Homo sapiens Protein: CDC42SE1
Summary
InnateDB Protein IDBP-102281.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CDC42SE1
Protein Name CDC42 small effector 1
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000349773
InnateDB Gene IDBG-102279 (CDC42SE1)
Protein Structure
UniProt Annotation
Function Probably involved in the organization of the actin cytoskeleton by acting downstream of CDC42, inducing actin filament assembly. Alters CDC42-induced cell shape changes. In activated T-cells, may play a role in CDC42-mediated F-actin accumulation at the immunological synapse. May play a role in early contractile events in phagocytosis in macrophages. {ECO:0000269PubMed:10816584, ECO:0000269PubMed:15840583, ECO:0000269PubMed:17045588}.
Subcellular Localization Cytoplasm, cytoskeleton. Cell membrane; Lipid-anchor. Note=Recruited to the activated TCR prior actin polymerization.
Disease Associations
Tissue Specificity Widely expressed. Expressed at higher level in T-lymphocytes, dendritic and whole blood cells. {ECO:0000269PubMed:15840583}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 6 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 6 [view]
Protein-Protein 5 [view]
Protein-DNA 0
Protein-RNA 1 [view]
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005095 GTPase inhibitor activity
Biological Process
GO:0006909 phagocytosis
GO:0007165 signal transduction
GO:0008360 regulation of cell shape
GO:0043086 negative regulation of catalytic activity
Cellular Component
GO:0005737 cytoplasm
GO:0005856 cytoskeleton
GO:0005886 plasma membrane
Protein Structure and Domains
PDB ID
InterPro IPR000095 CRIB domain
PFAM PF00786
PRINTS
PIRSF
SMART SM00285
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9NRR8
PhosphoSite PhosphoSite-Q9NRR8
TrEMBL
UniProt Splice Variant
Entrez Gene 56882
UniGene Hs.22065
RefSeq NP_064624
HUGO HGNC:17719
OMIM
CCDS CCDS981
HPRD 16694
IMGT
EMBL AF187845 AF286041 AF286592 AL590133 BC012796 BC041604 CH471121
GenPept AAF87597 AAF97248 AAG17723 AAH12796 AAH41604 CAI13349 EAW53477 EAW53478 EAW53479