Entity Details

Primary name MYO3A_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8NEV4
EntryNameMYO3A_HUMAN
FullNameMyosin-IIIa
TaxID9606
Evidenceevidence at protein level
Length1616
SequenceStatuscomplete
DateCreated2004-04-26
DateModified2021-06-02

Ontological Relatives

GenesMYO3A

GO terms

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GOName
GO:0000146 microfilament motor activity
GO:0003779 actin binding
GO:0004672 protein kinase activity
GO:0005516 calmodulin binding
GO:0005524 ATP binding
GO:0005737 cytoplasm
GO:0007601 visual perception
GO:0007605 sensory perception of sound
GO:0016459 myosin complex
GO:0030175 filopodium
GO:0031941 filamentous actin
GO:0032426 stereocilium tip
GO:0032433 filopodium tip
GO:0043531 ADP binding
GO:0046777 protein autophosphorylation
GO:0050896 response to stimulus
GO:0060002 plus-end directed microfilament motor activity
GO:0090103 cochlea morphogenesis
GO:0106310 protein serine kinase activity
GO:0106311 protein threonine kinase activity

Subcellular Location

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Subcellular Location
Cell projection
Cytoplasm

Domains

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DomainNameCategoryType
IPR000048 IQ motif, EF-hand binding siteSiteBinding site
IPR000719 Protein kinase domainDomainDomain
IPR001609 Myosin head, motor domainDomainDomain
IPR011009 Protein kinase-like domain superfamilyFamilyHomologous superfamily
IPR017441 Protein kinase, ATP binding siteSiteBinding site
IPR027417 P-loop containing nucleoside triphosphate hydrolaseFamilyHomologous superfamily
IPR036083 Class III myosin, motor domainDomainDomain

Diseases

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Disease IDSourceNameDescription
607101 OMIMDeafness, autosomal recessive, 30 (DFNB30)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. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB12010 FostamatinibDrugbanksmall molecule

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
MYO3A_HUMANMYZAP_HUMANBioGRID, IntAct16169070 details
MYO3A_HUMANGRL1A_HUMANBioGRID, HPRD, IntAct16169070 details
MYO3A_HUMANGL1AD_HUMANBioGRID, HPRD16169070 details
MYO3A_HUMANTGFR1_HUMANHPRD15761153 details