Homo sapiens Protein: MYO1A
Summary
InnateDB Protein IDBP-378322.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MYO1A
Protein Name myosin IA
Synonyms BBMI; DFNA48; MIHC; MYHL;
Species Homo sapiens
Ensembl Protein ENSP00000393392
InnateDB Gene IDBG-41918 (MYO1A)
Protein Structure
UniProt Annotation
Function Involved in directing the movement of organelles along actin filaments. {ECO:0000305}.
Subcellular Localization
Disease Associations Deafness, autosomal dominant, 48 (DFNA48) [MIM:607841]: 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:12736868}. 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 6 experimentally validated interaction(s) in this database.
Experimentally validated
Total 6 [view]
Protein-Protein 5 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003774 motor activity
GO:0003779 actin binding
GO:0005515 protein binding
GO:0005516 calmodulin binding
GO:0005524 ATP binding
Biological Process
GO:0007605 sensory perception of sound
GO:0008152 metabolic process
GO:0030030 cell projection organization
GO:0030033 microvillus assembly
GO:0051648 vesicle localization
Cellular Component
GO:0005737 cytoplasm
GO:0005902 microvillus
GO:0005903 brush border
GO:0009925 basal plasma membrane
GO:0016323 basolateral plasma membrane
GO:0016324 apical plasma membrane
GO:0016328 lateral plasma membrane
GO:0016459 myosin complex
GO:0030864 cortical actin cytoskeleton
GO:0031941 filamentous actin
Protein Structure and Domains
PDB ID
InterPro IPR000048 IQ motif, EF-hand binding site
IPR001609 Myosin head, motor domain
IPR010926 Myosin tail 2
IPR027417 P-loop containing nucleoside triphosphate hydrolase
PFAM PF00612
PF00063
PF06017
PRINTS PR00193
PIRSF
SMART SM00015
SM00242
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9UBC5
PhosphoSite PhosphoSite-Q9UBC5
TrEMBL Q13871
UniProt Splice Variant
Entrez Gene 4640
UniGene Hs.5394
RefSeq NP_001242970
HUGO HGNC:7595
OMIM 601478
CCDS CCDS8929
HPRD 08371
IMGT
EMBL AC026120 AF009961 AF105424 AF127026 BC059387 L29137
GenPept AAA20900 AAC27437 AAC78645 AAD31189 AAH59387