Homo sapiens Protein: KIF11
Summary
InnateDB Protein IDBP-82527.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol KIF11
Protein Name kinesin family member 11
Synonyms EG5; HKSP; KNSL1; MCLMR; TRIP5;
Species Homo sapiens
Ensembl Protein ENSP00000260731
InnateDB Gene IDBG-82525 (KIF11)
Protein Structure
UniProt Annotation
Function Motor protein required for establishing a bipolar spindle. Blocking of KIF11 prevents centrosome migration and arrest cells in mitosis with monoastral microtubule arrays. {ECO:0000269PubMed:19001501}.
Subcellular Localization Cytoplasm {ECO:0000269PubMed:19001501}. Cytoplasm, cytoskeleton, spindle pole {ECO:0000269PubMed:19001501}.
Disease Associations Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR) [MIM:152950]: An autosomal dominant disorder that involves an overlapping but variable spectrum of central nervous system and ocular developmental anomalies. Microcephaly ranges from mild to severe and is often associated with mild to moderate developmental delay and a characteristic facial phenotype with upslanting palpebral fissures, broad nose with rounded tip, long philtrum with thin upper lip, prominent chin, and prominent ears. Chorioretinopathy is the most common eye abnormality, but retinal folds, microphthalmia, and myopic and hypermetropic astigmatism have also been reported, and some individuals have no overt ocular phenotype. Congenital lymphedema, when present, is typically confined to the dorsa of the feet, and lymphoscintigraphy reveals the absence of radioactive isotope uptake from the webspaces between the toes. {ECO:0000269PubMed:22284827}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 26 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Experimentally validated
Total 26 [view]
Protein-Protein 23 [view]
Protein-DNA 3 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003777 microtubule motor activity
GO:0005524 ATP binding
GO:0008017 microtubule binding
GO:0019901 protein kinase binding
GO:0032403 protein complex binding
Biological Process
GO:0007018 microtubule-based movement
GO:0007051 spindle organization
GO:0007052 mitotic spindle organization
GO:0007067 mitotic nuclear division
GO:0007100 mitotic centrosome separation
GO:0007596 blood coagulation
GO:0008152 metabolic process
GO:0019886 antigen processing and presentation of exogenous peptide antigen via MHC class II
GO:0090307 spindle assembly involved in mitosis
Cellular Component
GO:0000922 spindle pole
GO:0005737 cytoplasm
GO:0005819 spindle
GO:0005829 cytosol
GO:0005871 kinesin complex
GO:0005874 microtubule
GO:0005876 spindle microtubule
GO:0016020 membrane
Protein Structure and Domains
PDB ID
InterPro IPR001752 Kinesin, motor domain
IPR027417 P-loop containing nucleoside triphosphate hydrolase
PFAM PF00225
PRINTS PR00380
PIRSF
SMART SM00129
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P52732
PhosphoSite PhosphoSite-P52732
TrEMBL
UniProt Splice Variant
Entrez Gene 3832
UniGene Hs.8878
RefSeq NP_004514
HUGO HGNC:6388
OMIM 148760
CCDS CCDS7422
HPRD 01023
IMGT
EMBL AL356128 AL360222 BC126211 BC136474 L40372 U37426 X85137
GenPept AAA86132 AAC41739 AAI26212 AAI36475 CAA59449 CAH72288 CAI13671