Homo sapiens Protein: MYO15A | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-33541.6 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | MYO15A | ||||||||||||||||||||||
Protein Name | myosin XVA | ||||||||||||||||||||||
Synonyms | |||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000205890 | ||||||||||||||||||||||
InnateDB Gene | IDBG-33539 (MYO15A) | ||||||||||||||||||||||
Protein Structure | |||||||||||||||||||||||
UniProt Annotation | |||||||||||||||||||||||
Function | Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments. Required for the arrangement of stereocilia in mature hair bundles (By similarity). {ECO:0000250}. | ||||||||||||||||||||||
Subcellular Localization | Cell projection, stereocilium {ECO:0000250}. Cytoplasm, cytoskeleton {ECO:0000250}. Note=Localizes to stereocilium tips in cochlear and vestibular hair cells. {ECO:0000250}. | ||||||||||||||||||||||
Disease Associations | Deafness, autosomal recessive, 3 (DFNB3) [MIM:600316]: A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. {ECO:0000269PubMed:11735029, ECO:0000269PubMed:9603736}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||||||
Tissue Specificity | Highly expressed in pituitary. Also expressed at lower levels in adult brain, kidney, liver, lung, pancreas, placenta and skeletal muscle. Not expressed in brain. In the pituitary, highly expressed in anterior gland cells. {ECO:0000269PubMed:10552926}. | ||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||
InterPro |
IPR000048
IQ motif, EF-hand binding site IPR000299 FERM domain IPR000857 MyTH4 domain IPR001452 SH3 domain IPR001609 Myosin head, motor domain IPR011511 Variant SH3 domain IPR019748 FERM central domain IPR019749 Band 4.1 domain IPR027417 P-loop containing nucleoside triphosphate hydrolase IPR029071 Ubiquitin-related domain |
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PFAM |
PF00612
PF00784 PF00018 PF14604 PF00063 PF07653 PF00373 |
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PRINTS |
PR00452
PR00193 |
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PIRSF | |||||||||||||||||||||||
SMART |
SM00015
SM00139 SM00326 SM00242 SM00295 |
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TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | Q9UKN7 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-Q9UKN7 | ||||||||||||||||||||||
TrEMBL | K7EQV1 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 51168 | ||||||||||||||||||||||
UniGene | Hs.462390 | ||||||||||||||||||||||
RefSeq | NP_057323 | ||||||||||||||||||||||
HUGO | HGNC:7594 | ||||||||||||||||||||||
OMIM | 602666 | ||||||||||||||||||||||
CCDS | CCDS42271 | ||||||||||||||||||||||
HPRD | 04049 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AC087164 AF051976 AF144094 | ||||||||||||||||||||||
GenPept | AAF05903 | ||||||||||||||||||||||