TCDB is operated by the Saier Lab Bioinformatics Group
TCIDNameDomainKingdom/PhylumProtein(s)
8.A.22.1.1









Voltage-dependent Ca2+ channel (VSCC) β1-subunit, CACNB1 of 597 aas.  VSCCs are composed of different subunits, α1, β, α2δ and γ, among which the cytosolic β subunit (Cavβ) controls the trafficking of the channel to the plasma membrane, its regulation and its gating properties. Many proteins interact with Cavβ, suggesting a multifunctional role of these proteins. Some of the newly assigned functions of Cavβ are independent of its role in the regulation of VGCC (Rima et al. 2016). Cavβ1 regulates T cell expansion and apoptosis independently of voltage-gated Ca2+ channel function(Erdogmus et al. 2022). The human ortholog is 98% identical to this mouse protein.

Eukaryota
Metazoa, Chordata
CACNB1 of Mus musculus (33146398)
8.A.22.1.2









Voltage-gated Ca2+ channel β2-subunit, CACNB2 of 660 aas and possibly 1 N-terminal TMS and others near the C-terminus of the protein.  It plays a role in diseases such as schizaphrenia and cancer (Kraft et al. 2024; Masuelli et al. 2023).

Eukaryota
Metazoa, Chordata
CACNB2 of Homo sapiens (18481641)
8.A.22.1.3









Dihydropyridine-sensitive L-type, Ca2+ channel β3-subunit, CACNB3. Oligomerization of Cavβ subunits is required for Ca2+ channel activity (Lao et al., 2010).

Eukaryota
Metazoa, Chordata
CACNB3 of Homo sapiens (1705683)
8.A.22.1.4









L-type Ca2+ channel, VGCC, voltage-dependent, β4-subunit, CACNB4, of 520 aas and possibly 0 TMSs.  The α1 subunit, comprises the ion-permeable channel, and there are three auxiliary subunits: β, α2δ, and γ. β is necessary for forward trafficking of the α1 subunit to the plasma membrane.  It increases peak calcium current, shifting the voltage dependencies of activation and inactivation, modulating G protein inhibition and controlling the alpha-1 subunit membrane targeting (Helton and Horne 2002).  Subunit β1b is enriched in the β4 interactome of male relative to female mice, and thus may have served to mitigate VGCC overexpression-mediated spine loss in male mice (Parker et al. 2024).

Eukaryota
Metazoa, Chordata
CACNB4 of Homo sapiens (4502537)