucial role in orchestrating a fine balance between cellular proliferation, cell death, and DNA repair in human embryonic stem cells (hESCs). Activity of CDK2 is maximal during S phase and G2; activated by interaction with cyclin E during the early stages of DNA synthesis to permit G1-S transition, and subsequently activated by cyclin A2 (cyclin A1 in germ cells) during the late stages of DNA replication to drive the transition from S phase to mitosis, the G2 phase. EZH2 phosphorylation promotes H3K27me3 maintenance and epigenetic gene silencing. Phosphorylates CABLES1 (By similarity). Cyclin E/CDK2 prevents oxidative stress-mediated Ras-induced senescence by phosphorylating MYC. Involved in G1-S phase DNA damage checkpoint that prevents cells with damaged DNA from initiating mitosis; regulates homologous recombination-dependent repair by phosphorylating BRCA2, this phosphorylation is low in S phase when recombination is active, but increases as cells progress towards mitosis. In response to DNA damage, double-strand break repair by homologous recombination a reduction of CDK2-mediated BRCA2 phosphorylation. Phosphorylation of RB1 disturbs its interaction with E2F1. NPM1 phosphorylation by cyclin E/CDK2 promotes its dissociates from unduplicated centrosomes, thus initiating centrosome duplication. Cyclin E/CDK2-mediated phosphorylation of NPAT at G1-S transition and until prophase stimulates the NPAT-mediated activation of histone gene transcription during S phase. Required for vitamin D-mediated growth inhibition by being itself inactivated. Involved in the nitric oxide- (NO) mediated signaling in a nitrosylation/activation-dependent manner. USP37 is activated by phosphorylation and thus triggers G1-S transition. CTNNB1 phosphorylation regulates insulin internalization. Phosphorylates FOXP3 and negatively regulates its transcriptional activity and protein stability (By similarity). Phosphorylates CDK2AP2 (PubMed:12944431). Phosphorylates ERCC6 which is essential for its chromatin remodeling activity at DNA double-strand breaks (PubMed:29203878).
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GO - Biological processes (BP):
anaphase-promoting complex-dependent catabolic process, cell division, cellular response to nitric oxide, centriole replication, centrosome duplication, DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest, DNA repair, DNA replication, G1/S transition of mito...
anaphase-promoting complex-dependent catabolic process, cell division, cellular response to nitric oxide, centriole replication, centrosome duplication, DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest, DNA repair, DNA replication, G1/S transition of mitotic cell cycle, G2/M transition of mitotic cell cycle, histone phosphorylation, meiotic cell cycle, mitotic G1 DNA damage checkpoint, multicellular organism development, negative regulation of transcription by RNA polymerase II, peptidyl-serine phosphorylation, positive regulation of cell population proliferation, positive regulation of DNA-dependent DNA replication initiation, positive regulation of transcription, DNA-templated, potassium ion transport, protein phosphorylation, Ras protein signal transduction, regulation of G2/M transition of mitotic cell cycle, regulation of gene expression, regulation of gene silencing, regulation of signal transduction by p53 class mediator
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GO - Molecular function (MF):
ATP binding, cyclin binding, cyclin-dependent protein kinase activity, cyclin-dependent protein serine/threonine kinase activity, magnesium ion binding, protein domain specific binding, protein serine/threonine kinase activity...
ATP binding, cyclin binding, cyclin-dependent protein kinase activity, cyclin-dependent protein serine/threonine kinase activity, magnesium ion binding, protein domain specific binding, protein serine/threonine kinase activity
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GO - Cellular component (CC):
centrosome, cytosol, endosome, Cajal body, nucleoplasm, nucleus, chromosome, telomeric region, condensed chromosome, cyclin A1-CDK2 complex, cyclin A2-CDK2 complex, cyclin E1-CDK2 complex, cyclin E2-CDK2 complex, cyclin-dependent protein kinase holoenzyme complex, cytoplasm, transcription factor com...
centrosome, cytosol, endosome, Cajal body, nucleoplasm, nucleus, chromosome, telomeric region, condensed chromosome, cyclin A1-CDK2 complex, cyclin A2-CDK2 complex, cyclin E1-CDK2 complex, cyclin E2-CDK2 complex, cyclin-dependent protein kinase holoenzyme complex, cytoplasm, transcription factor complex, X chromosome, Y chromosome
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