EKS-RAN-00055
Eukaryotic Protein Kinase & Protein Phosphatase Database
TagContent
EKPD IDEKS-RAN-00055
Classification
Group/FamilyScoreE-ValueStartEndDomain Length
CMGC/CDK413.74.3E-1244287284
StatusReviewed
Ensembl ProteinENSRNOP00000000783
UniProt AccessionP39951; Q5BJB4;
Protein NameCyclin-dependent kinase 1
Protein Synonyms/Alias CDK1; Cell division control protein 2 homolog; Cell division protein kinase 1; p34 protein kinase;
Gene NameCdk1
Gene Synonyms/Alias Cdk1; Cdc2, Cdc2a, Cdkn1;
Ensembl Information
Ensembl Gene IDEnsembl Protein IDEnsembl Transcript ID
ENSRNOG00000000632ENSRNOP00000000783ENSRNOT00000000783
OrganismRattus norvegicus
Functional DescriptionPlays a key role in the control of the eukaryotic cellcycle by modulating the centrosome cycle as well as mitotic onset; promotes G2-M transition, and regulates G1 progress and G1-S transition via association with multiple interphase cyclins. Required in higher cells for entry into S-phase and mitosis. Phosphorylates PARVA/actopaxin, APC, AMPH, APC, BARD1, Bcl- xL/BCL2L1, BRCA2, CALD1, CASP8, CDC7, CDC20, CDC25A, CDC25C, CC2D1A, CSNK2 proteins/CKII, FZR1/CDH1, CDK7, CEBPB, CHAMP1, DMD/dystrophin, EEF1 proteins/EF-1, EZH2, KIF11/EG5, EGFR, FANCG, FOS, GFAP, GOLGA2/GM130, GRASP1, UBE2A/hHR6A, HIST1H1 proteins/histone H1, HMGA1, HIVEP3/KRC, LMNA, LMNB, LMNC, LBR, LATS1, MAP1B, MAP4, MARCKS, MCM2, MCM4, MKLP1, MYB, NEFH, NFIC, NPC/nuclear pore complex, PITPNM1/NIR2, NPM1, NCL, NUCKS1, NPM1/numatrin, ORC1, PRKAR2A, EEF1E1/p18, EIF3F/p47, p53/TP53, NONO/p54NRB, PAPOLA, PLEC/plectin, RB1, UL40/R2, RAB4A, RAP1GAP, RCC1, RPS6KB1/S6K1, KHDRBS1/SAM68, ESPL1, SKI, BIRC5/survivin, STIP1, TEX14, beta-tubulins, MAPT/TAU, NEDD1, VIM/vimentin, TK1, FOXO1, RUNX1/AML1 and RUNX2. CDK1/CDC2-cyclin-B controls pronuclear union in interphase fertilized eggs. Essential for early stages of embryonic development. During G2 and early mitosis, CDC25A/B/C-mediated dephosphorylation activates CDK1/cyclin complexes which phosphorylate several substrates that trigger at least centrosome separation, Golgi dynamics, nuclear envelope breakdown and chromosome condensation. Once chromosomes are condensed and aligned at the metaphase plate, CDK1 activity is switched off by WEE1- and PKMYT1-mediated phosphorylation to allow sister chromatid separation, chromosome decondensation, reformation of the nuclear envelope and cytokinesis. Inactivated by PKR/EIF2AK2- and WEE1-mediated phosphorylation upon DNA damage to stop cell cycle and genome replication at the G2 checkpoint thus facilitating DNA repair. Reactivated after successful DNA repair through WIP1-dependent signaling leading to CDC25A/B/C- mediated dephosphorylation and restoring cell cycle progression. In proliferating cells, CDK1-mediated FOXO1 phosphorylation at the G2-M phase represses FOXO1 interaction with 14-3-3 proteins and thereby promotes FOXO1 nuclear accumulation and transcription factor activity, leading to cell death of postmitotic neurons. The phosphorylation of beta-tubulins regulates microtubule dynamics during mitosis. NEDD1 phosphorylation promotes PLK1-mediated NEDD1 phosphorylation and subsequent targeting of the gamma-tubulin ring complex (gTuRC) to the centrosome, an important step for spindle formation. In addition, CC2D1A phosphorylation regulates CC2D1A spindle pole localization and association with SCC1/RAD21 and centriole cohesion during mitosis. The phosphorylation of Bcl- xL/BCL2L1 after prolongated G2 arrest upon DNA damage triggers apoptosis. In contrast, CASP8 phosphorylation during mitosis prevents its activation by proteolysis and subsequent apoptosis. This phosphorylation occurs in cancer cell lines, as well as in primary breast tissues and lymphocytes. EZH2 phosphorylation promotes H3K27me3 maintenance and epigenetic gene silencing (By similarity). CALD1 phosphorylation promotes Schwann cell migration during peripheral nerve regeneration.
Protein Length297
Protein Sequence
(FASTA)
MEDYIKIEKI GEGTYGVVYK GRHRTTGQIV AMKKIRLESE EEGVPSTAIR EISLLKELRH 60
PNIVSLQDVL MQDSRLYLIF EFLSMDLKKY LDSIPPGQFM DSSLVKSYLY QILQGIVFCH 120
SRRVLHRDLK PQNLLIDDKG TIKLADFGLA RAFGIPIRVY THEVVTLWYR SPEVLLGSAR 180
YSTPVDIWSI GTIFAELATK KPLFHGDSEI DQLFRIFRAL GTPNNEVWPE VESLQDYKNT 240
FPKWKPGSLA SHVKNLDENG LDLLSKMLVY DPAKRISGKM ALKHPYFDDL DNQIKKM 297
Nucleotide Sequence
(FASTA)
ATGGAGGACT ATATCAAAAT AGAGAAAATC GGAGAAGGGA CTTATGGTGT GGTATATAAA 60
GGTAGACACA GGACTACTGG CCAGATCGTG GCCATGAAGA AAATCAGACT TGAAAGCGAG 120
GAAGAAGGAG TGCCCAGTAC GGCAATCCGG GAAATCTCTC TGTTAAAAGA ACTTCGACAT 180
CCAAATATAG TCAGCCTGCA GGATGTACTC ATGCAGGACT CCAGGCTGTA TCTCATCTTC 240
GAGTTCCTGT CCATGGATCT CAAGAAGTAC CTGGACTCTA TCCCTCCTGG CCAGTTCATG 300
GATTCTTCGC TCGTTAAGAG TTACTTGTAC CAAATCCTCC AGGGGATTGT GTTTTGTCAC 360
TCCCGACGAG TTCTTCACAG AGACTTGAAA CCTCAAAATC TATTGATTGA TGACAAAGGA 420
ACAATCAAAC TGGCAGATTT CGGCCTTGCC AGAGCGTTTG GAATACCGAT AAGAGTGTAC 480
ACACACGAGG TAGTGACGCT GTGGTACCGG TCGCCAGAGG TGTTGCTGGG CTCGGCTCGC 540
TACTCCACCC CGGTTGACAT CTGGAGCATA GGGACCATAT TTGCAGAGCT GGCGACCAAG 600
AAGCCGCTTT TCCACGGCGA CTCAGAGATT GACCAGCTCT TCAGGATCTT CAGAGCTCTG 660
GGCACCCCTA ACAACGAAGT GTGGCCAGAA GTAGAGTCCC TGCAGGACTA CAAGAACACT 720
TTCCCCAAGT GGAAGCCGGG GAGCCTCGCG TCCCACGTCA AGAACCTGGA TGAAAACGGC 780
TTGGACTTGC TCTCGAAAAT GCTGGTCTAT GATCCAGCCA AACGAATCTC TGGAAAAATG 840
GCCCTTAAGC ACCCATACTT TGACGACTTG GACAATCAGA TCAAGAAGAT GTAA 894
Domain Profile
S: 1     yeklekigeGtygkvykakdketgevvAlKkirlekekegvpitalrEisllkelkhkni  60
         y k+ekigeGtyg+vyk+++++tg++vA+Kkirle+e+egvp+ta+rEisllkel+h+ni
Q: 4     YIKIEKIGEGTYGVVYKGRHRTTGQIVAMKKIRLESEEEGVPSTAIREISLLKELRHPNI  63
         789*********************************************************
S: 61    vkLlevvakdkkklyLvfefleqdLkkllkkkkkk.klsleevkslllqlleglaylHsn  119
         v+L++v++ ++++lyL+fefl++dLkk+l++ +    ++++ vks+l+q+l+g+ ++Hs+
Q: 64    VSLQDVLM-QDSRLYLIFEFLSMDLKKYLDSIPPGqFMDSSLVKSYLYQILQGIVFCHSR  122
         ********.99********************98764789999******************
S: 120   kilHRDlKpqNlLiskegklklaDfGlarafssplktytkevvTlwYraPelLlgakeYs  179
         ++lHRDlKpqNlLi+++g++klaDfGlaraf+ p + yt+evvTlwYr+Pe+Llg+ +Ys
Q: 123   RVLHRDLKPQNLLIDDKGTIKLADFGLARAFGIPIRVYTHEVVTLWYRSPEVLLGSARYS  182
         ************************************************************
S: 180   tavDiWsvgcilaelltrkplfqgkseidqlerifkllgtpsekvwpevsklpeykksfp  239
         t vDiWs+g i+ael+t+kplf+g+seidql+rif+ lgtp+++vwpev++l++yk++fp
Q: 183   TPVDIWSIGTIFAELATKKPLFHGDSEIDQLFRIFRALGTPNNEVWPEVESLQDYKNTFP  242
         ************************************************************
S: 240   kkkkkklkekvkklkekaldllekllaldpkkRisakealqhkyf  284
         k+k+ +l+++vk+l+e++ldll+k+l +dp+kRis k al+h+yf
Q: 243   KWKPGSLASHVKNLDENGLDLLSKMLVYDPAKRISGKMALKHPYF  287
         ********************************************9
Domain Sequence
(FASTA)
YIKIEKIGEG TYGVVYKGRH RTTGQIVAMK KIRLESEEEG VPSTAIREIS LLKELRHPNI 60
VSLQDVLMQD SRLYLIFEFL SMDLKKYLDS IPPGQFMDSS LVKSYLYQIL QGIVFCHSRR 120
VLHRDLKPQN LLIDDKGTIK LADFGLARAF GIPIRVYTHE VVTLWYRSPE VLLGSARYST 180
PVDIWSIGTI FAELATKKPL FHGDSEIDQL FRIFRALGTP NNEVWPEVES LQDYKNTFPK 240
WKPGSLASHV KNLDENGLDL LSKMLVYDPA KRISGKMALK HPYF 284
KeywordAcetylation; Apoptosis; ATP-binding; Cell cycle; Cell division; Complete proteome; Cytoplasm; Cytoskeleton; Isopeptide bond; Kinase; Mitochondrion; Mitosis; Nucleotide-binding; Nucleus; Phosphoprotein; Reference proteome; Serine/threonine-protein kinase; Transferase; Ubl conjugation.
Sequence SourceEnsembl
Orthology
Ortholog group
Ailuropoda melanoleuca"; ?>Anolis carolinensis"; ?>Bos taurus"; ?>Caenorhabditis elegans"; ?>Callithrix jacchus"; ?>Canis familiaris"; ?>Cavia porcellus"; ?>Choloepus hoffmanni"; ?>Ciona savignyi"; ?>Danio rerio"; ?>Dasypus novemcinctus"; ?>Drosophila melanogaster"; ?>Echinops telfairi"; ?>Equus caballus"; ?>Erinaceus europaeus"; ?>Felis catus"; ?>Gadus morhua"; ?>Gallus gallus"; ?>Gasterosteus aculeatus"; ?>Gorilla gorilla"; ?>Homo sapiens"; ?>Ictidomys tridecemlineatus"; ?>Latimeria chalumnae"; ?>Loxodonta africana"; ?>Macaca mulatta"; ?>Meleagris gallopavo"; ?>Microcebus murinus"; ?>Monodelphis domestica"; ?>Mus musculus"; ?>Mustela putorius furo"; ?>Myotis lucifugus"; ?>Nomascus leucogenys"; ?>Ochotona princeps"; ?>Oreochromis niloticus"; ?>Ornithorhynchus anatinus"; ?>Oryctolagus cuniculus"; ?>Oryzias latipes"; ?>Otolemur garnettii"; ?>Pan troglodytes"; ?>Pelodiscus sinensis"; ?>Petromyzon marinus"; ?>Pongo abelii"; ?>Sarcophilus harrisii"; ?>Sus scrofa"; ?>Taeniopygia guttata"; ?>Takifugu rubripes"; ?>Tarsius syrichta"; ?>Tetraodon nigroviridis"; ?>Tursiops truncatus"; ?>Xenopus tropicalis"; ?>Xiphophorus maculatus"; ?>
EKS-AIM-00056
EKS-ANC-00049
EKS-BOT-00058
EKS-CAE-00040
EKS-CAJ-00057
EKS-CAF-00059
EKS-CAP-00072
EKS-CHH-00023
EKS-CIS-00061
EKS-DAR-00071
EKS-DAN-00020
EKS-DRM-00022
EKS-ECT-00040
EKS-EQC-00057
EKS-ERE-00033
EKS-FEC-00055
EKS-GAM-00025
EKS-GAG-00046
EKS-GAA-00074
EKS-GOG-00056
EKS-HOS-00058
EKS-ICT-00054
EKS-LAC-00061
EKS-LOA-00057
EKS-MAM-00057
EKS-MEG-00045
EKS-MIM-00028
EKS-MOD-00056
EKS-MUM-00057
EKS-MUP-00059
EKS-MYL-00059
EKS-NOL-00053
EKS-OCP-00039
EKS-ORN-00076
EKS-ORA-00047
EKS-ORC-00055
EKS-ORL-00069
EKS-OTG-00060
EKS-PAT-00053
EKS-PES-00051
EKS-PEM-00034
EKS-POA-00054
EKS-SAH-00053
EKS-SUS-00051
EKS-TAG-00050
EKS-TAR-00077
EKS-TAS-00025
EKS-TEN-00080
EKS-TUT-00056
EKS-XET-00064
EKS-XIM-00074
Gene Ontology
GO:0005737; C:cytoplasm
GO:0005815; C:microtubule organizing center
GO:0030496; C:midbody
GO:0005739; C:mitochondrion
GO:0005634; C:nucleus
GO:0005876; C:spindle microtubule
GO:0005524; F:ATP binding
GO:0004693; F:cyclin-dependent protein kinase activity
GO:0035173; F:histone kinase activity
GO:0008353; F:RNA polymerase II carboxy-terminal domain kinase activity
GO:0006915; P:apoptotic process
GO:0007569; P:cell aging
GO:0051301; P:cell division
GO:0070301; P:cellular response to hydrogen peroxide
GO:0030261; P:chromosome condensation
GO:0000080; P:G1 phase of mitotic cell cycle
GO:0007067; P:mitosis
GO:0007095; P:mitotic cell cycle G2/M transition DNA damage checkpoint
GO:0031100; P:organ regeneration
GO:0060045; P:positive regulation of cardiac muscle cell proliferation
GO:0045740; P:positive regulation of DNA replication
GO:0010628; P:positive regulation of gene expression
GO:0045931; P:positive regulation of mitotic cell cycle
GO:0033160; P:positive regulation of protein import into nucleus, translocation
GO:0006461; P:protein complex assembly
GO:0034501; P:protein localization to kinetochore
GO:0014823; P:response to activity
GO:0014075; P:response to amine stimulus
GO:0048678; P:response to axon injury
GO:0046686; P:response to cadmium ion
GO:0046688; P:response to copper ion
GO:0042493; P:response to drug
GO:0045471; P:response to ethanol
GO:0014070; P:response to organic cyclic compound
GO:0009636; P:response to toxin
GO:0055015; P:ventricular cardiac muscle cell development
KEGG
rno:54237;
InterPros
IPR011009; Kinase-like_dom.
IPR000719; Prot_kinase_cat_dom.
IPR017441; Protein_kinase_ATP_BS.
IPR002290; Ser/Thr_dual-sp_kinase_dom.
IPR008271; Ser/Thr_kinase_AS.
Pfam
PF00069; Pkinase; 1.
SMARTs
SM00220; S_TKc; 1.
Prosites
PS00107; PROTEIN_KINASE_ATP; 1.
PS50011; PROTEIN_KINASE_DOM; 1.
PS00108; PROTEIN_KINASE_ST; 1.
Prints
Created Date20-Feb-2013