Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 2.7.11.13 extracted from

  • Rajagopal, S.; Fang, H.; Patanavanich, S.; Sando, J.J.; Kamatchi, G.L.
    Protein kinase C isozyme-specific potentiation of expressed Cav 2.3 currents by acetyl-beta-methylcholine and phorbol-12-myristate,13-acetate (2008), Brain Res., 1210, 1-10.
    View publication on PubMedView publication on EuropePMC

Activating Compound

Activating Compound Comment Organism Structure
acetyl-beta-methylcholine
-
Xenopus laevis
phorbol 12-myristate 13-acetate
-
Xenopus laevis

Inhibitors

Inhibitors Comment Organism Structure
betaIIV5.3 0.01 mM, peptide translocation inhibitor of isozyme PKC betaII Xenopus laevis
CG53353 0.01 mM, isozyme PKC betaII antagonist Xenopus laevis
epsilonV1.2 0.01 mM, peptide translocation inhibitor of isozyme PKC epsilon Xenopus laevis
Go6976 0.01 mM Xenopus laevis

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
additional information
-
the molecular weight of the Xenopus PKC isozyme proteins varies from 75 to 90 kDa Xenopus laevis

Organism

Organism UniProt Comment Textmining
Xenopus laevis
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
oocyte
-
Xenopus laevis
-

Synonyms

Synonyms Comment Organism
PKC alpha isozyme Xenopus laevis
PKC betaII isozyme Xenopus laevis
PKC epsilon isozyme Xenopus laevis