Homo sapiens (human): 8440
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Entry
8440 CDS
T01001
Symbol
NCK2, GRB4, NCKbeta
Name
(RefSeq) cytoplasmic protein NCK2 isoform A
KO
K19862
NCK adaptor protein 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04012
ErbB signaling pathway
hsa04360
Axon guidance
hsa04517
IgSF CAM signaling
hsa04518
Integrin signaling
hsa04660
T cell receptor signaling pathway
hsa05130
Pathogenic Escherichia coli infection
Network
nt06180
Pathogenic Escherichia coli
nt06182
Shigella
Element
N01078
EGF-EGFR-Actin signaling pathway
N01092
Escherichia Eae/Tir to Actin signaling pathway
N01093
Escherichia EspJ/Tir to Actin signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04012 ErbB signaling pathway
8440 (NCK2)
09133 Signaling molecules and interaction
04517 IgSF CAM signaling
8440 (NCK2)
04518 Integrin signaling
8440 (NCK2)
09150 Organismal Systems
09151 Immune system
04660 T cell receptor signaling pathway
8440 (NCK2)
09158 Development and regeneration
04360 Axon guidance
8440 (NCK2)
09160 Human Diseases
09171 Infectious disease: bacterial
05130 Pathogenic Escherichia coli infection
8440 (NCK2)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
SH3_1
SH3_9
SH3_2
SH2
SH3_3
SH3_10
hSH3
SH2_2
Motif
Other DBs
NCBI-GeneID:
8440
NCBI-ProteinID:
NP_001004720
OMIM:
604930
HGNC:
7665
UniProt:
O43639
A0A0S2Z4M6
Structure
PDB
PDBj
LinkDB
All DBs
Position
2:105744453..105894272
Genome browser
AA seq
380 aa
AA seq
DB search
MTEEVIVIAKWDYTAQQDQELDIKKNERLWLLDDSKTWWRVRNAANRTGYVPSNYVERKN
SLKKGSLVKNLKDTLGLGKTRRKTSARDASPTPSTDAEYPANGSGADRIYDLNIPAFVKF
AYVAEREDELSLVKGSRVTVMEKCSDGWWRGSYNGQIGWFPSNYVLEEVDEAAAESPSFL
SLRKGASLSNGQGSRVLHVVQTLYPFSSVTEEELNFEKGETMEVIEKPENDPEWWKCKNA
RGQVGLVPKNYVVVLSDGPALHPAHAPQISYTGPSSSGRFAGREWYYGNVTRHQAECALN
ERGVEGDFLIRDSESSPSDFSVSLKASGKNKHFKVQLVDNVYCIGQRRFHTMDELVEHYK
KAPIFTSEHGEKLYLVRALQ
NT seq
1143 nt
NT seq
+upstream
nt +downstream
nt
atgacagaagaagttattgtgatagccaagtgggactacaccgcccagcaggaccaggag
ctggacatcaagaagaacgagcggctgtggttgctggacgactccaagacgtggtggcgg
gtgaggaacgcggccaacaggacgggctatgtaccgtccaactacgtggagcggaagaac
agcctgaagaagggctccctcgtgaagaacctgaaggacacactaggcctcggcaagacg
cgcaggaagaccagcgcgcgggatgcgtcccccacgcccagcacggacgccgagtacccc
gccaatggcagcggcgccgaccgcatctacgacctcaacatcccggccttcgtcaagttc
gcctatgtggccgagcgggaggatgagttgtccctggtgaaggggtcgcgcgtcaccgtc
atggagaagtgcagcgacggttggtggcggggcagctacaacgggcagatcggctggttc
ccctccaactacgtcttggaggaggtggacgaggcggctgcggagtccccaagcttcctg
agcctgcgcaagggcgcctcgctgagcaatggccagggctcccgcgtgctgcatgtggtc
cagacgctgtaccccttcagctcagtcaccgaggaggagctcaacttcgagaagggggag
accatggaggtgattgagaagccggagaacgaccccgagtggtggaaatgcaaaaatgcc
cggggccaggtgggcctcgtccccaaaaactacgtggtggtcctcagtgacgggcctgcc
ctgcaccctgcgcacgccccacagataagctacaccgggccctcgtccagcgggcgcttc
gcgggcagagagtggtactacgggaacgtgacgcggcaccaggccgagtgcgccctcaac
gagcggggcgtggagggcgacttcctcattagggacagcgagtcctcgcccagcgacttc
tccgtgtcccttaaagcgtcagggaagaacaaacacttcaaggtgcagctcgtggacaat
gtctactgcattgggcagcggcgcttccacaccatggacgagctggtggaacactacaaa
aaggcgcccatcttcaccagcgagcacggggagaagctctacctcgtcagggccctgcag
tga
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