KEGG   Homo sapiens (human): 1457Help
Entry
1457              CDS       T01001                                 

Gene name
CSNK2A1, CK2A1, CKII, CSNK2A3
Definition
casein kinase 2, alpha 1 polypeptide (EC:2.7.11.1)
Orthology
K03097  
casein kinase II subunit alpha [EC:2.7.11.1]
Organism
hsa  Homo sapiens (human)
Pathway
Ribosome biogenesis in eukaryotes
NF-kappa B signaling pathway
Wnt signaling pathway
Adherens junction
Tight junction
Measles
Herpes simplex infection
Epstein-Barr virus infection
Brite
KEGG Orthology (KO) [BR:hsa00001]
 Genetic Information Processing
  Translation
   03008 Ribosome biogenesis in eukaryotes
    1457 (CSNK2A1)
 Environmental Information Processing
  Signal transduction
   04310 Wnt signaling pathway
    1457 (CSNK2A1)
   04064 NF-kappa B signaling pathway
    1457 (CSNK2A1)
 Cellular Processes
  Cellular commiunity
   04520 Adherens junction
    1457 (CSNK2A1)
   04530 Tight junction
    1457 (CSNK2A1)
 Human Diseases
  Infectious diseases
   05162 Measles
    1457 (CSNK2A1)
   05168 Herpes simplex infection
    1457 (CSNK2A1)
   05169 Epstein-Barr virus infection
    1457 (CSNK2A1)
Enzymes [BR:hsa01000]
 2. Transferases
  2.7  Transferring phosphorus-containing groups
   2.7.11  Protein-serine/threonine kinases
    2.7.11.1  non-specific serine/threonine protein kinase
     1457 (CSNK2A1)
Protein kinases [BR:hsa01001]
 Serine/threonine protein kinases: Other group
  CK2 family
   1457 (CSNK2A1)
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif Motif
Other DBs
NCBI-GI: 
NCBI-GeneID: 
OMIM: 
HGNC: 
HPRD: 
UniProt: 
Structure
PDB: 

Jmol
Position
20p13
AA seq 391 aa AA seqDB search
MSGPVPSRARVYTDVNTHRPREYWDYESHVVEWGNQDDYQLVRKLGRGKYSEVFEAINIT
NNEKVVVKILKPVKKKKIKREIKILENLRGGPNIITLADIVKDPVSRTPALVFEHVNNTD
FKQLYQTLTDYDIRFYMYEILKALDYCHSMGIMHRDVKPHNVMIDHEHRKLRLIDWGLAE
FYHPGQEYNVRVASRYFKGPELLVDYQMYDYSLDMWSLGCMLASMIFRKEPFFHGHDNYD
QLVRIAKVLGTEDLYDYIDKYNIELDPRFNDILGRHSRKRWERFVHSENQHLVSPEALDF
LDKLLRYDHQSRLTAREAMEHPYFYTVVKDQARMGSSSMPGGSTPVSSANMMSGISSVPT
PSPLGPLAGSPVIAAANPLGMPVPAAAGAQQ
NT seq 1176 nt NT seq  +upstreamnt  +downstreamnt
atgtcgggacccgtgccaagcagggccagagtttacacagatgttaatacacacagacct
cgagaatactgggattacgagtcacatgtggtggaatggggaaatcaagatgactaccag
ctggttcgaaaattaggccgaggtaaatacagtgaagtatttgaagccatcaacatcaca
aataatgaaaaagttgttgttaaaattctcaagccagtaaaaaagaagaaaattaagcgt
gaaataaagattttggagaatttgagaggaggtcccaacatcatcacactggcagacatt
gtaaaagaccctgtgtcacgaacccccgccttggtttttgaacacgtaaacaacacagac
ttcaagcaattgtaccagacgttaacagactatgatattcgattttacatgtatgagatt
ctgaaggccctggattattgtcacagcatgggaattatgcacagagatgtcaagccccat
aatgtcatgattgatcatgagcacagaaagctacgactaatagactggggtttggctgag
ttttatcatcctggccaagaatataatgtccgagttgcttcccgatacttcaaaggtcct
gagctacttgtagactatcagatgtacgattatagtttggatatgtggagtttgggttgt
atgctggcaagtatgatctttcggaaggagccatttttccatggacatgacaattatgat
cagttggtgaggatagccaaggttctggggacagaagatttatatgactatattgacaaa
tacaacattgaattagatccacgtttcaatgatatcttgggcagacactctcgaaagcga
tgggaacgctttgtccacagtgaaaatcagcaccttgtcagccctgaggccttggatttc
ctggacaaactgctgcgatatgaccaccagtcacggcttactgcaagagaggcaatggag
cacccctatttctacactgttgtgaaggaccaggctcgaatgggttcatctagcatgcca
gggggcagtacgcccgtcagcagcgccaatatgatgtcagggatttcttcagtgccaacc
ccttcaccccttggacctctggcaggctcaccagtgattgctgctgccaacccccttggg
atgcctgttccagctgccgctggcgctcagcagtaa

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