EKS-MUM-00494
Eukaryotic Protein Kinase & Protein Phosphatase Database
TagContent
EKPD IDEKS-MUM-00494
Classification
Group/FamilyScoreE-ValueStartEndDomain Length
CMGC/MAPK430.85.6E-12923311289
StatusReviewed
Ensembl ProteinENSMUSP00000023462
UniProt AccessionP63085; P27703; Q3V1U6;
Protein NameMitogen-activated protein kinase 1
Protein Synonyms/Alias MAP kinase 1; MAPK 1; ERT1; Extracellular signal-regulated kinase 2; ERK-2; MAP kinase isoform p42; p42-MAPK; Mitogen-activated protein kinase 2; MAP kinase 2; MAPK 2;
Gene NameMapk1
Gene Synonyms/Alias Mapk1; Erk2, Mapk, Prkm1;
Ensembl Information
Ensembl Gene IDEnsembl Protein IDEnsembl Transcript ID
ENSMUSG00000063358ENSMUSP00000115125ENSMUST00000129477
ENSMUSG00000063358ENSMUSP00000111396ENSMUST00000115731
ENSMUSG00000063358ENSMUSP00000065983ENSMUST00000069107
ENSMUSG00000063358ENSMUSP00000023462ENSMUST00000023462
OrganismMus musculus
Functional DescriptionSerine/threonine kinase which acts as an essentialcomponent of the MAP kinase signal transduction pathway. MAPK1/ERK2 and MAPK3/ERK1 are the 2 MAPKs which play an important role in the MAPK/ERK cascade. They participate also in a signaling cascade initiated by activated KIT and KITLG/SCF. Depending on the cellular context, the MAPK/ERK cascade mediates diverse biological functions such as cell growth, adhesion, survival and differentiation through the regulation of transcription, translation, cytoskeletal rearrangements. The the MAPK/ERK cascade plays also a role in initiation and regulation of meiosis, mitosis, and postmitotic functions in differentiated cells by phosphorylating a number of transcription factors. About 160 substrates have already been discovered for ERKs. Many of these substrates are localized in the nucleus, and seem to participate in the regulation of transcription upon stimulation. However, other substrates are found in the cytosol as well as in other cellular organelles, and those are responsible for processes such as translation, mitosis and apoptosis. Moreover, the MAPK/ERK cascade is also involved in the regulation of the endosomal dynamics, including lysosome processing and endosome cycling through the perinuclear recycling compartment (PNRC); as well as in the fragmentation of the Golgi apparatus during mitosis. The substrates include transcription factors (such as ATF2, BCL6, ELK1, ERF, FOS, HSF4 or SPZ1), cytoskeletal elements (such as CANX, CTTN, GJA1, MAP2, MAPT, PXN, SORBS3 or STMN1), regulators of apoptosis (such as BAD, BTG2, CASP9, DAPK1, IER3, MCL1 or PPARG), regulators of translation (such as EIF4EBP1) and a variety of other signaling-related molecules (like ARHGEF2, DCC, FRS2 or GRB10). Protein kinases (such as RAF1, RPS6KA1/RSK1, RPS6KA3/RSK2, RPS6KA2/RSK3, RPS6KA6/RSK4, SYK, MKNK1/MNK1, MKNK2/MNK2, RPS6KA5/MSK1, RPS6KA4/MSK2, MAPKAPK3 or MAPKAPK5) and phosphatases (such as DUSP1, DUSP4, DUSP6 or DUSP16) are other substrates which enable the propagation the MAPK/ERK signal to additional cytosolic and nuclear targets, thereby extending the specificity of the cascade. Acts as a transcriptional repressor. Binds to a[GC]AAA[GC] consensus sequence. Repress the expression of interferon gamma-induced genes. Seems to bind to the promoter of CCL5, DMP1, IFIH1, IFITM1, IRF7, IRF9, LAMP3, OAS1, OAS2, OAS3 and STAT1. Transcriptional activity is independent of kinase activity (By similarity).
Protein Length358
Protein Sequence
(FASTA)
MAAAAAAGPE MVRGQVFDVG PRYTNLSYIG EGAYGMVCSA YDNLNKVRVA IKKISPFEHQ 60
TYCQRTLREI KILLRFRHEN IIGINDIIRA PTIEQMKDVY IVQDLMETDL YKLLKTQHLS 120
NDHICYFLYQ ILRGLKYIHS ANVLHRDLKP SNLLLNTTCD LKICDFGLAR VADPDHDHTG 180
FLTEYVATRW YRAPEIMLNS KGYTKSIDIW SVGCILAEML SNRPIFPGKH YLDQLNHILG 240
ILGSPSQEDL NCIINLKARN YLLSLPHKNK VPWNRLFPNA DSKALDLLDK MLTFNPHKRI 300
EVEQALAHPY LEQYYDPSDE PIAEAPFKFD MELDDLPKEK LKELIFEETA RFQPGYRS 358
Nucleotide Sequence
(FASTA)
ATGGCGGCGG CGGCGGCGGC GGGCCCGGAG ATGGTCCGCG GGCAGGTGTT CGACGTAGGG 60
CCGCGCTACA CCAACCTCTC GTACATCGGA GAAGGCGCCT ACGGCATGGT TTGCTCTGCT 120
TATGATAATC TCAACAAAGT TCGAGTTGCT ATCAAGAAAA TCAGTCCTTT TGAGCACCAG 180
ACCTACTGTC AAAGAACCCT AAGAGAGATA AAAATCTTAC TGCGCTTCAG ACATGAGAAC 240
ATCATTGGCA TCAATGACAT CATCCGGGCA CCAACCATTG AGCAAATGAA AGATGTATAT 300
ATAGTACAGG ACCTCATGGA GACGGACCTT TACAAGCTCT TGAAGACACA GCACCTCAGC 360
AATGACCACA TCTGCTATTT TCTTTATCAG ATCCTGAGAG GGCTAAAGTA TATCCATTCA 420
GCTAACGTTC TGCACCGTGA CCTCAAGCCT TCCAACCTCC TGCTGAACAC CACTTGTGAT 480
CTCAAGATCT GTGACTTTGG CCTTGCCCGT GTTGCAGATC CAGATCATGA TCACACAGGG 540
TTCTTGACAG AGTACGTAGC CACACGTTGG TACAGAGCTC CAGAAATTAT GTTGAATTCC 600
AAGGGTTATA CCAAGTCCAT TGATATTTGG TCTGTGGGCT GCATCCTGGC AGAGATGCTA 660
TCCAACAGGC CTATCTTCCC AGGAAAGCAT TACCTTGACC AGCTGAATCA CATCCTGGGT 720
ATTCTTGGAT CTCCATCACA GGAAGATCTG AATTGTATAA TAAATTTAAA AGCTAGAAAC 780
TATTTGCTTT CTCTCCCGCA CAAAAATAAG GTGCCATGGA ACAGGTTGTT CCCAAATGCT 840
GACTCCAAAG CTCTGGATTT ACTGGATAAA ATGTTGACAT TTAACCCTCA CAAGAGGATT 900
GAAGTTGAAC AGGCTCTGGC CCACCCATAC CTGGAGCAGT ATTATGACCC AAGTGATGAG 960
CCCATTGCTG AAGCGCCATT CAAGTTTGAC ATGGAGTTGG ACGACTTACC TAAGGAGAAG 1020
CTCAAAGAAC TCATTTTTGA AGAGACTGCT AGATTCCAGC CAGGATACAG ATCTTAA 1077
Domain Profile
S: 1     yeslkplgeGaygvvvsavdkrteervaikklsrpfqketsakrtlRElkllkelkheNi  60
         y++l+++geGayg+v+sa+d+ ++ rvaikk+s pf+++t ++rtlRE+k+l +++heNi
Q: 23    YTNLSYIGEGAYGMVCSAYDNLNKVRVAIKKIS-PFEHQTYCQRTLREIKILLRFRHENI  81
         78999***************************9.**************************
S: 61    iklldvftpeeeleelkdvYlvtelmetdLkkviksqklsdehiklllyqilrglkylHs  120
         i + d++++ + +e++kdvY+v++lmetdL+k++k+q+ls++hi ++lyqilrglky+Hs
Q: 82    IGINDIIRAPT-IEQMKDVYIVQDLMETDLYKLLKTQHLSNDHICYFLYQILRGLKYIHS  140
         ********999.************************************************
S: 121   anviHrDlKPsNllvnedcelkildFGlarsadkekekk..lteyvatrwYraPeillsl  178
         anv+HrDlKPsNll+n++c+lki+dFGlar+ad++++++  lteyvatrwYraPei+l++
Q: 141   ANVLHRDLKPSNLLLNTTCDLKICDFGLARVADPDHDHTgfLTEYVATRWYRAPEIMLNS  200
         ***********************************999999*******************
S: 179   keytkavDiWsvGCIlaElltgkplfpgkdeidqlekilevlgtpseeflkkieseearn  238
         k ytk++DiWsvGCIlaE+l+++p+fpgk+++dql++il +lg+ps+e+l++i + +arn
Q: 201   KGYTKSIDIWSVGCILAEMLSNRPIFPGKHYLDQLNHILGILGSPSQEDLNCIINLKARN  260
         ************************************************************
S: 239   yikslpkkkkkdfeelfpkaseealdLleklLvldpdkRisveeaLehpYl  289
         y+ slp+k+k ++++lfp+a+++aldLl+k+L+++p+kRi+ve+aL+hpYl
Q: 261   YLLSLPHKNKVPWNRLFPNADSKALDLLDKMLTFNPHKRIEVEQALAHPYL  311
         **************************************************7
Domain Sequence
(FASTA)
YTNLSYIGEG AYGMVCSAYD NLNKVRVAIK KISPFEHQTY CQRTLREIKI LLRFRHENII 60
GINDIIRAPT IEQMKDVYIV QDLMETDLYK LLKTQHLSND HICYFLYQIL RGLKYIHSAN 120
VLHRDLKPSN LLLNTTCDLK ICDFGLARVA DPDHDHTGFL TEYVATRWYR APEIMLNSKG 180
YTKSIDIWSV GCILAEMLSN RPIFPGKHYL DQLNHILGIL GSPSQEDLNC IINLKARNYL 240
LSLPHKNKVP WNRLFPNADS KALDLLDKML TFNPHKRIEV EQALAHPYL 289
KeywordAcetylation; Apoptosis; ATP-binding; Cell cycle; Complete proteome; Cytoplasm; Cytoskeleton; Direct protein sequencing; Kinase; Nucleotide-binding; Nucleus; Phosphoprotein; Reference proteome; Serine/threonine-protein kinase; Transferase.
Sequence SourceEnsembl
Orthology
Ortholog group
Ailuropoda melanoleuca"; ?>Anolis carolinensis"; ?>Bos taurus"; ?>Caenorhabditis elegans"; ?>Callithrix jacchus"; ?>Canis familiaris"; ?>Cavia porcellus"; ?>Ciona intestinalis"; ?>Ciona savignyi"; ?>Danio rerio"; ?>Drosophila melanogaster"; ?>Echinops telfairi"; ?>Equus caballus"; ?>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"; ?>Mustela putorius furo"; ?>Myotis lucifugus"; ?>Nomascus leucogenys"; ?>Ochotona princeps"; ?>Oreochromis niloticus"; ?>Oryctolagus cuniculus"; ?>Oryzias latipes"; ?>Otolemur garnettii"; ?>Pan troglodytes"; ?>Pelodiscus sinensis"; ?>Petromyzon marinus"; ?>Rattus norvegicus"; ?>Sarcophilus harrisii"; ?>Sus scrofa"; ?>Taeniopygia guttata"; ?>Takifugu rubripes"; ?>Tetraodon nigroviridis"; ?>Tursiops truncatus"; ?>Xenopus tropicalis"; ?>Xiphophorus maculatus"; ?>Saccharomyces cerevisiae"; ?>Schizosaccharomyces pombe"; ?>
EKS-AIM-00435
EKS-ANC-00450
EKS-BOT-00467
EKS-CAE-00385
EKS-CAJ-00466
EKS-CAF-00460
EKS-CAP-00498
EKS-CII-00260
EKS-CIS-00220
EKS-DAR-00868
EKS-DRM-00222
EKS-ECT-00060
EKS-EQC-00454
EKS-FEC-00439
EKS-GAM-00267
EKS-GAG-00389
EKS-GAA-00558
EKS-GOG-00450
EKS-HOS-00469
EKS-ICT-00444
EKS-LAC-00473
EKS-LOA-00473
EKS-MAM-00459
EKS-MEG-00382
EKS-MIM-00088
EKS-MOD-00452
EKS-MUP-00456
EKS-MYL-00461
EKS-NOL-00423
EKS-OCP-00120
EKS-ORN-00584
EKS-ORC-00441
EKS-ORL-00529
EKS-OTG-00474
EKS-PAT-00435
EKS-PES-00410
EKS-PEM-00252
EKS-RAN-00476
EKS-SAH-00435
EKS-SUS-00410
EKS-TAG-00529
EKS-TAR-00574
EKS-TEN-00574
EKS-TUT-00170
EKS-XET-00610
EKS-XIM-00573
EKS-SAC-00100
EKS-SCP-00101
Gene Ontology
GO:0033267; C:axon part
GO:0005901; C:caveola
GO:0005856; C:cytoskeleton
GO:0005829; C:cytosol
GO:0032839; C:dendrite cytoplasm
GO:0005769; C:early endosome
GO:0005925; C:focal adhesion
GO:0005794; C:Golgi apparatus
GO:0005770; C:late endosome
GO:0005815; C:microtubule organizing center
GO:0005739; C:mitochondrion
GO:0005654; C:nucleoplasm
GO:0043204; C:perikaryon
GO:0043234; C:protein complex
GO:0031143; C:pseudopodium
GO:0005524; F:ATP binding
GO:0004707; F:MAP kinase activity
GO:0001784; F:phosphotyrosine binding
GO:0008353; F:RNA polymerase II carboxy-terminal domain kinase activity
GO:0006915; P:apoptotic process
GO:0050853; P:B cell receptor signaling pathway
GO:0072584; P:caveolin-mediated endocytosis
GO:0007049; P:cell cycle
GO:0019858; P:cytosine metabolic process
GO:0070371; P:ERK1 and ERK2 cascade
GO:0060716; P:labyrinthine layer blood vessel development
GO:0031663; P:lipopolysaccharide-mediated signaling pathway
GO:0033598; P:mammary gland epithelial cell proliferation
GO:0000189; P:MAPK import into nucleus
GO:0045596; P:negative regulation of cell differentiation
GO:0009887; P:organ morphogenesis
GO:0018105; P:peptidyl-serine phosphorylation
GO:0030335; P:positive regulation of cell migration
GO:0008284; P:positive regulation of cell proliferation
GO:0010800; P:positive regulation of peptidyl-threonine phosphorylation
GO:0045893; P:positive regulation of transcription, DNA-dependent
GO:0045727; P:positive regulation of translation
GO:0051493; P:regulation of cytoskeleton organization
GO:2000641; P:regulation of early endosome to late endosome transport
GO:0090170; P:regulation of Golgi inheritance
GO:0051090; P:regulation of sequence-specific DNA binding transcription factor activity
GO:0032872; P:regulation of stress-activated MAPK cascade
GO:0006974; P:response to DNA damage stimulus
GO:0043627; P:response to estrogen stimulus
GO:0043330; P:response to exogenous dsRNA
GO:0009636; P:response to toxin
GO:0019233; P:sensory perception of pain
GO:0050852; P:T cell receptor signaling pathway
GO:0006351; P:transcription, DNA-dependent
KEGG
mmu:26413;
InterPros
IPR011009; Kinase-like_dom.
IPR003527; MAP_kinase_CS.
IPR008349; MAPK_ERK1/2.
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
PS01351; MAPK; 1.
PS00107; PROTEIN_KINASE_ATP; 1.
PS50011; PROTEIN_KINASE_DOM; 1.
PS00108; PROTEIN_KINASE_ST; 1.
Prints
PR01770; ERK1ERK2MAPK.
Created Date20-Feb-2013