Homo sapiens (human): 4751
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Entry
4751 CDS
T01001
Symbol
NEK2, HsPK21, NEK2A, NLK1, PPP1R111, RP67
Name
(RefSeq) NIMA related kinase 2
KO
K20872
serine/threonine-protein kinase Nek2 [EC:
2.7.11.1
]
Organism
hsa
Homo sapiens (human)
Disease
H00527
Retinitis pigmentosa
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09181 Protein families: metabolism
01001 Protein kinases [BR:
hsa01001
]
4751 (NEK2)
01009 Protein phosphatases and associated proteins [BR:
hsa01009
]
4751 (NEK2)
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
4751 (NEK2)
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
4751 (NEK2)
Protein kinases [BR:
hsa01001
]
Serine/threonine kinases: Other
NEK family
4751 (NEK2)
Protein phosphatases and associated proteins [BR:
hsa01009
]
Protein serine/threonine phosphatases
Phosphoprotein phosphatases (PPPs)
Protein phosphatase-1
PP1-interacting proteins (PIPs)
4751 (NEK2)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centromeric chromatin formation proteins
SAC (spindle assembly checkpoint) factors
Protein kinases
4751 (NEK2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Pkinase
PK_Tyr_Ser-Thr
Kinase-like
ABC1
APH
Motif
Other DBs
NCBI-GeneID:
4751
NCBI-ProteinID:
NP_002488
OMIM:
604043
HGNC:
7745
Ensembl:
ENSG00000117650
UniProt:
P51955
Structure
PDB
LinkDB
All DBs
Position
1:complement(211658256..211675621)
Genome browser
AA seq
445 aa
AA seq
DB search
MPSRAEDYEVLYTIGTGSYGRCQKIRRKSDGKILVWKELDYGSMTEAEKQMLVSEVNLLR
ELKHPNIVRYYDRIIDRTNTTLYIVMEYCEGGDLASVITKGTKERQYLDEEFVLRVMTQL
TLALKECHRRSDGGHTVLHRDLKPANVFLDGKQNVKLGDFGLARILNHDTSFAKTFVGTP
YYMSPEQMNRMSYNEKSDIWSLGCLLYELCALMPPFTAFSQKELAGKIREGKFRRIPYRY
SDELNEIITRMLNLKDYHRPSVEEILENPLIADLVADEQRRNLERRGRQLGEPEKSQDSS
PVLSELKLKEIQLQERERALKAREERLEQKEQELCVRERLAEDKLARAENLLKNYSLLKE
RKFLSLASNPELLNLPSSVIKKKVHFSGESKENIMRSENSESQLTSKSKCKDLKKRLHAA
QLRAQALSDIEKNYQLKSRQILGMR
NT seq
1338 nt
NT seq
+upstream
nt +downstream
nt
atgccttcccgggctgaggactatgaagtgttgtacaccattggcacaggctcctacggc
cgctgccagaagatccggaggaagagtgatggcaagatattagtttggaaagaacttgac
tatggctccatgacagaagctgagaaacagatgcttgtttctgaagtgaatttgcttcgt
gaactgaaacatccaaacatcgttcgttactatgatcggattattgaccggaccaataca
acactgtacattgtaatggaatattgtgaaggaggggatctggctagtgtaattacaaag
ggaaccaaggaaaggcaatacttagatgaagagtttgttcttcgagtgatgactcagttg
actctggccctgaaggaatgccacagacgaagtgatggtggtcataccgtattgcatcgg
gatctgaaaccagccaatgttttcctggatggcaagcaaaacgtcaagcttggagacttt
gggctagctagaatattaaaccatgacacgagttttgcaaaaacatttgttggcacacct
tattacatgtctcctgaacaaatgaatcgcatgtcctacaatgagaaatcagatatctgg
tcattgggctgcttgctgtatgagttatgtgcattaatgcctccatttacagcttttagc
cagaaagaactcgctgggaaaatcagagaaggcaaattcaggcgaattccataccgttac
tctgatgaattgaatgaaattattacgaggatgttaaacttaaaggattaccatcgacct
tctgttgaagaaattcttgagaaccctttaatagcagatttggttgcagacgagcaaaga
agaaatcttgagagaagagggcgacaattaggagagccagaaaaatcgcaggattccagc
cctgtattgagtgagctgaaactgaaggaaattcagttacaggagcgagagcgagctctc
aaagcaagagaagaaagattggagcagaaagaacaggagctttgtgttcgtgagagacta
gcagaggacaaactggctagagcagaaaatctgttgaagaactacagcttgctaaaggaa
cggaagttcctgtctctggcaagtaatccagaacttcttaatcttccatcctcagtaatt
aagaagaaagttcatttcagtggggaaagtaaagagaacatcatgaggagtgagaattct
gagagtcagctcacatctaagtccaagtgcaaggacctgaagaaaaggcttcacgctgcc
cagctgcgggctcaagccctgtcagatattgagaaaaattaccaactgaaaagcagacag
atcctgggcatgcgctag
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