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Protein Page:
IL17RB (human)
p Phosphorylation
a Acetylation
m Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
u Ubiquitination
s Sumoylation
n Neddylation
g O-GlcNAc
h Palmitoylation
ad Adenylylation
sn S-Nitrosylation
ca Caspase cleavage

Overview
IL17RB Receptor for the proinflammatory cytokines IL17B and IL17E. May play a role in controlling the growth and/or differentiation of hematopoietic cells. 2 isoforms of the human protein are produced by alternative splicing. Note: This description may include information from UniProtKB.
Protein type: Membrane protein, integral
Cellular Component: cell surface; membrane; integral to plasma membrane; cytoplasm; extracellular region
Molecular Function: hematopoietin/interferon-class (D200-domain) cytokine receptor activity
Biological Process: cytokine and chemokine mediated signaling pathway; defense response; regulation of cell growth
Reference #:  Q9NRM6 (UniProtKB)
Alt. Names/Synonyms: CRL4; cytokine receptor CRL4; Cytokine receptor-like 4; EVI27; I17RB; IL-17 receptor B; IL-17 receptor homolog 1; IL-17B receptor; IL-17RB; IL-17Rh1; IL17BR; IL17RB; IL17Rh1; interleukin 17 receptor B; interleukin 17 receptor homolog 1; interleukin 17B receptor; Interleukin-17 receptor B; Interleukin-17B receptor; MGC5245
Gene Symbols: IL17RB
Molecular weight: 55,885 Da
Basal Isoelectric point: 8.44  Predict pI for various phosphorylation states
CST Pathways:  PI3K/Akt Signaling
Select Structure to View Below

IL17RB

Protein Structure Not Found.


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Modification Sites and Domains Show Modification Legend
Click here to view phosphorylation modifications only

Modification Sites in Parent Protein, Orthologs, and Isoforms Show Modification Legend
 

Show Multiple Sequence Alignment


 SS 

SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 MS 

MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

 
0 1 Y310-p WVLVAGIyLMWRHER
0 1 K320 WRHERIKKtSFSTTT
0 1 T321-p RHERIKKtSFSTTTL
0 1 Y447-p LHKYVVVyFREIDTK
0 1 Y466-p ALSVCPKyHLMKDAT
  mouse

 
Y306 WVLAAGIYLTWRQGR
K316-u WRQGRSTkTSFPIST
T317 RQGRSTkTSFPISTM
Y444 LHKYLVVYLGGADLK
Y463 ALSVCPQYHLMKDAT
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