MYO3B encodes myosin IIIB, a class III actin-based motor with an amino-terminal kinase domain and retinal expression
[1]. Mechanistically, MYO3B reaches actin protrusion tips through espin-1 (ESPN1) cargo and promotes filopodia elongation in COS7 models
[2]. In sensory systems, MYO3A and MYO3B shape auditory hair bundles by limiting microvilli and stereocilia growth during cochlear development
[3]. MYO3B and related class III motors also influence stereocilia-staircase spacing through espin-1 and espin-like cargos
[4]. In mouse retina, Myo3B variants appear early in development, localize with Myo3A in photoreceptor inner segments, and show differential cone outer-segment distribution
[5]. Compared with MYO3A, MYO3B lacks tail actin-binding activity, depends more strongly on cargo-mediated actin binding, and shows weaker actin-protrusion elongation activity in comparative assays
[2][6]. Human MYO3A differs from MYO3B by an extended tail domain with an additional actin-binding motif, while MYO3A shows faster motor activity, higher ATPase activity, and stronger actin affinity
[6]. No well-established MYO3B-specific agonist or inhibitor was supported by the retrieved peer-reviewed evidence.