Homo sapiens Protein: MYO3A
Summary
InnateDB Protein IDBP-63449.4
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MYO3A
Protein Name myosin IIIA
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000265944
InnateDB Gene IDBG-63447 (MYO3A)
Protein Structure
UniProt Annotation
Function Probable actin-based motor with a protein kinase activity. Probably plays a role in vision and hearing. {ECO:0000269PubMed:12032315}.
Subcellular Localization Cytoplasm, cytoskeleton.
Disease Associations Deafness, autosomal recessive, 30 (DFNB30) [MIM:607101]: A form of non-syndromic deafness characterized by bilateral progressive hearing loss, which first affects the high frequencies. Hearing loss begins in the second decade, and by age 50 is severe in high and middle frequencies and moderate at low frequencies. {ECO:0000269PubMed:12032315}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Strongest expression in retina, retinal pigment epithelial cells, cochlea and pancreas.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000146 microfilament motor activity
GO:0003774 motor activity
GO:0004672 protein kinase activity
GO:0004674 protein serine/threonine kinase activity
GO:0004713 protein tyrosine kinase activity
GO:0005515 protein binding
GO:0005516 calmodulin binding
GO:0005524 ATP binding
GO:0016772 transferase activity, transferring phosphorus-containing groups
GO:0030898 actin-dependent ATPase activity
GO:0043531 ADP binding
GO:0051015 actin filament binding
GO:0060002 plus-end directed microfilament motor activity
Biological Process
GO:0006200 ATP catabolic process
GO:0006468 protein phosphorylation
GO:0007601 visual perception
GO:0007605 sensory perception of sound
GO:0018105 peptidyl-serine phosphorylation
GO:0018107 peptidyl-threonine phosphorylation
GO:0046777 protein autophosphorylation
GO:0048839 inner ear development
GO:0050896 response to stimulus
GO:0051491 positive regulation of filopodium assembly
Cellular Component
GO:0001917 photoreceptor inner segment
GO:0005737 cytoplasm
GO:0016459 myosin complex
GO:0030175 filopodium
GO:0031941 filamentous actin
GO:0032426 stereocilium bundle tip
GO:0032433 filopodium tip
Protein Structure and Domains
PDB ID
InterPro IPR000048 IQ motif, EF-hand binding site
IPR000719 Protein kinase domain
IPR001245 Serine-threonine/tyrosine-protein kinase catalytic domain
IPR001609 Myosin head, motor domain
IPR002290 Serine/threonine/dual specificity protein kinase, catalytic domain
IPR011009 Protein kinase-like domain
IPR020635 Tyrosine-protein kinase, catalytic domain
IPR027417 P-loop containing nucleoside triphosphate hydrolase
PFAM PF00612
PF00069
PF07714
PF00063
PRINTS PR00109
PR00193
PIRSF
SMART SM00015
SM00242
SM00220
SM00219
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8NEV4
PhosphoSite PhosphoSite-Q8NEV4
TrEMBL
UniProt Splice Variant
Entrez Gene 53904
UniGene Hs.662630
RefSeq NP_059129
HUGO HGNC:7601
OMIM 606808
CCDS CCDS7148
HPRD 06008
IMGT
EMBL AF229172 AL162503 AL358612 AL360217 AL391812 AY101367
GenPept AAF70861 AAM34500 CAD13206 CAH73661 CAH73814 CAI17380