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Protein Page:
ICAM1 (mouse)
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
ICAM1 a type I membrane protein of the immunoglobulin superfamily. Is a ligand for the leukocyte adhesion LFA-1 protein (Integrin alpha-L/beta-2) and a Rhinovirus receptor. Typically expressed on endothelial cells and cells of the immune system. ICAM1 binds to integrins of type CD11a / CD18, or CD11b / CD18. Its expression is activated by p53 in an NF-kappaB-independent manner. Induced by TNFalpha in a process that involves IKKbeta. Note: This description may include information from UniProtKB.
Protein type: Membrane protein, integral; Cell adhesion; Immunoglobulin superfamily
Cellular Component: extracellular space; cell surface; membrane; integral to membrane; plasma membrane; immunological synapse; external side of plasma membrane
Molecular Function: integrin binding; protein complex binding; cell surface binding
Biological Process: adhesion to symbiont; regulation of cell adhesion; virion attachment, binding of host cell surface receptor; negative regulation of calcium ion transport; positive regulation of nitric oxide biosynthetic process; T cell antigen processing and presentation; activation of NF-kappaB transcription factor; positive regulation of cellular extravasation; regulation of cell shape; leukocyte adhesion; cell-cell adhesion; T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell; positive regulation of vasoconstriction; cell adhesion mediated by integrin; cell adhesion
Reference #:  P13597 (UniProtKB)
Alt. Names/Synonyms: CD54; ICAM-1; Icam1; Intercellular adhesion molecule 1; Ly-47; MALA-2; MGC6195; MyD10
Gene Symbols: Icam1
Molecular weight: 58,844 Da
Basal Isoelectric point: 5.79  Predict pI for various phosphorylation states
Select Structure to View Below

ICAM1

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.


       mouse

 
0 1 R209 FSNVSEARSLRTFDL
0 1 T213 SEARSLRTFDLPATI
0 1 T219 RTFDLPATIPKLDTP
0 1 T225 ATIPKLDTPDLLEVG
0 1 L277 DSVSATALVEVTEEF
0 2 - gap
1 0 Y507 GLVMAASYVYNRQRK
5 2 Y518-p RQRKIRIyKLQkAQE
0 1 K522-u IRIyKLQkAQEEAIk
0 3 E525 yKLQkAQEEAIkLKG
0 3 E526 KLQkAQEEAIkLKGQ
0 29 K529-u kAQEEAIkLKGQAPP
0 3 P535 IkLKGQAPPP_____
  human

 
Y207-p FENTSAPyQLQtFVL
T211-p SAPyQLQtFVLPAtP
T217-p QtFVLPAtPPQLVsP
S223-p AtPPQLVsPRVLEVD
S275-p DSFSAKAsVSVTAED
K359-u PRAQLLLkATPEDNG
Y501-p GTAGLSTyLYNRQRK
Y512-p RQRKIKKyRLQQAQk
Q516 IKKyRLQQAQkGtPM
K519-u yRLQQAQkGtPMkPN
T521-p LQQAQkGtPMkPNTQ
K524-u AQkGtPMkPNTQAtP
T530-p MkPNTQAtPP_____
  rat

 
R207 FKNVSEVRQLRTFDL
T211 SEVRQLRTFDLPTRV
R217 RTFDLPTRVLKLDTP
T223 TRVLKLDTPDLLEVG
S275 DFVSATASVEVTEKL
- gap
Y515 FVIVASIYTYYRQRK
Y526 RQRKIRIYKLQKAQE
K530 IRIYKLQKAQEEALK
E533 YKLQKAQEEALKLKV
E534 KLQKAQEEALKLKVQ
K537 KAQEEALKLKVQAPP
P543 LKLKVQAPPP_____
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